{"id":18,"date":"2023-11-14T17:53:35","date_gmt":"2023-11-14T08:53:35","guid":{"rendered":"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/?page_id=18"},"modified":"2026-01-25T12:29:34","modified_gmt":"2026-01-25T03:29:34","slug":"publications","status":"publish","type":"page","link":"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/publications\/","title":{"rendered":"\u7814\u7a76\u696d\u7e3e"},"content":{"rendered":"\n<h2 class=\"wp-block-heading\">\u7814\u7a76\u696d\u7e3e<\/h2>\n\n\n\n<ul class=\"icon\">\n<li><a href=\"#1\">\u539f\u8457\u8ad6\u6587<\/a><\/li>\n\n\n\n<li><a href=\"#2\">\u7dcf\u8aac<\/a><\/li>\n\n\n\n<li><a href=\"#3\">\u8457\u66f8<\/a><\/li>\n\n\n\n<li><a href=\"#4\">\u4f9d\u983c\u89e3\u8aac\u8a18\u4e8b<\/a><\/li>\n<\/ul>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"1\">\u539f\u8457\u8ad6\u6587<\/h3>\n\n\n\n<ol reversed>\n<li>K. Oga, Y. Yamada, M. Nagatomo, H. Fujino, M. Inoue, &#8220;Collective Total Synthesis of 12 C4-Oxygenated Cladiellins and Structure Elucidation of Cladieunicellin D and Cladielloides A\/C,&#8221;<br><strong><em>J. Am. Chem. Soc<\/em><\/strong>. <strong>2026<\/strong>, <em>148<\/em>, 1812\u20131823.<br><br>(UTokyo FOCUS\u5185 press releases\u306b\u3066\u7d39\u4ecb\u3055\u308c\u307e\u3057\u305f\u3002<a href=\"https:\/\/www.u-tokyo.ac.jp\/focus\/ja\/press\/z0111_00095.html\" target=\"_blank\" rel=\"noreferrer noopener\">\u30ea\u30f3\u30af<\/a>)<br><br><img loading=\"lazy\" decoding=\"async\" width=\"992\" height=\"540\" class=\"wp-image-879\" style=\"width: 650px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2026\/01\/images_large_ja5c19112_0008.jpeg\" alt=\"\" srcset=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2026\/01\/images_large_ja5c19112_0008.jpeg 992w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2026\/01\/images_large_ja5c19112_0008-300x163.jpeg 300w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2026\/01\/images_large_ja5c19112_0008-768x418.jpeg 768w\" sizes=\"(max-width: 992px) 100vw, 992px\" \/><br><br>DOI: <a href=\"https:\/\/doi.org\/10.1021\/jacs.5c19112\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/jacs.5c19112<\/a><br><br><\/li>\n\n\n\n<li>K. Takaoka, D. Matsubara, M. Matsumoto, M. Nagatomo, K. Hagiwara, M. Inoue, &#8220;Total Synthesis of Trigocherrins A and C,&#8221;&nbsp;<br><strong><em>J. Am. Chem. Soc.<\/em><\/strong>&nbsp;<strong>2025<\/strong>,&nbsp;<em>147<\/em>, 45670\u201345679.<br><br>(UTokyo FOCUS\u5185 press releases\u306b\u3066\u7d39\u4ecb\u3055\u308c\u307e\u3057\u305f\u3002<a href=\"https:\/\/www.u-tokyo.ac.jp\/focus\/ja\/press\/z0111_00094.html\" target=\"_blank\" rel=\"noreferrer noopener\">\u30ea\u30f3\u30af<\/a>)<br>(Selected as Most Read Articles)<br><br><img loading=\"lazy\" decoding=\"async\" width=\"914\" height=\"558\" class=\"wp-image-859\" style=\"width: 650px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2025\/11\/images_large_ja5c17272_0008.jpeg\" alt=\"\" srcset=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2025\/11\/images_large_ja5c17272_0008.jpeg 914w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2025\/11\/images_large_ja5c17272_0008-300x183.jpeg 