{"id":366,"date":"2024-07-10T23:42:51","date_gmt":"2024-07-10T14:42:51","guid":{"rendered":"https:\/\/wwwchem.sci.hokudai.ac.jp\/~orgmet\/?page_id=366"},"modified":"2026-04-18T10:59:31","modified_gmt":"2026-04-18T01:59:31","slug":"shimizu","status":"publish","type":"page","link":"https:\/\/wwwchem.sci.hokudai.ac.jp\/~orgmet\/shimizu\/","title":{"rendered":"\u6e05\u6c34 \u6d0b\u5e73"},"content":{"rendered":"\n<h2 class=\"wp-block-heading\">\u6e05\u6c34 \u6d0b\u5e73\u3000Yohei Shimizu<\/h2>\n\n\n\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\" style=\"flex-basis:33.33%\"><div class=\"wp-block-image\">\n<figure class=\"aligncenter size-full is-resized\"><img loading=\"lazy\" decoding=\"async\" width=\"186\" height=\"204\" src=\"https:\/\/wwwchem.sci.hokudai.ac.jp\/~orgmet\/wp-content\/uploads\/2024\/07\/shimizu.png\" alt=\"\" class=\"wp-image-121\" style=\"width:200px\"\/><\/figure>\n<\/div><\/div>\n\n\n\n<div class=\"wp-block-column is-vertically-aligned-center is-layout-flow wp-block-column-is-layout-flow\" style=\"flex-basis:66.66%\">\n<h4 class=\"wp-block-heading\">\u51c6\u6559\u6388\u3000Associate Professor<\/h4>\n\n\n\n<p class=\"has-medium-font-size\">\u6e05\u6c34\u3000\u6d0b\u5e73\u3000Yohei Shimizu<\/p>\n\n\n\n<p>E-mail: shimizu-y[at]sci.hokudai.ac.jp<\/p>\n<\/div>\n<\/div>\n\n\n\n<h5 class=\"wp-block-heading\">\u7565\u6b74<\/h5>\n\n\n\n<ul class=\"wp-block-list list has-small-font-size\">\n<li>1984 \u9577\u91ce\u770c\u306b\u751f\u308c\u308b\u3000\u3000<br>Born in Nagano<\/li>\n\n\n\n<li>2002 \u9577\u91ce\u770c\u7acb\u9808\u5742\u9ad8\u6821\u3000\u5352\u696d<\/li>\n\n\n\n<li>2006 \u6771\u4eac\u5927\u5b66\u85ac\u5b66\u90e8\u3000\u5352\u696d<\/li>\n\n\n\n<li>2008 \u6771\u4eac\u5927\u5b66\u5927\u5b66\u9662\u85ac\u5b66\u7cfb\u7814\u7a76\u79d1\u5206\u5b50\u85ac\u5b66\u5c02\u653b\u4fee\u58eb\u8ab2\u7a0b\u3000\u4fee\u4e86<\/li>\n\n\n\n<li>2011 \u6771\u4eac\u5927\u5b66\u5927\u5b66\u9662\u85ac\u5b66\u7cfb\u7814\u7a76\u79d1\u5206\u5b50\u85ac\u5b66\u5c02\u653b\u535a\u58eb\u8ab2\u7a0b\u3000\u4fee\u4e86\u3000\u3000<br>         Ph.D. The University of Tokyo<\/li>\n\n\n\n<li>2011 \u6771\u4eac\u5927\u5b66\u5927\u5b66\u9662\u85ac\u5b66\u7cfb\u7814\u7a76\u79d1\u3000\u52a9\u6559\u3000\u3000<br>         Assistant Professor, The University of Tokyo<\/li>\n\n\n\n<li>2012 \u30b1\u30f3\u30d6\u30ea\u30c3\u30b8\u5927\u5b66\u5316\u5b66\u79d1\u3000\u77ed\u671f\u7559\u5b66\u3000\u3000<br>         Visiting Scientist, Department of Chemistry, University of Cambridge (Prof. Matthew J. Gaunt)<\/li>\n\n\n\n<li>2018 \u5317\u6d77\u9053\u5927\u5b66\u5927\u5b66\u9662\u7406\u5b66\u7814\u7a76\u9662\u5316\u5b66\u90e8\u9580\u3000\u8b1b\u5e2b\u3000\u3000<br>         Lecturer, Hokkaido University<\/li>\n\n\n\n<li>2020 \u540c \u51c6\u6559\u6388\u3000\u3000<br>         Associate Professor, Hokkaido University<\/li>\n\n\n\n<li>2024 &nbsp;JST-PRESTO\u300c\u6750\u6599\u306e\u5275\u88fd\u30fb\u5faa\u74b0\u300d\u9818\u57df\u7814\u7a76\u8005\uff08\u517c\u4efb\uff09<\/li>\n<\/ul>\n\n\n\n<h5 class=\"wp-block-heading\">\u53d7\u8cde\u6b74<\/h5>\n\n\n\n<ul class=\"wp-block-list has-small-font-size\">\n<li>2009 \u7b2c35\u56de\u53cd\u5fdc\u3068\u5408\u6210\u306e\u9032\u6b69\u30b7\u30f3\u30dd\u30b8\u30a6\u30e0\u3000\u512a\u79c0\u767a\u8868\u8cde\u3000\u3000<br>         Student Oral Presentation Award in 35th \u201cHannou to Gousei no Sinpo\u201d Symposium, Japan<\/li>\n\n\n\n<li>2013 Frontires in Chemistry, Armenia (ArmChemFront) Best Poster Prize<\/li>\n\n\n\n<li>2015 \u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a\u300c\u6771\u30ec\u300d\u7814\u7a76\u4f01\u753b\u8cde\u3000\u3000<br>         TORAY Award in Synthetic Organic Chemistry, Japan<\/li>\n\n\n\n<li>2018 \u65e5\u672c\u5316\u5b66\u4f1a \u7b2c98\u6625\u5b63\u5e74\u4f1a\u300e\u7b2c32\u56de\u82e5\u3044\u4e16\u4ee3\u306e\u7279\u5225\u8b1b\u6f14\u4f1a\u300f\u3000\u3000<br>         The Young Scholar Lectures of The Chemical Society of Japan<\/li>\n\n\n\n<li>2019 \u65e5\u672c\u85ac\u5b66\u4f1a\u5968\u52b1\u8cde\u3000\u3000<br>         The Pharmaceutical Society of Japan Award for Young Scientists<\/li>\n\n\n\n<li>2020 Thieme Chemistry Journals Award 2020<\/li>\n\n\n\n<li>2023 2022\u5e74\u5ea6\u65e5\u672c\u5316\u5b66\u4f1a\u5317\u6d77\u9053\u652f\u90e8\u5968\u52b1\u8cde<\/li>\n<\/ul>\n\n\n\n<h3 class=\"wp-block-heading\">Original papers<\/h3>\n\n\n\n<ol reversed class=\"wp-block-list\">\n<li><strong>Silver-Catalyzed<\/strong> <strong>Enantioselective Aldol Reaction of Isocyanoacetic Acid Derivatives with Prolinol-Phosphine-<em>sec<\/em>-Amine Chiral Ligand<\/strong><br>Sakai, S.; Maeda, K.; Shimizu, Y.; Sawamura, M. <br><em>Chem. Lett. <\/em> in press. (DOI: <a href=\"https:\/\/doi.org\/10.1093\/chemle\/upag060\" target=\"_blank\" rel=\"noreferrer noopener\">10.1093\/chemle\/upag060<\/a>)<\/li>\n\n\n\n<li><strong>Copper-Catalyzed Asymmetric Michael Reaction of \u03b1-Substituted Cyanoacetates with Acrylates and Acrylamides with Prolinol-phosphine-<em>sec<\/em>-amine Chiral Ligand.