{"id":42,"date":"2021-04-08T11:42:38","date_gmt":"2021-04-08T02:42:38","guid":{"rendered":"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/?page_id=42"},"modified":"2026-01-21T21:32:12","modified_gmt":"2026-01-21T12:32:12","slug":"work","status":"publish","type":"page","link":"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/work\/","title":{"rendered":"Publication"},"content":{"rendered":"\n<div class=\"wp-block-columns is-layout-flex wp-container-core-columns-is-layout-9d6595d7 wp-block-columns-is-layout-flex\">\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\">\n<p class=\"has-text-align-center has-background\" style=\"background-color:#fafbf9\"><a href=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-admin\/post.php?post=42&amp;action=edit#publications\">\u696d\u7e3e \/ \u8ad6\u6587<\/a><\/p>\n<\/div>\n\n\n\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\">\n<p class=\"has-text-align-center has-background\" style=\"background-color:#fafbf9\"><a href=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/work\/external\/\">Cover Picture<\/a><\/p>\n<\/div>\n\n\n\n<div class=\"wp-block-column is-layout-flow wp-block-column-is-layout-flow\">\n<p class=\"has-text-align-center has-background\" style=\"background-color:#fafbf9\"><a href=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/work\/joint\/\" data-type=\"URL\" data-id=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/work\/joint\/\">\u5171\u540c\u7814\u7a76\u5b9f\u7e3e<\/a><\/p>\n<\/div>\n<\/div>\n\n\n\n<div style=\"height:30px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h2 class=\"wp-block-heading\" id=\"publications\">\u696d\u7e3e \/ \u8ad6\u6587<\/h2>\n\n\n\n<div style=\"height:30px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"2024\">2025\u5e74<\/h3>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>\u5b66\u8853\u8ad6\u6587<\/strong><\/h4>\n\n\n\n<div class=\"wp-block-group\"><div class=\"wp-block-group__inner-container is-layout-constrained wp-block-group-is-layout-constrained\">\n<ol start=\"1\" class=\"wp-block-list\">\n<li><a href=\"https:\/\/doi.org\/10.1039\/D4RA08380F\">Nobuki Katayama, Kazuki Tabaru, Tatsuki Nagata, Miku Yamaguchi, Takeyuki Suzuki, Takashi Toyao, Yuan Jing, Zen Maeno, Ken-ichi Shimizu, Takeshi Watanabe, Yasushi Obora:<br><strong>Recyclable and air-stable colloidal manganese nanoparticles catalyzed hydrosilylation of alkenes with tertiary silane<\/strong>,<br><em>RSC Adv.<\/em>, <strong>2025<\/strong>, <em>15<\/em>, 1776-1781.<\/a><\/li>\n<\/ol>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-large is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"443\" src=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/01\/\u6700\u7d42_TOC-1024x443.png\" alt=\"\" class=\"wp-image-1027\" style=\"width:425px;height:auto\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/01\/\u6700\u7d42_TOC-1024x443.png 1024w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/01\/\u6700\u7d42_TOC-300x130.png 300w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/01\/\u6700\u7d42_TOC-768x332.png 768w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/01\/\u6700\u7d42_TOC-1536x664.png 1536w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/01\/\u6700\u7d42_TOC-2048x886.png 2048w\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" \/><\/figure>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-group\"><div class=\"wp-block-group__inner-container is-layout-constrained wp-block-group-is-layout-constrained\">\n<ol start=\"2\" class=\"wp-block-list\">\n<li><a href=\"https:\/\/doi.org\/10.1021\/acsomega.5c00230\">Mana Yamamoto, Kazuki Tabaru, Tatsuki Nagata, Yushi Kuroda, Takeyuki Suzuki, Tatsuo Yajima, Takashi Toyao, Yuan Jing, Zen Maeno, Ken-ichi Shimizu, Takeshi Watanabe, Yasushi Obora:<br><strong>Synthesis of Colloidal DMF-Protected Cobalt Nanoparticles for Alkene Hydrosilylation Catalyst: Effect of Cobalt Precursors and Recycling Process. <\/strong><br><em>ACS Omega<\/em>, <strong>2025<\/strong>, <em>10<\/em>, 8718\u20138728.<\/a><\/li>\n<\/ol>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"1000\" height=\"516\" src=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/04\/images_large_ao5c00230_0017.jpeg\" alt=\"\" class=\"wp-image-1052\" style=\"width:425px;height:auto\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/04\/images_large_ao5c00230_0017.jpeg 1000w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/04\/images_large_ao5c00230_0017-300x155.jpeg 300w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/04\/images_large_ao5c00230_0017-768x396.jpeg 768w\" sizes=\"auto, (max-width: 1000px) 100vw, 1000px\" \/><\/figure>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-group\"><div class=\"wp-block-group__inner-container is-layout-constrained wp-block-group-is-layout-constrained\">\n<ol start=\"3\" class=\"wp-block-list\">\n<li><a href=\"https:\/\/doi.org\/10.1093\/chemle\/upaf068\">Kazuki Tabaru&nbsp;,&nbsp;Haruka Nishimura&nbsp;,&nbsp;Takeyuki Suzuki&nbsp;,&nbsp;Yasushi Obora:<br><strong>Palladium Nanoparticles for Aerobic Oxidative Heck Arylation of Alkenes,<\/strong><br><em>Chem. Lett.,<\/em> <strong>2025<\/strong>, <em>54<\/em>, upaf068.<\/a><\/li>\n<\/ol>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"624\" height=\"167\" src=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/04\/\u753b\u50cf1.jpg\" alt=\"\" class=\"wp-image-1049\" style=\"width:501px;height:auto\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/04\/\u753b\u50cf1.jpg 624w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/04\/\u753b\u50cf1-300x80.jpg 300w\" sizes=\"auto, (max-width: 624px) 100vw, 624px\" \/><\/figure>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-group\"><div class=\"wp-block-group__inner-container is-layout-constrained wp-block-group-is-layout-constrained\">\n<ol start=\"4\" class=\"wp-block-list\">\n<li><a href=\"https:\/\/doi.org\/10.1021\/acscatal.5c02118\">Kazuki Tabaru, Nobuki Katayama, Takeyuki Suzuki, Duotian Chen, Takashi Toyao, Ken-ichi Shimizu, Hiromitsu Sogawa, Takeshi Watanabe, Fumio Sanda, Yasushi Obora:<br><strong>Dynamics of Cooperative Palladium\/Copper Catalysis for Aerobic Oxidative Difunctionalization of 1,3-Dienes with Aniline and Disilane,<\/strong><br><em>ACS Catal.,<\/em>&nbsp;<strong>2025<\/strong>, <em>15<\/em>, 10227\u201310238.<\/a><\/li>\n<\/ol>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"635\" height=\"414\" src=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/06\/images_large_cs5c02118_0018.jpeg\" alt=\"\" class=\"wp-image-1079\" style=\"width:425px;height:auto\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/06\/images_large_cs5c02118_0018.jpeg 635w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/06\/images_large_cs5c02118_0018-300x196.jpeg 300w\" sizes=\"auto, (max-width: 635px) 100vw, 635px\" \/><\/figure>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-group\"><div class=\"wp-block-group__inner-container is-layout-constrained wp-block-group-is-layout-constrained\">\n<ol start=\"5\" class=\"wp-block-list\">\n<li><a href=\"https:\/\/doi.org\/10.1016\/j.apcata.2025.120572\">Yukio&nbsp;Hamamoto,&nbsp;Yasushi&nbsp;Obora<br><strong>Direct Catalytic Synthesis of Functionalized Dienes from Simple 1,3-Dienes: A Review on Substitution of 1,3-Butadiene, Isoprene, and 2,3-Dimethyl-1,3-Butadiene with Metal Catalysts.<\/strong><br><em>Appl. Catal. A Gen.<\/em> <strong>2025<\/strong>, <em>708<\/em>, 120572.<\/a><\/li>\n<\/ol>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"2141\" height=\"886\" src=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/09\/1-s2.0-S0926860X25004740-ga1_lrg.jpg\" alt=\"\" class=\"wp-image-1219\" style=\"width:425px;height:auto\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/09\/1-s2.0-S0926860X25004740-ga1_lrg.jpg 2141w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/09\/1-s2.0-S0926860X25004740-ga1_lrg-300x124.jpg 300w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/09\/1-s2.0-S0926860X25004740-ga1_lrg-1024x424.jpg 1024w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/09\/1-s2.0-S0926860X25004740-ga1_lrg-768x318.jpg 768w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/09\/1-s2.0-S0926860X25004740-ga1_lrg-1536x636.jpg 1536w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/09\/1-s2.0-S0926860X25004740-ga1_lrg-2048x848.jpg 2048w\" sizes=\"auto, (max-width: 2141px) 100vw, 2141px\" \/><\/figure>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-group\"><div class=\"wp-block-group__inner-container is-layout-constrained wp-block-group-is-layout-constrained\">\n<ol start=\"6\" class=\"wp-block-list\">\n<li><a href=\"https:\/\/doi.org\/10.1002\/ajoc.202500610\">Nobuki Katayama,&nbsp;Akihiro Marutani,&nbsp;Masatoshi Safumi,&nbsp;Keiko Uchida,&nbsp;Takeyuki Suzuki,&nbsp;Yasushi Obora<br><strong>Synthesis of Hydroxynitriles by <em>N<\/em>,<em>N<\/em>\u2010dimethylformamide\u2010stabilized Ruthenium Nanoparticles\u2010catalyzed \u0391\u2010alkylation of Arylacetonitriles with Diols<\/strong><br><em>Asian J. Org. Chem.<\/em> <strong>2025<\/strong>, <em>14<\/em>, e00610.<\/a><\/li>\n<\/ol>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"2560\" height=\"769\" src=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/09\/TOC_1-scaled.png\" alt=\"\" class=\"wp-image-1220\" style=\"width:595px;height:auto\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/09\/TOC_1-scaled.png 2560w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/09\/TOC_1-300x90.png 300w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/09\/TOC_1-1024x307.png 1024w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/09\/TOC_1-768x231.png 768w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/09\/TOC_1-1536x461.png 1536w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/09\/TOC_1-2048x615.png 2048w\" sizes=\"auto, (max-width: 2560px) 100vw, 2560px\" \/><\/figure>\n<\/div><\/div><\/div>\n\n\n\n<div class=\"wp-block-group\"><div class=\"wp-block-group__inner-container is-layout-constrained wp-block-group-is-layout-constrained\">\n<ol start=\"7\" class=\"wp-block-list\">\n<li><a href=\"https:\/\/doi.org\/10.1039\/D5OB01744K\">Ayumi Yamaguchi<sup>\u2020<\/sup>, Nobuki Katayama<sup>\u2020<\/sup>, Kazuki Tabaru, Tetsuaki Fujihara, Yasushi Obora<br>(\u2020\u00a0These authors contributed equally to this work.)<br><strong>Synthesis of Morpholine Derivatives from 1,3-Dienes and N-Arylaminoalcohols by Palladium-Catalyzed Sequential C-N and C-O Bond Formation<\/strong><br><em>Org. Biomol. Chem.<\/em> <strong>2025<\/strong>,<strong> <\/strong><em>24<\/em>, 592-596.<\/a><\/li>\n<\/ol>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"2560\" height=\"1352\" src=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/12\/20251031_GA-scaled.png\" alt=\"\" class=\"wp-image-1302\" style=\"width:441px;height:auto\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/12\/20251031_GA-scaled.png 2560w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/12\/20251031_GA-300x158.png 300w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/12\/20251031_GA-1024x541.png 1024w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/12\/20251031_GA-768x406.png 768w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/12\/20251031_GA-1536x811.png 1536w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2025\/12\/20251031_GA-2048x1081.png 2048w\" sizes=\"auto, (max-width: 2560px) 100vw, 2560px\" \/><\/figure>\n<\/div><\/div><\/div>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"2024\">2024\u5e74<\/h3>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>\u5b66\u8853\u8ad6\u6587<\/strong><\/h4>\n\n\n\n<ol start=\"1\" class=\"wp-block-list\">\n<li><a href=\"https:\/\/doi.org\/10.1093\/chemle\/upae134\" data-type=\"link\" data-id=\"https:\/\/doi.org\/10.1016\/j.tetlet.2023.154798\">Nobuki Katayama, Yasushi Obora:<br><strong><strong>Developments in the synthesis of allylsilanes by transition metal\u2013catalyzed silylation of 1,3-dienes with disilanes<\/strong><\/strong>,<br><em>Chem. Lett.<\/em>, <strong>53<\/strong>, upae134 (2024).<\/a><\/li>\n<\/ol>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-large is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"314\" src=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2024\/07\/240519_CL_GA_2-1024x314.png\" alt=\"\" class=\"wp-image-814\" style=\"width:545px;height:auto\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2024\/07\/240519_CL_GA_2-1024x314.png 1024w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2024\/07\/240519_CL_GA_2-300x92.png 300w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2024\/07\/240519_CL_GA_2-768x235.png 768w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2024\/07\/240519_CL_GA_2-1536x471.png 1536w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2024\/07\/240519_CL_GA_2-2048x628.png 2048w\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" \/><\/figure>\n<\/div>\n\n\n<ol start=\"2\" class=\"wp-block-list\">\n<li><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.4c02518?goto=supporting-info\">Kazuki Tabaru, Tetsuaki Fujihara, Kazuyuki Torii, Takeyuki Suzuki, Yuan Jing, Takashi Toyao, Zen Maeno, Ken-ichi Shimizu, Takeshi Watanabe, Hiromitsu Sogawa, Fumio Sanda, Jun-ya Hasegawa, Yasushi Obora:<br><strong>Exploring Catalytic Intermediates in Pd-Catalyzed Aerobic Oxidative Amination of 1,3-Dienes: Multiple Metal Interactions of the Palladium Nanoclusters<\/strong>. <br><em>J. Am. Chem. Soc.<\/em>, <strong>146<\/strong>, 22993 (2024).<\/a><\/li>\n<\/ol>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"992\" height=\"523\" src=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2024\/08\/images_large_ja4c02518_0010-2.jpeg\" alt=\"\" class=\"wp-image-830\" style=\"width:457px;height:auto\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2024\/08\/images_large_ja4c02518_0010-2.jpeg 992w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2024\/08\/images_large_ja4c02518_0010-2-300x158.jpeg 300w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2024\/08\/images_large_ja4c02518_0010-2-768x405.jpeg 768w\" sizes=\"auto, (max-width: 992px) 100vw, 992px\" \/><\/figure>\n<\/div>\n\n\n<ol start=\"3\" class=\"wp-block-list\">\n<li><a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2024\/ma\/d4ma00674g\">Kazuki Tabaru, Kanji Okada, Tatsuki Nagata, Takeyuki Suzuki, Hiromitsu Sogawa, Fumio Sanda, Takeshi Watanabec and Yasuhi Obora:<br><strong>Synthesis of colloidal Pd nanoparticles immobilised on poly(N-vinylacetamide): characterisation and application in catalysis.<\/strong><br><em>Mater. Adv.<\/em>, <strong>5<\/strong>, 8439 (2024).<\/a><\/li>\n<\/ol>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"673\" height=\"302\" src=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2024\/11\/\u30b9\u30af\u30ea\u30fc\u30f3\u30b7\u30e7\u30c3\u30c8-2024-10-20-230504-1.png\" alt=\"\" class=\"wp-image-983\" style=\"width:480px;height:auto\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2024\/11\/\u30b9\u30af\u30ea\u30fc\u30f3\u30b7\u30e7\u30c3\u30c8-2024-10-20-230504-1.png 673w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2024\/11\/\u30b9\u30af\u30ea\u30fc\u30f3\u30b7\u30e7\u30c3\u30c8-2024-10-20-230504-1-300x135.png 300w\" sizes=\"auto, (max-width: 673px) 100vw, 673px\" \/><\/figure>\n<\/div>\n\n\n<h3 class=\"wp-block-heading\" id=\"2023\">2023\u5e74<\/h3>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>\u5b66\u8853\u8ad6\u6587<\/strong><\/h4>\n\n\n\n<ol start=\"1\" class=\"wp-block-list\">\n<li><a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S2468823123004765?via%3Dihub\" data-type=\"link\" data-id=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S2468823123004765?via%3Dihub\">Tatsuki Nagata, Shunsuke Aratani, Moegi Nomura, Maito Fuji, Taichi Sotani, Hiromitsu Sogawa, Fumio Sanda, Tatsuo Yajima, Yasushi Obora:<br><strong>Reactivity of niobium(V) pentaalkoxide complexes: Ring-opening metathesis polymerization of norbornene<\/strong>,<br><em>Molecular Catalysis<\/em>, <strong>547<\/strong>, 113393 (2023).<\/a><\/li>\n<\/ol>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"767\" height=\"277\" src=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2023\/12\/Nb.png\" alt=\"\" class=\"wp-image-792\" style=\"aspect-ratio:2.656;width:460px;height:auto\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2023\/12\/Nb.png 767w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2023\/12\/Nb-300x108.png 300w\" sizes=\"auto, (max-width: 767px) 100vw, 767px\" \/><\/figure>\n<\/div>\n\n\n<ol start=\"2\" class=\"wp-block-list\">\n<li><a href=\"https:\/\/doi.org\/10.1016\/j.tetlet.2023.154798\" data-type=\"link\" data-id=\"https:\/\/doi.org\/10.1016\/j.tetlet.2023.154798\">Nobuki Katayama, Yasushi Obora:<br><strong>Recent Developments in Alkene Hydrosilylation Utilizing Manganese Catalysts<\/strong>,<br><em>Tetrahedron Lett.<\/em>, <strong>132<\/strong>, 154798 (2023).<\/a><\/li>\n<\/ol>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-large is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"385\" src=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2023\/10\/1-s2.0-S0040403923005087-ga1_lrg-1024x385.jpg\" alt=\"\" class=\"wp-image-775\" style=\"aspect-ratio:2.656;width:510px;height:auto\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2023\/10\/1-s2.0-S0040403923005087-ga1_lrg-1024x385.jpg 1024w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2023\/10\/1-s2.0-S0040403923005087-ga1_lrg-300x113.jpg 300w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2023\/10\/1-s2.0-S0040403923005087-ga1_lrg-768x288.jpg 768w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2023\/10\/1-s2.0-S0040403923005087-ga1_lrg-1536x577.jpg 1536w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2023\/10\/1-s2.0-S0040403923005087-ga1_lrg-2048x769.jpg 2048w\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" \/><\/figure>\n<\/div>\n\n\n<ol start=\"3\" class=\"wp-block-list\">\n<li><a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/a-2227-1020\">Kazuki Tabaru, Yasushi Obora:<br><strong>Pd-catalyzed oxidative functionalization of alkenes, arenes, and 1,3-dienes using molecular oxygen as the terminal oxidant<\/strong><br><em>Synlett<\/em>, doi: 10.1055\/a-2227-1020<\/a><\/li>\n<\/ol>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"832\" height=\"374\" src=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2023\/12\/graphical_abstract-2.png\" alt=\"\" class=\"wp-image-797\" style=\"width:506px;height:auto\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2023\/12\/graphical_abstract-2.png 832w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2023\/12\/graphical_abstract-2-300x135.png 300w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2023\/12\/graphical_abstract-2-768x345.png 768w\" sizes=\"auto, (max-width: 832px) 100vw, 832px\" \/><\/figure>\n<\/div>\n\n\n<h3 class=\"wp-block-heading\" id=\"2022\">2022\u5e74<\/h3>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>\u5b66\u8853\u8ad6\u6587<\/strong><\/h4>\n\n\n\n<div class=\"wp-block-group\"><div class=\"wp-block-group__inner-container is-layout-constrained wp-block-group-is-layout-constrained\">\n<ol class=\"wp-block-list\">\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1021\/acsanm.2c01357\" target=\"_blank\">Honami Iguchi, Mitsuru Inada, Shunsuke Aratani, Moegi Nomura, Takeyuki Suzuki, Yuan Jing, Takashi Toyao, Zen Maeno, Ken-ichi Shimizu, Yasushi Obora:<br><strong>Application to Electroluminescence Devices with Dimethylformamide-Stabilized Niobium Oxide Nanoparticles<\/strong>,&nbsp;<br><em>ACS Appl. Nano Mater.<\/em>, <strong>5<\/strong>, 7658 (2022).<\/a><br><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1039\/D2RA02381D\" data-type=\"URL\" data-id=\"https:\/\/doi.org\/10.1039\/D2RA02381D\" target=\"_blank\">Tatsuki Nagata, Kanji Okada, Ryota Kondo, Takashi Toyao, Ken-ichi Shimizu, Takeyuki Suzuki, Yasushi Obora:<br><strong>N,N-Dimethylformamide-stabilized ruthenium nanoparticle catalyst for \u03b2-alkylated dimer alcohol formation via Guerbet reaction of primary alcohols<\/strong>,<br><em>RSC Adv.<\/em>, <strong>12<\/strong>, 16599 (2022).