{"id":368,"date":"2024-07-10T23:44:39","date_gmt":"2024-07-10T14:44:39","guid":{"rendered":"https:\/\/wwwchem.sci.hokudai.ac.jp\/~orgmet\/?page_id=368"},"modified":"2026-03-04T09:02:21","modified_gmt":"2026-03-04T00:02:21","slug":"masuda","status":"publish","type":"page","link":"https:\/\/wwwchem.sci.hokudai.ac.jp\/~orgmet\/masuda\/","title":{"rendered":"\u5897\u7530 \u4f91\u4eae"},"content":{"rendered":"\n<h2 class=\"wp-block-heading\">\u5897\u7530 \u4f91\u4eae\u3000Yusuke Masuda<\/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=\"156\" height=\"209\" src=\"https:\/\/wwwchem.sci.hokudai.ac.jp\/~orgmet\/wp-content\/uploads\/2024\/07\/Masuda.jpg\" alt=\"\" class=\"wp-image-122\" 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\">\u52a9\u6559\u3000Assistant Professor<\/h4>\n\n\n\n<p class=\"has-medium-font-size\">\u5897\u7530\u3000\u4f91\u4eae\u3000Yusuke Masuda<\/p>\n\n\n\n<p>E-mail: ymasuda[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>1990 \u5927\u962a\u5e9c\u306b\u751f\u307e\u308c\u308b\u3000\u3000Born in Osaka<\/li>\n\n\n\n<li>2008 \u5927\u962a\u5e9c\u7acb\u5929\u738b\u5bfa\u9ad8\u7b49\u5b66\u6821\u3000\u5352\u696d<\/li>\n\n\n\n<li>2012 \u4eac\u90fd\u5927\u5b66\u5de5\u5b66\u90e8\u5de5\u696d\u5316\u5b66\u79d1\u3000\u5352\u696d<\/li>\n\n\n\n<li>2014 \u4eac\u90fd\u5927\u5b66\u5927\u5b66\u9662\u5de5\u5b66\u7814\u7a76\u79d1\u3000\u5408\u6210\u30fb\u751f\u7269\u5316\u5b66\u5c02\u653b\u3000\u4fee\u58eb\u8ab2\u7a0b\u3000\u4fee\u4e86<\/li>\n\n\n\n<li>2017 \u4eac\u90fd\u5927\u5b66\u5927\u5b66\u9662\u5de5\u5b66\u7814\u7a76\u79d1\u3000\u5408\u6210\u30fb\u751f\u7269\u5316\u5b66\u5c02\u653b\u3000\u535a\u58eb\u8ab2\u7a0b \u4fee\u4e86\u3000\u3000Ph.D. Kyoto University<\/li>\n\n\n\n<li>2017 \u65e5\u672c\u5b66\u8853\u632f\u8208\u4f1a\u7279\u5225\u7814\u7a76\u54e1\u3000SPD\u3000\uff08\u6771\u4eac\u5927\u5b66\u5927\u5b66\u9662\u85ac\u5b66\u7cfb\u7814\u7a76\u79d1\uff09\u3000\u3000JSPS Research Fellow (SPD), The University of Tokyo<\/li>\n\n\n\n<li>2017 \u7c73\u56fd\u30fb\u30ab\u30ea\u30d5\u30a9\u30eb\u30cb\u30a2\u5de5\u79d1\u5927\u5b66\u3000\u7559\u5b66\u3000\u3000Visiting Scientist, California Institute of Technology<\/li>\n\n\n\n<li>2018 \u4eac\u90fd\u5927\u5b66\u5927\u5b66\u9662\u5de5\u5b66\u7814\u7a76\u79d1\u3000\u5408\u6210\u30fb\u751f\u7269\u5316\u5b66\u5c02\u653b \u7279\u5b9a\u52a9\u6559\u3000\u3000Assistant Professor, Kyoto University<\/li>\n\n\n\n<li>2021 \u5317\u6d77\u9053\u5927\u5b66\u5927\u5b66\u9662\u7406\u5b66\u7814\u7a76\u9662\u3000\u5316\u5b66\u90e8\u9580\u3000\u52a9\u6559\u3000\u3000Assistant Professor, Hokkaido University<\/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>2016 Reaxys PhD Prize Finalist<\/li>\n\n\n\n<li>2025 \u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a \u56db\u56fd\u5316\u6210\u5de5\u696d \u7814\u7a76\u4f01\u753b\u8cde\u3000\u3000Shikokukasei Award in Synthetic Organic Chemistry, Japan<\/li>\n\n\n\n<li>2025 \u65e5\u672c\u5316\u5b66\u4f1a \u7b2c75\u56de\u9032\u6b69\u8cde\u3000The Chemical Society of Japan Award for Young Chemists for 2025 <\/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>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\">10.1002\/ceur.202500436<\/a>).