<\/strong><br>Onizawa, M.; Sakai, S.; Qureshi, I.; Shimizu, Y.; Sawamura, M. <br><em>Eur. J. Org. Chem. (<a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/toc\/10.1002\/(ISSN)1099-0690.organometallics-in-organic-synthesis\" target=\"_blank\" rel=\"noreferrer noopener\">Special Collection: Organometallics in Organic Synthesis<\/a>)<\/em>, <em>Early View<\/em> (DOI: <a href=\"https:\/\/doi.org\/10.1002\/ejoc.202501226\" data-type=\"link\" data-id=\"https:\/\/doi.org\/10.1002\/ejoc.202501226\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/ejoc.202501226<\/a>)<\/li>\n\n\n\n<li><strong>Reductively Stable Platinum Catalyst Enabling Metallaphotoredox Reductive Allylation of Ketones, Aldehydes and Imines.<\/strong> <br>Shimosato, J.; Nishimura, K.; Fukuyo, B.; Shimizu, Y.; Sawamura, M.; Masuda, Y. <br><em>ChemistryEurope<\/em>, <strong>2026<\/strong>, <em>4<\/em>, e20250436. (DOI: <a href=\"https:\/\/doi.org\/10.1002\/ceur.202500436\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/ceur.202500436<\/a>)<\/li>\n\n\n\n<li><strong>Photoinduced Boron-Catalyzed Direct \u03b1-Aminoxylation of Carboxylic Acids.<\/strong> <br>Oyama, T.; Morisawa, T.; Yoshida, Y.; Heike, Y.; Sawamura, M.; Shimizu, Y. <br><em>ChemistryEurope,<\/em> <strong>2026<\/strong>, <em>4<\/em>, e202500316. (DOI: <a href=\"http:\/\/doi.org\/10.1002\/ceur.202500316\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/ceur.202500316<\/a>)<\/li>\n\n\n\n<li><strong>Ligand-Controlled Stereodivergent Proton Migration in Skipped Enynes<\/strong><br>Wu, T.; Fan, C.; Jin, W.; Xie, X.; Wang, S.; Wang, H.; Shi, G.; Gao, Y.; Sun, J.; Zhao, Y.; Shimizu Y.; Kanai, M.; Persson, K. A.; Ma, P.; Wei, X. <br><em>Cell. Rep. Phys. Sci. <\/em><strong>2025<\/strong>, <em>6<\/em>, 103020. (DOI: <a href=\"https:\/\/doi.org\/10.1016\/j.xcrp.2025.103020\" target=\"_blank\" rel=\"noreferrer noopener\">10.1016\/j.xcrp.2025.103020<\/a>)<\/li>\n\n\n\n<li><strong>Silver-Catalyzed Asymmetric Aldol Reaction of Nonactivated Ketones with \u03b1-Isocyanocarboxylic Acid Derivatives Enabled by Prolinol-phosphine-<em>sec<\/em>-amine Chiral Ligand.<br><\/strong>Sakai, S.; Uchiyama, K.; Imai, K; Yato, K.; Onizawa, M.; Higashida, K.; Sato, H.; Aoyama, Y.; <br>Shimizu, Y.; Sawamura, M.<br><em>ACS Catal.&nbsp;<\/em><strong>2025<\/strong>, <em>15<\/em>, 16039\u201316051. (DOI: <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acscatal.5c04986\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/acscatal.5c04986<\/a>)<\/li>\n\n\n\n<li><strong>Phosphorus Catalysis Enabling \u03b1-<em>sp<\/em>3-C\u2013H Amination of 2-Alkylpyridines<\/strong><br>Heike, Y.; Tagata, A.; Yada, A.; Nozawa-Kumada, K.; Sawamura, M.; Shimizu, Y.<br><em>Org. Chem. Front. &nbsp;<\/em><strong>2025<\/strong>, <em>12<\/em>, 6059\u20136069. (DOI:&nbsp;<a href=\"https:\/\/doi.org\/10.1039\/D5QO00960J\" target=\"_blank\" rel=\"noreferrer noopener\">10.1039\/D5QO00960J<\/a>)<\/li>\n\n\n\n<li><strong>Photoinduced Direct \u03b2-Allylation of Carboxylic Acids Enabled by Boron Catalysis with a Mixed Two-Ligand System<\/strong><br>Sun, K.; Heike, Y.; Yoshida, Y.; Sawamura, M.; Huang, C.-Y. D.; Shimizu, Y.<br><em>ChemCatChem<\/em>, <strong>2025<\/strong>, <em>17<\/em>, e202500091. (DOI:&nbsp;<a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/abs\/10.1002\/cctc.202500091\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/cctc.202500091<\/a>)<\/li>\n\n\n\n<li><strong>Copper(I)-Catalyzed Asymmetric Nucleophilic Addition to Aldehydes with Skipped Enynes.<\/strong><br>Peng, C.; Wu, T.; Yang, X.; Pei, M.; Wang, S.; Kanai, M.; Shimizu, Y.; Wei, X.<br><em>Org. Lett.