&nbsp;<\/a><br><\/li>\n\n\n\n<li><a href=\"https:\/\/doi.org\/10.1002\/ejoc.202200618\">Kazuki Tabaru, Yasushi Obora:<br><strong>Synergic Palladium Catalysis for Aerobic Oxidative Coupling<\/strong><br><em>Eur. J. Org. Chem.<\/em>,e202200618 (2022).<\/a><\/li>\n<\/ol>\n<\/div><\/div>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"325\" height=\"264\" src=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2022\/09\/image.png\" alt=\"\" class=\"wp-image-689\" style=\"aspect-ratio:1.2327044025157232;width:282px;height:auto\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2022\/09\/image.png 325w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2022\/09\/image-300x244.png 300w\" sizes=\"auto, (max-width: 325px) 100vw, 325px\" \/><\/figure>\n<\/div>\n\n\n<div class=\"wp-block-group\"><div class=\"wp-block-group__inner-container is-layout-constrained wp-block-group-is-layout-constrained\">\n<div class=\"wp-block-group\"><div class=\"wp-block-group__inner-container is-layout-constrained wp-block-group-is-layout-constrained\">\n<ol start=\"4\" class=\"wp-block-list\">\n<li><a href=\"https:\/\/doi.org\/10.1039\/D2CC04133B\">Honami Iguchi, Nobuki Katayama, Takeyuki Suzuki, Tetsuaki Fujihara,  Yuan Jing, Takashi Toyao,  Zen Maeno,  Ken-ichi Shimizu,  Yasushi Obora: <br><strong>Dimethylacetamide-stabilized ruthenium nanoparticles for catalysing \u03b1-alkylations of amides with alcohols<\/strong><br><em>Chem. Commum.<\/em>, <strong>58<\/strong>, 11851 (2022).<\/a><\/li>\n<\/ol>\n<\/div><\/div>\n<\/div><\/div>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"472\" height=\"228\" src=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2023\/04\/DMA-1.png\" alt=\"\" class=\"wp-image-757\" style=\"aspect-ratio:2.063380281690141;width:411px;height:auto\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2023\/04\/DMA-1.png 472w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2023\/04\/DMA-1-300x145.png 300w\" sizes=\"auto, (max-width: 472px) 100vw, 472px\" \/><\/figure>\n<\/div>\n\n\n<div class=\"wp-block-group\"><div class=\"wp-block-group__inner-container is-layout-constrained wp-block-group-is-layout-constrained\">\n<ol start=\"5\" class=\"wp-block-list\">\n<li><a href=\"https:\/\/doi.org\/10.1002\/cctc.202101672\" data-type=\"link\" data-id=\"https:\/\/doi.org\/10.1002\/cctc.202101672\">Nagata, T.; Tanaka, T.; Lin, X.; Kondo, R.; Suzuki, T.; Kanda, Y.; Toyao, T.; Shimizu, K.-I.; Obora, Y. <br><strong>N,N \u2010dimethylformamide\u2010protected Fe 2 O 3 Combined with Pt Nanoparticles: Characterization and Catalysis in Alkene Hydrosilylation.<\/strong><em>ChemCatChem<\/em>, <strong>14<\/strong>, e202101672 (2022).<\/a> <\/li>\n<\/ol>\n<\/div><\/div>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-large is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"1024\" height=\"370\" src=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2024\/04\/cctc202101672-toc-0001-m-1024x370.jpg\" alt=\"\" class=\"wp-image-806\" style=\"width:562px;height:auto\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2024\/04\/cctc202101672-toc-0001-m-1024x370.jpg 1024w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2024\/04\/cctc202101672-toc-0001-m-300x108.jpg 300w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2024\/04\/cctc202101672-toc-0001-m-768x277.jpg 768w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2024\/04\/cctc202101672-toc-0001-m-1536x554.jpg 1536w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2024\/04\/cctc202101672-toc-0001-m.jpg 1928w\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" \/><\/figure>\n<\/div>\n\n\n<p class=\"has-text-align-right\"><mark style=\"color:#89a06c\" class=\"has-inline-color\">\u25b2<\/mark> <a href=\"#top\">\u30da\u30fc\u30b8\u306eTOP\u3078<\/a><\/p>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"2021\">2021\u5e74<\/h3>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>\u5b66\u8853\u8ad6\u6587<\/strong><\/h4>\n\n\n\n<ol class=\"wp-block-list\">\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1002\/chem.202100043\" target=\"_blank\">K. Torii, A. Kawakubo, X. Lin, T, Fujihara, T. Yajima, Y. Obora:<br><strong>Palladium\u2010Catalyzed Difunctionalization of 1,3\u2010Diene with Amine and Disilane under a Mild Re\u2010oxidation System<\/strong>,&nbsp;<br><em>Chem. Eur. J.<\/em>, <strong>27<\/strong>, 4888 (2021).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"1267\" height=\"257\" class=\"wp-image-659\" style=\"width: 700px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/07\/TOC.png\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/07\/TOC.png 1267w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/07\/TOC-300x61.png 300w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/07\/TOC-1024x208.png 1024w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/07\/TOC-768x156.png 768w\" sizes=\"auto, (max-width: 1267px) 100vw, 1267px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1039\/D1OB00045D\" target=\"_blank\">M. Kobayashi, H. Yamaguchi, T. Suzuki, Y. Obora:<br><strong>Cross \u03b2-alkylation of primary alcohols catalysed by DMF-stabilized iridium nanoparticles<\/strong>,<br><em>Org. Biomol. Chem.<\/em>, <strong>19<\/strong>, 1950 (2021).&nbsp;<\/a><br><img decoding=\"async\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Cross-%CE%B2-alkylation-of-primary-alcohols-catalysed-by-DMF-stabilized-iridium-nanoparticles.jpg\" alt=\"\"><\/li>\n\n\n\n<li><a href=\"https:\/\/doi.org\/10.1039\/D1RA00915J\">Ismiyarto, N. Kishi,<sup> <\/sup>Y. Adachi, R. Jiang, T. Doi,<sup><em> <\/em><\/sup>D.-Y. Zhou, K. Asano, Y. Obora,&nbsp;T. Suzuki, H. Sasai,&nbsp;T. Suzuki:<br><strong>Catalytic enantioselective intramolecular Tishchenko reaction of&nbsp;<em>meso<\/em>-dialdehyde: synthesis of (<em>S<\/em>)-cedarmycins<\/strong><br><em>RSC Adv.<\/em>, <strong>11<\/strong>, 11606 (2021).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"517\" height=\"284\" class=\"wp-image-651\" style=\"width: 600px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/07\/tishchenko-1.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/07\/tishchenko-1.jpg 517w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/07\/tishchenko-1-300x165.jpg 300w\" sizes=\"auto, (max-width: 517px) 100vw, 517px\" \/><\/li>\n\n\n\n<li><a href=\"https:\/\/doi.org\/10.1039\/D1OB00369K\">K. Tabaru,<sup><em> <\/em><\/sup>M. Nakatsuji,<sup> <\/sup>S. Itoh,<sup><em> <\/em><\/sup>T. Suzuki,&nbsp;Y. Obora:<br><strong><em>N<\/em>,<em>N<\/em>-Dimethylformamide-stabilised palladium nanoparticles combined with bathophenanthroline as catalyst for transfer vinylation of alcohols from vinyl ether<\/strong><br><em>Org. Biomol. Chem.<\/em>, <strong>19<\/strong>, 3384 (2021).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"927\" height=\"497\" class=\"wp-image-652\" style=\"width: 500px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/07\/table-of-contents-image.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/07\/table-of-contents-image.jpg 927w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/07\/table-of-contents-image-300x161.jpg 300w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/07\/table-of-contents-image-768x412.jpg 768w\" sizes=\"auto, (max-width: 927px) 100vw, 927px\" \/><\/li>\n\n\n\n<li><a href=\"https:\/\/doi.org\/10.1039\/D1CC01388B\">M. Utsunomiya,<sup><em> <\/em><\/sup>R. Kondo, T. Oshima,<sup><em> <\/em><\/sup>M. Safumi, T. Suzuki&nbsp;Y. Obora:<br><strong>Cross \u03b2-arylmethylation of alcohols catalysed by recyclable Ti\u2013Pd alloys not requiring pre-activation<\/strong><br><em>Chem. Commun.<\/em>, <strong>57<\/strong>, 5139 (2021).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"846\" height=\"325\" class=\"wp-image-653\" style=\"width: 500px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/07\/210419_TOC.png\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/07\/210419_TOC.png 846w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/07\/210419_TOC-300x115.png 300w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/07\/210419_TOC-768x295.png 768w\" sizes=\"auto, (max-width: 846px) 100vw, 846px\" \/><\/li>\n\n\n\n<li><a href=\"https:\/\/doi.org\/10.1021\/acs.orglett.1c01648\">K. Torii, K. Tabaru, Y. Obora:<br><strong>Palladium-Catalyzed Three-Component Silylalkoxylation of 1,3-Diene with Alcohol and Disilane via Oxidative Coupling<\/strong><br><em>Org. Lett.<\/em>, <strong>23<\/strong>, 4898 (2021).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"714\" height=\"128\" class=\"wp-image-654\" style=\"width: 700px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/07\/organicletters.png\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/07\/organicletters.png 714w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/07\/organicletters-300x54.png 300w\" sizes=\"auto, (max-width: 714px) 100vw, 714px\" \/><\/li>\n<\/ol>\n\n\n\n<div style=\"height:20px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<p class=\"has-text-align-right\"><mark style=\"color:#89a06c\" class=\"has-inline-color\">\u25b2<\/mark> <a href=\"#top\">\u30da\u30fc\u30b8\u306eTOP\u3078<\/a><\/p>\n\n\n\n<div style=\"height:40px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"2020\">2020\u5e74<\/h3>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>\u5b66\u8853\u8ad6\u6587<\/strong><\/h4>\n\n\n\n<ol class=\"wp-block-list\">\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1002\/ajoc.202000240\" target=\"_blank\">T. Nagata, Y. Obora:<br><strong>Transition-Metal-Mediated\/Catalyzed Synthesis of Pyridines, Pyrimidines, and Triazines by [2+2+2] Cycloaddition Reaction<\/strong>,&nbsp;<\/a><br><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1002\/ajoc.202000240\" target=\"_blank\"><em>Asian J<\/em>.&nbsp;<em>Org<\/em>.&nbsp;<em>Chem<\/em>.,&nbsp;<strong>9<\/strong>, 1532 (2020).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"632\" height=\"747\" class=\"wp-image-239\" style=\"width: 400px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Transition-Metal-MediatedCatalyzed-Synthesis-of-Pyridines.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Transition-Metal-MediatedCatalyzed-Synthesis-of-Pyridines.jpg 632w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Transition-Metal-MediatedCatalyzed-Synthesis-of-Pyridines-254x300.jpg 254w\" sizes=\"auto, (max-width: 632px) 100vw, 632px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1021\/acsomega.0c01006\" target=\"_blank\">J. Ishida, S. Nakamichi, T. Nagata, H. Kawasaki, T. Suzuki, Y. Obora:<br><strong>Synthesis and Characterization of&nbsp;<em>N<\/em>,<em>N<\/em>-Dimethylformamide Protected Palladium Nanoparticles and Their Use in the Suzuki-Miyaura Cross-Coupling Reaction<\/strong>,&nbsp;<br><em>ACS Omega.<\/em>,&nbsp;<strong>5<\/strong>, 9598 (2020).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"531\" height=\"332\" class=\"wp-image-237\" style=\"width: 500px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Synthesis-and-Characterization-of-NN-Dimethylformamide-Protected-Palladium-Nanoparticles-and-Their-Use-in-the-Suzuki\u2013Miyaura-Cross-Coupling-Reaction.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Synthesis-and-Characterization-of-NN-Dimethylformamide-Protected-Palladium-Nanoparticles-and-Their-Use-in-the-Suzuki\u2013Miyaura-Cross-Coupling-Reaction.jpg 531w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Synthesis-and-Characterization-of-NN-Dimethylformamide-Protected-Palladium-Nanoparticles-and-Their-Use-in-the-Suzuki\u2013Miyaura-Cross-Coupling-Reaction-300x188.jpg 300w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Synthesis-and-Characterization-of-NN-Dimethylformamide-Protected-Palladium-Nanoparticles-and-Their-Use-in-the-Suzuki\u2013Miyaura-Cross-Coupling-Reaction-480x300.jpg 480w\" sizes=\"auto, (max-width: 531px) 100vw, 531px\" \/><br><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1021\/acsomega.9b03828\" target=\"_blank\">T. Nagata, Y. Obora:<br><em><strong>N<\/strong><\/em><strong>,<em>N<\/em>-Dimethylformamide-Protected Single-Size Metal Nanoparticles and Their Use as Catalysts for Organic Transformation<\/strong>,&nbsp;<br><em>ACS Omega.<\/em>,&nbsp;<strong>5<\/strong>, 98 (2020).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"528\" height=\"286\" class=\"wp-image-235\" style=\"width: 400px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/NN-Dimethylformamide-Protected-Single-Sized-Metal-Nanoparticles-and-Their-Use-as-Catalysts-for-Organic-Transformations-e1620796029183.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/NN-Dimethylformamide-Protected-Single-Sized-Metal-Nanoparticles-and-Their-Use-as-Catalysts-for-Organic-Transformations-e1620796029183.jpg 528w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/NN-Dimethylformamide-Protected-Single-Sized-Metal-Nanoparticles-and-Their-Use-as-Catalysts-for-Organic-Transformations-e1620796029183-300x163.jpg 300w\" sizes=\"auto, (max-width: 528px) 100vw, 528px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1246\/bcsj.20200115\" target=\"_blank\">P. Suktanarak, T. Tanaka, T. Nagata, R. Kondo, T. Suzuki, T. Tuntulani, P. Leeladee, Y. Obora:<br><strong>Effect of Water in Fabricating Copper Nanoparticles onto Reduced Graphene Oxide Nanosheets: Application in Catalytic Ullmann-Coupling Reactions<\/strong>,&nbsp;<br><em>Bull<\/em>.&nbsp;<em>Chem<\/em>.&nbsp;<em>Soc. Jpn.<\/em>,&nbsp;<strong>93<\/strong>, 1164 (2020).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"659\" height=\"425\" class=\"wp-image-233\" style=\"width: 480px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Effect-of-Water-in-Fabricating-Copper-Nanoparticles-onto-Reduced-Graphene-Oxide-Nanosheets-Application-in-Catalytic-Ullmann-Coupling-Reactions-e1620796387385.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Effect-of-Water-in-Fabricating-Copper-Nanoparticles-onto-Reduced-Graphene-Oxide-Nanosheets-Application-in-Catalytic-Ullmann-Coupling-Reactions-e1620796387385.jpg 659w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Effect-of-Water-in-Fabricating-Copper-Nanoparticles-onto-Reduced-Graphene-Oxide-Nanosheets-Application-in-Catalytic-Ullmann-Coupling-Reactions-e1620796387385-300x193.jpg 300w\" sizes=\"auto, (max-width: 659px) 100vw, 659px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1021\/acs.joc.0c01540\" target=\"_blank\">M. Kobayashi, S. Itoh, K. Yoshimura, Y. Tsukamoto, Y. Obora:<br><strong>Iridium Complex-Catalyzed C2-Extension of Primary Alcohols with Ethanol via a Hydrogen Autotransfer Reaction<\/strong>,&nbsp;<br><em>J. Org. Chem.<\/em>,&nbsp;<strong>85<\/strong>, 11952 (2020).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"531\" height=\"125\" class=\"wp-image-234\" style=\"width: 500px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-Complex-Catalyzed-C2-Extension-of-Primary-Alcohols-with-Ethanol-via-a-Hydrogen-Autotransfer-Reaction.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-Complex-Catalyzed-C2-Extension-of-Primary-Alcohols-with-Ethanol-via-a-Hydrogen-Autotransfer-Reaction.jpg 531w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-Complex-Catalyzed-C2-Extension-of-Primary-Alcohols-with-Ethanol-via-a-Hydrogen-Autotransfer-Reaction-300x71.jpg 300w\" sizes=\"auto, (max-width: 531px) 100vw, 531px\" \/><\/li>\n<\/ol>\n\n\n\n<div style=\"height:20px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<p class=\"has-text-align-right\"><mark style=\"color:#89a06c\" class=\"has-inline-color\">\u25b2<\/mark> <a href=\"#top\">\u30da\u30fc\u30b8\u306eTOP\u3078<\/a><\/p>\n\n\n\n<div style=\"height:40px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"2019\">2019\u5e74<\/h3>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>\u5b66\u8853\u8ad6\u6587<\/strong><\/h4>\n\n\n\n<ol class=\"wp-block-list\">\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1039\/C9RA02895A\" target=\"_blank\">T. Nagata, T. Inoue, X. Lin, S. Ishimoto, S. Nakamichi, H. Oka, R. Kondo, T. Suzuki, Y. Obora:<br><strong>Dimethylformamide-stabilised palladium nanoclusters catalysed coupling reactions of aryl halides with hydrosilanes\/disilanes<\/strong><br><em>RSC Adv.<\/em>,&nbsp;<strong>9<\/strong>, 17425 (2019).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"509\" height=\"195\" class=\"wp-image-240\" style=\"width: 500px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Dimethylformamide-stabilised-palladium-nanoclusters-catalysed-coupling-reactions-of-aryl-halides-with-hydrosilanesdisilanes.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Dimethylformamide-stabilised-palladium-nanoclusters-catalysed-coupling-reactions-of-aryl-halides-with-hydrosilanesdisilanes.jpg 509w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Dimethylformamide-stabilised-palladium-nanoclusters-catalysed-coupling-reactions-of-aryl-halides-with-hydrosilanesdisilanes-300x115.jpg 300w\" sizes=\"auto, (max-width: 509px) 100vw, 509px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1002\/cctc.201900318\" target=\"_blank\">Y. Takahashi, R. Kondo, M. Utsunomiya, T. Suzuki, H. T. Takeshita, Y. Obora:<br><strong>Ti\u2212Pd Alloys as Heterogeneous Catalysts for the Hydrogen Autotransfer Reaction and Catalytic Improvement by Hydrogenation Effects<\/strong>,&nbsp;<br><em>ChemCatChem.<\/em>,&nbsp;<strong>11<\/strong>, 2432 (2019).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"443\" height=\"373\" class=\"wp-image-238\" style=\"width: 320px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Ti-Pd-Alloys-as-Heterogeneous-Catalysts-for-the-Hydrogen.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Ti-Pd-Alloys-as-Heterogeneous-Catalysts-for-the-Hydrogen.jpg 443w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Ti-Pd-Alloys-as-Heterogeneous-Catalysts-for-the-Hydrogen-300x253.jpg 300w\" sizes=\"auto, (max-width: 443px) 100vw, 443px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1021\/acs.orglett.9b01025\" target=\"_blank\">Y. Tsukamoto, S. Itoh, M. Kobayashi, Y. Obora:<br><strong>Iridium-Catalyzed \u03b1-Methylation of \u03b1-Aryl Esters Using Methanol as the C1 Source<\/strong>,&nbsp;<br><em>Org. Lett.<\/em>,&nbsp;<strong>21<\/strong>, 3299 (2019).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"606\" height=\"210\" class=\"wp-image-241\" style=\"width: 450px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-Catalyzed-\u03b1-Methylation-of-\u03b1-Aryl-Esters-Using-Methanol-as-the-C1-Source.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-Catalyzed-\u03b1-Methylation-of-\u03b1-Aryl-Esters-Using-Methanol-as-the-C1-Source.jpg 606w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-Catalyzed-\u03b1-Methylation-of-\u03b1-Aryl-Esters-Using-Methanol-as-the-C1-Source-300x104.jpg 300w\" sizes=\"auto, (max-width: 606px) 100vw, 606px\" \/><\/li>\n<\/ol>\n\n\n\n<div style=\"height:20px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<p class=\"has-text-align-right\"><mark style=\"color:#89a06c\" class=\"has-inline-color\">\u25b2<\/mark> <a href=\"#top\">\u30da\u30fc\u30b8\u306eTOP\u3078<\/a><\/p>\n\n\n\n<div style=\"height:40px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"2018\">2018\u5e74<\/h3>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>\u5b66\u8853\u8ad6\u6587<\/strong><\/h4>\n\n\n\n<ol class=\"wp-block-list\">\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1055\/s-0037-1610671\" target=\"_blank\">T. Nagata, Y. Adachi, Y. Obora:<br><strong>Thiolate-Protected Gold Au25(SC2H4Ph)18 Nanoclusters as a Catalyst for Intermolecular Hydroamination of Terminal Alkynes<\/strong>,&nbsp;<br><em>Synlett<\/em>,&nbsp;<strong>29&nbsp;<\/strong>(20), 2655 (2018).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"957\" height=\"349\" class=\"wp-image-247\" style=\"width: 650px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Thiolate-Protected-Au25SC2H4Ph18-Nanoclusters-as-a-Catalyst-for-Intermolecular-Hydroamination-of-Terminal-Alkynes.