300w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2025\/11\/images_large_ja5c17272_0008-768x469.jpeg 768w\" sizes=\"(max-width: 914px) 100vw, 914px\" \/><br><br>DOI: <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.5c17272\" data-type=\"link\" data-id=\"https:\/\/pubs.acs.org\/doi\/10.1021\/jacs.5c17272\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/jacs.5c17272<\/a><br><br><\/li>\n\n\n\n<li>Y. Yamada, R. Yoshinaga, Y. Matsui, M. Nagatomo, H. Fujino, M. Inoue, &#8220;Et<sub>3<\/sub>Al\/Light-Promoted Radical-Polar Crossover Reactions of \u03b1-Alkoxyacyl Tellurides&#8221; <strong><em>J. Org. Chem.<\/em><\/strong> <strong>2024<\/strong>,<em> 89<\/em>, 11701\u201311706<em>.<\/em><br><br><img loading=\"lazy\" decoding=\"async\" width=\"997\" height=\"537\" class=\"wp-image-415\" style=\"width: 650px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2024\/08\/images_large_jo4c01445_0010.jpeg\" alt=\"\"><br><br>DOI: <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.joc.4c01445\" data-type=\"link\" data-id=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.joc.4c01445\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/acs.joc.4c01445<\/a><br><br><\/li>\n\n\n\n<li>A. Watanabe, Y. Hikone, M. Nagatomo, M. Inoue, &#8220;Conversion of Phorbol into Des-D-Ring Tricycle and Crotonianoid B via Peroxidation Reaction,&#8221; <strong><em>Org. Lett.<\/em><\/strong> <strong>2024<\/strong>, <em>26, <\/em>4335\u20134339.<br><br><img loading=\"lazy\" decoding=\"async\" width=\"1000\" height=\"558\" class=\"wp-image-376\" style=\"width: 650px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2024\/05\/images_large_ol4c01363_0004.jpeg\" alt=\"\"><br><br>DOI: <a href=\"https:\/\/pubs.acs.org\/doi\/full\/10.1021\/acs.orglett.4c01363\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/acs.orglett.4c01363<\/a><br><br><\/li>\n\n\n\n<li>A. Watanabe, M. Nagatomo, A. Hirose, Y. Hikone, N. Kishimoto, S. Miura, T. Yasutake, T. Abe, S. Misumi, M. Inoue, \u201cTotal Syntheses of Phorbol and 11 Tigliane Diterpenoids and Their Evaluation as HIV Latency-Reversing Agents,\u201d&nbsp;<em><strong>J. Am. Chem. Soc.&nbsp;<\/strong><\/em><strong>2024<\/strong>,&nbsp;<em>146<\/em>, 8746\u20138756.<br><br>(UTokyo FOCUS\u5185 press releases\u306b\u3066\u7d39\u4ecb\u3055\u308c\u307e\u3057\u305f\u3002<a href=\"https:\/\/www.u-tokyo.ac.jp\/focus\/ja\/press\/z0111_90051.html\" target=\"_blank\" rel=\"noreferrer noopener\">\u30ea\u30f3\u30af<\/a>)<br>(24\/3\/18 \u65e5\u672c\u7d4c\u6e08\u65b0\u805e\u306b\u3066\u5831\u9053\u3055\u308c\u307e\u3057\u305f\u3002<a href=\"https:\/\/www.nikkei.com\/article\/DGXZRSP669535_Y4A310C2000000\/\" target=\"_blank\" rel=\"noreferrer noopener\">\u30ea\u30f3\u30af<\/a>)<br><br><img loading=\"lazy\" decoding=\"async\" width=\"1000\" height=\"549\" class=\"wp-image-309\" style=\"width: 650px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2024\/03\/images_large_ja4c01589_0009.jpeg\" alt=\"\"><br><br>DOI: <a href=\"https:\/\/pubs.acs.org\/doi\/full\/10.1021\/jacs.4c01589\">10.1021\/jacs.4c01589<\/a><br><br><\/li>\n\n\n\n<li>T. Watanabe, K. Oga, H. Matoba, M. Nagatomo,&nbsp;M. Inoue, &#8220;Total Synthesis of Taxol Enabled by Intermolecular Radical Coupling and Pd-Catalyzed Cyclization,&#8221;&nbsp;<strong><em>J. Am. Chem. Soc.<\/em><\/strong>&nbsp;<strong>2023<\/strong>, <em>145<\/em>, 25894\u201325902.<br><br>(UTokyo FOCUS\u5185 press releases\u306b\u3066\u7d39\u4ecb\u3055\u308c\u307e\u3057\u305f\u3002<a href=\"https:\/\/www.u-tokyo.ac.jp\/focus\/ja\/press\/z0111_90042.html\" target=\"_blank\" rel=\"noreferrer noopener\">\u30ea\u30f3\u30af<\/a>)<br>(23\/11\/21 \u65e5\u672c\u7d4c\u6e08\u65b0\u805e\u306b\u3066\u5831\u9053\u3055\u308c\u307e\u3057\u305f\u3002<a href=\"https:\/\/www.nikkei.com\/article\/DGXZRSP664791_R21C23A1000000\/\" target=\"_blank\" rel=\"noreferrer noopener\">\u30ea\u30f3\u30af<\/a>)<br>(23\/12\/4 Selected as Most Read Articles)<br>(24\/1\/9 Featured in &#8220;<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.oprd.3c00496\" target=\"_blank\" rel=\"noreferrer noopener\">Some Items of Interest to Process R&amp;D Chemists and Engineers<\/a>&#8221; <em><strong>Org. Process. Res. Dev.<\/strong><\/em> <strong>2024<\/strong>, <em>28<\/em>, 1.)<br>(Featured in&nbsp;<a href=\"https:\/\/www.thieme-connect.de\/products\/ejournals\/html\/10.1055\/s-0043-1772968\" target=\"_blank\" rel=\"noreferrer noopener\">Synfacts<\/a>)<br>(<a href=\"https:\/\/www.chem-station.com\/blog\/2024\/02\/taxol.html\" target=\"_blank\" rel=\"noreferrer noopener\">Chem-Station<\/a>\u306b\u3066\u53d6\u308a\u4e0a\u3052\u3089\u308c\u307e\u3057\u305f\u3002)<br><br><img loading=\"lazy\" decoding=\"async\" width=\"1563\" height=\"454\" class=\"wp-image-96\" style=\"width: 700px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/36.jpg\" alt=\"\" srcset=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/36.jpg 1563w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/36-300x87.jpg 300w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/36-1024x297.jpg 1024w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/36-768x223.jpg 768w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/36-1536x446.jpg 1536w\" sizes=\"(max-width: 1563px) 100vw, 1563px\" \/><br><br>DOI:&nbsp;<a href=\"https:\/\/doi.org\/10.1021\/jacs.3c10658\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/jacs.3c10658<\/a><br><br><\/li>\n\n\n\n<li>Y. Imamura, K. Takaoka, Y. Komori,&nbsp;M. Nagatomo, M. Inoue, &#8220;Total Synthesis of Taxol Enabled by Inter- and Intramolecular Radical Coupling Reactions,&#8221;&nbsp;<strong><em>Angew. Chem. Int. Ed.<\/em><\/strong>&nbsp;<strong>2023<\/strong>,&nbsp;<em>62<\/em>, e202219114.<br><br>(UTokyo FOCUS\u5185 press releases\u306b\u3066\u7d39\u4ecb\u3055\u308c\u307e\u3057\u305f\u3002<a href=\"https:\/\/www.u-tokyo.ac.jp\/focus\/ja\/press\/z0111_90029.html\" target=\"_blank\" rel=\"noreferrer noopener\">\u30ea\u30f3\u30af<\/a>)<br>(23\/1\/23 \u65e5\u672c\u7d4c\u6e08\u65b0\u805e\u306b\u3066\u5831\u9053\u3055\u308c\u307e\u3057\u305f\u3002<a href=\"https:\/\/www.nikkei.com\/article\/DGXZRSP647980_T20C23A1000000\/\" target=\"_blank\" rel=\"noreferrer noopener\">\u30ea\u30f3\u30af<\/a>)<br>(Selected as Hot Paper)<br>(<a href=\"https:\/\/www.chem-station.com\/blog\/2023\/02\/taxol.html\" target=\"_blank\" rel=\"noreferrer noopener\">Chem-Station<\/a>\u306b\u3066\u53d6\u308a\u4e0a\u3052\u3089\u308c\u307e\u3057\u305f\u3002)<br>(Featured in&nbsp;<a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/html\/10.1055\/s-0042-1753430\" target=\"_blank\" rel=\"noreferrer noopener\">Synfacts<\/a>)<br><br><img loading=\"lazy\" decoding=\"async\" width=\"651\" height=\"138\" class=\"wp-image-97\" style=\"width: 900px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/35.jpg\" alt=\"\" srcset=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/35.jpg 651w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/35-300x64.jpg 300w\" sizes=\"(max-width: 651px) 100vw, 651px\" \/><br><br>DOI:&nbsp;<a href=\"https:\/\/doi.org\/10.1002\/anie.202219114\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/anie.202219114<\/a><br><br><\/li>\n\n\n\n<li>Y. Hikone, T. Kato,&nbsp;M. Nagatomo, M. Inoue, &#8220;Total Synthesis of Resiniferatoxin Enabled by Photocatalytic Decarboxylative Radical Cyclization,&#8221;&nbsp;<strong><em>Org. Lett.<\/em><\/strong>&nbsp;<strong>2022<\/strong>,&nbsp;<em>24<\/em>, 929\u2013933.<br><br>(Selected as Most Read Articles)<br><br><img loading=\"lazy\" decoding=\"async\" width=\"500\" height=\"243\" class=\"wp-image-98\" style=\"width: 500px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/34.jpg\" alt=\"\" srcset=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/34.jpg 500w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/34-300x146.jpg 300w\" sizes=\"(max-width: 500px) 100vw, 500px\" \/><br><br>DOI:&nbsp;<a href=\"https:\/\/doi.org\/10.1021\/acs.orglett.1c04286\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/acs.orglett.1c04286<\/a><br><br><\/li>\n\n\n\n<li>D. Kuwana, Y. Komori,&nbsp;M. Nagatomo, M. Inoue, &#8220;Photoinduced Decarboxylative Radical Coupling Reaction of Multiply Oxygenated Structures by Catalysis of Pt-Doped TiO<sub>2<\/sub>,&#8221;&nbsp;<strong><em>J. Org. Chem.<\/em><\/strong>&nbsp;<strong>2022<\/strong>,&nbsp;<em>87<\/em>, 730\u2013736.<br><br><img loading=\"lazy\" decoding=\"async\" width=\"1719\" height=\"909\" class=\"wp-image-99\" style=\"width: 500px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/33.png\" alt=\"\" srcset=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/33.png 1719w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/33-300x159.png 300w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/33-1024x541.png 1024w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/33-768x406.png 768w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/33-1536x812.png 1536w\" sizes=\"(max-width: 1719px) 100vw, 1719px\" \/><br><br>DOI:&nbsp;<a href=\"https:\/\/doi.org\/10.1021\/acs.joc.1c02736\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/acs.joc.1c02736<\/a><br><br><\/li>\n\n\n\n<li>A. Hirose, A. Watanabe, K. Ogino,&nbsp;M. Nagatomo, M. Inoue, &#8220;Unified Total Syntheses of Rhamnofolane, Tigliane, and Daphnane Diterpenoids,&#8221;&nbsp;<strong><em>J. Am. Chem. Soc.<\/em><\/strong>&nbsp;<strong>2021<\/strong>,&nbsp;<em>143<\/em>, 12387\u201312396.<br><br>(Featured in&nbsp;<a href=\"https:\/\/www.thieme-connect.de\/products\/ejournals\/abstract\/10.1055\/s-0040-1720188\" target=\"_blank\" rel=\"noreferrer noopener\">Synfacts<\/a>)<br>(Organic Chemistry Highlights\u3067\u7d39\u4ecb\u3055\u308c\u307e\u3057\u305f\u3002<a href=\"https:\/\/www.organic-chemistry.org\/Highlights\/2022\/29August.shtm\" target=\"_blank\" rel=\"noreferrer noopener\">\u30ea\u30f3\u30af<\/a>)<br><br><img loading=\"lazy\" decoding=\"async\" width=\"500\" height=\"270\" class=\"wp-image-100\" style=\"width: 500px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/32.jpg\" alt=\"\" srcset=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/32.jpg 500w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/32-300x162.jpg 300w\" sizes=\"(max-width: 500px) 100vw, 500px\" \/><br><br>DOI:&nbsp;<a href=\"https:\/\/doi.org\/10.1021\/jacs.1c06450\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/jacs.1c06450<\/a><br><br><\/li>\n\n\n\n<li>M. Nagatomo, K. Zhang, H. Fujino, M. Inoue, &#8220;Et3B\/Et2AlCl\/O2\u2010Mediated Radical Coupling Reaction between \u03b1\u2010Alkoxyacyl Tellurides and 2\u2010Hydroxybenzaldehyde Derivatives,&#8221;&nbsp;<strong><em>Chem. Asian. J.<\/em><\/strong>&nbsp;<strong>2020<\/strong>,&nbsp;<em>15<\/em>, 3820\u20133824.<br><br><img loading=\"lazy\" decoding=\"async\" width=\"465\" height=\"125\" class=\"wp-image-101\" style=\"width: 500px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/31.png\" alt=\"\" srcset=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/31.png 465w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/31-300x81.png 300w\" sizes=\"(max-width: 465px) 100vw, 465px\" \/><br><br>DOI:&nbsp;<a href=\"https:\/\/doi.org\/10.1002\/asia.202001090\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/asia.202001090<\/a><br><br><\/li>\n\n\n\n<li>T. Fukuda,&nbsp;M. Nagatomo, M. Inoue, &#8220;Total Synthesis of Diospyrodin and Its Three Diastereomers,&#8221;&nbsp;<strong><em>Org. Lett.<\/em><\/strong>&nbsp;<strong>2020<\/strong>,&nbsp;<em>22<\/em>, 6468\u20136472.<br><br><img loading=\"lazy\" decoding=\"async\" width=\"639\" height=\"274\" class=\"wp-image-102\" style=\"width: 500px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/30.jpg\" alt=\"\" srcset=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/30.jpg 639w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/30-300x129.jpg 300w\" sizes=\"(max-width: 639px) 100vw, 639px\" \/><br><br>DOI:&nbsp;<a href=\"https:\/\/doi.org\/10.1021\/acs.orglett.0c02280\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/acs.orglett.0c02280<\/a><br><br><\/li>\n\n\n\n<li>H. Fujino, T. Fukuda,&nbsp;M. Nagatomo, M. Inoue, &#8220;Convergent Total Synthesis of Hikizimycin Enabled by Intermolecular Radical Addition to Aldehyde,&#8221;&nbsp;<strong><em>J. Am. Chem. Soc.<\/em><\/strong>&nbsp;<strong>2020<\/strong>,&nbsp;<em>142<\/em>, 13227\u201313234.<br><br>(UTokyo FOCUS\u5185 articles\u306b\u3066\u7d39\u4ecb\u3055\u308c\u307e\u3057\u305f\u3002&nbsp;<a href=\"https:\/\/www.u-tokyo.ac.jp\/focus\/ja\/articles\/z0508_00058.html\" target=\"_blank\" rel=\"noreferrer noopener\">\u30ea\u30f3\u30af<\/a>)<br>(Organic Chemistry Highlights\u3067\u7d39\u4ecb\u3055\u308c\u307e\u3057\u305f\u3002<a href=\"https:\/\/www.organic-chemistry.org\/Highlights\/2021\/26July.shtm\" target=\"_blank\" rel=\"noreferrer noopener\">\u30ea\u30f3\u30af<\/a>)<br><br><img loading=\"lazy\" decoding=\"async\" width=\"1947\" height=\"923\" class=\"wp-image-103\" style=\"width: 600px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/29.png\" alt=\"\" srcset=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/29.png 1947w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/29-300x142.png 300w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/29-1024x485.png 1024w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/29-768x364.png 768w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/29-1536x728.png 1536w\" sizes=\"(max-width: 1947px) 100vw, 1947px\" \/><br><br>DOI:&nbsp;<a href=\"https:\/\/doi.org\/10.1021\/jacs.0c06354\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/jacs.0c06354<\/a><br><br><\/li>\n\n\n\n<li>D. Kuwana,&nbsp;M. Nagatomo, M. Inoue, &#8220;Total Synthesis of 5-epi-Eudesm-4(15)-ene-1\u03b2,6\u03b2-diol via Decarbonylative Radical Coupling Reaction,&#8221;&nbsp;<strong><em>Org. Lett.<\/em><\/strong>&nbsp;<strong>2019<\/strong>,&nbsp;<em>21<\/em>, 7619\u20137623.<br><br><img loading=\"lazy\" decoding=\"async\" width=\"500\" height=\"106\" class=\"wp-image-106\" style=\"width: 700px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/28.gif\" alt=\"\"><br><br>DOI:&nbsp;<a href=\"https:\/\/doi.org\/10.1021\/acs.orglett.9b02895\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/acs.orglett.9b02895<\/a><br><br><\/li>\n\n\n\n<li>Y. Imamura, S. Yoshioka,&nbsp;M. Nagatomo, M. Inoue, &#8220;Total Synthesis of 1\u2010Hydroxytaxinine,&#8221;&nbsp;<strong><em>Angew. Chem. Int. Ed.<\/em><\/strong>&nbsp;<strong>2019<\/strong>,&nbsp;<em>58<\/em>, 12159\u201312163.<br><br>(Selected as Hot Paper)<br>(UTokyo FOCUS\u5185 articles\u306b\u3066\u7d39\u4ecb\u3055\u308c\u307e\u3057\u305f\u3002&nbsp;<a href=\"https:\/\/www.u-tokyo.ac.jp\/focus\/ja\/articles\/z0508_00139.html\" target=\"_blank\" rel=\"noreferrer noopener\">\u30ea\u30f3\u30af<\/a>)<br>(Chem-Station\u3067\u7d39\u4ecb\u3055\u308c\u307e\u3057\u305f\u3002<a href=\"https:\/\/www.chem-station.com\/blog\/2019\/08\/1-hydroxytaxinine.html\" target=\"_blank\" rel=\"noreferrer noopener\">\u30ea\u30f3\u30af<\/a>)<br>(Organic Chemistry Highlights\u3067\u7d39\u4ecb\u3055\u308c\u307e\u3057\u305f\u3002<a href=\"https:\/\/www.organic-chemistry.org\/Highlights\/2020\/04May.shtm\" target=\"_blank\" rel=\"noreferrer noopener\">\u30ea\u30f3\u30af<\/a>)<br><br><img loading=\"lazy\" decoding=\"async\" width=\"784\" height=\"212\" class=\"wp-image-104\" style=\"width: 700px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/27.jpg\" alt=\"\" srcset=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/27.jpg 784w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/27-300x81.jpg 300w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/27-768x208.jpg 768w\" sizes=\"(max-width: 784px) 100vw, 784px\" \/><br><br>DOI:&nbsp;<a href=\"https:\/\/doi.org\/10.1002\/anie.201906872\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/anie.201906872<\/a><br><br><\/li>\n\n\n\n<li>D. Kuwana, B. Ovadia, D. Kamimura,&nbsp;M. Nagatomo, M. Inoue, &#8220;Installation of O\u2010Heterocycles to N\u2010Heteroarenes via an Et<sub>3<\/sub>B\/O<sub>2<\/sub>\u2010mediated Radical Reaction of \u03b1-Alkoxy and \u03b1-Alkoxyacyl Tellurides,&#8221;&nbsp;<strong><em>Asian J. Org. Chem.<\/em><\/strong>&nbsp;<strong>2019<\/strong>,&nbsp;<em>8<\/em>, 1088\u20131091.<br><br><img loading=\"lazy\" decoding=\"async\" width=\"1469\" height=\"340\" class=\"wp-image-107\" style=\"width: 700px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/26.png\" alt=\"\" srcset=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/26.png 1469w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/26-300x69.png 300w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/26-1024x237.png 1024w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/26-768x178.png 768w\" sizes=\"(max-width: 1469px) 100vw, 1469px\" \/><br><br>DOI:&nbsp;<a href=\"https:\/\/doi.org\/10.1002\/ajoc.201900170\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/ajoc.201900170<\/a><br><br><\/li>\n\n\n\n<li>M. Nagatomo, Y. Fujimoto, K. Masuda, M. Inoue, &#8220;Construction of a 6\/5\/9-membered tricyclic structure of cladiellins via radical-polar crossover reaction,&#8221;&nbsp;<strong><em>J. Antibiot.<\/em><\/strong>&nbsp;<strong>2019<\/strong>,&nbsp;<em>72<\/em>, 486\u2013489.<br>DOI:&nbsp;<a href=\"https:\/\/doi.org\/10.1038\/s41429-019-0150-7\" target=\"_blank\" rel=\"noreferrer noopener\">10.1038\/s41429-019-0150-7<\/a><br><br><\/li>\n\n\n\n<li>H. Matoba, T. Watanabe,&nbsp;M. Nagatomo, M. Inoue, &#8220;Convergent Synthesis of Taxol Skeleton via Decarbonylative Radical Coupling Reaction,&#8221;&nbsp;<strong><em>Org. Lett.<\/em><\/strong>&nbsp;<strong>2018<\/strong>,&nbsp;<em>20<\/em>, 7554\u20137557.<br><br>(Selected as Most Read Articles of the month)<br><br><img loading=\"lazy\" decoding=\"async\" width=\"500\" height=\"111\" class=\"wp-image-108\" style=\"width: 700px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/24.gif\" alt=\"\"><br><br>DOI:&nbsp;<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.8b03302\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/acs.orglett.8b03302<\/a><br><br><\/li>\n\n\n\n<li>T. Kawamata, A. Yamaguchi,&nbsp;M. Nagatomo, M. Inoue, &#8220;Convergent Total Synthesis of Asimicin via Decarbonylative Radical Dimerization,&#8221;&nbsp;<strong><em>Chem. Eur. J.<\/em><\/strong>&nbsp;<strong>2018<\/strong>,&nbsp;<em>24<\/em>, 18907\u201318912.<br><br><img loading=\"lazy\" decoding=\"async\" width=\"619\" height=\"119\" class=\"wp-image-109\" style=\"width: 800px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/23.jpg\" alt=\"\" srcset=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/23.jpg 619w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/23-300x58.jpg 300w\" sizes=\"(max-width: 619px) 100vw, 619px\" \/><br><br>DOI:&nbsp;<a href=\"https:\/\/doi.org\/10.1002\/chem.201805317\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/chem.201805317<\/a><br><br><\/li>\n\n\n\n<li>D. