{"id":2436,"date":"2022-08-29T14:32:22","date_gmt":"2022-08-29T05:32:22","guid":{"rendered":"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/?page_id=2436"},"modified":"2026-04-01T14:54:53","modified_gmt":"2026-04-01T05:54:53","slug":"publication","status":"publish","type":"page","link":"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/publication\/","title":{"rendered":"\u7814\u7a76\u696d\u7e3e"},"content":{"rendered":"\n<div class=\"wp-block-vk-blocks-table-of-contents-new vk_tableOfContents vk_tableOfContents-style-default tabs\"><div class=\"tab\"><div class=\"vk_tableOfContents_title\">\u76ee\u6b21<\/div><input type=\"checkbox\" id=\"chck1\"\/><label class=\"tab-label vk_tableOfContents_openCloseBtn button_status button_status-close\" for=\"chck1\"><\/label><ul class=\"vk_tableOfContents_list tab_content-close\"><li class=\"vk_tableOfContents_list_item vk_tableOfContents_list_item-h-2\" data-reactroot=\"\"><a href=\"#vk-htags-b7a170c3-a1d1-4852-a748-63fdcc8d7fe8\" class=\"vk_tableOfContents_list_item_link\"><span class=\"vk_tableOfContents_list_item_link_preNumber\">1. <\/span>2026<\/a><\/li><li class=\"vk_tableOfContents_list_item vk_tableOfContents_list_item-h-3\" data-reactroot=\"\"><a href=\"#vk-htags-ef4b196e-4b8a-44c0-bcae-51188b23842e\" class=\"vk_tableOfContents_list_item_link\"><span class=\"vk_tableOfContents_list_item_link_preNumber\">1.1. <\/span>\u539f\u8457\u8ad6\u6587<\/a><\/li><li class=\"vk_tableOfContents_list_item vk_tableOfContents_list_item-h-2\" data-reactroot=\"\"><a href=\"#vk-htags-b7a170c3-a1d1-4852-a748-63fdcc8d7fe8\" class=\"vk_tableOfContents_list_item_link\"><span class=\"vk_tableOfContents_list_item_link_preNumber\">2. <\/span>2025<\/a><\/li><li class=\"vk_tableOfContents_list_item vk_tableOfContents_list_item-h-3\" data-reactroot=\"\"><a href=\"#vk-htags-ef4b196e-4b8a-44c0-bcae-51188b23842e\" class=\"vk_tableOfContents_list_item_link\"><span class=\"vk_tableOfContents_list_item_link_preNumber\">2.1. <\/span>\u539f\u8457\u8ad6\u6587<\/a><\/li><li class=\"vk_tableOfContents_list_item vk_tableOfContents_list_item-h-3\" data-reactroot=\"\"><a href=\"#vk-htags-ef4b196e-4b8a-44c0-bcae-51188b23842e\" class=\"vk_tableOfContents_list_item_link\"><span class=\"vk_tableOfContents_list_item_link_preNumber\">2.2. <\/span>\u7dcf\u8aac\uff0f\u89e3\u8aac\uff0f\u5831\u544a<\/a><\/li><li class=\"vk_tableOfContents_list_item vk_tableOfContents_list_item-h-2\" data-reactroot=\"\"><a href=\"#vk-htags-b7a170c3-a1d1-4852-a748-63fdcc8d7fe8\" class=\"vk_tableOfContents_list_item_link\"><span class=\"vk_tableOfContents_list_item_link_preNumber\">3. <\/span>2024<\/a><\/li><li class=\"vk_tableOfContents_list_item vk_tableOfContents_list_item-h-3\" data-reactroot=\"\"><a href=\"#vk-htags-ef4b196e-4b8a-44c0-bcae-51188b23842e\" class=\"vk_tableOfContents_list_item_link\"><span class=\"vk_tableOfContents_list_item_link_preNumber\">3.1. <\/span>\u539f\u8457\u8ad6\u6587<\/a><\/li><li class=\"vk_tableOfContents_list_item vk_tableOfContents_list_item-h-2\" data-reactroot=\"\"><a href=\"#vk-htags-89323569-1126-47f8-aabb-331b70c4a96f\" class=\"vk_tableOfContents_list_item_link\"><span