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Thiolate-Protected-Au25SC2H4Ph18-Nanoclusters-as-a-Catalyst-for-Intermolecular-Hydroamination-of-Terminal-Alkynes.jpg 957w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Thiolate-Protected-Au25SC2H4Ph18-Nanoclusters-as-a-Catalyst-for-Intermolecular-Hydroamination-of-Terminal-Alkynes-300x109.jpg 300w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Thiolate-Protected-Au25SC2H4Ph18-Nanoclusters-as-a-Catalyst-for-Intermolecular-Hydroamination-of-Terminal-Alkynes-768x280.jpg 768w\" sizes=\"auto, (max-width: 957px) 100vw, 957px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1002\/cctc.201800161\" target=\"_blank\">R. Azuma, S. Nakamichi, J. Kimura, H. Yano, H. Kawasaki, T. Suzuki, R. Kondo, Y. Kanda, K. Shimizu, K. Kato, Y. Obora:<br><strong>Solution Synthesis of&nbsp;<em>N<\/em>,&nbsp;<em>N<\/em>-Dimethylformamide-stabilized Iron Oxide Nanoparticles as an Efficient and Recyclable Catalyst for Alkene Hydrosilylation<\/strong>,&nbsp;<br><em>ChamCatChem.<\/em>,&nbsp;<strong>10<\/strong>(11), 2378 (2018).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"408\" height=\"191\" class=\"wp-image-245\" style=\"width: 400px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Solution-Synthesis-of-NN-Dimethylformamide-Stabilized.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Solution-Synthesis-of-NN-Dimethylformamide-Stabilized.jpg 408w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Solution-Synthesis-of-NN-Dimethylformamide-Stabilized-300x140.jpg 300w\" sizes=\"auto, (max-width: 408px) 100vw, 408px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1016\/j.tetlet.2017.12.020\" target=\"_blank\">Y. Obora:<br><strong>Recent Advances in the Synthesis of N-Alkenyl Carbazoles<\/strong>,&nbsp;<br><em>Tetrahedron Lett.<\/em>,&nbsp;<strong>59<\/strong>(3), 167 (2018).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"685\" height=\"220\" class=\"wp-image-244\" style=\"width: 500px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Recent-advances-in-the-synthesis-of-N-alkenyl-carbazoles.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Recent-advances-in-the-synthesis-of-N-alkenyl-carbazoles.jpg 685w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Recent-advances-in-the-synthesis-of-N-alkenyl-carbazoles-300x96.jpg 300w\" sizes=\"auto, (max-width: 685px) 100vw, 685px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1039\/C8RA01410H\" target=\"_blank\">K. Onishi, K. Oikawa, H. Yano, T. Suzuki, Y. Obora:<br><em><strong>N<\/strong><\/em><strong>,&nbsp;<em>N<\/em>-Dimethylformamide-stabilized Palladium Nanoclusters as Catalyst for Larock Indole Synthesis<\/strong>,&nbsp;<br><em>RSC Adv.<\/em>,&nbsp;<strong>8<\/strong>(21), 11324 (2018).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"524\" height=\"177\" class=\"wp-image-243\" style=\"width: 500px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/NN-Dimethylformamide-stabilized-palladium-nanoclusters-as-a-catalyst-for-Larock-indole-synthesis.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/NN-Dimethylformamide-stabilized-palladium-nanoclusters-as-a-catalyst-for-Larock-indole-synthesis.jpg 524w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/NN-Dimethylformamide-stabilized-palladium-nanoclusters-as-a-catalyst-for-Larock-indole-synthesis-300x101.jpg 300w\" sizes=\"auto, (max-width: 524px) 100vw, 524px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1021\/acsomega.8b01642\" target=\"_blank\">M. Fuji, J. Chiwata, M. Ozaki, S. Aratani, Y. Obora:<br><em><strong>In Situ<\/strong><\/em><strong>-Generated Niobium-Catalyzed Synthesis of 3-Pyrroline Darivatives&nbsp;<em>via<\/em>&nbsp;Ring-Closing Metathesis Reactions<\/strong>,&nbsp;<br><em>ACS Omega<\/em>,&nbsp;<strong>3<\/strong>(8), 8865 (2018).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"532\" height=\"219\" class=\"wp-image-242\" style=\"width: 350px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/In-Situ-Generated-Niobium-Catalyzed-Synthesis-of-3-Pyrroline-Derivatives-via-Ring-Closing-Metathesis-Reactions.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/In-Situ-Generated-Niobium-Catalyzed-Synthesis-of-3-Pyrroline-Derivatives-via-Ring-Closing-Metathesis-Reactions.jpg 532w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/In-Situ-Generated-Niobium-Catalyzed-Synthesis-of-3-Pyrroline-Derivatives-via-Ring-Closing-Metathesis-Reactions-300x123.jpg 300w\" sizes=\"auto, (max-width: 532px) 100vw, 532px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.2320\/matertrans.M2018240\" target=\"_blank\">R. Kondo, S. Nakamichi, R. Azuma, Y. Takahashi, Y. Obora, H. T. Takeshita:<br><strong>Surface Properties of Air-exposed \u03b1-Ti-Pd Alloys via XPS and Cross-coupling Reaction<\/strong>,&nbsp;<br><em>Mater. Trans.<\/em>,&nbsp;<strong>59<\/strong>(12), 1911 (2018).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"641\" height=\"255\" class=\"wp-image-246\" style=\"width: 480px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Surface-Properties-of-Air-Exposed-\u03b1-Ti\u2013Pd-Alloys-via-XPS-and-Cross-Coupling-Reaction.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Surface-Properties-of-Air-Exposed-\u03b1-Ti\u2013Pd-Alloys-via-XPS-and-Cross-Coupling-Reaction.jpg 641w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Surface-Properties-of-Air-Exposed-\u03b1-Ti\u2013Pd-Alloys-via-XPS-and-Cross-Coupling-Reaction-300x119.jpg 300w\" sizes=\"auto, (max-width: 641px) 100vw, 641px\" \/><\/li>\n<\/ol>\n\n\n\n<div style=\"height:20px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<p class=\"has-text-align-right\"><mark style=\"color:#89a06c\" class=\"has-inline-color\">\u25b2<\/mark> <a href=\"#top\">\u30da\u30fc\u30b8\u306eTOP\u3078<\/a><\/p>\n\n\n\n<div style=\"height:40px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"2017\">2017\u5e74<\/h3>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>\u5b66\u8853\u8ad6\u6587<\/strong><\/h4>\n\n\n\n<ol class=\"wp-block-list\">\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1039\/C6CC09279A\" target=\"_blank\">K. Oikawa, S. Itoh, H. Yano, H. Kawasaki, Y. Obora:<br><strong>Preparation and use of DMF-stabilized iridium nanoclusters as methylation catalysts using methanol as the C1 source<\/strong>,&nbsp;<br><em>Chem. 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Oka, K. Kitai, T. Suzuki, Y. 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Obora:<br><strong>Niobium Complexes in Organic Transformations: From Stoichiometric Reactions to Catalytic [2+2+2] Cycloaddition Reactions<\/strong>,&nbsp;<br><em>Eur. J. Org. Chem.<\/em>,&nbsp;<strong>2015&nbsp;<\/strong>(23), 5041-5054 (2015).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"422\" height=\"400\" class=\"wp-image-256\" style=\"width: 300px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Niobium-Complexes-in-Organic-Transformations-From-Stoichiometric-Reactions-to-Catalytic-222-Cycloaddition-Reactions.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Niobium-Complexes-in-Organic-Transformations-From-Stoichiometric-Reactions-to-Catalytic-222-Cycloaddition-Reactions.jpg 422w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Niobium-Complexes-in-Organic-Transformations-From-Stoichiometric-Reactions-to-Catalytic-222-Cycloaddition-Reactions-300x284.jpg 300w\" sizes=\"auto, (max-width: 422px) 100vw, 422px\" \/><\/li>\n<\/ol>\n\n\n\n<div style=\"height:20px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<p class=\"has-text-align-right\"><mark style=\"color:#89a06c\" class=\"has-inline-color\">\u25b2<\/mark> <a href=\"#top\">\u30da\u30fc\u30b8\u306eTOP\u3078<\/a><\/p>\n\n\n\n<div style=\"height:40px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"2014\">2014\u5e74<\/h3>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>\u5b66\u8853\u8ad6\u6587<\/strong><\/h4>\n\n\n\n<ol class=\"wp-block-list\">\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1021\/cs501269d\" target=\"_blank\">Y. Obora:<br><strong>Recent Advances in \u03b1-Alkylation Reactions using Alcohols with Hydrogen Borrowing Methodologies<\/strong>,<br><em>ACS Catal<\/em>,&nbsp;<strong>4<\/strong>, 3972 (2014).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"530\" height=\"206\" class=\"wp-image-261\" style=\"width: 400px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Recent-Advances-in-\u03b1-Alkylation-Reactions-using-Alcohols-with-Hydrogen-Borrowing-Methodologies.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Recent-Advances-in-\u03b1-Alkylation-Reactions-using-Alcohols-with-Hydrogen-Borrowing-Methodologies.jpg 530w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Recent-Advances-in-\u03b1-Alkylation-Reactions-using-Alcohols-with-Hydrogen-Borrowing-Methodologies-300x117.jpg 300w\" sizes=\"auto, (max-width: 530px) 100vw, 530px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.5059\/yukigoseikyokaishi.72.257\" target=\"_blank\">\u4f50\u85e4 \u9756,&nbsp;\u5927\u6d1e \u5eb7\u55e3:<br>\u524d\u5468\u671f\u4f4e\u539f\u5b50\u4fa1\u30cb\u30aa\u30d6\u5316\u5408\u7269\u306e\u6709\u6a5f\u5909\u63db\u53cd\u5fdc\u3078\u306e\u5229\u7528\u3000\u2014\u91cf\u8ad6\u53cd\u5fdc\u304b\u3089\u89e6\u5a92\u53cd\u5fdc\u3078\u2014,<br>\u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a\u8a8c<em>,<\/em>&nbsp;<strong>72<\/strong>, 257 (2014).<\/a><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.5059\/yukigoseikyokaishi.72.257\" target=\"_blank\">Y. Satoh, Y. Obora:<br><strong>Synthesis of arylacetonitrile derivatives: Ni-catalyzed reaction of benzyl chlorides with trimethylsilyl cyanide under base-free conditions<\/strong>,<br><em>RSC Adv.<\/em>,&nbsp;<strong>4<\/strong>, 15736 (2014).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"525\" height=\"146\" class=\"wp-image-262\" style=\"width: 500px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Synthesis-of-arylacetonitrile-derivatives-Ni-catalyzed-reaction-of-benzyl-chlorides-with-trimethylsilyl-cyanide-under-base-free-conditions.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Synthesis-of-arylacetonitrile-derivatives-Ni-catalyzed-reaction-of-benzyl-chlorides-with-trimethylsilyl-cyanide-under-base-free-conditions.jpg 525w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Synthesis-of-arylacetonitrile-derivatives-Ni-catalyzed-reaction-of-benzyl-chlorides-with-trimethylsilyl-cyanide-under-base-free-conditions-300x83.jpg 300w\" sizes=\"auto, (max-width: 525px) 100vw, 525px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1039\/C3CC49626K\" target=\"_blank\">S. Ogawa, Y. Obora:<br><strong>Iridium-catalyzed selective a-methylation of ketones with methanol<\/strong>,<br><em>Chem. Commun.<\/em>,&nbsp;<strong>50<\/strong>, 2491 (2014).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"512\" height=\"244\" class=\"wp-image-260\" style=\"width: 500px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-catalyzed-selective-\u03b1-methylation-of-ketones-with-methanol.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-catalyzed-selective-\u03b1-methylation-of-ketones-with-methanol.jpg 512w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-catalyzed-selective-\u03b1-methylation-of-ketones-with-methanol-300x143.jpg 300w\" sizes=\"auto, (max-width: 512px) 100vw, 512px\" \/><\/li>\n<\/ol>\n\n\n\n<div style=\"height:20px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<p class=\"has-text-align-right\"><mark style=\"color:#89a06c\" class=\"has-inline-color\">\u25b2<\/mark> <a href=\"#top\">\u30da\u30fc\u30b8\u306eTOP\u3078<\/a><\/p>\n\n\n\n<div style=\"height:40px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"2013\">2013\u5e74<\/h3>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>\u5b66\u8853\u8ad6\u6587<\/strong><\/h4>\n\n\n\n<ol class=\"wp-block-list\">\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1021\/jo4010734\" target=\"_blank\">Y.&nbsp;Mizuta, K. Yasuda, Y. Obora:<br><strong>Palladium-Catalyzed Z-Selective Oxidative Amination of ortho-Substituted Primary Anilines with Olefins under an Open Air Atmosphere<\/strong>,<br><em>J. Org. Chem.<\/em>&nbsp;<strong>78&nbsp;<\/strong>(12), 6332-6337 (2013).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"532\" height=\"111\" class=\"wp-image-267\" style=\"width: 500px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Palladium-Catalyzed-Z-Selective-Oxidative-Amination-of-ortho-Substituted-Primary-Anilines-with-Olefins-under-an-Open-Air-Atmosphere.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Palladium-Catalyzed-Z-Selective-Oxidative-Amination-of-ortho-Substituted-Primary-Anilines-with-Olefins-under-an-Open-Air-Atmosphere.jpg 532w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Palladium-Catalyzed-Z-Selective-Oxidative-Amination-of-ortho-Substituted-Primary-Anilines-with-Olefins-under-an-Open-Air-Atmosphere-300x63.jpg 300w\" sizes=\"auto, (max-width: 532px) 100vw, 532px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1021\/jo401399y\" target=\"_blank\">Y. Satoh, Y. Obora:<br><strong>Low-Valent Niobium-Catalyzed Intermolecular [2 + 2 + 2] Cycloaddition of tert-Butylacetylene and Arylnitriles to Form 2,3,6-Trisubstituted Pyridine Derivatives<\/strong>,&nbsp;<br><em>J. Org. Chem.<\/em><strong>78&nbsp;<\/strong>(15), 7771-7776 (2013).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"533\" height=\"177\" class=\"wp-image-265\" style=\"width: 400px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Low-Valent-Niobium-Catalyzed-Intermolecular-2-2-2-Cycloaddition-of-tert-Butylacetylene-and-Arylnitriles-to-Form-236-Trisubstituted-Pyridine-Derivatives.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Low-Valent-Niobium-Catalyzed-Intermolecular-2-2-2-Cycloaddition-of-tert-Butylacetylene-and-Arylnitriles-to-Form-236-Trisubstituted-Pyridine-Derivatives.jpg 533w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Low-Valent-Niobium-Catalyzed-Intermolecular-2-2-2-Cycloaddition-of-tert-Butylacetylene-and-Arylnitriles-to-Form-236-Trisubstituted-Pyridine-Derivatives-300x100.jpg 300w\" sizes=\"auto, (max-width: 533px) 100vw, 533px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1002\/cctc.201200649\" target=\"_blank\">S. Harada, H. Yano, Y. Obora:<br><strong>Palladium-Catalyzed, Ligand-Controlled Chemoselective Oxidative Coupling Reactions of Benzene Derivatives with Acrylamides under an Oxygen Atmosphere<\/strong>,<br><em>ChemCatChem<\/em>,&nbsp;<strong>5&nbsp;<\/strong>(1), 121-125 (2013).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"679\" height=\"229\" class=\"wp-image-268\" style=\"width: 500px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Palladium\u2010Catalyzed-Ligand\u2010Controlled-Chemoselective-Oxidative-Coupling-Reactions-of-Benzene-Derivatives-with-Acrylamides-under-an-Oxygen-Atmosphere.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Palladium\u2010Catalyzed-Ligand\u2010Controlled-Chemoselective-Oxidative-Coupling-Reactions-of-Benzene-Derivatives-with-Acrylamides-under-an-Oxygen-Atmosphere.jpg 679w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Palladium\u2010Catalyzed-Ligand\u2010Controlled-Chemoselective-Oxidative-Coupling-Reactions-of-Benzene-Derivatives-with-Acrylamides-under-an-Oxygen-Atmosphere-300x101.jpg 300w\" sizes=\"auto, (max-width: 679px) 100vw, 679px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1055\/s-0033-1338510\" target=\"_blank\">Y. Obora, T. Sawaguchi, K. Tsubakimoto, H. Yoshida, S. Ogawa, Shintaro Hatanaka:<br><strong>Iridium-Catalyzed Synthesis of \u03c9-Hydroxy Homoallylic Alcohols<\/strong>,<br>Synthesis,&nbsp;<strong>45<\/strong>&nbsp;(15), 2115-2119 (2013).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"589\" height=\"141\" class=\"wp-image-264\" style=\"width: 500px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-Catalyzed-Synthesis-of-\u03c9-Hydroxy-Homoallylic-Alcohols.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-Catalyzed-Synthesis-of-\u03c9-Hydroxy-Homoallylic-Alcohols.jpg 589w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-Catalyzed-Synthesis-of-\u03c9-Hydroxy-Homoallylic-Alcohols-300x72.jpg 300w\" sizes=\"auto, (max-width: 589px) 100vw, 589px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1016\/j.jorganchem.2013.05.035\" target=\"_blank\">M. Ozaki, Y. Obora, Y. Tada, Y. Ishii:<br><strong>Generation of low-valent alkoxy niobium from Nb (OEt) 5 and Grignard reagents and their use as catalysts in the cyclotrimerization of isocyanates<\/strong>,&nbsp;<br><em>J. Organomet. Chem.<\/em>,<strong>&nbsp;741-742<\/strong>, 109-113&nbsp;(2013).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"685\" height=\"196\" class=\"wp-image-263\" style=\"width: 380px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Generation-of-low-valent-alkoxy-niobium-from-NbOEt5-and-Grignard-reagents-and-their-use-as-catalysts-in-the-cyclotrimerization-of-isocyanates.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Generation-of-low-valent-alkoxy-niobium-from-NbOEt5-and-Grignard-reagents-and-their-use-as-catalysts-in-the-cyclotrimerization-of-isocyanates.jpg 685w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Generation-of-low-valent-alkoxy-niobium-from-NbOEt5-and-Grignard-reagents-and-their-use-as-catalysts-in-the-cyclotrimerization-of-isocyanates-300x86.jpg 300w\" sizes=\"auto, (max-width: 685px) 100vw, 685px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1016\/j.jorganchem.2013.08.004\" target=\"_blank\">H. Yano, Y. Nakajima, Y. Obora:<br><strong>N,N-Dimethylformamide-stabilized palladium nanoclusters as catalyst for Migita-Kosugi-Stille cross-coupling reactions<\/strong>,<br><em>J. Organomet. Chem.<\/em>&nbsp;<strong>745-746<\/strong>, 258-261 (2013).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"574\" height=\"277\" class=\"wp-image-266\" style=\"width: 420px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/NN-Dimethylformamide-stabilized-palladium-nanoclusters-as-catalyst-for-Migita\u2013Kosugi\u2013Stille-cross-coupling-reactions.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/NN-Dimethylformamide-stabilized-palladium-nanoclusters-as-catalyst-for-Migita\u2013Kosugi\u2013Stille-cross-coupling-reactions.jpg 574w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/NN-Dimethylformamide-stabilized-palladium-nanoclusters-as-catalyst-for-Migita\u2013Kosugi\u2013Stille-cross-coupling-reactions-300x145.jpg 300w\" sizes=\"auto, (max-width: 574px) 100vw, 574px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1007\/s11051-012-1379-2\" target=\"_blank\">Y. Sugii, M. Inada, H. Yano, Y. Obora, Y. Iwasaki:<br><strong>Single nanosized FeO nanocrystals with photoluminescence properties<\/strong>,<br><em>J. Nanopart. Res.<\/em>,&nbsp;<strong>15<\/strong>(1) 1379 (2013).<\/a><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.3390\/catal3040794\" target=\"_blank\">Y. Obora, Y. Ishii:<br><strong>Palladium-Catalyzed Intermolecular Oxidative Amination of Alkenes with Amines, Using Molecular Oxygen as Terminal Oxidant<\/strong>,<br><em>Catalysis<\/em>,&nbsp;<strong>3<\/strong>&nbsp;(4), 794-810 (2013).<\/a><\/li>\n<\/ol>\n\n\n\n<div style=\"height:20px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<p class=\"has-text-align-right\"><mark style=\"color:#89a06c\" class=\"has-inline-color\">\u25b2<\/mark> <a href=\"#top\">\u30da\u30fc\u30b8\u306eTOP\u3078<\/a><\/p>\n\n\n\n<div style=\"height:40px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"2012\">2012\u5e74<\/h3>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>\u5b66\u8853\u8ad6\u6587<\/strong><\/h4>\n\n\n\n<ol class=\"wp-block-list\">\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1039\/C2NR30222E\" target=\"_blank\">H. Yamamoto, H. Yano, H. Kouchi, Y. Obora, R. Arakawa, H. Kawasaki:<br><strong>N,N-Dimethylformamide-stabilized gold nanoclusters as a catalyst for the reduction of 4-nitrophenol<\/strong>,<br><em>Nanoscale<\/em>,&nbsp;<strong>4<\/strong>, 4148\u20134154 (2012).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"770\" height=\"523\" class=\"wp-image-270\" style=\"width: 520px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/NN-Dimethylformamide-stabilized-gold-nanoclusters-as-a-catalyst-for-the-reduction-of-4-nitrophenol.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/NN-Dimethylformamide-stabilized-gold-nanoclusters-as-a-catalyst-for-the-reduction-of-4-nitrophenol.jpg 770w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/NN-Dimethylformamide-stabilized-gold-nanoclusters-as-a-catalyst-for-the-reduction-of-4-nitrophenol-300x204.jpg 300w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/NN-Dimethylformamide-stabilized-gold-nanoclusters-as-a-catalyst-for-the-reduction-of-4-nitrophenol-768x522.jpg 768w\" sizes=\"auto, (max-width: 770px) 100vw, 770px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1039\/C2CC30975K\" target=\"_blank\">Y. Isomura, T. Narushima, H. Kawasaki, T. Yonezawa, Y. Obora:<br><strong>Surfactant-free single-nano-sized colloidal Cu nanoparticles for use as an active catalyst in Ullmann-coupling reaction<\/strong>,<br><em>Chem. Commun.,<\/em>&nbsp;<strong>48<\/strong>, 3784-3786 (2012).