<\/em> <strong>2024<\/strong>, 26, 10072\u201310077. (DOI: <a href=\"https:\/\/doi.org\/10.1021\/acs.orglett.4c03449\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/acs.orglett.4c03449<\/a>)<\/li>\n\n\n\n<li><strong>Oxyamination of Alkenes Enabled by Direct Photoexcitation of Fluorenone Oxime Derivatives.<\/strong><br>Tagata, A.; Sawamura, M.; Shimizu, Y.<br><em>Chem. Lett. <\/em><strong>2024<\/strong>, <em>53<\/em>, upae216. (DOI: <a href=\"https:\/\/doi.org\/10.1093\/chemle\/upae216\" target=\"_blank\" rel=\"noreferrer noopener\">10.1093\/chemle\/upae216<\/a>)<\/li>\n\n\n\n<li><strong>Boron-Catalyzed Michael Reaction of Donor-Acceptor Carboxylic Acid Pairs Enabling Direct Synthesis of 1,5-Dicarboxylic Acids.<br><\/strong>Yoshida,&nbsp;Y.;&nbsp;Sawamura,&nbsp;M.;&nbsp;Shimizu,&nbsp;Y.&nbsp;<br><em>Org. Lett.,&nbsp;<\/em><strong>2024<\/strong>, <em>26<\/em>, 5425\u20135429. (DOI:&nbsp;<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.4c01542\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/acs.orglett.4c01542<\/a>)<\/li>\n\n\n\n<li><strong>Visible-Light-Induced Aminochlorination of Alkenes.<br><\/strong>Mejri,&nbsp;E.;&nbsp;Higashida,&nbsp;K.;&nbsp;Kondo,Y.;&nbsp;Nawachi,&nbsp;A.;&nbsp;Morimoto,&nbsp;H.;&nbsp;Ohshima,&nbsp;T.;&nbsp;Sawamura,&nbsp;M.;&nbsp;Shimizu,&nbsp;Y.&nbsp;<br><em>Org. Lett.<\/em>&nbsp;<strong>2023<\/strong>, <em>25<\/em>, 4581\u20134585. (DOI:&nbsp;<a href=\"https:\/\/doi.org\/10.1021\/acs.orglett.3c01645\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/acs.orglett.3c01645<\/a>)<\/li>\n\n\n\n<li><strong>Direct \u03b1-Trifluoromethylthiolation of Carboxylic Acids Enabled by Boron Catalysis.<br><\/strong>Sun, K.; Huang, C.-Y. (Dennis); Sawamura, M.; Shimizu, Y.<br><em>Synlett,<\/em>&nbsp;<strong>2023<\/strong>,&nbsp;2210\u20132214<em>.&nbsp;<\/em>(DOI: <a href=\"https:\/\/doi.org\/10.1055\/a-2071-4465\" target=\"_blank\" rel=\"noreferrer noopener\">10.1055\/a-2071-4465<\/a><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/adsc.202200327\"><\/a>)<\/li>\n\n\n\n<li><strong>Silver-Catalyzed Asymmetric Aldol Reaction of Isocyanoacetic&nbsp;Acid&nbsp;Derivatives Enabled&nbsp;by Cooperative Participation of Classical&nbsp;and&nbsp;Nonclassical&nbsp;Hydrogen Bonds.<br><\/strong>Sakai,&nbsp;S.; Fujioka,&nbsp;A.;&nbsp;Imai,&nbsp;K.;&nbsp;Uchiyama,&nbsp;K.;&nbsp;Shimizu,&nbsp;Y.;&nbsp;Higashida,&nbsp;K.;&nbsp;Sawamura,&nbsp;M.<br><em>Adv. Synth. Catal.<\/em>&nbsp;<strong>2022,<\/strong>&nbsp;<em>364<\/em>,&nbsp;2333-2339.&nbsp;(<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/adsc.202200327\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:10.1002\/adsc.202200327<\/a>)<\/li>\n\n\n\n<li><strong>Insights into the Mechanism of Enantioselective Copper-Catalyzed Ring-Opening Allylic Alkylation of Cyclopropanols.<\/strong><br>Kitabayashi, A.; Mizushima,&nbsp;S.;&nbsp;Higashida,&nbsp;K.;&nbsp;Yasuda,&nbsp;Y.;&nbsp;Shimizu,&nbsp;Y.;&nbsp;Sawamura,&nbsp;M.&nbsp;<br><em>Adv. Synth. Catal.&nbsp;<\/em><strong>2022<\/strong><em>,&nbsp;364,&nbsp;1855-1862.&nbsp;<\/em>(DOI:&nbsp;<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/adsc.202200157\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/adsc.202200157<\/a>)<\/li>\n\n\n\n<li><strong>Visible Light-Induced Reductive Alkynylation of Aldehydes by Umpolung Approach.<\/strong><br>Tanaka,&nbsp;I.;&nbsp;Sawamura,&nbsp;M.; Shimizu, Y.<br><em>Org. Lett.<\/em>&nbsp;<strong>2022<\/strong>, <em>24,<\/em>&nbsp;520\u2013524<em>. (<\/em>DOI:&nbsp;<a href=\"https:\/\/doi.org\/10.1021\/acs.orglett.1c03927\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/acs.orglett.1c03927<\/a>)<\/li>\n\n\n\n<li><strong>Synthesis of C,N,N-Cyclometalated Gold(III) Complexes with Anionic Amide Ligands<br><\/strong>Niizeki, R.; Higashida, K.; Mejri, E.; Sawamura, M.; Shimizu, Y.<br><em>Synlett,<\/em>&nbsp;<strong>2022<\/strong>,&nbsp;<em>32<\/em>, 288\u2013292. (<a href=\"https:\/\/doi.org\/10.1055\/a-1673-9236\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1055\/a-1673-9236<\/a>)<\/li>\n\n\n\n<li><strong>Data-Driven Catalyst Optimization for Stereodivergent Asymmetric Synthesis by Iridium\/Boron Hybrid Catalysis<br><\/strong>Chen, H.; Yamaguchi, S.; Morita, Y.; Nakao, H.; Zhai, X.-N.; Shimizu, Y.; Mitsunuma, H.; Kanai, M.<br><em>Cell Rep. Phys. Sci.&nbsp;<\/em><strong>2021<\/strong>,<em>&nbsp;2<\/em>, 100679.