class=\"vk_tableOfContents_list_item_link_preNumber\">4. <\/span>2023<\/a><\/li><li class=\"vk_tableOfContents_list_item vk_tableOfContents_list_item-h-3\" data-reactroot=\"\"><a href=\"#vk-htags-ef4b196e-4b8a-44c0-bcae-51188b23842e\" class=\"vk_tableOfContents_list_item_link\"><span class=\"vk_tableOfContents_list_item_link_preNumber\">4.1. <\/span>\u7dcf\u8aac\uff0f\u89e3\u8aac\uff0f\u5831\u544a<\/a><\/li><li class=\"vk_tableOfContents_list_item vk_tableOfContents_list_item-h-2\" data-reactroot=\"\"><a href=\"#vk-htags-89323569-1126-47f8-aabb-331b70c4a96f\" class=\"vk_tableOfContents_list_item_link\"><span class=\"vk_tableOfContents_list_item_link_preNumber\">5. <\/span>2022<\/a><\/li><li class=\"vk_tableOfContents_list_item vk_tableOfContents_list_item-h-3\" data-reactroot=\"\"><a href=\"#vk-htags-33ab8f8f-7f8d-4052-b72d-2c469c57f4ab\" class=\"vk_tableOfContents_list_item_link\"><span class=\"vk_tableOfContents_list_item_link_preNumber\">5.1. <\/span>\u7dcf\u8aac\uff0f\u89e3\u8aac\uff0f\u5831\u544a<\/a><\/li><li class=\"vk_tableOfContents_list_item vk_tableOfContents_list_item-h-2\" data-reactroot=\"\"><a href=\"#vk-htags-35d434c0-4679-47bb-a4f5-4884eb1e66fe\" class=\"vk_tableOfContents_list_item_link\"><span class=\"vk_tableOfContents_list_item_link_preNumber\">6. <\/span>2021<\/a><\/li><li class=\"vk_tableOfContents_list_item vk_tableOfContents_list_item-h-3\" data-reactroot=\"\"><a href=\"#vk-htags-18f8a1dd-8826-48cb-b27c-1f59e5fd97de\" class=\"vk_tableOfContents_list_item_link\"><span class=\"vk_tableOfContents_list_item_link_preNumber\">6.1. <\/span>\u539f\u8457\u8ad6\u6587<\/a><\/li><li class=\"vk_tableOfContents_list_item vk_tableOfContents_list_item-h-3\" data-reactroot=\"\"><a href=\"#vk-htags-acc683d4-0a0b-40c2-889f-74a2c4d88c9c\" class=\"vk_tableOfContents_list_item_link\"><span class=\"vk_tableOfContents_list_item_link_preNumber\">6.2. <\/span>\u8457\u66f8<\/a><\/li><li class=\"vk_tableOfContents_list_item vk_tableOfContents_list_item-h-3\" data-reactroot=\"\"><a href=\"#vk-htags-f04688be-99b5-4e35-a716-6b9d598281e8\" class=\"vk_tableOfContents_list_item_link\"><span class=\"vk_tableOfContents_list_item_link_preNumber\">6.3. <\/span>\u7dcf\u8aac\uff0f\u89e3\u8aac\uff0f\u5831\u544a<\/a><\/li><li class=\"vk_tableOfContents_list_item vk_tableOfContents_list_item-h-3\" data-reactroot=\"\"><a href=\"#vk-htags-c6b70f11-9daf-4f72-983c-413cc33c1b2c\" class=\"vk_tableOfContents_list_item_link\"><span class=\"vk_tableOfContents_list_item_link_preNumber\">6.4. <\/span>\u62db\u5f85\uff0f\u57fa\u8abf\uff0f\u4f9d\u983c\u8b1b\u6f14\u30fb\u56fd\u969b\u4f1a\u8b70<\/a><\/li><\/ul><\/div><\/div>\n\n\n\n<h2 id=\"vk-htags-b7a170c3-a1d1-4852-a748-63fdcc8d7fe8\">2026<\/h2>\n\n\n\n<h3 id=\"vk-htags-ef4b196e-4b8a-44c0-bcae-51188b23842e\" style=\"font-size:20px\">\u539f\u8457\u8ad6\u6587<\/h3>\n\n\n\n<ul class=\"is-style-vk-triangle-mark\"><li>Ono, Y.; Matsumoto, A.; Shimozawa, S.; Uraguchi, D.; Asano, K. Asymmetric 1,3-Dioxane Synthesis by Using Bifunctional Thiourea Catalysis <a rel=\"noreferrer noopener\" href=\"https:\/\/aces.onlinelibrary.wiley.com\/doi\/10.1002\/asia.70698\" target=\"_blank\"><em>Chem.\u2014Asian J. <\/em><strong>2026<\/strong>, <em>21<\/em>, e70698.<\/a><\/li><\/ul>\n\n\n\n<h2 id=\"vk-htags-b7a170c3-a1d1-4852-a748-63fdcc8d7fe8\">2025<\/h2>\n\n\n\n<h3 id=\"vk-htags-ef4b196e-4b8a-44c0-bcae-51188b23842e\" style=\"font-size:20px\">\u539f\u8457\u8ad6\u6587<\/h3>\n\n\n\n<ul class=\"is-style-vk-triangle-mark\"><li>Sakaguchi, R.; Shimazu, T.; Yoshida, R.; Nagano, T.; Matsubara, S.; Uraguchi, D.; Asano, K. Olefin-Catalyzed Aromatic Bromination toward Biocompatible Tyrosine Modification <a rel=\"noreferrer noopener\" href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/10.1002\/chem.202501554\" target=\"_blank\"><em>Chem.\u2014Eur. J.<\/em>  <strong>2025<\/strong>, <em>31<\/em>, e202501554.<\/a><\/li><\/ul>\n\n\n\n<ul class=\"is-style-vk-triangle-mark\"><li>Nagano, T.; Shimazu, T.; Ono, Y.; Kaneko, K.; Matsubara, S.; Yamanaka, M.; Uraguchi, D.; Asano, K. Mechanism-Guided Development of Bifunctional Cyclooctenes as Active, Practical, and Light-Gated Bromination Catalysts. <a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/10.1002\/chem.202404011\" target=\"_blank\" rel=\"noreferrer noopener\"><em>Chem.\u2014Eur. J<\/em>. <strong>2025<\/strong>, <em>31<\/em>, e202404011<\/a>.<\/li><\/ul>\n\n\n\n<ul class=\"is-style-vk-triangle-mark\"><li>Murata, R.; Yoshida, R.; Uraguchi, D.; Asano, K.  Synthesis of Substituted Cyclooctenes through Cross-Coupling Reactions.  <a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/a-2330-0819\" target=\"_blank\" rel=\"noreferrer noopener\"><em>Synlett<\/em> <strong>2025, <\/strong><em>36<\/em><strong>, <\/strong>69\u201374<\/a>.<\/li><\/ul>\n\n\n\n<h3 id=\"vk-htags-ef4b196e-4b8a-44c0-bcae-51188b23842e\" style=\"font-size:20px\">\u7dcf\u8aac\uff0f\u89e3\u8aac\uff0f\u5831\u544a<\/h3>\n\n\n\n<ul class=\"is-style-vk-triangle-mark\"><li>\u6d45\u91ce \u572d\u4f51, \u4f4e\u30a8\u30cd\u30eb\u30ae\u30fc\u5149\u89e6\u5a92\u3092\u5229\u7528\u3059\u308b\u8fd1\u63a5\u4f9d\u5b58\u6027\u6a19\u8b58, <a href=\"https:\/\/kinka.or.jp\/om\/omnews_archive\/2025_01.html\" target=\"_blank\" rel=\"noreferrer noopener\"><em>Organometallic News<\/em> <strong>2025<\/strong>, 47<\/a>.<\/li><\/ul>\n\n\n\n<h2 id=\"vk-htags-b7a170c3-a1d1-4852-a748-63fdcc8d7fe8\">2024<\/h2>\n\n\n\n<h3 id=\"vk-htags-ef4b196e-4b8a-44c0-bcae-51188b23842e\" style=\"font-size:20px\">\u539f\u8457\u8ad6\u6587<\/h3>\n\n\n\n<ul class=\"is-style-vk-triangle-mark\"><li>Yoshida, R.; Hori, Y.; Uraguchi, D.; Asano, K. BODNs as biocompatible brominating reagents: visible-light photocatalytic tyrosine modification under physiologically favorable conditions. <a rel=\"noreferrer noopener\" href=\"https:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2024\/CC\/D4CC04171B\" target=\"_blank\"><em>Chem. Commun<\/em>. <strong>2024<\/strong>, <em>60<\/em>, 12381-12384.<\/a><br><br><strong>Highlighted in<\/strong> <a rel=\"noreferrer noopener\" href=\"https:\/\/www.thieme-connect.de\/products\/ejournals\/abstract\/10.1055\/a-2467-5538\" target=\"_blank\"><em>Synfacts<\/em> <strong>2025<\/strong>, <em>21<\/em>, 98<\/a>.