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"512\" height=\"181\" class=\"wp-image-273\" style=\"width: 520px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Surfactant-free-single-nano-sized-colloidal-Cu-nanoparticles-for-use-as-an-active-catalyst-in-Ullmann-coupling-reaction.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Surfactant-free-single-nano-sized-colloidal-Cu-nanoparticles-for-use-as-an-active-catalyst-in-Ullmann-coupling-reaction.jpg 512w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Surfactant-free-single-nano-sized-colloidal-Cu-nanoparticles-for-use-as-an-active-catalyst-in-Ullmann-coupling-reaction-300x106.jpg 300w\" sizes=\"auto, (max-width: 512px) 100vw, 512px\" \/><\/li>\n\n\n\n<li><a href=\"https:\/\/doi.org\/10.1039\/C2CC32787B\">Y. Obora, K. Nakamura, S. Hatanaka:<br><strong>Iridium-catalyzed reaction of enones with alcohols affording 1,3-diketones<\/strong>,<br><em>Chem. Commun.<\/em>,&nbsp;<strong>48<\/strong>, 6720-6722 (2012).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"517\" height=\"115\" class=\"wp-image-269\" style=\"width: 500px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-catalyzed-reaction-of-enones-with-alcohols-affording-13-diketones.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-catalyzed-reaction-of-enones-with-alcohols-affording-13-diketones.jpg 517w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-catalyzed-reaction-of-enones-with-alcohols-affording-13-diketones-300x67.jpg 300w\" sizes=\"auto, (max-width: 517px) 100vw, 517px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1021\/jo3019347\" target=\"_blank\">Y. Obora, S. Ogawa, N. Yamamoto:<br><strong>Iridium-Catalyzed Alkylation of Methylquinolines with Alcohols<\/strong>,<br><em>J. Org. Chem.<\/em>,&nbsp;<strong>77&nbsp;<\/strong>(20), 9429-9433 (2012).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"532\" height=\"103\" class=\"wp-image-274\" style=\"width: 500px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-Catalyzed-Alkylation-of-Methylquinolines-with-Alcohols.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-Catalyzed-Alkylation-of-Methylquinolines-with-Alcohols.jpg 532w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-Catalyzed-Alkylation-of-Methylquinolines-with-Alcohols-300x58.jpg 300w\" sizes=\"auto, (max-width: 532px) 100vw, 532px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1002\/cctc.201100375\" target=\"_blank\">Y. Mizuta, Y. Obora, Y. Shimizu, Y. Ishii:<br><strong>para\u2010Selective Aerobic Oxidative C\u2014H Olefination of Aminobenzenes Catalyzed by Palladium\/Molybdovanadophosphoric acid\/2, 4, 6\u2010Trimethylbenzoic Acid System<\/strong>,&nbsp;<br><em>ChemCatChem<\/em>,&nbsp;<strong>4<\/strong>, 187-191 (2012).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"477\" height=\"380\" class=\"wp-image-271\" style=\"width: 360px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/para\u2010Selective-Aerobic-Oxidative-C\uf8ffH-Olefination-of-Aminobenzenes-Catalyzed-by-PalladiumMolybdovanadophosphoric-acid246\u2010Trimethylbenzoic-Acid-System.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/para\u2010Selective-Aerobic-Oxidative-C\uf8ffH-Olefination-of-Aminobenzenes-Catalyzed-by-PalladiumMolybdovanadophosphoric-acid246\u2010Trimethylbenzoic-Acid-System.jpg 477w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/para\u2010Selective-Aerobic-Oxidative-C\uf8ffH-Olefination-of-Aminobenzenes-Catalyzed-by-PalladiumMolybdovanadophosphoric-acid246\u2010Trimethylbenzoic-Acid-System-300x239.jpg 300w\" sizes=\"auto, (max-width: 477px) 100vw, 477px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1021\/om300669s\" target=\"_blank\">Y. Satoh, K. Yasuda, Y. Obora:<br><strong>Strategy for the Synthesis of Pyrimidine Derivatives: NbCl5-Mediated Cycloaddition of Alkynes and Nitriles<\/strong>,&nbsp;<br><em>Organometallics<\/em>,<strong>&nbsp;31&nbsp;<\/strong>(15), 5235-5238&nbsp;(2012).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"532\" height=\"150\" class=\"wp-image-272\" style=\"width: 420px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Strategy-for-the-Synthesis-of-Pyrimidine-Derivatives-NbCl5-Mediated-Cycloaddition-of-Alkynes-and-Nitriles.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Strategy-for-the-Synthesis-of-Pyrimidine-Derivatives-NbCl5-Mediated-Cycloaddition-of-Alkynes-and-Nitriles.jpg 532w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Strategy-for-the-Synthesis-of-Pyrimidine-Derivatives-NbCl5-Mediated-Cycloaddition-of-Alkynes-and-Nitriles-300x85.jpg 300w\" sizes=\"auto, (max-width: 532px) 100vw, 532px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1002\/0471264229.os089.30\" target=\"_blank\">Y. Obora, Y. Ishii:<br><strong>Discussion addendum for: Iridium-catalyzed synthesis of vinyl ethers from alcohols and vinyl acetate<\/strong>,&nbsp;<br><em>Org<\/em>.<em>&nbsp;Syn<\/em>.,&nbsp;<strong>89<\/strong>, 307-310 (2012).<\/a><\/li>\n<\/ol>\n\n\n\n<div style=\"height:20px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<p class=\"has-text-align-right\"><mark style=\"color:#89a06c\" class=\"has-inline-color\">\u25b2<\/mark> <a href=\"#top\">\u30da\u30fc\u30b8\u306eTOP\u3078<\/a><\/p>\n\n\n\n<div style=\"height:40px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"2011\">2011\u5e74<\/h3>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>\u5b66\u8853\u8ad6\u6587<\/strong><\/h4>\n\n\n\n<ol class=\"wp-block-list\">\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1002\/anie.201104452\" target=\"_blank\">Y. Obora, Y. Anno<sup>D<\/sup>, R. Okamoto<sup>B<\/sup>, T. Matsu-ura<sup>D<\/sup>, Y. Ishii:<br><strong>Iridium-catalyzed Reactions of \u03c9-Arylalkanols to \u03b1,\u03c9-Diarylalkanes,<\/strong><br>Angew. Chem. Int. Ed., 50 (37), 8618-8622 (2011).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"552\" height=\"179\" class=\"wp-image-276\" style=\"width: 500px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium\u2010Catalyzed-Reactions-of-\u03c9\u2010Arylalkanols-to-\u03b1\u03c9\u2010Diarylalkanes.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium\u2010Catalyzed-Reactions-of-\u03c9\u2010Arylalkanols-to-\u03b1\u03c9\u2010Diarylalkanes.jpg 552w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium\u2010Catalyzed-Reactions-of-\u03c9\u2010Arylalkanols-to-\u03b1\u03c9\u2010Diarylalkanes-300x97.jpg 300w\" sizes=\"auto, (max-width: 552px) 100vw, 552px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1246\/cl.2011.1055\" target=\"_blank\">T. Sawaguchi<sup>D<\/sup>, Y. Obora:<br><strong>Iridium-catalyzed \u03b1-Alkylation of Acetonitrile with Primary and Secondary Alcohols,<\/strong><br>Chem. Lett., 40 (9), 1055-1057 (2011).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"603\" height=\"148\" class=\"wp-image-277\" style=\"width: 500px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-catalyzed-\u03b1-Alkylation-of-Acetonitrile-with-Primary-and-Secondary-Alcohols.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-catalyzed-\u03b1-Alkylation-of-Acetonitrile-with-Primary-and-Secondary-Alcohols.jpg 603w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-catalyzed-\u03b1-Alkylation-of-Acetonitrile-with-Primary-and-Secondary-Alcohols-300x74.jpg 300w\" sizes=\"auto, (max-width: 603px) 100vw, 603px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1021\/jo201757w\" target=\"_blank\">Y. Satoh<sup>D<\/sup>, Y. Obora:<br><strong>Active Low-valent Niobium Catalysts from NbCl<sub>5<\/sub>&nbsp;and Hydrosilanes for Selective Intermolecular Cycloadditions,<\/strong><br>J. Org. Chem.,76 (20), 8569-8573 (2011).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"532\" height=\"135\" class=\"wp-image-275\" style=\"width: 500px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Active-Low-Valent-Niobium-Catalysts-from-NbCl5-and-Hydrosilanes-for-Selective-Intermolecular-Cycloadditions.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Active-Low-Valent-Niobium-Catalysts-from-NbCl5-and-Hydrosilanes-for-Selective-Intermolecular-Cycloadditions.jpg 532w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Active-Low-Valent-Niobium-Catalysts-from-NbCl5-and-Hydrosilanes-for-Selective-Intermolecular-Cycloadditions-300x76.jpg 300w\" sizes=\"auto, (max-width: 532px) 100vw, 532px\" \/><\/li>\n<\/ol>\n\n\n\n<div style=\"height:30px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>\u56fd\u969b\u4f1a\u8b70<\/strong><\/h4>\n\n\n\n<ol class=\"wp-block-list\">\n<li>Y. Isomura<sup>D<\/sup>, M. Hyotanishi<sup>D<\/sup>, T. Narushima (Hokkaido U.), H. Kawasaki, T. Yonezawa (Hokkaido U.), Y. Obora:<br><strong>Surfactant-free Synthesis of Copper and Palladium Nanoclusters for Their Use in Catalytic Cross-Coupling Reactions,<\/strong><br>16th IUPAC International Symposium on Organometallic Chemistry Directed Towards Organic Synthesis (OMCOS 16), P-270, Shanghai International Conference Center, Shanghai, China (2011.7.25).<\/li>\n\n\n\n<li>T. Sawaguchi<sup>D<\/sup>, Y. Obora:<br><strong>Iridium-catalyzed \u03b1-Alkylation of Acetonitrile with Alcohols and Diols,<\/strong><br>16th IUPAC International Symposium on Organometallic Chemistry Directed Towards Organic Synthesis (OMCOS 16), P-271, Shanghai International Conference Center, Shanghai, China (2011.7.25).<\/li>\n\n\n\n<li>T. Arai<sup>D<\/sup>, Y. Obora:<br><strong>Palladium-catalyzed Reaction of Internal Alkynes, Acid Chlorides, and Disilanes to Cyclopentenone Derivatives,<\/strong><br>16th IUPAC International Symposium on Organometallic Chemistry Directed Towards Organic Synthesis (OMCOS 16), P-272, Shanghai International Conference Center, Shanghai, China (2011.7.25).<\/li>\n\n\n\n<li>Y. Mizuta<sup>D<\/sup>, Y. Obora, Y. Shimizu<sup>D<\/sup>, Y. Ishii:<br><strong>Aerobic Oxidative Coupling Reaction of Aminobenzenes with Olefins Catalyzed by Pd\/HPMoV\/O<sub>2<\/sub>&nbsp;System,<\/strong><br>16th IUPAC International Symposium on Organometallic Chemistry Directed Towards Organic Synthesis (OMCOS 16), P-273, Shanghai International Conference Center, Shanghai, China (2011.7.25).<\/li>\n\n\n\n<li>Y. Obora:<br><strong>Development of Efficient Catalytic Transformations Using Simple Olefins and Alcohols,<\/strong>&nbsp;14th Asian Chemical Congress 2011 Contemporary Chemistry for Sustainability and Economic Sufficiency, INV-G4-62, Queen Sirikit National Convention Center, Bangkok, Thailand (2011.9.7) (Invited Lecture),.<\/li>\n\n\n\n<li>Y. Obora:<br><strong>Iridium-catalyzed Reactions Using Simple Alkynes and Alcohols,<\/strong><br>International Symposium on Catalysis and Fine Chemicals 2011 (C&amp;FC 2011), IL-38, Nara Prefectural New Public Hall, Nara, Japan (2011.12.8) (Invited Lecture).<\/li>\n\n\n\n<li>Y. Obora:<br><strong>Innovative Catalytic Transformations from Monofunctionalized Chemical Feedstocks,<\/strong><br>The 11th Youngnam-Kinki Joint Symposium on Organometallic Chemistry, Kyoto University, Kyoto, Japan (2012.1.31) (Invited Lecture).<\/li>\n<\/ol>\n\n\n\n<div style=\"height:30px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>\u5b66\u4f1a\u767a\u8868<\/strong><\/h4>\n\n\n\n<ol class=\"wp-block-list\">\n<li>\u5927\u6d1e\u5eb7\u55e3\uff1a<br><strong>\u91d1\u5c5e\u89e6\u5a92\u306e\u8d85\u9ad8\u5ea6\u5229\u7528\u306b\u57fa\u3065\u304f\u65b0\u898f\u5206\u5b50\u5909\u63db\u53cd\u5fdc\uff0c<\/strong><br>\u5e73\u6210\uff12\uff13\u5e74\u5ea6\u7b2c\uff11\u56de\u30ad\u30e3\u30bf\u30ea\u30b9\u30c8\u30af\u30e9\u30d6\u4f8b\u4f1a\uff0c\u5927\u962a\u5927\u5b66\u4e2d\u4e4b\u5cf6\u30bb\u30f3\u30bf\u30fc\uff082011.5.13\uff09(\u62db\u5f85\u8b1b\u6f14).<\/li>\n\n\n\n<li>\u5927\u6d1e\u5eb7\u55e3\uff1a<br><strong>\u91d1\u5c5e\u89e6\u5a92\u306e\u8d85\u9ad8\u5ea6\u5229\u7528\u3092\u57fa\u8ef8\u3068\u3059\u308b\u52b9\u7387\u7684\u5206\u5b50\u5909\u63db\u53cd\u5fdc\uff0c<\/strong><br>\u7b2c\uff13\uff18\u56de\u6709\u6a5f\u53cd\u5fdc\u61c7\u8ac7\u4f1a\uff0c\u5927\u962a\u5e9c\u7acb\u5927\u5b66 (2011.8.3) (\u62db\u5f85\u8b1b\u6f14).<\/li>\n\n\n\n<li>\u4f50\u85e4\u9756<sup>D<\/sup>\uff0c<br><strong>\u5927\u6d1e\u5eb7\u55e3\uff1a\u30d2\u30c9\u30ed\u30b7\u30e9\u30f3\u3092\u9084\u5143\u5264\u3068\u3057\u3066\u5229\u7528\u3057\u305f\u65b0\u898f\u6d3b\u6027\u5316\u30cb\u30aa\u30d6\u89e6\u5a92\u306b\u3088\u308b\u9ad8\u9078\u629e\u7684\u74b0\u5316\u4ed8\u52a0\u53cd\u5fdc,<\/strong><br>\u7b2c\uff13\uff18\u56de\u6709\u6a5f\u53cd\u5fdc\u61c7\u8ac7\u4f1a\uff0c\u5927\u962a\u5e9c\u7acb\u5927\u5b66 P-01 (2011.8.3).<\/li>\n\n\n\n<li>\u65b0\u5c45\u502b\u6210<sup>D<\/sup>\uff0c\u5927\u6d1e\u5eb7\u55e3\uff1a<br><strong>\u30d1\u30e9\u30b8\u30a6\u30e0\u89e6\u5a92\u3092\u7528\u3044\u305f\u9178\u5869\u5316\u7269\uff0c\u30a2\u30eb\u30ad\u30f3\u304a\u3088\u3073\u30b8\u30b7\u30e9\u30f3\u306b\u3088\u308b\u30b7\u30af\u30ed\u30da\u30f3\u30c6\u30ce\u30f3\u8a98\u5c0e\u4f53\u306e\u5408\u6210,<\/strong><br>\u7b2c\uff13\uff18\u56de\u6709\u6a5f\u53cd\u5fdc\u61c7\u8ac7\u4f1a\uff0c\u5927\u962a\u5e9c\u7acb\u5927\u5b66 P-04 (2011.8.3).<\/li>\n\n\n\n<li>\u77f3\u6a4b\u512a<sup>D<\/sup>\uff0c\u963f\u6b66\u7531\u52a0<sup>D<\/sup>\uff0c\u677e\u6d66\u8c4a\u7f8e<sup>D<\/sup>\uff0c\u4e2d\u5ddd\u4e9c\u7d00\u5b50<sup>B<\/sup>\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c\uff1a<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u89e6\u5a92\u3092\u7528\u3044\u305f\u30a2\u30eb\u30b3\u30fc\u30eb\u304b\u3089\u306e\u30c6\u30c8\u30e9\u30ea\u30f3\u8a98\u5c0e\u4f53\u306e\u5408\u6210\u53ca\u3073\u591a\u5206\u5c90\u30dd\u30ea\u30aa\u30fc\u30eb\u306e\u5408\u6210,<\/strong><br>\u7b2c\uff13\uff18\u56de\u6709\u6a5f\u53cd\u5fdc\u61c7\u8ac7\u4f1a\uff0c\u5927\u962a\u5e9c\u7acb\u5927\u5b66 P-08 (2011.8.3).<\/li>\n\n\n\n<li>\u6fa4\u53e3\u62d3\u77e2<sup>D<\/sup>\uff0c\u5927\u6d1e\u5eb7\u55e3\uff1a<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u932f\u4f53\u89e6\u5a92\u306b\u3088\u308b\u30a2\u30bb\u30c8\u30cb\u30c8\u30ea\u30eb\u3068\u30a2\u30eb\u30b3\u30fc\u30eb\u307e\u305f\u306f\u30b8\u30aa\u30fc\u30eb\u3092\u7528\u3044\u305f\u03b1-\u30a2\u30eb\u30ad\u30eb\u5316\u53cd\u5fdc,<\/strong><br>\u7b2c\uff13\uff18\u56de\u6709\u6a5f\u53cd\u5fdc\u61c7\u8ac7\u4f1a\uff0c\u5927\u962a\u5e9c\u7acb\u5927\u5b66 P-12 (2011.8.3).<\/li>\n\n\n\n<li>\u539f\u7530\u8056\u4e00\u6717<sup>D<\/sup>\uff0c\u5927\u6d1e\u5eb7\u55e3\uff1a<br><strong>\u30d1\u30e9\u30b8\u30a6\u30e0\u89e6\u5a92\u306e\u3088\u308b\u82b3\u9999\u65cf\u5316\u5408\u7269\u3068\u30a2\u30af\u30ea\u30eb\u30a2\u30df\u30c9\u306e\u9178\u5316\u7684\u30ab\u30c3\u30d7\u30ea\u30f3\u30b0\u53cd\u5fdc,<\/strong><br>\u7b2c\uff13\uff18\u56de\u6709\u6a5f\u53cd\u5fdc\u61c7\u8ac7\u4f1a\uff0c\u5927\u962a\u5e9c\u7acb\u5927\u5b66 P-15 (2011.8.3).<\/li>\n\n\n\n<li>\u6c34\u7530\u5eb8\u5e73<sup>D<\/sup>\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u6e05\u6c34\u6d0b\u4f51<sup>D<\/sup>\uff0c\u77f3\u4e95\u5eb7\u656c\uff1a<br><strong>\u30d1\u30e9\u30b8\u30a6\u30e0\u3001\u30e2\u30ea\u30d6\u30c9\u30d0\u30ca\u30c9\u30ea\u30f3\u9178\u89e6\u5a92\u7cfb\u306b\u3088\u308b\u30a2\u30df\u30ce\u30d9\u30f3\u30bc\u30f3\u3068\u30aa\u30ec\u30d5\u30a3\u30f3\u306e\u30c0\u30a4\u30ec\u30af\u30c8\u30ab\u30c3\u30d7\u30ea\u30f3\u30b0\u53cd\u5fdc,<\/strong><br>\u7b2c\uff13\uff18\u56de\u6709\u6a5f\u53cd\u5fdc\u61c7\u8ac7\u4f1a\uff0c\u5927\u962a\u5e9c\u7acb\u5927\u5b66 P-18 (2011.8.3).<\/li>\n\n\n\n<li>\u78ef\u6751\u512a\u4ec1<sup>D<\/sup>\uff0c\u5175\u4e39\u77f3\u6075<sup>D<\/sup>\uff0c\u6210\u5cf6\u9686(\u5317\u6d77\u9053\u5927)\uff0c\u5ddd\ufa11\u82f1\u4e5f\uff0c\u7c73\u6fa4\u5fb9\uff08\u5317\u6d77\u9053\u5927\uff09\uff0c\u5927\u6d1e\u5eb7\u55e3\uff1a<br><strong>Cu\u304a\u3088\u3073Pd\u5fae\u7c92\u5b50\u3092\u7528\u3044\u305f\u30af\u30ed\u30b9\u30ab\u30c3\u30d7\u30ea\u30f3\u30b0\u53cd\u5fdc,<\/strong><br>\u7b2c\uff13\uff18\u56de\u6709\u6a5f\u53cd\u5fdc\u61c7\u8ac7\u4f1a\uff0c\u5927\u962a\u5e9c\u7acb\u5927\u5b66 P-21 (2011.8.3).<\/li>\n\n\n\n<li>\u5c3e\u5d0e\u8aa0<sup>D<\/sup>\uff0c\u4f50\u85e4\u9756<sup>D<\/sup>\uff0c\u591a\u7530\u88d5\u4eae<sup>D<\/sup>\uff0c\u897f\u91ce\u6f64\u4e00<sup>D<\/sup>\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c\uff1a<br><strong>\u65b0\u898f\u9ad8\u6d3b\u6027\u30cb\u30aa\u30d6\u7a2e\u306e\u8abf\u88fd\u3068\u305d\u308c\u3092\u7528\u3044\u305f\u89e6\u5a92\u53cd\u5fdc\u3078\u306e\u5229\u7528,<\/strong><br>\u7b2c\uff13\uff18\u56de\u6709\u6a5f\u53cd\u5fdc\u61c7\u8ac7\u4f1a\uff0c\u5927\u962a\u5e9c\u7acb\u5927\u5b66 P-25 (2011.8.3).<\/li>\n\n\n\n<li>\u83ca\u672c\u7fd4\u592a<sup>D<\/sup>\uff0c\u6fa4\u53e3\u62d3\u77e2<sup>D<\/sup>\uff0c\u4e95\u5185\u6d0b\u4ecb<sup>D<\/sup>\uff0c\u5927\u6d1e\u5eb7\u55e3\uff1a<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u932f\u4f53\u89e6\u5a92\u306b\u3088\u308b\u30a2\u30eb\u30b3\u30fc\u30eb\u3092\u7528\u3044\u305f\u30a2\u30bb\u30c8\u30a2\u30df\u30c9\u306e\u03b1-\u30a2\u30eb\u30ad\u30eb\u5316\u53cd\u5fdc,<\/strong><br>\u7b2c\uff13\uff18\u56de\u6709\u6a5f\u53cd\u5fdc\u61c7\u8ac7\u4f1a\uff0c\u5927\u962a\u5e9c\u7acb\u5927\u5b66 P-27 (2011.8.3).<\/li>\n\n\n\n<li>\u4e2d\u4e95\u4fca\u5fd7<sup>D<\/sup>\uff0c\u6e05\u6c34\u6d0b\u4f51<sup>D<\/sup>\uff0c\u5927\u6d1e\u5eb7\u55e3\uff1a<br><strong>\u30d1\u30e9\u30b8\u30a6\u30e0\u89e6\u5a92\u306b\u3088\u308b\u5358\u7d14\u30a2\u30eb\u30b1\u30f3\u304b\u3089\u306e\u30a2\u30ea\u30eb\u30b7\u30e9\u30f3\u306e\u5408\u6210,<\/strong><br>\u7b2c\uff13\uff18\u56de\u6709\u6a5f\u53cd\u5fdc\u61c7\u8ac7\u4f1a\uff0c\u5927\u962a\u5e9c\u7acb\u5927\u5b66 P-30 (2011.8.3).<\/li>\n\n\n\n<li>\u4e2d\u6751\u4e00\u88d5<sup>D<\/sup>\uff0c\u7551\u4e2d\u614e\u592a\u90ce<sup>D<\/sup>\uff0c\u5927\u6d1e\u5eb7\u55e3\uff1a<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u932f\u4f53\u89e6\u5a92\u306b\u3088\u308b\u30a2\u30eb\u30b3\u30fc\u30eb\u3068\u30a8\u30ce\u30f3\u3092\u7528\u3044\u305f1,3-\u30b8\u30b1\u30c8\u30f3\u306e\u5408\u6210,<\/strong><br>\u7b2c\uff13\uff18\u56de\u6709\u6a5f\u53cd\u5fdc\u61c7\u8ac7\u4f1a\uff0c\u5927\u962a\u5e9c\u7acb\u5927\u5b66 P-34 (2011.8.3).<\/li>\n\n\n\n<li>\u65b0\u5c45\u502b\u6210<sup>D<\/sup>\uff0c\u5927\u6d1e\u5eb7\u55e3:<br><strong>\u30d1\u30e9\u30b8\u30a6\u30e0\u89e6\u5a92\u3092\u7528\u3044\u305f\u5185\u90e8\u30a2\u30eb\u30ad\u30f3\u3001\u9178\u5869\u5316\u7269\u304a\u3088\u3073\u30b8\u30b7\u30e9\u30f3\u3068\u306e\u53cd\u5fdc\u306b\u3088\u308b\u30b7\u30af\u30ed\u30da\u30f3\u30c6\u30ce\u30f3\u8a98\u5c0e\u4f53\u306e\u5408\u6210,<\/strong><br>\u7b2c58\u56de\u6709\u6a5f\u91d1\u5c5e\u5316\u5b66\u8a0e\u8ad6\u4f1a\uff0c\u540d\u53e4\u5c4b\u5927\u5b66\uff0cP3A-19 (2011.9.9).<\/li>\n\n\n\n<li>\u4e2d\u4e95\u4fca\u5fd7<sup>D<\/sup>\uff0c\u6e05\u6c34\u6d0b\u4f51<sup>D<\/sup>\uff0c\u5927\u6d1e\u5eb7\u55e3:<br><strong>\u30d1\u30e9\u30b8\u30a6\u30e0\u89e6\u5a92\u3092\u7528\u3044\u305f\u5358\u7d14\u30a2\u30eb\u30b1\u30f3\u3068\u30b8\u30b7\u30e9\u30f3\u3068\u306e\u9178\u5316\u7684\u30ab\u30c3\u30d7\u30ea\u30f3\u30b0\u53cd\u5fdc\u306b\u3088\u308b\u30a2\u30ea\u30eb\u30b7\u30e9\u30f3\u306e\u5408\u6210,<\/strong><br>\u7b2c58\u56de\u6709\u6a5f\u91d1\u5c5e\u5316\u5b66\u8a0e\u8ad6\u4f1a\uff0c\u540d\u53e4\u5c4b\u5927\u5b66\uff0cP3A-20 (2011.9.9).<\/li>\n\n\n\n<li>\u78ef\u6751\u512a\u4ec1<sup>D<\/sup>, \u5175\u4e39\u77f3\u6075<sup>D<\/sup>,\u6210\u5cf6\u9686(\u5317\u6d77\u9053\u5927)\uff0c \u5ddd\u5d0e\u82f1\u4e5f, \u7c73\u6fa4\u5fb9\uff08\u5317\u6d77\u9053\u5927\uff09, \u5927\u6d1e\u5eb7\u55e3:<br><strong>\u9077\u79fb\u91d1\u5c5e\u30ca\u30ce\u30af\u30e9\u30b9\u30bf\u30fc\u306e\u5408\u6210\u306a\u3089\u3073\u306b\u305d\u306e\u89e6\u5a92\u4f5c\u7528,<\/strong><br>\u7b2c58\u56de\u6709\u6a5f\u91d1\u5c5e\u5316\u5b66\u8a0e\u8ad6\u4f1a\uff0c\u540d\u53e4\u5c4b\u5927\u5b66\uff0cP3B-08 (2011.9.9).<\/li>\n\n\n\n<li>\u4e2d\u6751\u4e00\u88d5<sup>D<\/sup>\uff0c\u7551\u4e2d\u614e\u592a\u90ce<sup>D<\/sup>\uff0c\u5927\u6d1e\u5eb7\u55e3\uff1a<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u932f\u4f53\u3092\u89e6\u5a92\u3068\u3059\u308b\u30a2\u30eb\u30b3\u30fc\u30eb\u3068\u30a8\u30ce\u30f3\u3068\u306e\u30ab\u30c3\u30d7\u30ea\u30f3\u30b0\u53cd\u5fdc,<\/strong><br>\u7b2c108\u56de\u89e6\u5a92\u8a0e\u8ad6\u4f1a\uff0c\u5317\u898b\u5de5\u696d\u5927\u5b66\uff0c1H04 (2011.9.20).