<\/li>\n\n\n\n<li><strong>Machine-learning-guided Screening of Organic Photosensitizers Accelerated by Domain Adaptation.<\/strong> <br>Ikemura, H.; Noto, N.; Akiba, R.; Rohlfs, T.; Masuda, Y.; Sumida, Y.; Manche\u00f1o, O. G.; Hosoya, T.; Ohmiya, H.; Sawamura, M.; Saito, S. <br><em>Cell Rep. Phys. Sci.<\/em>, <strong>2026<\/strong>, <em>7<\/em>, 103141. (DOI: <a href=\"https:\/\/doi.org\/10.1016\/j.xcrp.2026.103141\" target=\"_blank\" rel=\"noreferrer noopener\">10.1016\/j.xcrp.2026.103141<\/a>)<\/li>\n\n\n\n<li><strong>\u03b2-Vinylated Tri(1-adamantyl)phosphine: Synthesis, Characterization, and Application in Gold Catalysis.<\/strong> <br>Tulipkaliyev, A.; Sawamura, M.; Masuda, Y. <br><em>Chem. Asian J<\/em>. <strong>2026<\/strong>, <em>21<\/em>, e70542. (Special Collection: Asian Core Program) (DOI: <a href=\"https:\/\/aces.onlinelibrary.wiley.com\/doi\/10.1002\/asia.70542\">10.1002\/asia.70542<\/a>)<\/li>\n\n\n\n<li><strong>Synthesis of Imidoyltrialkylphosphonium Salts through Photocatalytic Reactions between Isocyanides and Tri-<em>t<\/em>-butylphosphine<\/strong><br>Sakurada, A.; Sawamura, M.; Masuda, Y. <br><em>Chem. Lett.<\/em>&nbsp;<strong>2025<\/strong>, <em>54<\/em>, upaf134. (Editor&#8217;s Choice) (DOI: <a href=\"https:\/\/academic.oup.com\/chemlett\/advance-article\/doi\/10.1093\/chemle\/upaf134\/8194504\">10.1093\/chemle\/upaf134<\/a>)<\/li>\n\n\n\n<li><strong>Photocatalytic Cyclization of 2-Phosphinobiaryls to Trivalent Dibenzophospholes<\/strong><br>Masuda, Y.; Harabuchi, Y.; Kawamura, Y.; Morooka, N.; Maeda, S.; Sawamura, M.<br><em>ACS Catal.<\/em>,&nbsp;<strong>2025<\/strong>, <em>15<\/em>, 6514\u20136524. (DOI:&nbsp;<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acscatal.5c01369\">10.1021\/acscatal.5c01369<\/a>)<\/li>\n\n\n\n<li><strong>Photocatalytic Alkene-Migrative Chain Elongation of 2-Phosphinostyrenes with Aldehydes<\/strong><br>Mori, H.; Sakurada, A.; Sawamura, M.; Masuda, Y.<br><em>Org. Lett.<\/em>,&nbsp;<strong>2025<\/strong>,&nbsp;<em>27<\/em>, 439\u2013443. (DOI:&nbsp;<a href=\"https:\/\/pubs.acs.org\/doi\/full\/10.1021\/acs.orglett.4c04424\">10.1021\/acs.orglett.4c04424<\/a>)<\/li>\n\n\n\n<li><strong>Photoinduced Enantioselective Triplet Radical Reaction on Metal: Copper-Catalyzed Conjugate Addition of Acylsilanes to \u03b1,\u03b2-Unsaturated Ketones and Aldehydes<\/strong><br>Masuda, Y.; Ueda, Y.; Sueki, A.; Shimosato, J.; Nishimura, K.; Gao, M.; Hasegawa, J.; Sawamura, M. <em>Chem. Eur. J., <\/em><strong>2024<\/strong>, <em>30<\/em>, e202402564. (DOI: <a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/abs\/10.1002\/chem.202402564\">10.1002\/chem.202402564<\/a>)<br>Front Cover: DOI:&nbsp;<a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/10.1002\/chem.202486501\">10.1002\/chem.202486501<\/a><\/li>\n\n\n\n<li><strong>Photoinduced Platinum-catalyzed Reductive Allylation of \u03b1-Diketones with Allylic Carbonates<\/strong><br>Shimosato,&nbsp;J.;&nbsp;Sawamura,&nbsp;M.;&nbsp;Masuda,&nbsp;Y.&nbsp;&nbsp;<br><em><em>Org. Lett.,<\/em>&nbsp;<\/em><strong>2024<\/strong>, <em>26<\/em>, 2023\u20132028. (DOI:&nbsp;<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.4c00091\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/acs.orglett.4c00091<\/a>)&nbsp;&nbsp;<\/li>\n\n\n\n<li><strong>Photocatalytic Aldehyde C\u2013H Bond Phosphonioethylation with Vinylphosphonium Bromide<\/strong><br>Mori,&nbsp;H.;&nbsp;Yoshida,&nbsp;M.;&nbsp;Sawamura,&nbsp;M.; Masuda,&nbsp;Y.&nbsp;<br><em>Asian J. Org. Chem., <\/em><strong>2024<\/strong>, <em>13<\/em>, e202300532. (DOI:<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/ajoc.202300532\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/ajoc.202300532<\/a>)<\/li>\n\n\n\n<li><strong><strong>Photocatalytic 1,2-Phosphorus-Migrative [3+2] Cycloaddition of&nbsp;Tri(<em>t<\/em>-butyl)phosphine with Terminal Alkynes<\/strong><br><\/strong>Masuda,&nbsp;Y.;&nbsp;Ikeshita,&nbsp;D.;&nbsp;Higashida,&nbsp;K.;&nbsp;Yoshida,&nbsp;M.;&nbsp;Ishida,&nbsp;N.;&nbsp;Murakami,&nbsp;M.;&nbsp;Sawamura,&nbsp;M.<br><em>J. Am. Chem. Soc.,&nbsp;<\/em><strong>2023<\/strong>,&nbsp;<em>145<\/em>, 19060\u201319066. (DOI:<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.3c06760\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/jacs.3c06760<\/a>)<\/li>\n\n\n\n<li><strong><strong>Sequence-selective Three-component Reactions of Alkyltrifluoroborates with \u03b1,\u03b2-Unsaturated Carbonyl Compounds and Vinylphosphonium Salts<\/strong><\/strong><br>Yoshida,M. ; Sawamura,&nbsp;M. ;&nbsp;Masuda,&nbsp;Y.&nbsp;&nbsp;<br><em>Org. Chem. Front.,<\/em><strong>&nbsp;2023<\/strong>, <em>10<\/em>, 3654\u20133661.&nbsp;(DOI:&nbsp;<a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2023\/qo\/d3qo00631j\" target=\"_blank\" rel=\"noreferrer noopener\">10.1039\/D3QO00631J<\/a>)<\/li>\n\n\n\n<li><strong>Nickel-Catalyzed Defluorophosphonylation of Aryl Fluorides<\/strong><br>You, Z.; Masuda, Y.; Iwai, T.; Higashida, K.;&nbsp; Sawamura, M.&nbsp;<br><em><em>J. Org. Chem.,<\/em><strong>&nbsp;<\/strong><\/em><strong>2022,<\/strong><em><strong>&nbsp;<\/strong>87,<\/em> 14731\u201314737 (DOI:&nbsp;<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.joc.2c02048\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/acs.joc.2c02048<\/a>)<\/li>\n\n\n\n<li><strong>Photoinduced Alcoholic \u03b1-C\u2013H Bond Anti-Markovnikov Addition to Vinylphosphonium Bromides Followed by Wittig Olefination: Two-step Protocol for \u03b1-C\u2013H Allylic Alkylation of Alcohols<\/strong><br>Yoshida, M.;&nbsp;Sawamura, M.;&nbsp;Masuda,&nbsp;Y.&nbsp;<br><em><em>ChemCatChem.,<\/em><strong>&nbsp;<\/strong><\/em><strong>2022,&nbsp;<\/strong><em>14, <\/em>e202200744. (VIP) (DOI: <a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/full\/10.1002\/cctc.202200744\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/cctc.202200744<\/a>)&nbsp;<\/li>\n\n\n\n<li><strong>Synthesis of Tetraarylphosphonium Salts from Triarylphosphines and Aryl Bromides Exploiting Light and Palladium<br><\/strong>Ikeshita, D.; Shimura, H.; Miyakawa, S.; Masuda, Y.; Ishida, N.; Murakami, M.<br><em>Chem. Lett.<\/em>, <strong>2022<\/strong>, <em>51<\/em>, 522\u2013524. (DOI: <a href=\"https:\/\/www.journal.csj.jp\/doi\/abs\/10.1246\/cl.220067\" target=\"_blank\" rel=\"noreferrer noopener\">10.1246\/cl.220067<\/a>)<\/li>\n\n\n\n<li><strong>Photoinduced Hydrophosphination of Terminal Alkynes with Tri(<em>o<\/em>-tolyl)phosphine: Synthesis of Alkenylphosphonium Salts<br><\/strong>Ikeshita, D.; Masuda, Y.; Ishida, N.; Murakami, M.<br><em>Org. Lett.<\/em>, <strong>2022<\/strong>, <em>24<\/em>, 2504\u20132508. (DOI: <a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.orglett.2c00634\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/acs.orglett.2c00634<\/a>)<\/li>\n\n\n\n<li><strong><strong>Photoinduced Copper-Catalyzed Asymmetric Acylation of Allylic Phosphates with Acylsilanes<br><\/strong><\/strong>Ueda,&nbsp;Y.;&nbsp;Masuda,&nbsp;Y.;&nbsp;Iwai,&nbsp;T.;&nbsp;Imaeda,&nbsp;K.;&nbsp;Takeuchi,&nbsp;H.;&nbsp;Ueno,&nbsp;K.;&nbsp;Gao,&nbsp;M.;&nbsp;Hasegawa,&nbsp;J.;&nbsp;Sawamura,&nbsp;M.<br><em>J. Am. Chem. Soc.<\/em>,&nbsp;<strong>2022<\/strong>, <em>144,<\/em>&nbsp;2218\u20132224<em>.<\/em> (DOI: <a href=\"https:\/\/doi.org\/10.1021\/jacs.1c11526\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/jacs.1c11526<\/a>)&nbsp;<\/li>\n\n\n\n<li><strong>Photoinduced Reaction of Triarylphosphines with Alkenes Forming Fused Tricyclic Phosphonium Salts<br><\/strong>Masuda, Y.; Uno, M.; Murakami, M.<br><em>Org. Lett.<\/em>, <strong>2021<\/strong>, <em>23<\/em>, 8445\u20138449. (DOI: <a href=\"http:\/\/dx.doi.org\/10.1021\/acs.orglett.1c03168\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/acs.orglett.1c03168<\/a>)<\/li>\n\n\n\n<li><strong>Photocatalytic Cycloaddition Reaction of Triarylphosphines with Alkynes Forming Cyclic Phosphonium Salts<br><\/strong>Masuda, Y.; Ikeshita, D.; Murakami, M.<br><em>Chem. Lett.<\/em>, <strong>2021<\/strong>, <em>50<\/em>, 1691\u20131694<strong>. <\/strong>(DOI: <a href=\"http:\/\/dx.doi.org\/10.1246\/cl.210361\" target=\"_blank\" rel=\"noreferrer noopener\">10.1246\/cl.210361<\/a>)<\/li>\n\n\n\n<li><strong>Isomerization of Unprotected Aldoses to 2-Deoxyaldonic Acids Induced by Visible Light\/Quinuclidine\/Water-Soluble Iridium Complex in Water<br><\/strong>Masuda, Y.; Tsuda, H.; Murakami, M.<br><em>Bull. Chem. Soc. Jpn.<\/em>, <strong>2021<\/strong>, <em>94<\/em>, 1702\u20131704<strong>.<\/strong> (DOI: <a href=\"http:\/\/dx.doi.org\/10.1246\/bcsj.20210098\" target=\"_blank\" rel=\"noreferrer noopener\">10.1246\/bcsj.20210098<\/a>)<\/li>\n\n\n\n<li><strong>Dehydrative\/Decarboxylative Coupling of Carboxylic Acids with Allylic Alcohols<br><\/strong>Masuda, Y.; Ito, M.; Murakami, M.<br><em>Chem. Lett.<\/em>,<strong> <strong>2021<\/strong><\/strong>, <em>50<\/em>, 1030\u20131033. (DOI: <a href=\"http:\/\/dx.doi.org\/10.1246\/cl.210036\" target=\"_blank\" rel=\"noreferrer noopener\">10.1246\/cl.210036<\/a>)<\/li>\n\n\n\n<li><strong>Photo-induced Dihydroxylation of Alkenes with Diacetyl, Oxygen, and Water<br><\/strong>Masuda, Y.; Ikeshita, D.; Murakami, M.<br><em>Helv. Chim. Acta<\/em>, <strong>2021<\/strong>,&nbsp;<em>104<\/em>, e20000228. (DOI: <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/hlca.202000228\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/hlca.202000228<\/a>)<\/li>\n\n\n\n<li><strong>Photo-induced Dearomatizing Three-component Coupling of Arylphosphines, Alkenes, and Water<br><\/strong>Masuda, Y.; Tsuda, H.; Murakami, M.<br><em>Angew. Chem. Int. Ed.<\/em>,&nbsp;<strong>2021<\/strong>, <em>60<\/em>, 3551\u20133555. (DOI: <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/anie.202013215\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/anie.202013215<\/a>)<\/li>\n\n\n\n<li><strong>Degradation of Unprotected Aldohexonic Acids to Aldopentoses Promoted by Light and Oxygen<\/strong><br>Masuda, Y.; Ito, M.; Murakami, M.<br><em>Chem. Lett<\/em>., <strong>2020<\/strong>, <em>49<\/em>, 1309\u20131311. (DOI: <a href=\"https:\/\/www.journal.csj.jp\/doi\/full\/10.1246\/cl.200517\" target=\"_blank\" rel=\"noreferrer noopener\">10.1246\/cl.200517<\/a>)<\/li>\n\n\n\n<li><strong>Dehydrative Allylation of \u03b1 C(sp3)\u2212H Bonds of Alkylamines with Allylic Alcohols<br><\/strong>Masuda, Y.; Ito, M.; Murakami, M.<br><em>Org. Lett.<\/em>, <strong>2020<\/strong>, <em>22<\/em>, 4467\u20134470. (DOI: <a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.orglett.0c01464\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/acs.orglett.0c01464<\/a>)<\/li>\n\n\n\n<li><strong>Dehydrative Allylation of 2-Alkylbenzophenones with Allylic Alcohols<br><\/strong>Masuda, Y.; Makita, K.; Murakami, M.<br><em>Chem. Lett<\/em>., <strong>2020<\/strong>, <em>49<\/em>, 616\u2013618. (DOI:<a href=\"https:\/\/www.journal.csj.jp\/doi\/full\/10.1246\/cl.200123\" target=\"_blank\" rel=\"noreferrer noopener\">10.1246\/cl.200123<\/a>)<\/li>\n\n\n\n<li><strong>C-1 Oxidation\/C-2 Reduction Isomerization of Unprotected Aldoses Induced by Light\/Ketone<br><\/strong>Masuda, Y.; Tsuda, H.; Murakami, M.<br><em>Angew. Chem., Int. Ed.<\/em>,<strong> 2020<\/strong>, <em>59<\/em>, 2755\u20132759 (DOI:<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/anie.201914242\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/anie.201914242<\/a>)<\/li>\n\n\n\n<li><strong>Carboxylation of Benzylic and Aliphatic C-H Bonds with CO2 Induced by Light\/Ketone\/Nickel<br><\/strong>Ishida, N.; Masuda, Y.; Imamura, Y.; Yamazaki, K.; Murakami, M.<br><em>J. Am. Chem. Soc.<\/em>,<strong> 2019<\/strong>, <em>141,<\/em> 19611\u201319615. (DOI: <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.9b12529\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/jacs.9b12529<\/a>)<\/li>\n\n\n\n<li><strong><strong>Synthesis of Tofisopam by Way of Photoinduced CO2 Fixation<br><\/strong><\/strong>Masuda, Y.; Makita, K.; Ishida, N.; Murakami, M.<br><em>Chem. Asian J.<\/em>, <strong>2019,<\/strong> <em>14<\/em>, 4189\u20134192. (DOI: <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/asia.201901431\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/asia.201901431<\/a>)<\/li>\n\n\n\n<li><strong><strong>Photo-Assisted Fixation of CO2 onto Aryl Bromides Producing Aromatic Esters<br><\/strong><\/strong>Ishida, N.; Masuda, Y.; Liao, W.; Murakami, M.<br><em>Chem. Lett.<\/em>, <strong>2019<\/strong>, <em>48,<\/em> 1316\u20131318. &nbsp;(DOI: <a href=\"https:\/\/www.journal.csj.jp\/doi\/full\/10.1246\/cl.190563\" target=\"_blank\" rel=\"noreferrer noopener\">10.1246\/cl.190563<\/a>)<\/li>\n\n\n\n<li><strong><strong>A Strained Vicinal Diol as a Reductant for Coupling of Organyl Halides<\/strong><\/strong><br>Ishida, N.; Masuda, Y.; Sun, F.; Kamae, Y.; Murakami, M.<br><em>Chem. Lett.,<\/em> <strong>2019<\/strong>, <em>48<\/em>, 1042\u20131045.&nbsp;(DOI: <a href=\"https:\/\/www.journal.csj.jp\/doi\/full\/10.1246\/cl.190403\" target=\"_blank\" rel=\"noreferrer noopener\">10.1246\/cl.190403<\/a>)<\/li>\n\n\n\n<li><strong><strong>Light\/Palladium-Promoted Benzylic C\u2013H Acylation Using a Benzoyl Group as the Photo-Directing Group<br><\/strong><\/strong>Masuda, Y.; Ishida, N.; Murakami, M.<br><em>Chem. Asian J., <\/em><strong>2019<em>, <\/em><\/strong><em>14, <\/em>403\u2013406<em>.<\/em>(DOI: <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/asia.201801881\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/asia.201801881<\/a>)<\/li>\n\n\n\n<li><strong>Cooperation of a Nickel-Bipyridine Complex with Light for Benzylic C\u2013H Arylation of Toluene Derivatives<\/strong><br>Ishida, N.; Masuda, Y.; Ishikawa, N.; Murakami, M.<br><em>Asian J. Org. Chem., <\/em><strong>2017<\/strong><em><strong>, <\/strong>6, <\/em>669\u2013672<em>.<\/em> (DOI: <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/ajoc.201700115\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/ajoc.201700115<\/a>)<\/li>\n\n\n\n<li><strong><strong>Aryl Ketones as Single-Electron-Transfer Photoredox Catalysts in the Nickel-Catalyzed Homocoupling of Aryl Halides<\/strong><br><\/strong>Masuda, Y.; Ishida, N.; Murakami, M.<br><em>Eur. J. Org. Chem., <\/em><strong>2016<em>, <\/em><\/strong><em>2016<\/em>, 5822\u20135825<strong><em>.<\/em><\/strong>(DOI: <a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/full\/10.1002\/ejoc.201601352\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/ejoc.201601352<\/a>)<\/li>\n\n\n\n<li><strong><strong>A Light\/Ketone\/Copper System for Carboxylation of Allylic C\u2013H Bonds of Alkenes with CO2<\/strong><br><\/strong>Ishida, N.; Masuda, Y.; Uemoto, S.; Murakami, M.<br><em>Chem. Eur. J.<\/em>, <strong>2016<\/strong>, <em>22<\/em>, 6524\u20136527. &nbsp;(DOI:&nbsp;<a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/full\/10.1002\/chem.201600682\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/chem.201600682<\/a>)<\/li>\n\n\n\n<li><strong><strong>Light-Driven Carboxylation of o-Alkylphenyl Ketones with CO2<br><\/strong><\/strong>Masuda, Y.; Ishida, N.; Murakami, M.<br><em>J. Am. Chem. Soc., <\/em><strong>2015<\/strong><em><strong>, <\/strong>137, <\/em>14063\u201314066<strong>.<\/strong> (DOI: <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.5b10032\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/jacs.5b10032<\/a>)<\/li>\n\n\n\n<li><strong><strong>Enantioselective Construction of 3-Hydroxypiperidine Scaffolds by Sequential Action of Light and Rhodium upon N-Allylglyoxylamides<br><\/strong><\/strong>Ishida, N.; Ne\u010das, D.; Masuda, Y.; Murakami, M.<br><em>Angew. Chem., Int. Ed., <\/em><strong>2015<\/strong><em><strong>,<\/strong> 54<\/em>, 7418\u20137421. (DOI:&nbsp;<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/anie.201502584\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/anie.201502584<\/a>)<\/li>\n\n\n\n<li><strong>Construction of tetralin skeletons based on rhodium-catalysed site-selective ring opening of benzocyclobutenols<\/strong><br>Ishida, N.; Ishikawa, N.; Sawano, S.; Masuda, Y.; Murakami, M.<br><em>Chem. Commun.<\/em>, <strong>2015<\/strong>, <em>51<\/em>, 1882\u20131885. (DOI: <a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2015\/cc\/c4cc09327e\">10.1039\/C4CC09327E<\/a>)<\/li>\n\n\n\n<li><strong>Synthesis of Acylphosphonates by a Palladium-Catalyzed Phosphonocarbonylation Reaction of Aryl Iodides with Phosphites<\/strong><br>Masuda, Y.; Ishida, N.; Murakami, M.<br><em>Chem. Asian J., <\/em><strong>2015<em>, <\/em><\/strong><em>10, <\/em>321\u2013324. (DOI:&nbsp;<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/asia.201403260\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/asia.201403260<\/a>)<\/li>\n\n\n\n<li><strong><strong>Oxidative Addition of a Strained C\u2212C Bond onto Electron-Rich Rhodium(I) at Room Temperature<br><\/strong><\/strong>Masuda, Y.; Hasegawa, M.; Yamashita, M.; Nozaki, K.; Ishida, N.; Murakami, M.<br><em>J. Am. Chem. Soc., <\/em><strong>2013<\/strong><em><strong>, <\/strong>135, <\/em>7142\u20137145<em>.<\/em> (DOI:&nbsp;<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/ja403461f\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/ja403461f)<\/a><\/li>\n\n\n\n<li><strong><strong>Rhodium-Catalyzed Ring Opening of Benzocyclobutenols with Site-Selectivity Complementary to Thermal Ring Opening<br><\/strong><\/strong>Ishida, N.; Sawano, S.; Masuda, Y.; Murakami, M.<br><em>J. Am. Chem. Soc., <\/em><strong>2012<em>,<\/em><\/strong><em> 134, <\/em>17502\u201317504<em>.<\/em>&nbsp;(DOI: <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/ja309013a\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/ja309013a<\/a>)<\/li>\n<\/ol>\n\n\n\n<h3 class=\"wp-block-heading\">Reviews<br><\/h3>\n\n\n\n<ol reversed class=\"wp-block-list\">\n<li><strong>Photocatalytic Transformations of Tertiary Phosphines through Precise Control of Organophosphorus Radicals<br><\/strong>Masuda, Y.<br><em>Chem. Lett.<\/em> <strong>2025<\/strong>, <em>54<\/em>, upaf214. (<a href=\"https:\/\/doi.org\/10.1093\/chemle\/upaf214\" target=\"_blank\" rel=\"noreferrer noopener\">DOI:&nbsp;10.1093\/chemle\/upaf214<\/a>)<\/li>\n<\/ol>\n","protected":false},"excerpt":{"rendered":"<p>\u5897\u7530 \u4f91\u4eae\u3000Yusuke Masuda \u52a9\u6559\u3000Assistant Professor \u5897\u7530\u3000\u4f91\u4eae\u3000Yusuke Masuda E-mail: ymasuda[a &#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-368","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/wwwchem.sci.hokudai.ac.jp\/~orgmet\/wp-json\/wp\/v2\/pages\/368","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=368"}],"version-history":[{"count":34,"href":"https:\/\/wwwchem.sci.hokudai.ac.jp\/~orgmet\/wp-json\/wp\/v2\/pages\/368\/revisions"}],"predecessor-version":[{"id":1578,"href":"https:\/\/wwwchem.sci.hokudai.ac.jp\/~orgmet\/wp-json\/wp\/v2\/pages\/368\/revisions\/1578"}],"wp:attachment":[{"href":"https:\/\/wwwchem.sci.hokudai.ac.jp\/~orgmet\/wp-json\/wp\/v2\/media?parent=368"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}