<\/li><\/ul>\n\n\n\n<ul class=\"is-style-vk-triangle-mark\"><li>Murata, R.; Shitamichi, K.; Hiramatsu, M.; Matsubara, S.; Uraguchi, D.; Asano, K.  <em>trans<\/em>-Cyclooctenes as Scavengers of Bromine Involved in Catalytic Bromination.  <a rel=\"noreferrer noopener\" href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/10.1002\/chem.202303399\" target=\"_blank\"><em>Chem.\u2014Eur. J. <\/em> <strong>2024<\/strong>, <em>30<\/em>, e202303399.<\/a><br><br><strong>Selected as<\/strong><a rel=\"noreferrer noopener\" href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/10.1002\/chem.202400128\" target=\"_blank\"> the Cover Feature<\/a>.<\/li><\/ul>\n\n\n\n<h2 class=\"is-style-vk-heading-default\" id=\"vk-htags-89323569-1126-47f8-aabb-331b70c4a96f\">2023<\/h2>\n\n\n\n<h3 id=\"vk-htags-ef4b196e-4b8a-44c0-bcae-51188b23842e\" style=\"font-size:20px\">\u7dcf\u8aac\uff0f\u89e3\u8aac\uff0f\u5831\u544a<\/h3>\n\n\n\n<ul class=\"is-style-vk-triangle-mark\"><li>Asano, K.; Matsubara, S.  Organocatalytic Access to Tetrasubstituted Chiral Carbons Integrating Functional Groups.  <a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/tcr.202200200\" target=\"_blank\" rel=\"noreferrer noopener\"><em>Chem. Rec.<\/em> <strong><strong>2023<\/strong>, <em>23<\/em><\/strong>, e202200200.<\/a><\/li><\/ul>\n\n\n\n<h2 class=\"is-style-vk-heading-default\" id=\"vk-htags-89323569-1126-47f8-aabb-331b70c4a96f\">2022<\/h2>\n\n\n\n<h3 id=\"vk-htags-33ab8f8f-7f8d-4052-b72d-2c469c57f4ab\" style=\"font-size:20px\">\u7dcf\u8aac\uff0f\u89e3\u8aac\uff0f\u5831\u544a<\/h3>\n\n\n\n<ul class=\"is-style-vk-triangle-mark\"><li>\u751f\u9577 \u5e78\u4e4b\u52a9, \u6d45\u91ce \u572d\u4f51, \u4e0a\u7530 \u5584\u5f18  \u6709\u6a5f\u89e6\u5a92\u63a2\u7d22\u304b\u3089\u306e\u8a08\u753b\u7684\u30bb\u30ec\u30f3\u30c7\u30a3\u30d4\u30c6\u30a3, <a href=\"http:\/\/hdl.handle.net\/2433\/275957\" target=\"_blank\" rel=\"noreferrer noopener\">\u533b\u5b66\u306e\u3042\u3086\u307f <strong>2022<\/strong>, <em>282<\/em>, 23261-23263<\/a>.<\/li><\/ul>\n\n\n\n<h2 id=\"vk-htags-35d434c0-4679-47bb-a4f5-4884eb1e66fe\">2021<\/h2>\n\n\n\n<h3 class=\"is-style-vk-heading-default\" id=\"vk-htags-18f8a1dd-8826-48cb-b27c-1f59e5fd97de\" style=\"font-size:20px\">\u539f\u8457\u8ad6\u6587<\/h3>\n\n\n\n<ul class=\"is-style-vk-triangle-mark\"><li>Kato, K.; Uraguchi, D.; Ooi, T.  <em>o<\/em>-Quinone Methide with Overcrowded Olefinic Core as a Catalytically-Active Surrogate of Triarylmethylium Salt for Dehydridative Oxidation of Benzylic Alcohols under Aeroboc Photoirradiation Conditions.<em>  <\/em><a href=\"https:\/\/www.sciencedirect.com\/search\/advanced?pub=Tetrahedron&amp;volume=100&amp;page=132459\" target=\"_blank\" rel=\"noreferrer noopener\"><em>Tetrahedron<\/em> <strong>2021<\/strong>, 100, 132459<\/a>.<\/li><li>\u6d66\u53e3 \u5927\u8f14, \u5927\u4e95 \u8cb4\u53f2  \u591a\u91cd\u9078\u629e\u6027\u5236\u5fa1\u3092\u53ef\u80fd\u306b\u3059\u308b\u30ad\u30e9\u30eb\u30a4\u30df\u30ce\u30db\u30b9\u30db\u30e9\u30f3\u306e\u89e6\u5a92\u4f5c\u7528\uff1a\u5b9f\u9a13\u7684\u304a\u3088\u3073\u7406\u8ad6\u7684\u8003\u5bdf, <em>\u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a\u8a8c<\/em> <strong>2021<\/strong>, <em>79<\/em>, 406-416.<\/li><\/ul>\n\n\n\n<h3 class=\"is-style-vk-heading-default\" id=\"vk-htags-acc683d4-0a0b-40c2-889f-74a2c4d88c9c\" style=\"font-size:20px\">\u8457\u66f8<\/h3>\n\n\n\n<ul class=\"is-style-vk-triangle-mark\"><li>\u6d66\u53e3 \u5927\u8f14, \u5927\u4e95 \u8cb4\u53f2  \u5149\u96fb\u5b50\u79fb\u52d5\u6761\u4ef6\u4e0b\u3067\u306e\u6709\u6a5f\u30a4\u30aa\u30f3\u5bfe\u89e6\u5a92\u306b\u3088\u308b\u7acb\u4f53\u5236\u5fa1, CSJ\u30ab\u30ec\u30f3\u30c8\u30ec\u30d3\u30e5\u30fc\u300c\u6709\u6a5f\u5149\u5316\u5b66\u53cd\u5fdc\u306e\u65b0\u5c55\u958b\u300d, \u5316\u5b66\u540c\u4eba, \u6771\u4eac, 49-55(2022).<\/li><li>Ohmatsu, K.; Uraguchi, D.; Ooi, T.  Assembled Ionic Molecular Catalysis and Ligands.  <em>Supramolecular Catalysis<\/em> <strong>2022<\/strong>, Wiley-VCH, 43-53.<\/li><\/ul>\n\n\n\n<h3 class=\"is-style-vk-heading-default\" id=\"vk-htags-f04688be-99b5-4e35-a716-6b9d598281e8\" style=\"font-size:20px\">\u7dcf\u8aac\uff0f\u89e3\u8aac\uff0f\u5831\u544a<\/h3>\n\n\n\n<ul class=\"is-style-vk-triangle-mark\"><li>\u8d99 \u5f37, \u6d66\u53e3 \u5927\u8f14, \u30b9\u30e9\u30a4\u30e0\u306e\u9032\u5316\u5148\u306f\u6709\u6a5f\u89e6\u5a92\uff01\uff1f, \u6708\u520a\u300c\u5316\u5b66\u300d, 77 (2022).<\/li><\/ul>\n\n\n\n<h3 class=\"is-style-vk-heading-default\" id=\"vk-htags-c6b70f11-9daf-4f72-983c-413cc33c1b2c\" style=\"font-size:20px\">\u62db\u5f85\uff0f\u57fa\u8abf\uff0f\u4f9d\u983c\u8b1b\u6f14\u30fb\u56fd\u969b\u4f1a\u8b70<\/h3>\n\n\n\n<ul class=\"is-style-vk-triangle-mark\"><li>\u6d66\u53e3 \u5927\u8f14\uff1a\u300c\u30ad\u30e9\u30eb\u6709\u6a5f\u30a4\u30aa\u30f3\u5bfe\u306e\u89e6\u5a92\u5316\u5b66\u300d, 2021\u5e74\u5ea6\u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a\u4e5d\u5dde\u5c71\u53e3\u652f\u90e8\u8b1b\u6f14\u4f1a\u300c\u5408\u6210\u6709\u6a5f\u5316\u5b66\u306e\u30d5\u30ed\u30f3\u30c6\u30a3\u30a2\u300d, \u30aa\u30f3\u30e9\u30a4\u30f3, (2021\/6\/4)\uff3b\u4f9d\u983c\u8b1b\u6f14\uff3d<\/li><\/ul>\n","protected":false},"excerpt":{"rendered":"<p>2026 \u539f\u8457\u8ad6\u6587 Ono, Y.; Matsumoto, A.; Shimozawa, S.; Uraguchi, D.; Asano, K. Asymmetric 1,3-Dioxane Synthesis by U [&hellip;]<\/p>\n","protected":false},"author":8,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_lightning_design_setting":{"layout":"default","header_trans":"default","section_base":"default"},"vkexunit_cta_each_option":""},"_links":{"self":[{"href":"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-json\/wp\/v2\/pages\/2436"}],"collection":[{"href":"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-json\/wp\/v2\/users\/8"}],"replies":[{"embeddable":true,"href":"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-json\/wp\/v2\/comments?post=2436"}],"version-history":[{"count":43,"href":"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-json\/wp\/v2\/pages\/2436\/revisions"}],"predecessor-version":[{"id":3231,"href":"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-json\/wp\/v2\/pages\/2436\/revisions\/3231"}],"wp:attachment":[{"href":"https:\/\/www.cat.hokudai.ac.jp\/uraguchi\/wp-json\/wp\/v2\/media?parent=2436"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}