<\/li>\n\n\n\n<li>\u539f\u7530\u8056\u4e00\u6717<sup>D<\/sup>\uff0c\u5927\u6d1e\u5eb7\u55e3:<br><strong>\u30d1\u30e9\u30b8\u30a6\u30e0\u89e6\u5a92\u3092\u7528\u3044\u305f\u30d9\u30f3\u30bc\u30f3\u985e\u3068\u6d3b\u6027\u30aa\u30ec\u30d5\u30a3\u30f3\u306e\u9178\u5316\u7684\u30ab\u30c3\u30d7\u30ea\u30f3\u30b0\u53cd\u5fdc,<\/strong><br>\u7b2c108\u56de\u89e6\u5a92\u8a0e\u8ad6\u4f1a\uff0c\u5317\u898b\u5de5\u696d\u5927\u5b66\uff0c1H09 (2011.9.20).<\/li>\n\n\n\n<li>\u4f50\u85e4\u9756<sup>\uff24<\/sup>\uff0c\u5927\u6d1e\u5eb7\u55e3:<br><strong>\u30d2\u30c9\u30ed\u30b7\u30e9\u30f3\u5316\u5408\u7269\u3092\u9084\u5143\u5264\u3068\u3057\u3066\u7528\u3044\u305f\u65b0\u898f\u6d3b\u6027\u5316Nb\u306e\u767a\u751f\u6cd5\u306a\u3089\u3073\u306b\u9ad8\u9078\u629e\u7684\u89e6\u5a92\u53cd\u5fdc\u306e\u958b\u767a,<\/strong><br>\u7b2c108\u56de\u89e6\u5a92\u8a0e\u8ad6\u4f1a\uff0c\u5317\u898b\u5de5\u696d\u5927\u5b66\uff0c1H20 (2011.9.20).<\/li>\n\n\n\n<li>\u5927\u6d1e\u5eb7\u55e3\uff1a<br><strong>\u932f\u4f53\u306e\u89e6\u5a92\u4f5c\u7528-\u9077\u79fb\u91d1\u5c5e\u932f\u4f53\u306e\u57fa\u790e\u3068\u6709\u6a5f\u5408\u6210\u53cd\u5fdc\u306b\u304a\u3051\u308b\u5229\u7528\uff0c<\/strong><br>\u8fd1\u757f\u79d1\u5b66\u5354\u4f1a\u89e6\u5a92\u30fb\u8868\u9762\u90e8\u4f1a\u3000\u5e73\u6210\uff12\uff13\u5e74\u5ea6\u5165\u9580\u89e6\u5a92\u79d1\u5b66\u30bb\u30df\u30ca\u30fc\uff0c\u5927\u962a\u79d1\u5b66\u6280\u8853\u30bb\u30f3\u30bf\u30fc (2011.10.28)(\u4f9d\u983c\u8b1b\u6f14).<\/li>\n\n\n\n<li>\u6fa4\u53e3\u62d3\u77e2<sup>D<\/sup>\uff0c\u5927\u6d1e\u5eb7\u55e3\uff1a<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u932f\u4f53\u89e6\u5a92\u306b\u3088\u308b\u30a2\u30eb\u30b3\u30fc\u30eb\u304a\u3088\u3073\u30b8\u30aa\u30fc\u30eb\u3092\u30a2\u30eb\u30ad\u30eb\u5316\u5264\u3068\u3057\u3066\u7528\u3044\u305f\u30a2\u30bb\u30c8\u30cb\u30c8\u30ea\u30eb\u306e\u03b1-\u30a2\u30eb\u30ad\u30eb\u5316\u53cd\u5fdc,<\/strong><br>\u7b2c\uff11\u56de\uff23\uff33\uff2a\u5316\u5b66\u30d5\u30a7\u30b9\u30bf\uff0c\u65e9\u7a32\u7530\u5927\u5b66\uff0c P6-23 (2011.11.15).<\/li>\n\n\n\n<li>\u6c34\u7530\u5eb8\u5e73<sup>D<\/sup>\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u6e05\u6c34\u6d0b\u4f51<sup>D<\/sup>\uff0c\u77f3\u4e95\u5eb7\u656c:&lt;<br><strong>\u30d1\u30e9\u30b8\u30a6\u30e0\u89e6\u5a92\u306b\u3088\u308b\u30a2\u30df\u30ce\u30d9\u30f3\u30bc\u30f3\u3068\u30aa\u30ec\u30d5\u30a3\u30f3\u3068\u306e\u30d1\u30e9\u9078\u629e\u7684\u9178\u5316\u7684C-H\u30aa\u30ec\u30d5\u30a3\u30f3\u5316\u53cd\u5fdc,&nbsp;<\/strong>\u7b2c\uff11\u56de\uff23\uff33\uff2a\u5316\u5b66\u30d5\u30a7\u30b9\u30bf\uff0c\u65e9\u7a32\u7530\u5927\u5b66\uff0c P6-30 (2011.11.15).<\/li>\n\n\n\n<li>\u65b0\u5c45\u502b\u6210D\uff0c\u5927\u6d1e\u5eb7\u55e3:<br><strong>\u30d1\u30e9\u30b8\u30a6\u30e0\u89e6\u5a92\u3092\u7528\u3044\u305f\uff0c\u9178\u5869\u5316\u7269\uff0c\u30a2\u30eb\u30ad\u30f3\u306a\u3089\u3073\u306b\u30b8\u30b7\u30e9\u30f3\u306b\u3088\u308b\u30b7\u30af\u30ed\u30da\u30f3\u30c6\u30ce\u30f3\u8a98\u5c0e\u4f53\u306e\u5408\u6210,<\/strong><br>\u77f3\u6cb9\u5b66\u4f1a\u95a2\u897f\u652f\u90e8\u7b2c20\u56de\u7814\u7a76\u767a\u8868\u4f1a\u65e5\u672c\u30a8\u30cd\u30eb\u30ae\u30fc\u5b66\u4f1a\u95a2\u897f\u652f\u90e8\u7b2c56\u56de\u5408\u540c\u7814\u7a76\u767a\u8868\u4f1a\uff0c\u4eac\u90fd\u6559\u80b2\u6587\u5316\u30bb\u30f3\u30bf\u30fc\uff0c\uff12 (2011.12.2).<\/li>\n\n\n\n<li>\u6fa4\u53e3\u62d3\u77e2<sup>D<\/sup>\uff0c\u5927\u6d1e\u5eb7\u55e3\uff1a<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u932f\u4f53\u89e6\u5a92\u306b\u3088\u308b\u30a2\u30bb\u30c8\u30cb\u30c8\u30ea\u30eb\u53ca\u3073\u30a2\u30eb\u30b3\u30fc\u30eb\u3092\u7528\u3044\u305f\u6c34\u7d20\u79fb\u52d5\u578b\u53cd\u5fdc,<\/strong><br>\u77f3\u6cb9\u5b66\u4f1a\u95a2\u897f\u652f\u90e8\u7b2c20\u56de\u7814\u7a76\u767a\u8868\u4f1a\u65e5\u672c\u30a8\u30cd\u30eb\u30ae\u30fc\u5b66\u4f1a\u95a2\u897f\u652f\u90e8\u7b2c56\u56de\u5408\u540c\u7814\u7a76\u767a\u8868\u4f1a\uff0c\u4eac\u90fd\u6559\u80b2\u6587\u5316\u30bb\u30f3\u30bf\u30fc\uff0cP05 (2011.12.2).<\/li>\n\n\n\n<li>\u77f3\u6a4b\u512a<sup>D<\/sup>\uff0c\u963f\u6b66\u7531\u52a0<sup>D<\/sup>\uff0c\u677e\u6d66\u8c4a\u7f8e<sup>D<\/sup>\uff0c\u4e2d\u5ddd\u4e9c\u7d00\u5b50<sup>B<\/sup>\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c\uff1a<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u89e6\u5a92\u3092\u7528\u3044\u305f\u30a2\u30eb\u30b3\u30fc\u30eb\u304b\u3089\u306e\u591a\u5206\u5c90\u30dd\u30ea\u30aa\u30fc\u30eb\u306e\u5408\u6210\uff0c<\/strong><br>\u77f3\u6cb9\u5b66\u4f1a\u95a2\u897f\u652f\u90e8\u7b2c20\u56de\u7814\u7a76\u767a\u8868\u4f1a\u65e5\u672c\u30a8\u30cd\u30eb\u30ae\u30fc\u5b66\u4f1a\u95a2\u897f\u652f\u90e8\u7b2c56\u56de\u5408\u540c\u7814\u7a76\u767a\u8868\u4f1a\uff0c\u4eac\u90fd\u6559\u80b2\u6587\u5316\u30bb\u30f3\u30bf\u30fc\uff0cP06 (2011.12.2).<\/li>\n\n\n\n<li>\u77e2\u91ce\u656c\u898f<sup>B<\/sup>\uff0c\u5ddd\ufa11\u82f1\u4e5f\uff0c\u5927\u6d1e\u5eb7\u55e3\uff1a<br><strong>\u9077\u79fb\u91d1\u5c5e\u30ca\u30ce\u30af\u30e9\u30b9\u30bf-\u3092\u7528\u3044\u305f\u89e6\u5a92\u53cd\u5fdc\uff0c<\/strong><br>\u7b2c\uff19\uff12\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a\uff0c\u6176\u5fdc\u7fa9\u587e\u5927\u5b66\uff0c1K8-43\uff082012.3.25).<\/li>\n\n\n\n<li>\u4e2d\u6751\u4e00\u88d5<sup>D<\/sup>\uff0c\u7551\u4e2d\u614e\u592a\u90ce<sup>D<\/sup>\uff0c\u5927\u6d1e\u5eb7\u55e3\uff1a<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u932f\u4f53\u89e6\u5a92\u3092\u7528\u3044\u305f\u30a2\u30eb\u30b3\u30fc\u30eb\u3068\u30a8\u30ce\u30f3\u3068\u306e\u53cd\u5fdc\u306b\u3088\u308b1,3-\u30b8\u30b1\u30c8\u30f3\u306e\u5408\u6210,<\/strong><br>\u7b2c\uff19\uff12\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a\uff0c\u6176\u5fdc\u7fa9\u587e\u5927\u5b66\uff0c1L1-01\uff082012.3.25).<\/li>\n\n\n\n<li>\u5317\u6751\u6d69\u58eb<sup>B<\/sup>\uff0c\u5ddd\ufa11\u82f1\u4e5f\uff0c\u5927\u6d1e\u5eb7\u55e3\uff1a<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u30ca\u30ce\u30af\u30e9\u30b9\u30bf-\u89e6\u5a92\u3092\u7528\u3044\u305f\u7b2c\u4e00\u7d1a\u30a2\u30eb\u30b3\u30fc\u30eb\u306eGuerbet\u53cd\u5fdc,<\/strong><br>\u7b2c\uff19\uff12\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a\uff0c\u6176\u5fdc\u7fa9\u587e\u5927\u5b66\uff0c1L1-02\uff082012.3.25).<\/li>\n\n\n\n<li>\u5c0f\u5ddd\u771f\u53f8<sup>B<\/sup>\uff0c\u5c71\u672c\u4fe1\u884c<sup>D<\/sup>\uff0c\u5927\u6d1e\u5eb7\u55e3\uff1a<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u89e6\u5a92\u306b\u3088\u308b\u30e1\u30c1\u30eb\u30ad\u30ce\u30ea\u30f3\u306e\u30a2\u30eb\u30b3\u30fc\u30eb\u3092\u7528\u3044\u305f\u03b1\u30a2\u30eb\u30ad\u30eb\u5316\u53cd\u5fdc,<\/strong><br>\u7b2c\uff19\uff12\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a\uff0c\u6176\u5fdc\u7fa9\u587e\u5927\u5b66\uff0c1L1-03\uff082012.3.25).<\/li>\n\n\n\n<li>\u6e9d\u8fba\u53cb\u6643<sup>B<\/sup>\uff0c\u671d\u6bd4\u5948\u7ae0<sup>B<\/sup>\uff0c\u5927\u6d1e\u5eb7\u55e3\uff1a<br><strong>\u30d1\u30e9\u30b8\u30a6\u30e0\u932f\u4f53\u89e6\u5a92\u306b\u3088\u308b\u30d9\u30f3\u30be\u30d5\u30e9\u30f3\u8a98\u5c0e\u4f53\u3068\u5358\u7d14\u30a2\u30eb\u30b1\u30f3\u306e\u9178\u5316\u7684\u30ab\u30c3\u30d7\u30ea\u30f3\u30b0\u53cd\u5fdc,<\/strong><br>\u7b2c\uff19\uff12\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a\uff0c\u6176\u5fdc\u7fa9\u587e\u5927\u5b66\uff0c2K8-33\uff082012.3.26).<\/li>\n\n\n\n<li>\u5b89\u7530\u99a8<sup>B<\/sup>\uff0c\u4f50\u85e4\u9756<sup>D<\/sup>\uff0c\u5927\u6d1e\u5eb7\u55e3\uff1a<br><strong>NbCl<sub>5<\/sub>\u3092\u7528\u3044\u305f\u30a2\u30eb\u30ad\u30f3\u3068\u30cb\u30c8\u30ea\u30eb\u304b\u3089\u306e\u30d4\u30ea\u30df\u30b8\u30f3\u8a98\u5c0e\u4f53\u5408\u6210,<\/strong><br>\u7b2c\uff19\uff12\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a\uff0c\u6176\u5fdc\u7fa9\u587e\u5927\u5b66\uff0c2L2-43\uff082012.3.26).<\/li>\n\n\n\n<li>\u4f50\u85e4\u9756<sup>\uff24<\/sup>\uff0c\u5927\u6d1e\u5eb7\u55e3:<br><strong>\u4f4e\u539f\u5b50\u4fa1\u30cb\u30aa\u30d6\u89e6\u5a92\u3092\u7528\u3044\u305f\u30a2\u30eb\u30ad\u30f3\u3068\u30aa\u30ec\u30d5\u30a3\u30f3\u3068\u306e[2+2+2]\u74b0\u5316\u4ed8\u52a0\u53cd\u5fdc\u306b\u3088\u308b\u9ad8\u9078\u629e\u76841,3-\u30b7\u30af\u30ed\u30d8\u30ad\u30b5\u30b8\u30a8\u30f3\u8a98\u5c0e\u4f53\u306e\u5408\u6210\uff0c<\/strong><br>\u7b2c\uff19\uff12\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a\uff0c\u6176\u5fdc\u7fa9\u587e\u5927\u5b66\uff0c2L2-44\uff082012.3.26).<\/li>\n\n\n\n<li>\u78ef\u6751\u512a\u4ec1<sup>D<\/sup>, \u5175\u4e39\u77f3\u6075<sup>D<\/sup>,\u6210\u5cf6\u9686(\u5317\u6d77\u9053\u5927)\uff0c \u7c73\u6fa4\u5fb9\uff08\u5317\u6d77\u9053\u5927\uff09, \u5ddd\u5d0e\u82f1\u4e5f, \u5927\u6d1e\u5eb7\u55e3:<br><strong>\u4fdd\u8b77\u5264\u30d5\u30ea\u30fc\u9285\u30ca\u30ce\u7c92\u5b50\u306e\u5408\u6210\u306a\u3089\u3073\u306b\u9ad8\u6d3b\u6027Ullmann\u53cd\u5fdc\u89e6\u5a92\u3068\u3057\u3066\u306e\u5229\u7528\uff0c<\/strong><br>\u7b2c\uff19\uff12\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a\uff0c\u6176\u5fdc\u7fa9\u587e\u5927\u5b66\uff0c3PA-092\uff082012.3.27).<\/li>\n\n\n\n<li>\u83ca\u672c\u7fd4\u592a<sup>D<\/sup>\uff0c\u4e95\u5185\u6d0b\u4ecb<sup>D<\/sup>\uff0c\u5927\u6d1e\u5eb7\u55e3\uff1a<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u89e6\u5a92\u306b\u3088\u308b\u30a2\u30eb\u30b3\u30fc\u30eb\u3092\u7528\u3044\u305f\u30a2\u30bb\u30c8\u30a2\u30df\u30c9\u306e\u03b1-\u30a2\u30eb\u30ad\u30eb\u5316\u53cd\u5fdc,<\/strong><br>\u7b2c\uff19\uff12\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a\uff0c\u6176\u5fdc\u7fa9\u587e\u5927\u5b66\uff0c3PA-095\uff082012.3.27).<\/li>\n\n\n\n<li>\u5c3e\u5d0e\u8aa0<sup>D<\/sup>\uff0c\u591a\u7530\u88d5\u4eae<sup>D<\/sup>\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c\uff1a<br><strong>\u30da\u30f3\u30bf\u30a2\u30eb\u30b3\u30ad\u30b7\u30cb\u30aa\u30d6\u304b\u3089\u306e\u4f4e\u539f\u5b50\u4fa1\u30cb\u30aa\u30d6\u7a2e\u306e\u8abf\u88fd\u3068\u6709\u6a5f\u5909\u63db\u53cd\u5fdc\u3078\u306e\u5229\u7528,<\/strong><br>\u7b2c\uff19\uff12\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a\uff0c\u6176\u5fdc\u7fa9\u587e\u5927\u5b66\uff0c3PA-101\uff082012.3.27).<\/li>\n\n\n\n<li>\u4e2d\u4e95\u4fca\u5fd7<sup>D<\/sup>\uff0c\u6e05\u6c34\u6d0b\u4f51<sup>D<\/sup>\uff0c\u5927\u6d1e\u5eb7\u55e3\uff1a<br><strong>\u30d1\u30e9\u30b8\u30a6\u30e0\u89e6\u5a92\u3092\u7528\u3044\u305f\u30b8\u30b7\u30e9\u30f3\u3068\u5358\u7d14\u30a2\u30eb\u30b1\u30f3\u3068\u306e\u9178\u5316\u7684\u30ab\u30c3\u30d7\u30ea\u30f3\u30b0\u53cd\u5fdc\u306b\u3088\u308b\u30a2\u30ea\u30eb\u30b7\u30e9\u30f3\u306e\u5408\u6210,<\/strong><br>\u7b2c\uff19\uff12\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a\uff0c\u6176\u5fdc\u7fa9\u587e\u5927\u5b66\uff0c4K8-18\uff082012.3.28).<\/li>\n<\/ol>\n\n\n\n<div style=\"height:20px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<p class=\"has-text-align-right\"><mark style=\"color:#89a06c\" class=\"has-inline-color\">\u25b2<\/mark> <a href=\"#top\">\u30da\u30fc\u30b8\u306eTOP\u3078<\/a><\/p>\n\n\n\n<div style=\"height:40px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"2010\">2010\u5e74<\/h3>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>\u5b66\u8853\u8ad6\u6587<\/strong><\/h4>\n\n\n\n<ol class=\"wp-block-list\">\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1039\/C0OB00176G\" target=\"_blank\">Y. Obora,* Y. Okabe, Y. Ishii*<br><strong>Direct Oxidative Coupling of Benzenes with Acrylonitriles to Cinnamonitriles Catalyzed by Pd(OAc)2\/HPMoV\/O2&nbsp;System<\/strong><br><em>Org. Biomol. Chem.&nbsp;<\/em>8 (18), 4071-4073 (2010.9).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"523\" height=\"125\" class=\"wp-image-278\" style=\"width: 500px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Direct-oxidative-coupling-of-benzenes-with-acrylonitriles-to-cinnamonitriles-catalyzed-by.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Direct-oxidative-coupling-of-benzenes-with-acrylonitriles-to-cinnamonitriles-catalyzed-by.jpg 523w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Direct-oxidative-coupling-of-benzenes-with-acrylonitriles-to-cinnamonitriles-catalyzed-by-300x72.jpg 300w\" sizes=\"auto, (max-width: 523px) 100vw, 523px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1021\/jo101229u\" target=\"_blank\">Y. Obora,* Y. Satoh, Y. Ishii*<br><strong>NbCl3-Catalyzed Intermolecular [2+2+2] Cycloaddition of Alkynes and \u03b1,\u03c9-Dienes: Highly Chemo- and Regioselective Formation of 5-\u03c9-Alkenyl-1,4-substituted-1,3-cyclohexadiene Derivatives<\/strong><br><em>J. Org. Chem.&nbsp;<\/em>75 (17) 6046-6049 (2010.9).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"529\" height=\"251\" class=\"wp-image-281\" style=\"width: 400px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/NbCl3-Catalyzed-Intermolecular-222-Cycloaddition-of-Alkynes-and-\u03b1\u03c9-Dienes-Highly-Chemo-and-Regioselective-Formation-of-5-\u03c9-Alkenyl-14-substituted-13-cyclohexadiene-Derivatives.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/NbCl3-Catalyzed-Intermolecular-222-Cycloaddition-of-Alkynes-and-\u03b1\u03c9-Dienes-Highly-Chemo-and-Regioselective-Formation-of-5-\u03c9-Alkenyl-14-substituted-13-cyclohexadiene-Derivatives.jpg 529w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/NbCl3-Catalyzed-Intermolecular-222-Cycloaddition-of-Alkynes-and-\u03b1\u03c9-Dienes-Highly-Chemo-and-Regioselective-Formation-of-5-\u03c9-Alkenyl-14-substituted-13-cyclohexadiene-Derivatives-300x142.jpg 300w\" sizes=\"auto, (max-width: 529px) 100vw, 529px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1055\/s-0030-1259094\" target=\"_blank\">Y. Obora,* Y. Ishii*<br><strong>Iridium-Catalyzed Reactions Involving Transfer Hydrogenation, Additon, N-Heterocyclization, and Alkylation Using Alcohols and Diols as Key Substrates<\/strong><br><em>Synlett.&nbsp;<\/em>(1), 30-51 (2011.1).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"504\" height=\"113\" class=\"wp-image-280\" style=\"width: 460px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-Catalyzed-Reactions-Involving-Transfer-Hydrogenation-Addition-N-Heterocyclization-and-Alkylation-Using-Alcohols-and-Diols-as-Key-Substrates.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-Catalyzed-Reactions-Involving-Transfer-Hydrogenation-Addition-N-Heterocyclization-and-Alkylation-Using-Alcohols-and-Diols-as-Key-Substrates.jpg 504w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-Catalyzed-Reactions-Involving-Transfer-Hydrogenation-Addition-N-Heterocyclization-and-Alkylation-Using-Alcohols-and-Diols-as-Key-Substrates-300x67.jpg 300w\" sizes=\"auto, (max-width: 504px) 100vw, 504px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1055\/s-0030-1259681\" target=\"_blank\">N. Horikawa, Y. Obora,* Y. Ishii*<br><strong>Selective Synthesis of 2-Aryl-2<em>H<\/em>&#8211; and 4-Aryl-4-<em>H<\/em>-3,5-Diformylpyrans from Acetal with Aromatic Aldehydes Catalyzed by Lewis Acids<\/strong><br><em>Synlett.&nbsp;<\/em>(6), 857-861 (2011.2).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"413\" height=\"227\" class=\"wp-image-283\" style=\"width: 400px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Selective-Synthesis-of-2-Aryl-2H-and-4-Aryl-4H-35-diformylpyrans-from-Acetal-with-Aromatic-Aldehydes-Catalyzed-by-Lewis-Acids.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Selective-Synthesis-of-2-Aryl-2H-and-4-Aryl-4H-35-diformylpyrans-from-Acetal-with-Aromatic-Aldehydes-Catalyzed-by-Lewis-Acids.jpg 413w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Selective-Synthesis-of-2-Aryl-2H-and-4-Aryl-4H-35-diformylpyrans-from-Acetal-with-Aromatic-Aldehydes-Catalyzed-by-Lewis-Acids-300x165.jpg 300w\" sizes=\"auto, (max-width: 413px) 100vw, 413px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1021\/jo2003264\" target=\"_blank\">N. Yamamoto, Y. Obora,* Y. Ishii*<br><strong>Iridium-Catalyzed Oxidative Methyl Esterification of Primary Alcohols and Diols with Methanol<\/strong><br><em>J. Org. Chem.&nbsp;<\/em>76(8), 2937-2941 (2011.3).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"531\" height=\"126\" class=\"wp-image-279\" style=\"width: 400px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-Catalyzed-Oxidative-Methyl-Esterification-of-Primary-Alcohols-and-Diols-with-Methanol.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-Catalyzed-Oxidative-Methyl-Esterification-of-Primary-Alcohols-and-Diols-with-Methanol.jpg 531w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-Catalyzed-Oxidative-Methyl-Esterification-of-Primary-Alcohols-and-Diols-with-Methanol-300x71.jpg 300w\" sizes=\"auto, (max-width: 531px) 100vw, 531px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1039\/C1CC11487E\" target=\"_blank\">M. Hyotanishi, Y. Isomura, H. Yamamoto, H. Kawasaki, Y. Obora*<br><strong>Surfactant-free Synthesis of Palladium Nanoclusters for Their Use in Catalytic Cross-Coupling Reactions<\/strong><br><em>Chem. Commun.<\/em>, 47 (20), 5750-5752 (2011.4).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"519\" height=\"187\" class=\"wp-image-284\" style=\"width: 400px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Surfactant-free-synthesis-of-palladium-nanoclusters-for-their-use-in-catalytic-cross-coupling-reactions.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Surfactant-free-synthesis-of-palladium-nanoclusters-for-their-use-in-catalytic-cross-coupling-reactions.jpg 519w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Surfactant-free-synthesis-of-palladium-nanoclusters-for-their-use-in-catalytic-cross-coupling-reactions-300x108.jpg 300w\" sizes=\"auto, (max-width: 519px) 100vw, 519px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1021\/ol200662e\" target=\"_blank\">Y. Satoh, Y. Obora*<br><strong>NbCl3-Catalyzed Three-Component [2+2+2] Cycloaddition Reaction of Terminal Alkynes, Internal Alkynes, and Alkenes to 1,3,4,5-Tetrasubstituted 1,3-Cyclohexadienes<\/strong><br><em>Org. Lett.<\/em>&nbsp;13 (10), 2568-2571 (2011.4).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"533\" height=\"150\" class=\"wp-image-282\" style=\"width: 400px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/NbCl3-Catalyzed-Three-Component-2-2-2-Cycloaddition-Reaction-of-Terminal-Alkynes-Internal-Alkynes-and-Alkenes-to-1345-Tetrasubstituted-13-Cyclohexadienes.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/NbCl3-Catalyzed-Three-Component-2-2-2-Cycloaddition-Reaction-of-Terminal-Alkynes-Internal-Alkynes-and-Alkenes-to-1345-Tetrasubstituted-13-Cyclohexadienes.jpg 533w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/NbCl3-Catalyzed-Three-Component-2-2-2-Cycloaddition-Reaction-of-Terminal-Alkynes-Internal-Alkynes-and-Alkenes-to-1345-Tetrasubstituted-13-Cyclohexadienes-300x84.jpg 300w\" sizes=\"auto, (max-width: 533px) 100vw, 533px\" \/><\/li>\n<\/ol>\n\n\n\n<div style=\"height:30px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>\u7279\u8a31\u51fa\u9858<\/strong><\/h4>\n\n\n\n<ol class=\"wp-block-list\">\n<li>\u5927\u6d1e\u5eb7\u55e3\uff0c\u4f50\u85e4\u9756<br><strong>\u4f4e\u539f\u5b50\u4fa1\u524d\u5468\u671f\u91d1\u5c5e\u5316\u5408\u7269\u3092\u7528\u3044\u305f\u30a2\u30eb\u30ad\u30f3\u3068\u30a2\u30eb\u30b1\u30f3\u304b\u3089\u306e\u30b7\u30af\u30ed\u30d8\u30ad\u30b5\u30b8\u30a8\u30f3\u985e\u306e\u88fd\u9020\u65b9\u6cd5<br><\/strong>\uff08\u51fa\u9858\u4eba\uff1a\u5b66\u6821\u6cd5\u4eba\u95a2\u897f\u5927\u5b66\uff09<br>\u7279\u98582010-114257 (2010.5.18).<\/li>\n\n\n\n<li>\u5927\u6d1e\u5eb7\u55e3\uff0c\u5ddd\u5d0e\u82f1\u4e5f\uff0c\u5175\u4e39\u77f3\u6075\uff0c\u5c71\u672c\u5bdb\u5b50<br><strong>\u9077\u79fb\u91d1\u5c5e\u8d85\u5fae\u7c92\u5b50\u304b\u3089\u306a\u308b\u30af\u30ed\u30b9\u30ab\u30c3\u30d7\u30ea\u30f3\u30b0\u7528\u89e6\u5a92\u304a\u3088\u3073\u305d\u308c\u3092\u7528\u3044\u305f\u30af\u30ed\u30b9\u30ab\u30c3\u30d7\u30ea\u30f3\u30b0\u6cd5<\/strong><br>\uff08\u51fa\u9858\u4eba\uff1a\u5b66\u6821\u6cd5\u4eba\u95a2\u897f\u5927\u5b66\uff09<br>\u7279\u98582010-139638 (2010.6.18).<\/li>\n\n\n\n<li>\u5927\u6d1e\u5eb7\u55e3\uff0c\u4e2d\u4e95\u4fca\u5fd7<br><strong>\u30a2\u30ea\u30eb\u30b7\u30e9\u30f3\u985e\u306e\u88fd\u9020\u65b9\u6cd5<\/strong><br>\uff08\u51fa\u9858\u4eba\uff1a\u5b66\u6821\u6cd5\u4eba\u95a2\u897f\u5927\u5b66\uff09<br>\u7279\u98582011-15146 (2011.1.27).<\/li>\n<\/ol>\n\n\n\n<div style=\"height:30px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>\u5b66\u4f1a\u767a\u8868<\/strong><\/h4>\n\n\n\n<ol class=\"wp-block-list\">\n<li>\u6fa4\u53e3\u62d3\u77e2, \u4e95\u5185\u6d0b\u4ecb\uff0c\u83ca\u672c\u7fd4\u592a\uff0c\u5927\u6d1e\u5eb7\u55e3<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u932f\u4f53\u89e6\u5a92\u3092\u7528\u3044\u305f\u30a2\u30eb\u30b3\u30fc\u30eb\u306b\u3088\u308b\u30a2\u30bb\u30c8\u30cb\u30c8\u30ea\u30eb\u53ca\u3073\u30a2\u30bb\u30c8\u30a2\u30df\u30c9\u306e\u03b1-\u30a2\u30eb\u30ad\u30eb\u5316\u53cd\u5fdc<\/strong><br><em>\u7b2c57\u56de\u6709\u6a5f\u91d1\u5c5e\u5316\u5b66\u8a0e\u8ad6\u4f1a\u8981\u65e8\u96c6<\/em>\uff0c\u4e2d\u592e\u5927\u5b66\uff0cP1A-26 (2010.9.16).<\/li>\n\n\n\n<li>\u5175\u4e39\u77f3\u6075\uff0c\u78ef\u6751\u512a\u4ec1\uff0c\u4e2d\u5cf6\u7531\u4f9d\uff0c\u5c71\u672c\u5bdb\u5b50\uff0c\u5ddd\u5d0e\u82f1\u4e5f\uff0c\u5927\u6d1e\u5eb7\u55e3<br><strong>\u5f8c\u5468\u671f\u9077\u79fb\u91d1\u5c5e\u8d85\u5fae\u7c92\u5b50\u306e\u5408\u6210\u306a\u3089\u3073\u306b\u305d\u306e\u89e6\u5a92\u4f5c\u7528<\/strong><br><em>\u7b2c57\u56de\u6709\u6a5f\u91d1\u5c5e\u5316\u5b66\u8a0e\u8ad6\u4f1a\u8981\u65e8\u96c6<\/em>\uff0c\u4e2d\u592e\u5927\u5b66\uff0cP1B-14 (2010.9.16).<\/li>\n\n\n\n<li>\u4f50\u85e4\u9756, \u5927\u6d1e\u5eb7\u55e3<br><strong>\u4e09\u5869\u5316\u30cb\u30aa\u30d6\u89e6\u5a92\u3092\u7528\u3044\u305f\u672b\u7aef\u30a2\u30eb\u30ad\u30f3\u3068\u5185\u90e8\u30a2\u30eb\u30ad\u30f3\u3068\u30a2\u30eb\u30b1\u30f3\u3068\u306e\u4e09\u6210\u5206[2+2+2]\u74b0\u5316\u4ed8\u52a0\u53cd\u5fdc\u306b\u3088\u308b\u56db\u7f6e\u63db\uff11\uff0c\uff13\uff0d\u30b7\u30af\u30ed\u30d8\u30ad\u30b5\u30b8\u30a8\u30f3\u8a98\u5c0e\u4f53\u306e\u5408\u6210<\/strong><br><em>\u7b2c57\u56de\u6709\u6a5f\u91d1\u5c5e\u5316\u5b66\u8a0e\u8ad6\u4f1a\u8981\u65e8\u96c6<\/em>\uff0c\u4e2d\u592e\u5927\u5b66\uff0cP1B-25 (2009.9.16).<\/li>\n\n\n\n<li>\u963f\u6b66\u7531\u52a0\uff0c\u5ca1\u672c\u7adc\u5e73\uff0c\u677e\u6d66\u8c4a\u7f8e\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u932f\u4f53\u89e6\u5a92\u306b\u3088\u308b\u30a2\u30eb\u30b3\u30fc\u30eb\u304b\u3089\u306e\u30dd\u30ea\u30aa\u30fc\u30eb\u306a\u3089\u3073\u306b\u03b1,\u03c9-\u30b8\u30a2\u30ea\u30fc\u30eb\u30a2\u30eb\u30ab\u30f3\u306e\u5408\u6210<\/strong><br><em>\u7b2c\uff11\uff10\uff16\u56de\u89e6\u5a92\u8a0e\u8ad6\u4f1a<\/em>\uff0c\u5c71\u68a8\u5927\u5b66\uff0c3G18 (2010.9.17).<\/li>\n\n\n\n<li>\u6c34\u7530\u5eb8\u5e73\uff0c\u6e05\u6c34\u6d0b\u4f51\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c<br><strong>\u30d1\u30e9\u30b8\u30a6\u30e0\/\u30e2\u30ea\u30d6\u30c9\u30d0\u30ca\u30c9\u30ea\u30f3\u9178\/\u9178\u7d20\u7cfb\u3092\u7528\u3044\u305f\u30aa\u30ec\u30d5\u30a3\u30f3\u3068\u30a2\u30df\u30ce\u30d9\u30f3\u30bc\u30f3\u985e\u306e\u9178\u5316\u7684\u30ab\u30c3\u30d7\u30ea\u30f3\u30b0\u53cd\u5fdc<\/strong><br><em>\u7b2c\uff11\uff10\uff16\u56de\u89e6\u5a92\u8a0e\u8ad6\u4f1a<\/em>\uff0c\u5c71\u68a8\u5927\u5b66\uff0c3G19 (2010.9.17).<\/li>\n\n\n\n<li>\u5800\u5ddd\u5178\u79c0\u3001\u5927\u6d1e\u5eb7\u55e3\u3001\u77f3\u4e95\u5eb7\u656c<br><strong>\u30eb\u30a4\u30b9\u9178\u89e6\u5a92\u3092\u7528\u3044\u305f\u30a2\u30bb\u30bf\u30fc\u30eb\u3068\u30a2\u30eb\u30c7\u30d2\u30c9\u304b\u3089\u306e2-\u30a2\u30ea\u30fc\u30eb-2<em>H<\/em>-\u53ca\u30734-\u30a2\u30ea\u30fc\u30eb-4<em>H<\/em>-3,5-\u30b8\u30db\u30eb\u30df\u30eb\u30d4\u30e9\u30f3\u306e\u9078\u629e\u7684\u5408\u6210<\/strong><br>\u7b2c\uff13\uff10\u56de\u6709\u6a5f\u5408\u6210\u82e5\u624b\u30bb\u30df\u30ca\u30fc\uff0d\u660e\u65e5\u306e\u6709\u6a5f\u5408\u6210\u3092\u62c5\u3046\u4eba\u306e\u305f\u3081\u306b\uff0c\u5927\u962a\u5e9c\u7acb\u5927\u5b66\uff0cP-11 (2010.11.10).<\/li>\n\n\n\n<li>\u5c71\u672c\u4fe1\u884c, \u5927\u6d1e\u5eb7\u55e3, \u77f3\u4e95\u5eb7\u656c<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u932f\u4f53\u89e6\u5a92\u3092\u7528\u3044\u308b\u7b2c1\u7d1a\u30a2\u30eb\u30b3\u30fc\u30eb\u3068\u30e1\u30bf\u30ce\u30fc\u30eb\u306b\u3088\u308b\u30e1\u30c1\u30eb\u30a8\u30b9\u30c6\u30eb\u985e\u306e\u5408\u6210<\/strong><br>\u7b2c\uff13\uff10\u56de\u6709\u6a5f\u5408\u6210\u82e5\u624b\u30bb\u30df\u30ca\u30fc\uff0d\u660e\u65e5\u306e\u6709\u6a5f\u5408\u6210\u3092\u62c5\u3046\u4eba\u306e\u305f\u3081\u306b\uff0c\u5927\u962a\u5e9c\u7acb\u5927\u5b66\uff0cP-12 (2010.11.10).<\/li>\n\n\n\n<li>\u897f\u91ce\u6f64\u4e00\uff0c\u5927\u6d1e\u5eb7\u55e3<br><strong>\u30eb\u30a4\u30b9\u9178\u89e6\u5a92\u3092\u7528\u3044\u305f\u30a2\u30ea\u30eb\u30a2\u30eb\u30b3\u30fc\u30eb\u306e\u76f4\u63a5\u30a2\u30df\u30ce\u5316\u53cd\u5fdc<\/strong><br>\u7b2c\uff13\uff10\u56de\u6709\u6a5f\u5408\u6210\u82e5\u624b\u30bb\u30df\u30ca\u30fc\uff0d\u660e\u65e5\u306e\u6709\u6a5f\u5408\u6210\u3092\u62c5\u3046\u4eba\u306e\u305f\u3081\u306b\uff0c\u5927\u962a\u5e9c\u7acb\u5927\u5b66\uff0cP-15 (2010.11.10).<\/li>\n\n\n\n<li>\u5800\u5ddd\u5178\u79c0\u3001\u5927\u6d1e\u5eb7\u55e3\u3001\u77f3\u4e95\u5eb7\u656c<br><strong>\u30eb\u30a4\u30b9\u9178\u89e6\u5a92\u306b\u3088\u308b\u30a2\u30bb\u30bf\u30fc\u30eb\u3068\u82b3\u9999\u65cf\u30a2\u30eb\u30c7\u30d2\u30c9\u304b\u3089\u306e2<em>H<\/em>-\u53ca\u30734<em>H<\/em>-3,5-\u30b8\u30db\u30eb\u30df\u30eb\u30d4\u30e9\u30f3\u8a98\u5c0e\u4f53\u306e\u9078\u629e\u7684\u5408\u6210<\/strong><br><em>\u77f3\u6cb9\u5b66\u4f1a\u95a2\u897f\u652f\u90e8\u7b2c\uff11\uff19\u56de\u7814\u7a76\u767a\u8868\u4f1a\u65e5\u672c\u30a8\u30cd\u30eb\u30ae\u30fc\u5b66\u4f1a\u95a2\u897f\u652f\u90e8<br>\u7b2c\uff15\uff15\u56de\u5408\u540c\u7814\u7a76\u767a\u8868\u4f1a<\/em>\uff0c\u795e\u6238\u56fd\u969b\u4f1a\u8b70\u5834\uff0c6 (2010.11.25).<\/li>\n\n\n\n<li>\u5c71\u672c\u4fe1\u884c, \u5927\u6d1e\u5eb7\u55e3, \u77f3\u4e95\u5eb7\u656c<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u89e6\u5a92\u306b\u3088\u308b\u30a2\u30eb\u30b3\u30fc\u30eb\u3092\u7528\u3044\u308b\u30e1\u30c1\u30eb\u30a8\u30b9\u30c6\u30eb\u985e\u306e\u5408\u6210<\/strong><br><em>\u77f3\u6cb9\u5b66\u4f1a\u95a2\u897f\u652f\u90e8\u7b2c\uff11\uff19\u56de\u7814\u7a76\u767a\u8868\u4f1a\u65e5\u672c\u30a8\u30cd\u30eb\u30ae\u30fc\u5b66\u4f1a\u95a2\u897f\u652f\u90e8<br>\u7b2c\uff15\uff15\u56de\u5408\u540c\u7814\u7a76\u767a\u8868\u4f1a<\/em>\uff0c\u795e\u6238\u56fd\u969b\u4f1a\u8b70\u5834\uff0c7 (2010.11.25).<\/li>\n\n\n\n<li>\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c\uff0c\u5ddd\ufa11\u82f1\u4e5f<br><strong>\u91d1\u5c5e\u89e6\u5a92\u306e\u8d85\u9ad8\u5ea6\u5229\u7528\u3092\u57fa\u8ef8\u3068\u3059\u308b\u5358\u5b98\u80fd\u57fa\u30d5\u30a3\u30fc\u30c9\u30b9\u30c8\u30c3\u30af\u306e\u52b9\u7387\u7684\u6709\u6a5f\u5909\u63db\u53cd\u5fdc\u958b\u767a<\/strong><br><em>\u7b2c\uff11\uff15\u56de\u95a2\u897f\u5927\u5148\u7aef\u79d1\u5b66\u6280\u8853\u30b7\u30f3\u30dd\u30b8\u30a6\u30e0<\/em>\uff0c\u95a2\u897f\u5927\u5b66 (2011.1.13).<\/li>\n\n\n\n<li>\u6fa4\u53e3\u62d3\u77e2\uff0c\u5927\u6d1e\u5eb7\u55e3<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u932f\u4f53\u89e6\u5a92\u306b\u3088\u308b\u30a2\u30eb\u30b3\u30fc\u30eb\u3068\u30a2\u30bb\u30c8\u30cb\u30c8\u30ea\u30eb\u306e\u30ab\u30c3\u30d7\u30ea\u30f3\u30b0\u5316\u53cd\u5fdc<\/strong><br><em>\u7b2c\uff11\uff15\u56de\u95a2\u897f\u5927\u5148\u7aef\u79d1\u5b66\u6280\u8853\u30b7\u30f3\u30dd\u30b8\u30a6\u30e0\u30dd\u30b9\u30bf\u30fc\u30bb\u30c3\u30b7\u30e7\u30f3(\u5408\u6210\u89e6\u5a92\u30fb\u9ad8\u6a5f\u80fd\u6750\u6599\u3068\u3057\u3066\u306e\u5e0c\u5c11\u91d1\u5c5e\u8cc7\u6e90\u306e\u8d85\u9ad8\u5ea6\u5229\u7528\u7814\u7a76\u4f1a)<\/em>\uff0c6, \u95a2\u897f\u5927\u5b66 (2011.1.14).<\/li>\n\n\n\n<li>\u5175\u4e39\u77f3\u6075\uff0c\u5c71\u672c\u5bdb\u5b50\uff0c\u5ddd\u5d0e\u82f1\u4e5f\uff0c\u5927\u6d1e\u5eb7\u55e3<br><strong>\u30b5\u30d6\u30ca\u30ce\u30b5\u30a4\u30ba\u30d1\u30e9\u30b8\u30a6\u30e0\u5fae\u7c92\u5b50\u3092\u89e6\u5a92\u3068\u3057\u3066\u7528\u3044\u305f\u52b9\u7387\u7684\u30af\u30ed\u30b9\u30ab\u30c3\u30d7\u30ea\u30f3\u30b0\u53cd\u5fdc\u306e\u958b\u62d3<\/strong><br><em>\u7b2c\uff11\uff15\u56de\u95a2\u897f\u5927\u5148\u7aef\u79d1\u5b66\u6280\u8853\u30b7\u30f3\u30dd\u30b8\u30a6\u30e0\u30dd\u30b9\u30bf\u30fc\u30bb\u30c3\u30b7\u30e7\u30f3(\u5408\u6210\u89e6\u5a92\u30fb\u9ad8\u6a5f\u80fd\u6750\u6599\u3068\u3057\u3066\u306e\u5e0c\u5c11\u91d1\u5c5e\u8cc7\u6e90\u306e\u8d85\u9ad8\u5ea6\u5229\u7528\u7814\u7a76\u4f1a)<\/em>\uff0c7, \u95a2\u897f\u5927\u5b66 (2011.1.14).<\/li>\n\n\n\n<li>\u6c34\u7530\u5eb8\u5e73\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c<br><strong>\u30d1\u30e9\u30b8\u30a6\u30e0\/\u30e2\u30ea\u30d6\u30c9\u30d0\u30ca\u30c9\u30ea\u30f3\u9178\/\u9178\u7d20\u7cfb\u3092\u7528\u3044\u305f\u30a2\u30cb\u30ea\u30f3\u8a98\u5c0e\u4f53\u3068\u30aa\u30ec\u30d5\u30a3\u30f3\u3068\u306e\u9178\u5316\u7684\u30ab\u30c3\u30d7\u30ea\u30f3\u30b0\u53cd\u5fdc<\/strong><br><em>\u7b2c\uff11\uff15\u56de\u95a2\u897f\u5927\u5148\u7aef\u79d1\u5b66\u6280\u8853\u30b7\u30f3\u30dd\u30b8\u30a6\u30e0\u30dd\u30b9\u30bf\u30fc\u30bb\u30c3\u30b7\u30e7\u30f3(\u5408\u6210\u89e6\u5a92\u30fb\u9ad8\u6a5f\u80fd\u6750\u6599\u3068\u3057\u3066\u306e\u5e0c\u5c11\u91d1\u5c5e\u8cc7\u6e90\u306e\u8d85\u9ad8\u5ea6\u5229\u7528\u7814\u7a76\u4f1a)<\/em>\uff0c8, \u95a2\u897f\u5927\u5b66 (2011.1.14).<\/li>\n\n\n\n<li>\u4f50\u85e4\u9756, \u5927\u6d1e\u5eb7\u55e3<br><strong>\u4e09\u5869\u5316\u30cb\u30aa\u30d6\u89e6\u5a92\u3092\u7528\u3044\u305f\u30a2\u30eb\u30ad\u30f3\u3068\u30a2\u30eb\u30b1\u30f3\u304b\u3089\u306e\uff11\uff0c\uff13\uff0d\u30b7\u30af\u30ed\u30d8\u30ad\u30b5\u30b8\u30a8\u30f3\u8a98\u5c0e\u4f53\u306e\u5408\u6210<\/strong><br><em>\u7b2c\uff11\uff15\u56de\u95a2\u897f\u5927\u5148\u7aef\u79d1\u5b66\u6280\u8853\u30b7\u30f3\u30dd\u30b8\u30a6\u30e0\u30dd\u30b9\u30bf\u30fc\u30bb\u30c3\u30b7\u30e7\u30f3(\u6226\u7565\u57fa\u76e4\uff1a\u6b21\u4e16\u4ee3\u533b\u7642\u3092\u9769\u65b0\u3059\u308b\u30b9\u30de\u30fc\u30c8\u30d0\u30a4\u30aa\u30de\u30c6\u30ea\u30a2\u30eb\u306e\u5275\u51fa)<\/em>\uff0c74, \u95a2\u897f\u5927\u5b66 (2011.1.14).<\/li>\n\n\n\n<li>\u963f\u6b66\u7531\u52a0\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u932f\u4f53\u89e6\u5a92\u306b\u3088\u308bGuerbet\u53cd\u5fdc\u3092\u5229\u7528\u3057\u305f\u03b1,\u03c9-\u30b8\u30aa\u30fc\u30eb\u304b\u3089\u306e\u591a\u5206\u5c90\u30dd\u30ea\u30aa\u30fc\u30eb\u306e\u5408\u6210<\/strong><br><em>\u7b2c\uff11\uff15\u56de\u95a2\u897f\u5927\u5148\u7aef\u79d1\u5b66\u6280\u8853\u30b7\u30f3\u30dd\u30b8\u30a6\u30e0\u30dd\u30b9\u30bf\u30fc\u30bb\u30c3\u30b7\u30e7\u30f3(\u6226\u7565\u57fa\u76e4\uff1a\u6b21\u4e16\u4ee3\u533b\u7642\u3092\u9769\u65b0\u3059\u308b\u30b9\u30de\u30fc\u30c8\u30d0\u30a4\u30aa\u30de\u30c6\u30ea\u30a2\u30eb\u306e\u5275\u51fa)<\/em>\uff0c75, \u95a2\u897f\u5927\u5b66 (2011.1.14).<\/li>\n\n\n\n<li>\u4f50\u85e4\u9756\uff0c\u5927\u6d1e\u5eb7\u55e3<br><strong>\u4e94\u5869\u5316\u30cb\u30aa\u30d6\/\u30d2\u30c9\u30ed\u30b7\u30e9\u30f3\u89e6\u5a92\u7cfb\u3092\u7528\u3044\u305f\u74b0\u5316\u4ed8\u52a0\u53cd\u5fdc<\/strong><br><em>\u7b2c\uff191\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a<\/em>\uff0c\u795e\u5948\u5ddd\u5927\u5b66\uff0c1C7-14\uff082011.3.26).<\/li>\n\n\n\n<li>\u5c3e\u5d0e\u8aa0\uff0c\u4f50\u85e4\u9756\uff0c\u5927\u6d1e\u5eb7\u55e3<br><strong>\u4e94\u5869\u5316\u30cb\u30aa\u30d6\u304b\u3089\u306e\u4f4e\u539f\u5b50\u4fa1\u30cb\u30aa\u30d6\u7a2e\u306e\u8abf\u88fd\u3068\u30aa\u30ec\u30d5\u30a3\u30f3\u3092\u7528\u3044\u305f\u89e6\u5a92\u53cd\u5fdc\u3078\u306e\u5229\u7528<\/strong><br><em>\u7b2c\uff191\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a<\/em>\uff0c\u795e\u5948\u5ddd\u5927\u5b66\uff0c1C7-15\uff082011.3.26).<\/li>\n\n\n\n<li>\u4e2d\u4e95\u4fca\u5fd7\uff0c\u6e05\u6c34\u6d0b\u4f51\uff0c\u5927\u6d1e\u5eb7\u55e3<br><strong>\u30d1\u30e9\u30b8\u30a6\u30e0\u89e6\u5a92\u3092\u7528\u3044\u305f\u30b8\u30b7\u30e9\u30f3\u3068\u672b\u7aef\u30a2\u30eb\u30b1\u30f3\u306e\u53cd\u5fdc\u306b\u3088\u308b\u30a2\u30ea\u30eb\u30b7\u30e9\u30f3\u306e\u5408\u6210<\/strong><br><em>\u7b2c\uff191\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a<\/em>\uff0c\u795e\u5948\u5ddd\u5927\u5b66\uff0c1C9-20\uff082011.3.26).<\/li>\n\n\n\n<li>\u6c34\u7530\u5eb8\u5e73\uff0c\u6e05\u6c34\u6d0b\u4f51\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c<br><strong>Pd\/HPMoV\/O2\u7cfb\u306b\u3088\u308b\u542b\u7a92\u7d20\u82b3\u9999\u65cf\u5316\u5408\u7269\u3092\u7528\u3044\u305f\u9178\u5316\u7684\u30ab\u30c3\u30d7\u30ea\u30f3\u30b0\u53cd\u5fdc<\/strong><br><em>\u7b2c\uff191\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a<\/em>\uff0c\u795e\u5948\u5ddd\u5927\u5b66\uff0c1C9-37\uff082011.3.26).<\/li>\n\n\n\n<li>\u539f\u7530\u8056\u4e00\u6717\uff0c\u671d\u6bd4\u5948\u7ae0\uff0c\u5927\u6d1e\u5eb7\u55e3<br><strong>\u30d1\u30e9\u30b8\u30a6\u30e0\u89e6\u5a92\u3092\u7528\u3044\u305f\u82b3\u9999\u65cf\u5316\u5408\u7269\u3068\u30aa\u30ec\u30d5\u30a3\u30f3\u3068\u306e\u9178\u5316\u7684\u30ab\u30c3\u30d7\u30ea\u30f3\u30b0\u53cd\u5fdc<\/strong><br><em>\u7b2c\uff191\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a<\/em>\uff0c\u795e\u5948\u5ddd\u5927\u5b66\uff0c1C9-38\uff082011.3.26).<\/li>\n\n\n\n<li>\u65b0\u5c45\u502b\u6210\uff0c\u5927\u6d1e\u5eb7\u55e3<br><strong>\u30d1\u30e9\u30b8\u30a6\u30e0\u89e6\u5a92\u3092\u7528\u3044\u305f\u9178\u5869\u5316\u7269\uff0c\u30a2\u30eb\u30ad\u30f3\u304a\u3088\u3073\u30b8\u30b7\u30e9\u30f3\u306b\u3088\u308b\u30b7\u30af\u30ed\u30da\u30f3\u30c6\u30ce\u30f3\u8a98\u5c0e\u4f53\u306e\u5408\u6210<\/strong><br><em>\u7b2c\uff191\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a<\/em>\uff0c\u795e\u5948\u5ddd\u5927\u5b66\uff0c1C9-39\uff082011.3.26).<\/li>\n\n\n\n<li>\u4e2d\u6751\u4e00\u88d5\uff0c\u7551\u4e2d\u614e\u592a\u90ce\uff0c\u5927\u6d1e\u5eb7\u55e3<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u932f\u4f53\u89e6\u5a92\u3092\u7528\u3044\u305f\u30a2\u30eb\u30b3\u30fc\u30eb\u3068\u30a8\u30ce\u30f3\u304b\u3089\u306e1,3-\u30b8\u30b1\u30c8\u30f3\u306e\u5408\u6210<\/strong><br><em>\u7b2c\uff191\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a<\/em>\uff0c\u795e\u5948\u5ddd\u5927\u5b66\uff0c4C5-36\uff082011.3.29).<\/li>\n\n\n\n<li>\u6fa4\u53e3\u62d3\u77e2\uff0c\u5927\u6d1e\u5eb7\u55e3<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u932f\u4f53\u89e6\u5a92\u3092\u7528\u3044\u305f\u30a2\u30eb\u30b3\u30fc\u30eb\u306b\u3088\u308b\u30a2\u30bb\u30c8\u30cb\u30c8\u30ea\u30eb\u306e\u03b1-\u30a2\u30eb\u30ad\u30eb\u5316<\/strong><br><em>\u7b2c\uff191\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a<\/em>\uff0c\u795e\u5948\u5ddd\u5927\u5b66\uff0c4C5-39\uff082011.3.29).<\/li>\n\n\n\n<li>\u83ca\u672c\u7fd4\u592a\uff0c\u6fa4\u53e3\u62d3\u77e2\uff0c\u4e95\u5185\u6d0b\u4ecb\uff0c\u5927\u6d1e\u5eb7\u55e3<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u89e6\u5a92\u306b\u3088\u308b\u30a2\u30eb\u30ad\u30eb\u30a2\u30df\u30c9\u306e\u30a2\u30eb\u30b3\u30fc\u30eb\u3092\u7528\u3044\u305f\u03b1-\u30a2\u30eb\u30ad\u30eb\u5316\u53cd\u5fdc<\/strong><br><em>\u7b2c\uff191\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a<\/em>\uff0c\u795e\u5948\u5ddd\u5927\u5b66\uff0c4C5-40\uff082011.3.29).<\/li>\n\n\n\n<li>\u77f3\u6a4b\u512a\uff0c\u963f\u6b66\u7531\u52a0\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u89e6\u5a92\u306b\u3088\u308b\u30a2\u30eb\u30b3\u30fc\u30eb\u304b\u3089\u306e\u30c6\u30c8\u30e9\u30ea\u30f3\u8a98\u5c0e\u4f53\u306e\u5408\u6210\u304a\u3088\u3073\u591a\u5206\u5c90\u30dd\u30ea\u30aa\u30fc\u30eb\u306e\u5408\u6210<\/strong><br><em>\u7b2c\uff191\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a<\/em>\uff0c\u795e\u5948\u5ddd\u5927\u5b66\uff0c4C5-41\uff082011.3.29).<\/li>\n\n\n\n<li>\u78ef\u6751\u512a\u4ec1\uff0c\u5175\u4e39\u77f3\u6075\uff0c\u4e2d\u5cf6\u7531\u4f9d\uff0c\u5ddd\ufa11\u82f1\u4e5f\uff0c\u5927\u6d1e\u5eb7\u55e3<br><strong>\u30ec\u30a2\u30e1\u30bf\u30eb\u30ca\u30ce\u30af\u30e9\u30b9\u30bf\u30fc\u306e\u5408\u6210\u306a\u3089\u3073\u306b\u305d\u306e\u89e6\u5a92\u4f5c\u7528<\/strong><br><em>\u7b2c\uff191\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a<\/em>\uff0c\u795e\u5948\u5ddd\u5927\u5b66\uff0c4C9-12\uff082011.3.29).<\/li>\n<\/ol>\n\n\n\n<div style=\"height:30px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>\u8457\u66f8<\/strong><\/h4>\n\n\n\n<ol class=\"wp-block-list\">\n<li>Y. Ishii, S. Sakaguchi, Y. Obora<br><strong>Aerobic Oxidations and Related Reactions Catalyzed by N-Hydroxyphthalimide<\/strong><br><em>Modern Oxidation Methods<\/em>, 2nd completely revised and enlarged edition, Ed. by J.-E. B\u00e4ckvall, Wiley-VCH, Weinheim, Germany, chapter 6, pp. 187-240 [482] (2010. 12).<\/li>\n<\/ol>\n\n\n\n<div style=\"height:30px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>\u56fd\u969b\u4f1a\u8b70<\/strong><\/h4>\n\n\n\n<ol class=\"wp-block-list\">\n<li>Y. Obora, S. Hatanaka, Y. Ishii<br><strong>Coupling reaction of primary alcohols with 2-alkynes catalyzed by iridium complex<\/strong><br><em>2010 International Chemical Congress of Pacific Basin Societies, 1076 (Oral Presentation),<\/em>&nbsp;Hilton, Honolulu, United States (2010.12.18).<\/li>\n\n\n\n<li>Y. Mizuta, Y. Shimizu, Y. Obora, Y. Ishii<br><strong>Oxidative coupling reaction of aminobenzenes with olefins catalyzed by Pd(II)\/HPMoV\/O2&nbsp;system<\/strong><br><em>2010 International Chemical Congress of Pacific Basin Societies, 1405 (Poster Presentation),<\/em>&nbsp;Honolulu Convention Center, Honolulu, United States (2010.12.18).<\/li>\n\n\n\n<li>Y. Obora, Y. Shimizu, Y. Ishii<br><strong>Intermolecular aerobic oxidative amination of alkenes with amines catalyzed by the Pd\/NPMoV\/O2&nbsp;system<\/strong><br><em>2010 International Chemical Congress of Pacific Basin Societies, 1410 (Poster Presentation),<\/em>&nbsp;Honolulu Convention Center, Honolulu, United States (2010.12.18).<\/li>\n\n\n\n<li>M. Hyotanishi, H. Yamamoto, H. Kawasaki, Y. Obora<br><strong>Surfactant-free synthesis of sub-nanometer-sized transition-metal nanoclusters and their use in catalysis<\/strong><br><em>2010 International Chemical Congress of Pacific Basin Societies, 1411 (Poster Presentation),<\/em>&nbsp;Honolulu Convention Center, Honolulu, United States (2010.12.18).<\/li>\n\n\n\n<li>Y. Satoh, Y. Obora<br><strong>NbCl3-catalyzed [2+2+2] three-component cycloaddition reaction of terminal alkynes, internal alkynes and alkenes leading to tetrasubstituted-1,3-cyclohexadienes<\/strong><br><em>2010 International Chemical Congress of Pacific Basin Societies, 1412 (Poster Presentation),<\/em>&nbsp;Honolulu Convention Center, Honolulu, United States (2010.12.18).<\/li>\n\n\n\n<li>N. Horikawa, K. Tamaso, Y. Obora, Y. Ishii<br><strong>Synthesis of 3-formylfuranes and diformylpyrans from acetals with aldehydes using Lewis acid as a key catalyst<\/strong><br><em>2010 International Chemical Congress of Pacific Basin Societies, 1415 (Poster Presentation),<\/em>&nbsp;Honolulu Convention Center, Honolulu, United States (2010.12.18).<\/li>\n\n\n\n<li>Y. Anno, Y. Obora, Y. Ishii<br><strong>Iridium complex catalyzed Guerbet reaction of \u03b1,\u03c9-diols<\/strong><br><em>2010 International Chemical Congress of Pacific Basin Societies, 1420 (Poster Presentation),<\/em>&nbsp;Honolulu Convention Center, Honolulu, United States (2010.12.18).<\/li>\n\n\n\n<li>T. Sawaguchi, Y. Obora<br><strong>\u03b1-Alkylation of acetnitrile with alcohols by iridium complex<\/strong><br><em>2010 International Chemical Congress of Pacific Basin Societies, 1422 (Poster Presentation),<\/em>&nbsp;Honolulu Convention Center, Honolulu, United States (2010.12.18).<\/li>\n<\/ol>\n\n\n\n<div style=\"height:30px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>\u4f9d\u983c\u8b1b\u6f14\u3001\u8b1b\u7fd2\u4f1a\u3001\u305d\u306e\u4ed6<\/strong><\/h4>\n\n\n\n<ol class=\"wp-block-list\">\n<li>\u5927\u6d1e\u5eb7\u55e3<br><strong>\u91d1\u5c5e\u89e6\u5a92\u306e\u8d85\u9ad8\u5ea6\u5229\u7528\u306b\u57fa\u3065\u304f\u65b0\u898f\u6709\u6a5f\u5408\u6210\u30d7\u30ed\u30bb\u30b9<\/strong><br>\u95a2\u897f\u5927\u5b66\u6280\u8853\u4ea4\u6d41\u30bb\u30df\u30ca\u30fc\uff12\uff10\uff11\uff10\uff0c\u95a2\u897f\u5927\u5b66\u6771\u4eac\u30bb\u30f3\u30bf\u30fc (2010.6.30)\uff08\u4f9d\u983c\u8b1b\u6f14\uff09<\/li>\n\n\n\n<li>\u5927\u6d1e\u5eb7\u55e3<br><strong>\u5358\u5b98\u80fd\u57fa\u30d5\u30a3\u30fc\u30c9\u30b9\u30c8\u30c3\u30af\u3092\u7528\u3044\u305f\u9ad8\u52b9\u7387\u7684\u89e6\u5a92\u5909\u63db\u53cd\u5fdc\u958b\u767a (Development of Efficient Catalytic Transformations Using Monofunctionalized Chemical Feedstock)<\/strong><br>\u95a2\u897f\u5927\u5b66\u5148\u7aef\u79d1\u5b66\u6280\u8853\u63a8\u9032\u6a5f\u69cb\u3000\u7b2c29\u56de\u7814\u7a76\u90e8\u9580\u5225\u767a\u8868\u4f1a\uff0c(2010.9.6)<\/li>\n<\/ol>\n\n\n\n<div style=\"height:30px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>\u7814\u7a76\u7d39\u4ecb\u8a18\u4e8b<\/strong><\/h4>\n\n\n\n<ol class=\"wp-block-list\">\n<li>\u65e5\u672c\u7d4c\u6e08\u65b0\u805e\u300c\u30af\u30ed\u30b9\u30ab\u30c3\u30d7\u30ea\u30f3\u30b0\u300d\u9032\u5316\uff0d\u95a2\u5927\u3000\u5fae\u7c92\u5b50\u89e6\u5a92\u3067\u52b9\u7387\u6539\u5584 (2011.2.7)<\/li>\n<\/ol>\n\n\n\n<p><\/p>\n\n\n\n<div style=\"height:20px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<p class=\"has-text-align-right\"><mark style=\"color:#89a06c\" class=\"has-inline-color\">\u25b2<\/mark> <a href=\"#top\">\u30da\u30fc\u30b8\u306eTOP\u3078<\/a><\/p>\n\n\n\n<div style=\"height:40px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"2009\">2009\u5e74<\/h3>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>\u5b66\u8853\u8ad6\u6587<\/strong><\/h4>\n\n\n\n<ol class=\"wp-block-list\">\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1016\/j.tet.2009.03.013\" target=\"_blank\">R. Nakamura, Y. Obora, Y. Ishii<br><strong>Synthesis of 6-Hydroxy-2-Naphthoic Acid from 2,6-Diisopropylnaphthalene Using NHPI as a Key Catalyst<\/strong><br><em>Tetrahedron<\/em>&nbsp;65 (18), 3577-3581 (2009.5.2).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"661\" height=\"199\" class=\"wp-image-294\" style=\"width: 500px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Synthesis-of-6-hydroxy-2-naphthoic-acid-from-26-diisopropylnaphthalene-using-NHPI-as-a-key-catalyst.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Synthesis-of-6-hydroxy-2-naphthoic-acid-from-26-diisopropylnaphthalene-using-NHPI-as-a-key-catalyst.jpg 661w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Synthesis-of-6-hydroxy-2-naphthoic-acid-from-26-diisopropylnaphthalene-using-NHPI-as-a-key-catalyst-300x90.jpg 300w\" sizes=\"auto, (max-width: 661px) 100vw, 661px\" \/><\/li>\n<\/ol>\n\n\n\n<ol start=\"2\" class=\"wp-block-list\">\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1021\/op800258s\" target=\"_blank\">M. Hashimoto, Y. Obora, Y. Ishii<br><strong>An Efficient Catalytic Method for the Beckmann Rearrangement of Ketoxime to Lactams by Cyanuric Chloride and Phosphazene Catalyst<\/strong><br><em>Org. Process Res. Dev..&nbsp;<\/em>13 (3) 411-414 (2009.5).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"523\" height=\"358\" class=\"wp-image-298\" style=\"width: 320px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/An-Efficient-Catalytic-Method-for-the-Beckmann-Rearrangement-of-Ketoximes-to-Lactams-by-Cyanuric-Chloride-and-Phosphazene-Catalysts.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/An-Efficient-Catalytic-Method-for-the-Beckmann-Rearrangement-of-Ketoximes-to-Lactams-by-Cyanuric-Chloride-and-Phosphazene-Catalysts.jpg 523w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/An-Efficient-Catalytic-Method-for-the-Beckmann-Rearrangement-of-Ketoximes-to-Lactams-by-Cyanuric-Chloride-and-Phosphazene-Catalysts-300x205.jpg 300w\" sizes=\"auto, (max-width: 523px) 100vw, 523px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1002\/adsc.200900099\" target=\"_blank\">R. Nakamura, Y. Obora, Y. Ishii<br><strong>Selective Oxidation of Acetophenones Bearing Various Functional Groups to Benzoic Acid Derivatives with Molecular Oxygen<\/strong><br><em>Adv. Synth. Catal.&nbsp;<\/em>351(10), 1677-1684 (2009.7).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"604\" height=\"96\" class=\"wp-image-293\" style=\"width: 500px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Selective-Oxidation-of-Acetophenones-Bearing-Various.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Selective-Oxidation-of-Acetophenones-Bearing-Various.jpg 604w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Selective-Oxidation-of-Acetophenones-Bearing-Various-300x48.jpg 300w\" sizes=\"auto, (max-width: 604px) 100vw, 604px\" \/><\/li>\n<\/ol>\n\n\n\n<ol start=\"4\" class=\"wp-block-list\">\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1246\/bcsj.82.891\" target=\"_blank\">K. Kamae, Y. Obora, Y. Ishii<br><strong>Baeyer-Villiger Oxidation of Cycloalkanones with in situ Generated Hydrogen Peroxide from Alcohols and Molecular Oxygen Using NHPI as a Key Catalyst<\/strong><br><em>Bull. Chem. Soc. Jpn.&nbsp;<\/em>82 (7), 891-895 (2009.7.15).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"308\" height=\"194\" class=\"wp-image-285\" style=\"width: 300px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Baeyer\u2013Villiger-Oxidation-of-Cycloalkanones-with-In-Situ-Generated-Hydrogen-Peroxide-from-Alcohols-and-Molecular-Oxygen-Using-NHPI-as-a-Key-Catalyst.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Baeyer\u2013Villiger-Oxidation-of-Cycloalkanones-with-In-Situ-Generated-Hydrogen-Peroxide-from-Alcohols-and-Molecular-Oxygen-Using-NHPI-as-a-Key-Catalyst.jpg 308w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Baeyer\u2013Villiger-Oxidation-of-Cycloalkanones-with-In-Situ-Generated-Hydrogen-Peroxide-from-Alcohols-and-Molecular-Oxygen-Using-NHPI-as-a-Key-Catalyst-300x189.jpg 300w\" sizes=\"auto, (max-width: 308px) 100vw, 308px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1002\/ejoc.200900432\" target=\"_blank\">S. Maeda, Y. Obora, Y. Ishii<br><strong>Selective Cyclodimerization and Cyclotrimerization of Acetals Bearing Electron-Withdrawing Groups Catalyzed by Lewis Acids<\/strong>,<br><em>Eur. J. Org. Chem.&nbsp;<\/em>(24), 4067-4072 (2009.8).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"431\" height=\"233\" class=\"wp-image-292\" style=\"width: 300px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Selective-Cyclodimerization-and-Cyclotrimerization-of-Acetals-Bearing-Electron\u2010Withdrawing-Groups-Catalyzed-by-Lewis-Acids.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Selective-Cyclodimerization-and-Cyclotrimerization-of-Acetals-Bearing-Electron\u2010Withdrawing-Groups-Catalyzed-by-Lewis-Acids.jpg 431w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Selective-Cyclodimerization-and-Cyclotrimerization-of-Acetals-Bearing-Electron\u2010Withdrawing-Groups-Catalyzed-by-Lewis-Acids-300x162.jpg 300w\" sizes=\"auto, (max-width: 431px) 100vw, 431px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1246\/cl.2009.838\" target=\"_blank\">K. Koda, T. Matsu-ura, Y. Obora, Y. Ishii<br><strong>Guerbet Reaction of Ethanol to n-Butanol Catalyzed by Iridium Complexes<\/strong><br><em>Chem. Lett.<\/em>, 38 (8), 838-839 (2009.8.5).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"591\" height=\"203\" class=\"wp-image-286\" style=\"width: 450px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Guerbet-Reaction-of-Ethanol-to-n-Butanol-Catalyzed-by-Iridium-Complexes.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Guerbet-Reaction-of-Ethanol-to-n-Butanol-Catalyzed-by-Iridium-Complexes.jpg 591w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Guerbet-Reaction-of-Ethanol-to-n-Butanol-Catalyzed-by-Iridium-Complexes-300x103.jpg 300w\" sizes=\"auto, (max-width: 591px) 100vw, 591px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1021\/ol901366q\" target=\"_blank\">Y. Obora, S. Hatanaka, Y. Ishii<br><strong>Iridium-Catalyzed Coupling Reaction of Primary Alcohols with 1-Aryl-1-Propynes Leading to Secondary Homoallylic Alcohols<\/strong><br><em>Org. Lett.&nbsp;<\/em>11 (15), 3510-3513 (2009.8.6).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"531\" height=\"148\" class=\"wp-image-289\" style=\"width: 400px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-Catalyzed-Coupling-Reaction-of-Primary-Alcohols-with-1-Aryl-1-propynes-Leading-to-Secondary-Homoallylic-Alcohols.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-Catalyzed-Coupling-Reaction-of-Primary-Alcohols-with-1-Aryl-1-propynes-Leading-to-Secondary-Homoallylic-Alcohols.jpg 531w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-Catalyzed-Coupling-Reaction-of-Primary-Alcohols-with-1-Aryl-1-propynes-Leading-to-Secondary-Homoallylic-Alcohols-300x84.jpg 300w\" sizes=\"auto, (max-width: 531px) 100vw, 531px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1021\/ol902052z\" target=\"_blank\">Y. Obora, Y. Shimizu, Y. Ishii<br><strong>Intermolecular Oxidative Amination of Olefins with Amines Catalyzed by Pd(II)\/NPMoV\/O<sub>2<\/sub>&nbsp;System<\/strong><br><em>Org. Lett.<\/em>, 11 (21), 5058-5061 (2009.11.5).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"530\" height=\"142\" class=\"wp-image-288\" style=\"width: 420px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Intermolecular-Oxidative-Amination-of-Olefins-with-Amines-Catalyzed-by-the.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Intermolecular-Oxidative-Amination-of-Olefins-with-Amines-Catalyzed-by-the.jpg 530w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Intermolecular-Oxidative-Amination-of-Olefins-with-Amines-Catalyzed-by-the-300x80.jpg 300w\" sizes=\"auto, (max-width: 530px) 100vw, 530px\" \/><\/li>\n<\/ol>\n\n\n\n<ol start=\"9\" class=\"wp-block-list\">\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1246\/cl.2009.1106\" target=\"_blank\">N. Yamamoto, Y. Obora, Y. Ishii<br><strong>The Direct Conversion of Ethanol to Ethyl and Methyl Acetates Catalyzed by Iridium Complex<\/strong><br><em>Chem. Lett.<\/em>&nbsp;38 (11), 1106-1107 (2009.11).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"594\" height=\"146\" class=\"wp-image-297\" style=\"width: 460px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/The-Direct-Conversion-of-Ethanol-to-Ethyl-and-Methyl-Acetates-Catalyzed-by-Iridium-Complex.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/The-Direct-Conversion-of-Ethanol-to-Ethyl-and-Methyl-Acetates-Catalyzed-by-Iridium-Complex.jpg 594w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/The-Direct-Conversion-of-Ethanol-to-Ethyl-and-Methyl-Acetates-Catalyzed-by-Iridium-Complex-300x74.jpg 300w\" sizes=\"auto, (max-width: 594px) 100vw, 594px\" \/><\/li>\n<\/ol>\n\n\n\n<ol start=\"10\" class=\"wp-block-list\">\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1021\/jo9021293\" target=\"_blank\">S. Maeda, N. Horikawa, Y. Obora, Y. Ishii<br><strong>Synthesis of \u03b1-Cyanocinnamaldehydes from Acrylonitrile and Benzaldehydes Catalyzed by Pd(OAc)<sub>2<\/sub>\/HPMoV\/FeCl<sub>3<\/sub>\/O<sub>2<\/sub>&nbsp;System<\/strong><br><em>J. Org. Chem.,<\/em>&nbsp;74 (24), 9558-9561 (2009.12.18).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"532\" height=\"152\" class=\"wp-image-295\" style=\"width: 500px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Synthesis-of-\u03b1-Cyanocinnamaldehydes-from-Acrylonitrile-and-Benzaldehydes-Catalyzed.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Synthesis-of-\u03b1-Cyanocinnamaldehydes-from-Acrylonitrile-and-Benzaldehydes-Catalyzed.jpg 532w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Synthesis-of-\u03b1-Cyanocinnamaldehydes-from-Acrylonitrile-and-Benzaldehydes-Catalyzed-300x86.jpg 300w\" sizes=\"auto, (max-width: 532px) 100vw, 532px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1002\/chem.200902646\" target=\"_blank\">S. Hatanaka, Y. Obora, Y. Ishii<br><strong>Iridium-Catalyzed Coupling Reaction of Primary Alcohols with 2-Alkynes Leading to Hydroacylation Products<\/strong><br><em>Chem.-Eur. J.<\/em>&nbsp;16(6), 1883-1888 (2010.2.8).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"334\" height=\"103\" class=\"wp-image-290\" style=\"width: 380px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-Catalyzed-Coupling-Reaction-of-Primary-Alcohols-with-2-Alkynes.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-Catalyzed-Coupling-Reaction-of-Primary-Alcohols-with-2-Alkynes.jpg 334w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-Catalyzed-Coupling-Reaction-of-Primary-Alcohols-with-2-Alkynes-300x93.jpg 300w\" sizes=\"auto, (max-width: 334px) 100vw, 334px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1021\/ja9106989\" target=\"_blank\">Y. Iuchi, Y. Obora, Y. Ishii<br><strong>Iridium-Catalyzed a-Alkylation of Acetates with Alcohols and Diols<\/strong><br><em>J. Am. Chem. Soc.&nbsp;<\/em>132(8), 2536-2537 (2010.3.3).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"531\" height=\"149\" class=\"wp-image-291\" style=\"width: 400px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-Catalyzed-\u03b1-Alkylation-of-Acetates-with-Primary-Alcohols-and-Diols.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-Catalyzed-\u03b1-Alkylation-of-Acetates-with-Primary-Alcohols-and-Diols.jpg 531w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Iridium-Catalyzed-\u03b1-Alkylation-of-Acetates-with-Primary-Alcohols-and-Diols-300x84.jpg 300w\" sizes=\"auto, (max-width: 531px) 100vw, 531px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1021\/jo9027165\" target=\"_blank\">Y. Iuchi, M. Hyotanishi, B. E. Miller, K. Maeda, Y. Obora, Y. Ishii<br><strong>Synthesis of \u03c9-Hydroxy Carboxylic Acids and \u03b1,\u03c9-Dimethyl Ketones Using \u03b1,\u03c9-Diols as Alkylating Agents<\/strong><br><em>J. Org. Chem.<\/em>&nbsp;75(5), 1803-1806 (2010. 3.5).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"532\" height=\"162\" class=\"wp-image-296\" style=\"width: 450px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Synthesis-of-\u03c9-Hydroxy-Carboxylic-Acids-and-\u03b1\u03c9-Dimethyl-Ketones-Using-\u03b1\u03c9-Diols-As-Alkylating-Agents.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Synthesis-of-\u03c9-Hydroxy-Carboxylic-Acids-and-\u03b1\u03c9-Dimethyl-Ketones-Using-\u03b1\u03c9-Diols-As-Alkylating-Agents.jpg 532w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Synthesis-of-\u03c9-Hydroxy-Carboxylic-Acids-and-\u03b1\u03c9-Dimethyl-Ketones-Using-\u03b1\u03c9-Diols-As-Alkylating-Agents-300x91.jpg 300w\" sizes=\"auto, (max-width: 532px) 100vw, 532px\" \/><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.3390\/molecules15031487\" target=\"_blank\">Y. Obora, Y. Ishii<br><strong>Pd(II)\/HPMoV-Catalyzed Direct Oxidative Coupling Reaction of Benzenes with Olefins<\/strong><br><em>Molecules<\/em>&nbsp;15(3), 1487-1500 (2010.3.9).<\/a><\/li>\n\n\n\n<li><a rel=\"noreferrer noopener\" href=\"https:\/\/doi.org\/10.1021\/ol100292g\" target=\"_blank\">Y. Shimizu, Y. Obora, Y. Ishii<br><strong>Intermolecular Aerobic Oxidative Allylic Amination of Simple Alkenes with Diarylamines Catalyzed by the Pd(OCOCF<sub>3<\/sub>)<sub>2<\/sub>\/NPMoV\/O<sub>2<\/sub>&nbsp;System<\/strong><br><em>Org. Lett.&nbsp;<\/em>12(6), 1372-1374 (2010. 3. 19).<\/a><br><img loading=\"lazy\" decoding=\"async\" width=\"531\" height=\"145\" class=\"wp-image-287\" style=\"width: 420px\" src=\"http:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Intermolecular-Aerobic-Oxidative-Allylic-Amination-of-Simple-Alkenes-with-Diarylamines.jpg\" alt=\"\" srcset=\"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Intermolecular-Aerobic-Oxidative-Allylic-Amination-of-Simple-Alkenes-with-Diarylamines.jpg 531w, https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-content\/uploads\/sites\/217\/2021\/05\/Intermolecular-Aerobic-Oxidative-Allylic-Amination-of-Simple-Alkenes-with-Diarylamines-300x82.jpg 300w\" sizes=\"auto, (max-width: 531px) 100vw, 531px\" \/><\/li>\n<\/ol>\n\n\n\n<div style=\"height:30px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>\u5b66\u4f1a\u767a\u8868<\/strong><\/h4>\n\n\n\n<ol class=\"wp-block-list\">\n<li>\u4e95\u5185\u6d0b\u4ecb\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u932f\u4f53\u89e6\u5a92\u306b\u3088\u308b\u9162\u9178\u30a8\u30b9\u30c6\u30eb\u306e\u03b1\uff0d\u30a2\u30eb\u30ad\u30eb\u5316\u53cd\u5fdc<\/strong><br><em>\u7b2c\uff13\uff16\u56de\u6709\u6a5f\u53cd\u5fdc\u61c7\u8ac7\u4f1a\u8981\u65e8\u96c6<\/em>\uff0c\u95a2\u897f\u5b66\u9662\u5927\u5b66\uff0c13 (2009.8.3).<\/li>\n\n\n\n<li>\u5ca1\u8fba\u4f73\u4e45\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c<br><strong>Pd\/\u30e2\u30ea\u30d6\u30c9\u30d0\u30ca\u30c9\u30ea\u30f3\u9178\/\u9178\u7d20\u7cfb\u3092\u7528\u3044\u305f\u30d9\u30f3\u30bc\u30f3\u3068\u30a2\u30af\u30ea\u30ed\u30cb\u30c8\u30ea\u30eb\u985e\u306e\u76f4\u63a5\u7684\u30ab\u30c3\u30d7\u30ea\u30f3\u30b0\u53cd\u5fdc<\/strong><br><em>\u7b2c\uff13\uff16\u56de\u6709\u6a5f\u53cd\u5fdc\u61c7\u8ac7\u4f1a\u8981\u65e8\u96c6<\/em>\uff0c\u95a2\u897f\u5b66\u9662\u5927\u5b66\uff0c14 (2009.8.3).<\/li>\n\n\n\n<li>\u5ddd\u5cf6\u76f4\u502b\uff0c\u672c\u5e84\u7f8e\u9999, \u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c<br><strong>\u65b0\u898f\u74b0\u72b6\u304a\u3088\u3073\u975e\u74b0\u72b6\u30a2\u30ea\u30fc\u30eb\u30a8\u30fc\u30c6\u30eb\u90e8\u4f4d\u3092\u6709\u3059\u308b\u30db\u30b9\u30d5\u30a3\u30f3\u914d\u4f4d\u5b50\u306e\u5408\u6210\u3068\u9078\u629e\u7684\u89e6\u5a92\u53cd\u5fdc\u3078\u306e\u5229\u7528<\/strong><br><em>\u7b2c\uff13\uff16\u56de\u6709\u6a5f\u53cd\u5fdc\u61c7\u8ac7\u4f1a\u8981\u65e8\u96c6<\/em>\uff0c\u95a2\u897f\u5b66\u9662\u5927\u5b66\uff0c15 (2009.8.3).<\/li>\n\n\n\n<li>\u5b50\u7530\u4f73\u592a\u90ce\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u89e6\u5a92\u3092\u7528\u3044\u308b\u30a8\u30bf\u30ce\u30fc\u30eb\u306e\u4e8c\u91cf\u5316\u53cd\u5fdc\u306b\u3088\u308b\u30d6\u30bf\u30ce\u30fc\u30eb\u306e\u5408\u6210<\/strong><br><em>\u7b2c\uff13\uff16\u56de\u6709\u6a5f\u53cd\u5fdc\u61c7\u8ac7\u4f1a\u8981\u65e8\u96c6<\/em>\uff0c\u95a2\u897f\u5b66\u9662\u5927\u5b66\uff0c16 (2009.8.3).<\/li>\n\n\n\n<li>\u6e05\u6c34\u6d0b\u4f51\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c<br><strong>Pd(\u2161)\/NPMoV\/O<sub>2<\/sub>\u7cfb\u3092\u7528\u3044\u305f\u30a2\u30eb\u30b1\u30f3\u306e\u9178\u5316\u7684\u30a2\u30df\u30ce\u5316\u53cd\u5fdc<\/strong><br><em>\u7b2c\uff13\uff16\u56de\u6709\u6a5f\u53cd\u5fdc\u61c7\u8ac7\u4f1a\u8981\u65e8\u96c6<\/em>\uff0c\u95a2\u897f\u5b66\u9662\u5927\u5b66\uff0c17 (2009.8.3).<\/li>\n\n\n\n<li>\u7551\u4e2d\u614e\u592a\u90ce\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u932f\u4f53\u89e6\u5a92\u3092\u7528\u3044\u305f\u30a2\u30eb\u30ad\u30f3\u306e\u30d2\u30c9\u30ed\u30a2\u30b7\u30eb\u5316\u53cd\u5fdc<\/strong><br><em>\u7b2c\uff13\uff16\u56de\u6709\u6a5f\u53cd\u5fdc\u61c7\u8ac7\u4f1a\u8981\u65e8\u96c6<\/em>\uff0c\u95a2\u897f\u5b66\u9662\u5927\u5b66\uff0c18 (2009.8.3).<\/li>\n\n\n\n<li>\u5897\u5ddd\u6e96\u4e5f\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c<br><strong>\uff30\uff44\u89e6\u5a92\u3092\u7528\u3044\u308b\u82b3\u9999\u65cf\u74b0\u306e\u76f4\u63a5C-H\u7d50\u5408\u6d3b\u6027\u5316\u3092\u4f34\u3046\u30d9\u30f3\u30bc\u30f3\u3068\u03b1\uff0c\u03b2\uff0d\u4e0d\u98fd\u548c\u30ab\u30eb\u30dc\u30cb\u30eb\u3068\u306e\u30d2\u30c9\u30ed\u30a2\u30ea\u30fc\u30eb\u5316\u53cd\u5fdc<\/strong><br><em>\u7b2c\uff13\uff16\u56de\u6709\u6a5f\u53cd\u5fdc\u61c7\u8ac7\u4f1a\u8981\u65e8\u96c6<\/em>\uff0c\u95a2\u897f\u5b66\u9662\u5927\u5b66\uff0c19 (2009.8.3).<\/li>\n\n\n\n<li>\u963f\u6b66\u7531\u52a0\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u932f\u4f53\u89e6\u5a92\u3092\u7528\u3044\u305f\u03b1,\u03c9\uff0d\u30b8\u30aa\u30fc\u30eb\u306e\u03b2\uff0d\u30a2\u30eb\u30ad\u30eb\u5316\u53cd\u5fdc\u306b\u3088\u308b\u30aa\u30ea\u30b4\u30aa\u30fc\u30eb\u306e\u5408\u6210<\/strong><br><em>\u7b2c\uff13\uff16\u56de\u6709\u6a5f\u53cd\u5fdc\u61c7\u8ac7\u4f1a\u8981\u65e8\u96c6<\/em>\uff0c\u95a2\u897f\u5b66\u9662\u5927\u5b66\uff0c20 (2009.8.3).<\/li>\n\n\n\n<li>\u4f50\u85e4\u9756\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c<br><strong>\u4e09\u5869\u5316\u30cb\u30aa\u30d6\u932f\u4f53\u3092\u7528\u3044\u305f\u03b1,\u03c9\uff0d\u975e\u5171\u5f79\u30b8\u30a8\u30f3\u3068\u672b\u7aef\u30a2\u30eb\u30ad\u30f3\u306e\u9ad8\u9078\u629e\u7684[2+2+2]\u4ed8\u52a0\u74b0\u5316\u53cd\u5fdc<\/strong><br><em>\u7b2c\uff13\uff16\u56de\u6709\u6a5f\u53cd\u5fdc\u61c7\u8ac7\u4f1a\u8981\u65e8\u96c6<\/em>\uff0c\u95a2\u897f\u5b66\u9662\u5927\u5b66\uff0c21 (2009.8.3).<\/li>\n\n\n\n<li>\u897f\u91ce\u6f64\u4e00\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c<br><strong>\u4f4e\u539f\u5b50\u4fa1\u30cb\u30aa\u30d6\u89e6\u5a92\u3092\u7528\u3044\u305f\u30a2\u30eb\u30b1\u30f3\u3068\u30a2\u30df\u30f3\u306e\u30d2\u30c9\u30ed\u30a2\u30df\u30ce\u5316\u53cd\u5fdc<\/strong><br><em>\u7b2c\uff13\uff16\u56de\u6709\u6a5f\u53cd\u5fdc\u61c7\u8ac7\u4f1a\u8981\u65e8\u96c6<\/em>\uff0c\u95a2\u897f\u5b66\u9662\u5927\u5b66\uff0c22 (2009.8.3).<\/li>\n\n\n\n<li>\u5175\u4e39\u77f3\u6075\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u932f\u4f53\u89e6\u5a92\u306b\u3088\u308b\u30b7\u30a2\u30ce\u9162\u9178\u30a8\u30b9\u30c6\u30eb\u306e\u03b1\uff0d\u30a2\u30eb\u30ad\u30eb\u5316\u3092\u7528\u3044\u305f\u30e0\u30b9\u30af\u524d\u99c6\u4f53\u306e\u65b0\u898f\u5408\u6210\u6cd5\u306e\u958b\u767a<\/strong><br><em>\u7b2c\uff13\uff16\u56de\u6709\u6a5f\u53cd\u5fdc\u61c7\u8ac7\u4f1a\u8981\u65e8\u96c6<\/em>\uff0c\u95a2\u897f\u5b66\u9662\u5927\u5b66\uff0c23 (2009.8.3).<\/li>\n\n\n\n<li>\u5800\u5ddd\u5178\u79c0\uff0c\u7389\u7956\u5065\u4e00\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c<br><strong>Pd\u89e6\u5a92\u306b\u3088\u308b\u30a2\u30bb\u30bf\u30fc\u30eb\u3092\u9375\u4e2d\u9593\u4f53\u3068\u3057\u305f3-\u30d5\u30e9\u30a2\u30eb\u30c7\u30d2\u30c9\u8a98\u5c0e\u4f53\u306e\u5408\u6210<\/strong><br><em>\u7b2c\uff13\uff16\u56de\u6709\u6a5f\u53cd\u5fdc\u61c7\u8ac7\u4f1a\u8981\u65e8\u96c6<\/em>\uff0c\u95a2\u897f\u5b66\u9662\u5927\u5b66\uff0c24 (2009.8.3).<\/li>\n\n\n\n<li>\u5c71\u672c\u4fe1\u884c\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u932f\u4f53\u89e6\u5a92\u306b\u3088\u308b\u30a8\u30bf\u30ce\u30fc\u30eb\u304b\u3089\u9162\u9178\u30a8\u30c1\u30eb\u306e\u4e00\u6bb5\u968e\u5408\u6210<\/strong><br><em>\u7b2c\uff13\uff16\u56de\u6709\u6a5f\u53cd\u5fdc\u61c7\u8ac7\u4f1a\u8981\u65e8\u96c6<\/em>\uff0c\u95a2\u897f\u5b66\u9662\u5927\u5b66\uff0c25 (2009.8.3).<\/li>\n\n\n\n<li>\u7551\u4e2d\u614e\u592a\u90ce, \u5927\u6d1e\u5eb7\u55e3, \u77f3\u4e95\u5eb7\u656c<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u932f\u4f53\u89e6\u5a92\u3092\u7528\u3044\u305f\u82b3\u9999\u65cf\u30a2\u30eb\u30b3\u30fc\u30eb\u30682-\u30a2\u30eb\u30ad\u30f3\u3068\u306e\u30d2\u30c9\u30ed\u30a2\u30b7\u30eb\u5316\u53cd\u5fdc<\/strong><br><em>\u7b2c56\u56de\u6709\u6a5f\u91d1\u5c5e\u5316\u5b66\u8a0e\u8ad6\u4f1a\u8981\u65e8\u96c6<\/em>\uff0c\u540c\u5fd7\u793e\u5927\u5b66\uff0cP2B-36 (2009.9.10).<\/li>\n\n\n\n<li>\u5927\u6d1e\u5eb7\u55e3,\u672c\u5e84\u7f8e\u9999,\u5ddd\u5cf6\u76f4\u502b, \u77f3\u4e95\u5eb7\u656c<br><strong>\u74b0\u72b6\u304a\u3088\u3073\u975e\u74b0\u72b6\u30a2\u30ea\u30fc\u30eb\u30a8\u30fc\u30c6\u30eb\u90e8\u4f4d\u3092\u6709\u3059\u308b\u65b0\u898f\u30db\u30b9\u30d5\u30a3\u30f3\u914d\u4f4d\u5b50\u306e\u5408\u6210\u3068\u57fa\u8cea\u9078\u629e\u7684\u89e6\u5a92\u53cd\u5fdc\u3078\u306e\u5fdc\u7528<\/strong><br><em>\u7b2c56\u56de\u6709\u6a5f\u91d1\u5c5e\u5316\u5b66\u8a0e\u8ad6\u4f1a\u8981\u65e8\u96c6<\/em>\uff0c\u540c\u5fd7\u793e\u5927\u5b66\uff0cP3A-22 (2009.9.11).<\/li>\n\n\n\n<li>\u6e05\u6c34\u6d0b\u4f51, \u5927\u6d1e\u5eb7\u55e3, \u77f3\u4e95\u5eb7\u656c<br><strong>Pd(II)\/\u30e2\u30ea\u30d6\u30c9\u30d0\u30ca\u30c9\u30ea\u30f3\u9178\u5869\/\u9178\u7d20\u89e6\u5a92\u7cfb\u306b\u3088\u308b\u6d3b\u6027\u30aa\u30ec\u30d5\u30a3\u30f3\u304a\u3088\u3073\u5358\u7d14\u30aa\u30ec\u30d5\u30a3\u30f3\u306e\u9178\u5316\u7684\u30a2\u30df\u30ce\u5316\u53cd\u5fdc<\/strong><br><em>\u7b2c56\u56de\u6709\u6a5f\u91d1\u5c5e\u5316\u5b66\u8a0e\u8ad6\u4f1a\u8981\u65e8\u96c6<\/em>\uff0c\u540c\u5fd7\u793e\u5927\u5b66\uff0cP3A-27 (2009.9.10).<\/li>\n\n\n\n<li>\u5927\u6d1e\u5eb7\u55e3<br><strong>\u6709\u6a5f\u91d1\u5c5e\u5316\u5408\u7269\u306e\u7279\u6027\u3092\u6d3b\u304b\u3057\u305f\u5747\u4e00\u7cfb\u89e6\u5a92\u53cd\u5fdc\u958b\u767a<\/strong><br>\u30a4\u30ce\u30d9\u30fc\u30b7\u30e7\u30f3\u30b8\u30e3\u30d1\u30f3\uff12\uff10\uff10\uff19\u5927\u5b66\u898b\u672c\u5e02\uff0c\u6771\u4eac\u56fd\u969b\u30d5\u30a9\u30fc\u30e9\u30e0PZ-11 (2009.9.18).<\/li>\n\n\n\n<li>\u5800\u5ddd\u5178\u79c0,\u7389\u7956\u5065\u4e00,\u5927\u6d1e\u5eb7\u55e3, \u77f3\u4e95\u5eb7\u656c<br><strong>Pd \/ HPMoV \/ CeCl<sub>3<\/sub>&nbsp;\/ O<sub>2<\/sub>\u7cfb\u306b\u3088\u308b\u30a2\u30bb\u30bf\u30fc\u30eb\u3092\u9375\u4e2d\u9593\u4f53\u3068\u3057\u305f\u30a2\u30eb\u30c7\u30d2\u30c9\u304b\u3089\u306e\u65b0\u898f\u5408\u6210\u53cd\u5fdc\u306e\u958b\u767a<\/strong><br><em>\u7b2c\uff11\uff10\uff14\u56de\u89e6\u5a92\u8a0e\u8ad6\u4f1a\uff21\u4e88\u7a3f\u96c6<\/em>\uff0c\u5bae\u5d0e\u5927\u5b66\uff0c3J02 (2009.9.29).<\/li>\n\n\n\n<li>\u5c71\u672c\u4fe1\u884c,\u5927\u6d1e\u5eb7\u55e3, \u77f3\u4e95\u5eb7\u656c<br><strong>Ir\u89e6\u5a92\u306e\u6c34\u7d20\u79fb\u52d5\u80fd\u3092\u7528\u3044\u305f\u30a8\u30bf\u30ce\u30fc\u30eb\u304b\u3089\u9162\u9178\u30a8\u30c1\u30eb\u306e\u65b0\u898f\u5408\u6210\u6cd5\u306e\u958b\u767a<\/strong><br><em>\u7b2c\uff11\uff10\uff14\u56de\u89e6\u5a92\u8a0e\u8ad6\u4f1a\uff21\u4e88\u7a3f\u96c6<\/em>\uff0c\u5bae\u5d0e\u5927\u5b66\uff0c3J02 (2009.9.29).<\/li>\n\n\n\n<li>\u5175\u4e39\u77f3\u6075\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u932f\u4f53\u89e6\u5a92\u306b\u3088\u308b\u30b8\u30aa\u30fc\u30eb\u3092\u30a2\u30eb\u30ad\u30eb\u5316\u5264\u3068\u3057\u3066\u7528\u3044\u305f\u30e0\u30b9\u30af\u524d\u99c6\u4f53\u306e\u5408\u6210<\/strong><br><em>\u7b2c\uff15\uff13\u56de\u9999\u6599\u30fb\u30c6\u30eb\u30da\u30f3\u304a\u3088\u3073\u7cbe\u6cb9\u5316\u5b66\u306b\u95a2\u3059\u308b\u8a0e\u8ad6\u4f1a\u8b1b\u6f14\u8981\u65e8\u96c6<\/em>\uff0c\u5948\u826f\u5148\u7aef\u79d1\u5b66\u6280\u8853\u5927\u5b66\u9662\u5927\u5b66\uff0c2PIV-5 (2009.11.8).<\/li>\n\n\n\n<li>\u5897\u5ddd\u6e96\u4e5f\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c<br><strong>\uff30\uff44\u89e6\u5a92\u306b\u3088\u308b\u82b3\u9999\u65cf\u74b0\u306e\u76f4\u63a5\uff23\uff0d\uff28\u7d50\u5408\u6d3b\u6027\u5316\u30d7\u30ed\u30bb\u30b9\u3092\u4f34\u3046\u30d9\u30f3\u30bc\u30f3\u3068\u03b1\uff0c\u03b2\uff0d\u4e0d\u98fd\u548c\u30ab\u30eb\u30dc\u30cb\u30eb\u3068\u306e\u30d2\u30c9\u30ed\u30a2\u30ea\u30fc\u30eb\u5316\u53cd\u5fdc<\/strong><br><em>\u7b2c\uff14\uff12\u56de\u9178\u5316\u53cd\u5fdc\u8a0e\u8ad6\u4f1a\u8b1b\u6f14\u8981\u65e8\u96c6<\/em>\uff0c\u6771\u5317\u5927\u5b66\uff0cP-07 (2009.11.15).<\/li>\n\n\n\n<li>\u4e95\u5185\u6d0b\u4ecb\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u932f\u4f53\u89e6\u5a92\u306b\u3088\u308b\u30a2\u30bb\u30c8\u30f3\u304a\u3088\u3073\u9162\u9178\u30a8\u30b9\u30c6\u30eb\u306e\u03b1\uff0d\u30a2\u30eb\u30ad\u30eb\u5316\u53cd\u5fdc\uff1a\u30e0\u30b9\u30af\u524d\u99c6\u4f53\u5408\u6210\u3078\u306e\u5229\u7528<\/strong><br><em>\u77f3\u6cb9\u5b66\u4f1a\u95a2\u897f\u652f\u90e8\u7b2c\uff11\uff18\u56de\u7814\u7a76\u767a\u8868\u4f1a\u65e5\u672c\u30a8\u30cd\u30eb\u30ae\u30fc\u5b66\u4f1a\u95a2\u897f\u652f\u90e8<br>\u7b2c\uff15\uff14\u56de\u7814\u7a76\u767a\u8868\u4f1a\u5408\u540c\u7814\u7a76\u767a\u8868\u4f1a\u8b1b\u6f14\u8981\u65e8\u96c6<\/em>\uff0c\u795e\u6238\u5927\u5b66\uff0c1 (2009.12.4).<\/li>\n\n\n\n<li>\u5ca1\u8fba\u4f73\u4e45\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c<br><strong>Pd\/HPMoV\/O<sub>2<\/sub>\u89e6\u5a92\u7cfb\u3092\u7528\u3044\u305fC-H\u7d50\u5408\u6d3b\u6027\u5316\u306b\u3088\u308b\u82b3\u9999\u65cf\u5316\u5408\u7269\u3068\u30a2\u30af\u30ea\u30ed\u30cb\u30c8\u30ea\u30eb\u985e\u304a\u3088\u3073\u30d3\u30cb\u30eb\u30a8\u30b9\u30c6\u30eb\u985e\u306e\u9178\u5316\u7684\u30ab\u30c3\u30d7\u30ea\u30f3\u30b0\u53cd\u5fdc<\/strong><br><em>\u77f3\u6cb9\u5b66\u4f1a\u95a2\u897f\u652f\u90e8\u7b2c\uff11\uff18\u56de\u7814\u7a76\u767a\u8868\u4f1a\u65e5\u672c\u30a8\u30cd\u30eb\u30ae\u30fc\u5b66\u4f1a\u95a2\u897f\u652f\u90e8<br>\u7b2c\uff15\uff14\u56de\u7814\u7a76\u767a\u8868\u4f1a\u5408\u540c\u7814\u7a76\u767a\u8868\u4f1a\u8b1b\u6f14\u8981\u65e8\u96c6<\/em>\uff0c\u795e\u6238\u5927\u5b66\uff0c2 (2009.12.4).<\/li>\n\n\n\n<li>\u4f50\u85e4\u9756\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c<br><strong>\u4f4e\u539f\u5b50\u4fa1\u30cb\u30aa\u30d6\u89e6\u5a92\u3092\u7528\u3044\u305f\u03b1,\u03c9\uff0d\u30b8\u30a8\u30f3\u3068\u30a2\u30eb\u30ad\u30f3\u306b\u3088\u308b\u9ad8\u4f4d\u7f6e\u7acb\u4f53\u9078\u629e\u7684\uff15\uff0d\u03c9\uff0d\u30a2\u30eb\u30b1\u30cb\u30eb\uff0d\uff11\uff0c\uff13\uff0d\u30b7\u30af\u30ed\u30d8\u30ad\u30b5\u30b8\u30a8\u30f3\u8a98\u5c0e\u4f53\u306e\u5408\u6210<\/strong><br><em>\u77f3\u6cb9\u5b66\u4f1a\u95a2\u897f\u652f\u90e8\u7b2c\uff11\uff18\u56de\u7814\u7a76\u767a\u8868\u4f1a\u65e5\u672c\u30a8\u30cd\u30eb\u30ae\u30fc\u5b66\u4f1a\u95a2\u897f\u652f\u90e8<br>\u7b2c\uff15\uff14\u56de\u7814\u7a76\u767a\u8868\u4f1a\u5408\u540c\u7814\u7a76\u767a\u8868\u4f1a\u8b1b\u6f14\u8981\u65e8\u96c6<\/em>\uff0c\u795e\u6238\u5927\u5b66\uff0c3 (2009.12.4).<\/li>\n\n\n\n<li>\u6c34\u7530\u5eb8\u5e73\uff0c\u6e05\u6c34\u6d0b\u7950\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c<br><strong>Pd(II)\/HPMoV\/O<sub>2<\/sub>\u7cfb\u3092\u7528\u3044\u305f\u30a2\u30df\u30ce\u30d9\u30f3\u30bc\u30f3\u985e\u3068\u30aa\u30ec\u30d5\u30a3\u30f3\u3068\u306e\u9178\u5316\u7684\u30ab\u30c3\u30d7\u30ea\u30f3\u30b0\u53cd\u5fdc<\/strong><br><em>\u7b2c\uff19\uff10\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a\u8b1b\u6f14\u8981\u65e8\u96c6<\/em>\uff0c\u8fd1\u757f\u5927\u5b66\uff0c2F1-41\uff082010.3.27).<\/li>\n\n\n\n<li>\u897f\u91ce\u6f64\u4e00\uff0c\u5927\u6d1e\u5eb7\u55e3<br><strong>\u4f4e\u539f\u5b50\u4fa1\u30cb\u30aa\u30d6\u89e6\u5a92\u3092\u7528\u3044\u305f\u30a2\u30ea\u30eb\u30a2\u30eb\u30b3\u30fc\u30eb\u985e\u306e\u53cd\u5fdc<\/strong><br><em>\u7b2c\uff19\uff10\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a\u8b1b\u6f14\u8981\u65e8\u96c6<\/em>\uff0c\u8fd1\u757f\u5927\u5b66\uff0c2PB-176\uff082010.3.27).<\/li>\n\n\n\n<li>\u539f\u7530\u8056\u4e00\u6717\uff0c\u5927\u6d1e\u5eb7\u55e3<br><strong>\u30cb\u30aa\u30d6\u89e6\u5a92\u3092\u7528\u3044\u308b\u30a4\u30df\u30f3\u3068\u30aa\u30ec\u30d5\u30a3\u30f3\u985e\u3068\u306e\u30ab\u30c3\u30d7\u30ea\u30f3\u30b0\u53cd\u5fdc<\/strong><br><em>\u7b2c\uff19\uff10\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a\u8b1b\u6f14\u8981\u65e8\u96c6<\/em>\uff0c\u8fd1\u757f\u5927\u5b66\u30012PB-177\uff082010.3.27).<\/li>\n\n\n\n<li>\u65b0\u5c45\u502b\u6210\uff0c\u5927\u6d1e\u5eb7\u55e3<br><strong>\u30d1\u30e9\u30b8\u30a6\u30e0\u89e6\u5a92\u306b\u3088\u308b\u9178\u5869\u5316\u7269\uff0c\u30a2\u30eb\u30ad\u30f3\u304a\u3088\u3073\u30b8\u30b7\u30e9\u30f3\u3068\u306e\u53cd\u5fdc<\/strong><br><em>\u7b2c\uff19\uff10\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a\u8b1b\u6f14\u8981\u65e8\u96c6<\/em>\uff0c\u8fd1\u757f\u5927\u5b66\uff0c2PB-179\uff082010.3.27).<\/li>\n\n\n\n<li>\u4f50\u85e4\u9756\uff0c\u5927\u6d1e\u5eb7\u55e3<br><strong>\u4e09\u5869\u5316\u30cb\u30aa\u30d6\u89e6\u5a92\u3092\u7528\u3044\u305f\u672b\u7aef\u30a2\u30eb\u30ad\u30f3\uff0c\u5185\u90e8\u30a2\u30eb\u30ad\u30f3\u304a\u3088\u3073\u5358\u7d14\u30a2\u30eb\u30b1\u30f3\u3068\u306e\u4e09\u6210\u5206[2+2+2]\u74b0\u5316\u4ed8\u52a0\u53cd\u5fdc<\/strong><br><em>\u7b2c\uff19\uff10\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a\u8b1b\u6f14\u8981\u65e8\u96c6<\/em>\uff0c\u8fd1\u757f\u5927\u5b66\uff0c3F3-19\uff082010.3.28).<\/li>\n\n\n\n<li>\u963f\u6b66\u7531\u52a0\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u89e6\u5a92\u3092\u7528\u3044\u305f\u03b1,\u03c9\uff0d\u30b8\u30aa\u30fc\u30eb\u306eGuerbet\u53cd\u5fdc<\/strong><br><em>\u7b2c\uff19\uff10\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a\u8b1b\u6f14\u8981\u65e8\u96c6<\/em>\uff0c\u8fd1\u757f\u5927\u5b66\uff0c3F1-32\uff082010.3.28).<\/li>\n\n\n\n<li>\u6fa4\u53e3\u62d3\u77e2\uff0c\u5927\u6d1e\u5eb7\u55e3<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u89e6\u5a92\u306b\u3088\u308b\u30a2\u30bb\u30c8\u30cb\u30c8\u30ea\u30eb\u306e\u30a2\u30eb\u30b3\u30fc\u30eb\u3092\u7528\u3044\u305f\u03b1\uff0d\u30a2\u30eb\u30ad\u30eb\u5316\u53cd\u5fdc<\/strong><br><em>\u7b2c\uff19\uff10\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a\u8b1b\u6f14\u8981\u65e8\u96c6<\/em>\uff0c\u8fd1\u757f\u5927\u5b66\uff0c3F1-33\uff082010.3.28).<\/li>\n\n\n\n<li>\u77f3\u6a4b\u512a\uff0c\u5927\u6d1e\u5eb7\u55e3<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u89e6\u5a92\u306b\u3088\u308b\uff14\uff0d\u30a2\u30ea\u30fc\u30eb\u30d6\u30bf\u30ce\u30fc\u30eb\u985e\u306e\u5206\u5b50\u5185\u74b0\u5316\u53cd\u5fdc<\/strong><br><em>\u7b2c\uff19\uff10\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a\u8b1b\u6f14\u8981\u65e8\u96c6<\/em>\uff0c\u8fd1\u757f\u5927\u5b66\uff0c3F1-34\uff082010.3.28).<\/li>\n\n\n\n<li>\u5c71\u672c\u4fe1\u884c\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u89e6\u5a92\u3092\u7528\u3044\u305f\u7b2c\u4e00\u7d1a\u30a2\u30eb\u30b3\u30fc\u30eb\u3068\u30e1\u30bf\u30ce\u30fc\u30eb\u304b\u3089\u306e\u30e1\u30c1\u30eb\u30a8\u30b9\u30c6\u30eb\u985e\u306e\u5408\u6210<\/strong><br><em>\u7b2c\uff19\uff10\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a\u8b1b\u6f14\u8981\u65e8\u96c6<\/em>\uff0c\u8fd1\u757f\u5927\u5b66\uff0c3F1-38\uff082010.3.28).<\/li>\n\n\n\n<li>\u5409\u7530\u5146\u5fd7\uff0c\u7551\u4e2d\u614e\u592a\u90ce\uff0c\u5927\u6d1e\u5eb7\u55e3<br><strong>\u30a4\u30ea\u30b8\u30a6\u30e0\u89e6\u5a92\u306b\u3088\u308b\uff12\uff0d\u30a2\u30eb\u30ad\u30f3\u3068\u03b1,\u03c9\uff0d\u30b8\u30aa\u30fc\u30eb\u3068\u306e\u53cd\u5fdc<\/strong><br><em>\u7b2c\uff19\uff10\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a\u8b1b\u6f14\u8981\u65e8\u96c6<\/em>\uff0c\u8fd1\u757f\u5927\u5b66\uff0c3F1-38\uff082010.3.28).<\/li>\n\n\n\n<li>\u5175\u4e39\u77f3\u6075\uff0c\u897f\u91ce\u6f64\u4e00\uff0c\u5c71\u672c\u5bdb\u5b50\uff0c\u5ddd\u5d0e\u82f1\u4e5f\uff0c\u5927\u6d1e\u5eb7\u55e3<br><strong>\u30b5\u30d6\u30ca\u30ce\u30b5\u30a4\u30ba\u767d\u91d1\u304a\u3088\u3073\u30d1\u30e9\u30b8\u30a6\u30e0\u5fae\u7c92\u5b50\u306e\u5408\u6210\u304a\u3088\u3073\u89e6\u5a92\u3068\u3057\u3066\u306e\u5229\u7528<\/strong><br><em>\u7b2c\uff19\uff10\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a\u8b1b\u6f14\u8981\u65e8\u96c6<\/em>\uff0c\u8fd1\u757f\u5927\u5b66\uff0c4F1-20\uff082010.3.29).<\/li>\n\n\n\n<li>\u5800\u5ddd\u5178\u79c0\uff0c\u524d\u7530\u5f69\u7531\u7d00\uff0c\u5927\u6d1e\u5eb7\u55e3\uff0c\u77f3\u4e95\u5eb7\u656c<br><strong>\u30eb\u30a4\u30b9\u9178\u89e6\u5a92\u3092\u7528\u3044\u305f\u30a2\u30bb\u30bf\u30fc\u30eb\u304b\u3089\u306e\u591a\u7f6e\u63db\u82b3\u9999\u65cf\u5316\u5408\u7269\u306e\u5408\u6210<\/strong><br><em>\u7b2c\uff19\uff10\u65e5\u672c\u5316\u5b66\u4f1a\u6625\u5b63\u5e74\u4f1a\u8b1b\u6f14\u8981\u65e8\u96c6<\/em>\uff0c\u8fd1\u757f\u5927\u5b66\uff0c4F1-21\uff082010.3.29).<\/li>\n<\/ol>\n\n\n\n<div style=\"height:30px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>\u8457\u66f8<\/strong><\/h4>\n\n\n\n<ol class=\"wp-block-list\">\n<li>\u77f3\u4e95\u5eb7\u656c, \u5927\u6d1e\u5eb7\u55e3<br><strong>\u9178\u7d20\u9178\u5316\u5264\u3000\u5316\u5b66\u30d5\u30ed\u30f3\u30c6\u30a3\u30a2\uff12\uff11\u3000\u9032\u5316\u3092\u7d9a\u3051\u308b\u6709\u6a5f\u89e6\u5a92\uff0d\u6709\u6a5f\u5408\u6210\u3092\u9769\u65b0\u3059\u308b\u7b2c\u4e09\u306e\u89e6\u5a92<\/strong><br>\u4e38\u5ca1\u5553\u4e8c\u7de8\u5316\u5b66\u540c\u4eba, 177-184 [234](2009.7.30).<\/li>\n\n\n\n<li>\u77f3\u4e95\u5eb7\u656c, \u5927\u6d1e\u5eb7\u55e3<br><strong>\u4f7f\u3048\u308b\uff01\u6709\u6a5f\u5408\u6210\u53cd\u5fdc\uff12\uff14\uff11\u5b9f\u8df5\u30ac\u30a4\u30c9<\/strong><br>\u4e38\u5ca1\u5553\u4e8c, \u91ce\u5d0e\u4eac\u5b50, \u77f3\u4e95\u5eb7\u656c, \u5927\u5bfa\u7d14\u8535, \u5bcc\u5ca1\u6e05\u7de8, \u5316\u5b66\u540c\u4eba\uff0c346-347, 462-463 [504] (2010.4.1)<\/li>\n<\/ol>\n\n\n\n<div style=\"height:30px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>\u56fd\u969b\u4f1a\u8b70<\/strong><\/h4>\n\n\n\n<ol class=\"wp-block-list\">\n<li>S. Hatanaka, Y. Obora, Y. Ishii<br><strong>Iridium-catalyzed coupling of primary alcohols with 2-alkenes leading to hydroacylation products<\/strong><br><em>4th International Symposium in Science and Technology at Kansai University 2009<\/em>, LP-43, Kansai University, Suita (2009.8.25).<\/li>\n\n\n\n<li>Y. Shimizu, Y. Obora, Y. Ishii<br><strong>Pd\/molybdovanadophosphate salt catalyzed aerobic oxidative amination of alkenes with amines<\/strong><br><em>4th International Symposium in Science and Technology at Kansai University 2009<\/em>, LP-44, Kansai University, Suita (2009.8.25).<\/li>\n\n\n\n<li>Y. Obora, K. Takeshita, Y. Sato, Y. Ishii<br><strong>NbCl<sub>3<\/sub>-catalyzed [2+2+2] intermolecular cycloaddition of alkynes and alkenes leading to 1,3-cyclohexadiene derivatives<\/strong><br><em>The Eleventh International Kyoto Conference on New Aspects of Organic Chemistry (IKCOC-11)<\/em>, PB-055, Rihga Royal Hotel Kyoto, Kyoto (2009.11.11).<\/li>\n\n\n\n<li>Y. Obora, S. Hatanaka, Y. Ishii<br><strong>Iridium-catalyzed coupling reaction of primary alcohols with 2-alkynes<\/strong><br><em>CRC International Symposium on \u201cInnovation Driven by Catalysis-past, Present and Future\u201d-Dedicated to the 20 th Anniversary of CRC<\/em>, P-10, Hokkaido University, Sapporo (2009.12.7).<\/li>\n<\/ol>\n\n\n\n<div style=\"height:30px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>\u4f9d\u983c\u8b1b\u6f14\u3001\u8b1b\u7fd2\u4f1a\u3001\u305d\u306e\u4ed6<\/strong><\/h4>\n\n\n\n<ol class=\"wp-block-list\">\n<li>\u77f3\u4e95\u5eb7\u656c,\u5927\u6d1e\u5eb7\u55e3<br><strong>\u98fd\u548c\u304a\u3088\u3073\u4e0d\u98fd\u548c\u70ad\u7d20\u5206\u5b50\u306e\u70ad\u7d20\uff0d\u6c34\u7d20\u7d50\u5408\u306e\u9ad8\u5ea6\u9178\u5316\u624b\u6cd5\u306e\u958b\u767a<\/strong><br><em>\u7279\u5b9a\u9818\u57df\u7814\u7a76\u300c\u70ad\u7d20\u8cc7\u6e90\u306e\u9ad8\u5ea6\u5206\u5b50\u5909\u63db\u300d\u53d6\u308a\u7e8f\u3081\u30b7\u30f3\u30dd\u30b8\u30a6\u30e0\u3000\u30d7\u30ed\u30bb\u30b9\u5316\u5b66\u3092\u6307\u5411\u3059\u308b\u7cbe\u5bc6\u6709\u6a5f\u5408\u6210\u5316\u5b66\u8b1b\u6f14\u8981\u65e8\u96c6<\/em>\uff0c\u4eac\u90fd\u30c6\u30eb\u30b5\uff0c77-80 (2009.6.1)\uff08\u4f9d\u983c\u8b1b\u6f14\uff09.<\/li>\n\n\n\n<li>\u77f3\u4e95\u5eb7\u656c<br><strong>\u9178\u7d20\u9178\u5316\u53cd\u5fdc\uff0d\u5de5\u696d\u5316\u6280\u8853\u3092\u76ee\u6307\u3057\u3066\uff0d<\/strong><br><em>2009\u5e74\u5ea6\u30d5\u30a1\u30a4\u30f3\u30b1\u30df\u30ab\u30eb\u30ba\u5408\u6210\u89e6\u5a92\u7814\u7a76\u4f1a\u30b7\u30f3\u30dd\u30b8\u30a6\u30e0\uff0d\u65b0\u3057\u3044\u5408\u6210\u30d7\u30ed\u30bb\u30b9\u306e\u5275\u6210\uff0d<\/em>,\u30c0\u30a4\u30bb\u30eb\u5316\u5b66\u5de5\u696d\uff08\u682a\uff09\u7dcf\u5408\u7814\u7a76\u6240\uff0c(2009.6.5)(\u4f9d\u983c\u8b1b\u6f14).<\/li>\n\n\n\n<li>\u5927\u6d1e\u5eb7\u55e3<br><strong>\u9077\u79fb\u91d1\u5c5e\u932f\u4f53\u89e6\u5a92\u53cd\u5fdc\u306e\u57fa\u790e<\/strong><br>\u7b2c\uff13\uff16\u56de\u6709\u6a5f\u91d1\u5c5e\u30bb\u30df\u30ca\u30fc\uff1a\u6709\u6a5f\u91d1\u5c5e\u5316\u5408\u7269\u306e\u4f7f\u3044\u65b9\u3068\u30b3\u30c4, \u30ad\u30e3\u30f3\u30d1\u30b9\u30d7\u30e9\u30b6\u4eac\u90fd (2009.6.19) (\u4f9d\u983c\u8b1b\u6f14).<\/li>\n<\/ol>\n\n\n\n<div style=\"height:30px\" aria-hidden=\"true\" class=\"wp-block-spacer\"><\/div>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>\u7814\u7a76\u7d39\u4ecb\u8a18\u4e8b<\/strong><\/h4>\n\n\n\n<ol class=\"wp-block-list\">\n<li>\u5927\u6d1e\u5eb7\u55e3<br><strong>\u5358\u7d14\u30aa\u30ec\u30d5\u30a3\u30f3\u3092\u7528\u3044\u305f\u5206\u5b50\u9593\u9178\u5316\u7684\u30a2\u30df\u30ce\u5316\u53cd\u5fdc<\/strong><br>Organometallic News 167 (4), (2009.12.15).<\/li>\n\n\n\n<li>\u5927\u6d1e\u5eb7\u55e3<br><strong>\u6709\u6a5f\u91d1\u5c5e\u5316\u5408\u7269\u306e\u7279\u6027\u3092\u6d3b\u304b\u3057\u305f\u5747\u4e00\u7cfb\u89e6\u5a92\u53cd\u5fdc<\/strong><br>\u30b1\u30df\u30ab\u30eb\u30a8\u30f3\u30b8\u30cb\u30a2\u30ea\u30f3\u30b0\uff08\u5316\u5b66\u5de5\u696d\u793e\uff09\uff0c55 (3), 180-184 (2010.3.1).<\/li>\n<\/ol>\n","protected":false},"excerpt":{"rendered":"<p>Work<\/p>\n","protected":false},"author":220,"featured_media":0,"parent":0,"menu_order":4,"comment_status":"closed","ping_status":"closed","template":"template-fullwidth.php","meta":{"_monsterinsights_skip_tracking":false,"_monsterinsights_sitenote_active":false,"_monsterinsights_sitenote_note":"","_monsterinsights_sitenote_category":0,"footnotes":""},"class_list":["post-42","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-json\/wp\/v2\/pages\/42","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-json\/wp\/v2\/users\/220"}],"replies":[{"embeddable":true,"href":"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-json\/wp\/v2\/comments?post=42"}],"version-history":[{"count":247,"href":"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-json\/wp\/v2\/pages\/42\/revisions"}],"predecessor-version":[{"id":1314,"href":"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-json\/wp\/v2\/pages\/42\/revisions\/1314"}],"wp:attachment":[{"href":"https:\/\/wps.itc.kansai-u.ac.jp\/cataly\/wp-json\/wp\/v2\/media?parent=42"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}