&nbsp;(<a href=\"https:\/\/doi.org\/10.1016\/j.xcrp.2021.100679\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1016\/j.xcrp.2021.100679<\/a>)<\/li>\n\n\n\n<li><strong>Visible-Light-Driven \u03b1-Allylation of Carboxylic Acids<br><\/strong>Sun, K. ; Ueno, M. ; Imaeda, K. ; Ueno, K. ; Sawamura, M. ; Shimizu, Y.<br><em>ACS Catal.<\/em>&nbsp;<strong>2021<\/strong>,&nbsp;<em>11,<\/em> 9722\u20139728. (<a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acscatal.1c02558\" target=\"_blank\" rel=\"noreferrer noopener\">DOI: 10.1021\/acscatal.1c02558<\/a>)<\/li>\n\n\n\n<li><strong>Iridium-Catalyzed Enantioselective Transfer Hydrogenation of Ketones Controlled by Alcohol Hydrogen-Bonding and sp3-C\u2013H Noncovalent Interactions<br><\/strong>Murayama, H.; Heike, Y.; Higashida, K.; Shimizu, Y.; Yodsin, N.; Wongnongwa, Y.; Jungsuttiwong, S.;&nbsp; Mori, S.; Sawamura, M.<br><em>Adv. Synth. Catal.&nbsp;<\/em><strong>2020<\/strong>,<em>&nbsp;362, <\/em>4655\u20134661.&nbsp;(<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/adsc.202000615\" target=\"_blank\" rel=\"noreferrer noopener\">DOI: 10.1002\/adsc.202000615<\/a>)<\/li>\n\n\n\n<li><strong>Copper-Catalyzed Enantioselective Conjugate Reduction of \u03b1,\u03b2-Unsaturated Esters with Phenol-Carbene Chiral Ligand<br><\/strong>Mimura, S.; Mizushima, S.; Shimizu, Y.; Sawamura, M.<br><em>Beilstein J. Org. Chem. <\/em><strong>2020<\/strong><em>, 16,&nbsp;<\/em>537\u2013543.&nbsp;(<a href=\"https:\/\/doi.org\/10.3762\/bjoc.16.50\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:10.3762\/bjoc.16.50<\/a>)<\/li>\n\n\n\n<li><strong>A Stable and Cleavable&nbsp;<em>O<\/em>-Linked Spacer for Drug Delivery Systems<br><\/strong>Ito, K.; Tatsumi, T.; Takahashi, K.; Shimizu, Y.; Yamatsugu, K.; Kanai, M.<br><em>Chem. Pharm. Bull.&nbsp;<\/em><strong>2020<\/strong>,&nbsp;<em>68<\/em>, 212\u2013215. (<a href=\"https:\/\/doi.org\/10.1248\/cpb.c19-00376\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1248\/cpb.c19-00376<\/a>)<\/li>\n\n\n\n<li><strong>Boron-Catalyzed \u03b1-Amination of Carboxylic Acids<br><\/strong>Morisawa, T.; Sawamura, M.; Shimizu, Y.<br><em>Org. Lett.&nbsp;<\/em><strong>2019<\/strong>,&nbsp;<em>21<\/em>, 7466\u20137469.&nbsp;(<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.9b02769\" target=\"_blank\" rel=\"noreferrer noopener\">DOI: 10.1021\/acs.orglett.9b02769<\/a>)<\/li>\n\n\n\n<li><strong>Copper(I)-Catalyzed Stereodivergent Propargylation of N-Acetyl Mannosamine for Protecting-Group-Minimal Synthesis of C3-Substituted Sialic Acids<br><\/strong>Ishizawa, K.; Majima, S.; Wei, X.-F.; Mitsunuma, H.; Shimizu, Y.; Kanai, M.<br><em>J. Org. Chem.&nbsp;<\/em><strong>2019<\/strong><em>,<\/em> <em>84<\/em>, 10615\u201310628. (<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.joc.9b00887\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1021\/acs.joc.9b00887<\/a><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.9b00276\"><\/a>)<\/li>\n\n\n\n<li><strong>Asymmetric Synthesis of \u03b1-Alkylidene-\u03b2-Lactams through Copper Catalysis with a Prolinol-Phosphine Chiral Ligand<br><\/strong>Imai, K.; Takayama, H.; Murayama, H., Ohmiya, H.; Shimizu, Y.; Sawamura, M.<br><em>Org. Lett. <\/em><strong>2019<\/strong><em>, 21,&nbsp;<\/em>1717\u20131721<em>.<\/em>&nbsp;(<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.9b00276\" target=\"_blank\" rel=\"noreferrer noopener\">DOI: 10.1021\/acs.orglett.9b00276<\/a>)<\/li>\n\n\n\n<li><strong>Catalytic Regio- and Enantioselective Proton Migration from Skipped Enynes to Allenes<br><\/strong>Wei, X.-F.; Wakaki, T.; Itoh, T.; Li, H.-L.; Yoshimura, T.; Miyazaki, A.; Oisaki, K.; Hatanaka, M.; Shimizu, Y.; Kanai, M.<br><em>Chem<\/em>&nbsp;<strong>2019<\/strong><em>,<\/em> <em>5<\/em>, 585\u2013599.(<a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S2451929418305394?via%3Dihub\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1016\/j.chempr.2018.11.022<\/a>)<\/li>\n\n\n\n<li><strong>Copper(I)-Catalyzed Enantio- and Diastereodivergent Borylative Coupling of Styrenes and Imines<br><\/strong>Itoh, T.; Kanzaki, Y.; Shimizu, Y.; Kanai, M.<br><em>Angew. Chem. Int. Ed.<\/em>&nbsp;<strong>2018<\/strong>, <em>57<\/em>, 8265\u20138269.&nbsp;(<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/anie.201804117\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1002\/anie.201804117<\/a>)<\/li>\n\n\n\n<li><strong>Chemo- and Enantioselective Pd\/B Hybrid Catalysis forthe Construction of Acyclic Quaternary Carbons: Migratory Allylation of&nbsp;<em>O<\/em>-Allyl Esters to \u03b1-<em>C<\/em>-Allyl Carboxylic Acids<br><\/strong>Fujita, T.; Yamamoto, T.; Morita, Y.; Chen, H.; Shimizu, Y.; Kanai, M.<br><em>J. Am. Chem. Soc.<\/em>&nbsp;<strong>2018<\/strong>,&nbsp;<em>140<\/em>, 5899\u20135903<em>.<\/em>&nbsp;(<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.8b02783\">DOI:&nbsp;10.1<\/a><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.8b02783\" target=\"_blank\" rel=\"noreferrer noopener\">0<\/a><a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.8b02783\">21\/jacs.8b02783<\/a>)<\/li>\n\n\n\n<li><strong>Boron-Catalyzed Carboxylic Acid-Selective Aldol Reaction with Trifluoromethyl Ketones<\/strong><br>Ishizawa, K.; Nagai, H.; Shimizu, Y.; Kanai, M.<br><em>Chem. Pharm. Bull.<\/em>&nbsp;<strong>2018<\/strong>,&nbsp;<em>66<\/em>, 231\u2013234. (<a href=\"https:\/\/www.jstage.jst.go.jp\/article\/cpb\/advpub\/0\/advpub_c17-00545\/_article\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1248\/cpb.c17-00545)<\/a><\/li>\n\n\n\n<li><strong>Copper(I)-Catalyzed Enantioselective Addition of Enynes to Ketones<br><\/strong>Wei, X.-F.; Xie, X.-W.; Shimizu, Y.; Kanai, M.<br><em>J. Am. Chem. Soc. <\/em><strong>2017<\/strong>, <em>139<\/em>, 4647\u20134650. (<a href=\"http:\/\/pubs.acs.org\/doi\/10.1021\/jacs.7b01254\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1021\/jacs.7b01254)<\/a><\/li>\n\n\n\n<li><strong>Copper(I)-Catalyzed Dehydrative <em>C<\/em>-Glycosidation of Unprotected Pyranoses with Ketones<\/strong><br>Wei, X.-F.; Shi, S.-L.; Xie, X.-W.; Shimizu, Y.; Kanai, M.<br><em>ACS Catal. <\/em><strong>2016<\/strong>, <em>6<\/em>, 6718\u20136722. (<a href=\"http:\/\/pubs.acs.org\/doi\/10.1021\/acscatal.6b02106\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1021\/acscatal.6b02106<\/a>)<\/li>\n\n\n\n<li><strong>Ligand-Enabled, Copper-Catalyzed Regio- and Stereoselective Synthesis of Trialkylsubstituted Alkenylboronates from Unactivated Internal Alkynes<br><\/strong>Itoh, T.; Shimizu, Y.; Kanai, M.<br><em>J. Am. Chem. Soc. <\/em><strong>2016<\/strong><em>, 138, <\/em>7528\u20137531<em>.<\/em>&nbsp;(<a href=\"http:\/\/pubs.acs.org\/doi\/10.1021\/jacs.6b04646\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1021\/jacs.6b04646<\/a>)<\/li>\n\n\n\n<li><strong>Ligand-Promoted, Boron-Mediated Chemoselective Carboxylic Acid Aldol Reaction<br><\/strong>Nagai, H.; Morita, Y.;Shimizu, Y.; Kanai, M.<br><em>Org. Lett. <\/em><strong>2016<\/strong>,<em> 18, <\/em>2076\u20132079. (<a href=\"http:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.6b00914\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1021\/acs.orglett.6b00914<\/a>)<\/li>\n\n\n\n<li><strong>An Expeditious Synthesis of Sialic Acid Derivatives by Copper(I)-Catalyzed Stereodivergent Propargylation of Unprotected Aldoses<br><\/strong>Wei, X.-F.; Shimizu, Y.; Kanai, M.<br><em>ACS Cent. Sci. <\/em><strong>2016<\/strong>,<em> 2<\/em>, 21\u201326. (<a href=\"http:\/\/pubs.acs.org\/doi\/10.1021\/acscentsci.5b00360\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1021\/acscentsci.5b00360<\/a>)<\/li>\n\n\n\n<li><strong>Cu-Catalyzed Oxyboration of Unactivated Alkenes<br><\/strong>Itoh, T.; Matsueda, T.; Shimizu, Y.; Kanai, M.<br><em>Chem. Eur. J. <\/em><strong>2015<\/strong>,<em> 21<\/em>, 15955\u201315959.&nbsp;(<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/chem.201503329\/abstract\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1002\/chem.201503329<\/a><a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/chem.201503329\/abstract\"><\/a>)<\/li>\n\n\n\n<li><strong>Chemoselective Boron-Catalyzed Nucleophilic Activation of Carboxylic Acids for Mannich-Type Reactions<br><\/strong>Morita Y.; Yamamoto T.; Nagai H.; Shimizu Y.; Kanai M.<br><em>J. Am. Chem. Soc. <\/em><strong>2015<\/strong><em>, 137, <\/em>7075\u20137078. (<a href=\"http:\/\/pubs.acs.org\/doi\/10.1021\/jacs.5b04175\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1021\/jacs.5b04175<\/a>)<\/li>\n\n\n\n<li><strong>Structure-based design of a streptavidin mutant specific for an artificial biotin analogue<br><\/strong>Kawato T.; Mizohata E.; Shimizu Y.; Meshizuka T.; Yamamoto T.; Takasu N.; Matsuoka M.; Matsumura H.; Kodama T.; Kanai M.; Doi H.; Inoue T.; Sugiyama A.<br><em>J. Biochem.<\/em> <strong>2015<\/strong>, <em>157<\/em>, 467\u2013475. (<a href=\"https:\/\/academic.oup.com\/jb\/article\/157\/6\/467\/772589\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1093\/jb\/mvv004<\/a>)<\/li>\n\n\n\n<li><strong>Design and synthesis of biotin analogues reversibly binding with streptavidin<br><\/strong>Yamamoto T.; Aoki K.; Sugiyama A.; Doi H.; Kodama T.; Shimizu Y.; Kanai M.<br><em>Chem. Asian. J. <\/em><strong>2015<\/strong><em>, 10, <\/em>1071\u20131078. (<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/asia.201500120\/abstract\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1002\/asia.201500120<\/a>)<\/li>\n\n\n\n<li><strong>Structure-based design and synthesis of a bivalent iminobiotin analog showing strong affinity toward a low immunogenic streptavidin mutant<br><\/strong>Kawato T.; Mizohata E.; Shimizu Y.; Meshizuka T.; Yamamoto T.; Takasu N.; Matsuoka M.; Matsumura H.; Kodama T.; Kanai M.; Doi H.; Inoue T.; Sugiyama A.<br><em>Biosci. Biotechnol. Biochem. <\/em><strong>2015<\/strong>, <em>79<\/em>, 640\u2013642. (<a href=\"http:\/\/www.tandfonline.com\/doi\/full\/10.1080\/09168451.2014.991692\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1080\/09168451.2014.991692<\/a>)<\/li>\n\n\n\n<li><strong>Copper-Catalyzed Regio- and Stereoselective Intermolecular Three-Component Oxyarylation of Allenes<br><\/strong>Itoh T.; Shimizu Y.; Kanai M.<br><em>Org. Lett.<\/em> <strong>2014<\/strong>, <em>16<\/em>, 2736\u20132739. (<a href=\"http:\/\/pubs.acs.org\/doi\/10.1021\/ol501022d\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1021\/ol501022d<\/a>)<\/li>\n\n\n\n<li><strong>Catalytic enantioselective synthesis of 2-(2-hydroxyethyl)indole scaffolds via consecutive intramolecular amido-cupration of allenes and asymmetric addition of carbonyl compounds<\/strong>&nbsp;<br>Chikkade P. K.; Shimizu Y.; Kanai M.<br><em>Chem. Sci. <\/em><strong>2014<\/strong><em>,&nbsp;5,&nbsp;<\/em>1585\u20131590. (<a href=\"http:\/\/pubs.rsc.org\/en\/Content\/ArticleLanding\/2014\/SC\/c3sc52803k#!divAbstract\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1039\/C3SC52803K<\/a>)<\/li>\n\n\n\n<li><strong>A Catalytic C-C Bond-Formation with Minimal Use of Protecting Groups: Construction of Functionalized Isotetronic Acid Derivatives<\/strong><br>Shimizu Y.; Yasuda K.; Kanai M.<br><em>HETEROCYCLES<\/em> <strong>2014<\/strong>, <em>88<\/em>, 919\u2013927. (<a href=\"https:\/\/www.heterocycles.jp\/newlibrary\/libraries\/abst\/23204\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.3987\/COM-13-S(S)81<\/a>)<\/li>\n\n\n\n<li><strong>Catalytic Anomeric Aminoalkynylation of Unprotected Aldoses<\/strong><br>Kimura, Y.; Ito, S.; Shimizu, Y.; Kanai, M.<br><em>Org. Lett.<\/em> <strong>2013<\/strong>, <em>15<\/em>, 4130\u20134133. (<a href=\"http:\/\/pubs.acs.org\/doi\/10.1021\/ol401810b\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1021\/ol401810b<\/a>)<\/li>\n\n\n\n<li><strong><em>In situ<\/em> Catalytic Generation of Allylcopper Species for Asymmetric Allylation: Toward 1<em>H<\/em>-Isochromene Skeletons<\/strong><br>Kawai, J.; Chikkade, P. K.; Shimizu, Y.; Kanai, M.<br><em>Angew. Chem. Int. Ed.<\/em> <strong>2013<\/strong>, 52, 7177\u20137180. (<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.201302027\/abstract\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1002\/anie.201302027<\/a>)<\/li>\n\n\n\n<li><strong>Copper(I)-Catalyzed Enantioselective Incorporation of Ketones to Cyclic Hemiaminals for the Synthesis of Versatile Alkaloid Precursors<\/strong><br>Shi, S.-L.; Wei, X.-F.; Shimizu, Y.; Kanai, M.<br><em>J. Am. Chem. Soc. <\/em><strong>2012<\/strong><em>, 134, <\/em>17019\u201317022. (<a href=\"http:\/\/pubs.acs.org\/doi\/10.1021\/ja308872z\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1021\/ja308872z<\/a>)<\/li>\n\n\n\n<li><strong>Cu(I)-catalyzed a-alkylation of ketones with styrene derivatives<\/strong><br>Majima, S.; Shimizu, Y.; Kanai, M.<br><em>Tetrahedron Lett.<\/em> <strong>2012<\/strong>, <em>53<\/em>, 4381\u20134384. (<a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040403912009926?via%3Dihub\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1016\/j.tetlet.2012.06.019<\/a>)<\/li>\n\n\n\n<li><strong>Catalytic Asymmetric Synthesis of R207910<br><\/strong>Saga, Y.; Motoki, R.; Makino, S.; Shimizu, Y.; Kanai, M.; Shibasaki, M.<strong><br><\/strong><em>J. Am. Chem. Soc. <\/em><strong>2010<\/strong>, <em>132<\/em>, 7905\u20137907.&nbsp;(<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja103183r\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1021\/ja103183r<\/a>)<\/li>\n\n\n\n<li><strong>The first catalytic asymmetric total synthesis of <em>ent-<\/em>hyperforin<\/strong><br>Shimizu, Y.; Shi, S.\u2013L.; Usuda, H.; Kanai, M.; Shibasaki, M.<br><em>Tetrahedron<\/em> <strong>2010<\/strong>, <em>66<\/em>, 6569\u20136584. (<a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040402010008409?via%3Dihub\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1016\/j.tet.2010.05.086<\/a>)<\/li>\n\n\n\n<li><strong>Catalytic Asymmetric Total Synthesis of <em>ent-<\/em>Hyperforin<\/strong><br>Shimizu, Y.; Shi, S. \u2013L.; Usuda, H.; Kanai, M.; Shibasaki, M.<br><em>Angew. Chem. Int. Ed.<\/em> <strong>2010<\/strong>, <em>49<\/em>, 1103\u20131106. (<a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.200906678\/abstract\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1002\/anie.200906678<\/a>)<\/li>\n\n\n\n<li><strong>Asymmetric Reductive Mannich Reaction to Ketoimines Catalyzed by a Cu(I) Complex<\/strong><br>Du, Y.; Xu, L. \u2013W.; Shimizu, Y.; Oisaki, K.; Kanai, M.; Shibasaki, M.<br><em>J. Am. Chem. Soc. <\/em><strong>2008<\/strong>,<em> 130, <\/em>16146\u201316147. (<a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ja8069727\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1021\/ja8069727<\/a>)<\/li>\n\n\n\n<li><strong>New Approach for Construction of a Highly Congested Bicyclic System in Polycyclic Polyprenylated Acylphloroglucinols (PPAPs)<\/strong><br>Shimizu, Y.; Kuramochi, A.; Usuda, H.; Kanai, M.; Shibasaki, M.<br><em>Tetrahedron Lett.<\/em>&nbsp;<strong>2007<\/strong>, <em>48<\/em>, 4173\u20134177. (<a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S004040390700740X?via%3Dihub\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1016\/j.tetlet.2007.04.080<\/a>)<\/li>\n<\/ol>\n\n\n\n<h3 class=\"wp-block-heading\">Reviews<\/h3>\n\n\n\n<ol reversed class=\"wp-block-list\">\n<li><strong>MHAT\u306b\u57fa\u3065\u3044\u305f\u7b2c\u56db\u7d1a\u70ad\u7d20\u69cb\u7bc9\u53cd\u5fdc<\/strong><br>\u6e05\u6c34\u6d0b\u5e73<br><em>Organometallic News\u300c\u6709\u6a5f\u91d1\u5c5e\u30cf\u30a4\u30e9\u30a4\u30c8\u300d, <\/em><strong>2024<\/strong>, <em>3<\/em>, 100.<\/li>\n\n\n\n<li><strong>Enabling \u03b1-Functionalization of Carboxylic Acids by Boron Compounds<\/strong><br>Shimizu, Y.<br><em>J. Synth. Org. Chem. Jpn. <\/em><strong>2024<\/strong>, <em>82<\/em>, 802-813. (<a href=\"https:\/\/doi.org\/10.5059\/yukigoseikyokaishi.82.802\">DOI: 10.5059\/yukigoseikyokaishi.82.802<\/a>)<\/li>\n\n\n\n<li><strong>The Aldol Reaction: Group XIII Enolates<\/strong><br>Sawamura, M.; Shimizu, Y.<br><em>Comprehenseive Organic Synthesis<\/em> (Third Edition), <strong>2025<\/strong>, 2, 402-424. (<a href=\"https:\/\/doi.org\/10.1016\/B978-0-323-96025-0.00048-X\" target=\"_blank\" rel=\"noreferrer noopener\">DOI: 10.1016\/B978-0-323-96025-0.00048-X<\/a>)<\/li>\n\n\n\n<li><strong>Synthesis of Carboxylic Acids with Retention of the Functional Group (Update 2024)<\/strong><br>Sawamura, M.; Shimizu, Y.<br><em>Science of Synthesis Knowledge Updates<\/em>, <strong>2024<\/strong>, <em>2<\/em>, 201. (<a href=\"https:\/\/doi.org\/10.1055\/sos-SD-120-00214\" target=\"_blank\" rel=\"noreferrer noopener\">DOI: 10.1055\/sos-SD-120-00214<\/a>)<\/li>\n\n\n\n<li><strong><strong>Boron-Catalyzed \u03b1-Functionalizations of Carboxylic<\/strong> Acids<\/strong><br>Shimizu, Y.; Kanai, M.<br><em>Chem. Rec.&nbsp;<\/em><strong>2023<\/strong>, e202200273<em>.<\/em> (<a href=\"https:\/\/doi.org\/10.1002\/tcr.202200273\" target=\"_blank\" rel=\"noreferrer noopener\">DOI: 10.1002\/tcr.202200273<\/a>)<\/li>\n\n\n\n<li><strong><strong>Boron Catalysis in the Transformation of Carboxylic Acids and Carboxylic Acid Derivatives&nbsp;<br><\/strong><\/strong>Sawamura, M.; Shimizu, Y.<br><em>Eur. J. Org. Chem.<\/em>&nbsp;<strong>2023<\/strong>,&nbsp;<em>26<\/em>, e202201249. (<a href=\"https:\/\/doi.org\/10.1002\/ejoc.202201249\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1002\/ejoc.202201249<\/a>)<\/li>\n\n\n\n<li><strong><strong>Development of Copper-Catalyzed Chemoselective Reactions<br><\/strong><\/strong>Shimizu, Y.<br><em><em>Chem. Pharm. Bull. <\/em><\/em><strong>2020<\/strong>,<em> <em>68<\/em><\/em>, 405\u2013420.(<a href=\"https:\/\/doi.org\/10.1248\/cpb.c19-00739\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1248\/cpb.c19-00739<\/a>)<\/li>\n\n\n\n<li><strong><strong>Cupid and Psyche system for the diagnosis and treatment of advanced<\/strong> cancer<\/strong><br>Sugiyama, A.; Kawamura, T.; Tanaka, T.; Doi, H.; Yamashita, T.; Shinoda, K.; Fujitani, H.; Yamatsugu, K.;&nbsp;Shimizu, Y.; Tatsumi, T.; Takahashi, K.; Kanai, M.; Mizohata, E.; Kawato, T.; Doi, T.; Inoue, T.; Kodama, T.<br><em>Proc. Jpn. Acad., Ser. B&nbsp;<\/em><strong>2019<\/strong>,<em>&nbsp;95<\/em>, 602\u2013611.&nbsp;(<a href=\"https:\/\/doi.org\/10.2183\/pjab.95.041\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.2183\/pjab.95.041<\/a>)<\/li>\n\n\n\n<li><strong><strong>\u30ab\u30eb\u30dc\u30f3\u9178\u9078\u629e\u7684\u6c42\u6838\u7684\u6d3b\u6027\u5316\u6cd5\u306e\u958b\u767a\u2015\u5358\u7d14\u306a\u8a66\u85ac\u306e\u65b0\u3057\u3044\u5229\u7528\u6cd5<br><\/strong><\/strong>\u6e05\u6c34\u6d0b\u5e73<br><em>\u5316\u5b66\u3068\u5de5\u696d\uff08\u98db\u7fd4\u3059\u308b\u82e5\u624b\uff09<\/em><strong>2018<\/strong>,&nbsp;<em>71<\/em>, 871-872.<\/li>\n\n\n\n<li><strong><strong>Catalytic Asymmetric Addition Reactions of Cu(I)-Conjugated Soft Carbon Nucleophiles<br><\/strong><\/strong>Wei, X.-F.; Shimizu, Y.; Kanai, M.<br><em><em>Topics in Organometallic Chemistry<\/em><\/em> <strong>2016<\/strong>,<em> <em>58<\/em>,<\/em> 169\u2013182<em>. <\/em>(<a href=\"https:\/\/link.springer.com\/chapter\/10.1007%2F3418_2015_163\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1007\/3418_2015_163<\/a>)<\/li>\n\n\n\n<li><strong>Recent progress in copper-catalyzed difunctionalization of unactivated carbon-carbon multiple bonds<\/strong><br>Shimizu, Y.; Kanai, M.<br><em>Tetrahedron Lett.<\/em> <strong>2014<\/strong>,&nbsp;<em>55,&nbsp;<\/em>3727\u20133737. (<a href=\"https:\/\/link.springer.com\/chapter\/10.1007%2F3418_2015_163\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1016\/j.tetlet.2014.05.077<\/a>)<\/li>\n\n\n\n<li><strong>\u6709\u6a5f\u89e6\u5a92\u306e\u529b\u3000\u30ab\u30eb\u30dc\u30cb\u30eb\u2010\u30aa\u30ec\u30d5\u30a3\u30f3\u30e1\u30bf\u30bb\u30b7\u30b9<br><\/strong>\u6e05\u6c34\u6d0b\u5e73<br>\u30d5\u30a1\u30eb\u30de\u30b7\u30a2&nbsp;<strong>2013<\/strong>, <em>49<\/em>, 695. (<a href=\"https:\/\/www.jstage.jst.go.jp\/article\/faruawpsj\/49\/7\/49_KJ00010109747\/_article\/-char\/ja\/\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10. 10.14894\/faruawpsj.49.7_695<\/a>)<\/li>\n\n\n\n<li><strong>Carbon\u2013Carbon Bond-Formations Promoted by Redox-Active Metal Catalysts<br><\/strong>Kanai, M.; Matsunaga, S.; Oisaki, K.; Shimizu, Y.<br><em>J. Synth. Org. Chem. Jpn.<\/em> <strong>2013<\/strong>, <em>71<\/em>, 433\u2013442. (<a href=\"https:\/\/www.jstage.jst.go.jp\/article\/yukigoseikyokaishi\/71\/5\/71_433\/_article\/-char\/ja\/\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.5059\/yukigoseikyokaishi.71.433<\/a>)<\/li>\n<\/ol>\n","protected":false},"excerpt":{"rendered":"<p>\u6e05\u6c34 \u6d0b\u5e73\u3000Yohei Shimizu \u51c6\u6559\u6388\u3000Associate Professor \u6e05\u6c34\u3000\u6d0b\u5e73\u3000Yohei Shimizu E-mail: shimizu- &#8230; <\/p>\n","protected":false},"author":4,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-366","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/wwwchem.sci.hokudai.ac.jp\/~orgmet\/wp-json\/wp\/v2\/pages\/366","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/wwwchem.sci.hokudai.ac.jp\/~orgmet\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/wwwchem.sci.hokudai.ac.jp\/~orgmet\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/wwwchem.sci.hokudai.ac.jp\/~orgmet\/wp-json\/wp\/v2\/users\/4"}],"replies":[{"embeddable":true,"href":"https:\/\/wwwchem.sci.hokudai.ac.jp\/~orgmet\/wp-json\/wp\/v2\/comments?post=366"}],"version-history":[{"count":44,"href":"https:\/\/wwwchem.sci.hokudai.ac.jp\/~orgmet\/wp-json\/wp\/v2\/pages\/366\/revisions"}],"predecessor-version":[{"id":1627,"href":"https:\/\/wwwchem.sci.hokudai.ac.jp\/~orgmet\/wp-json\/wp\/v2\/pages\/366\/revisions\/1627"}],"wp:attachment":[{"href":"https:\/\/wwwchem.sci.hokudai.ac.jp\/~orgmet\/wp-json\/wp\/v2\/media?parent=366"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}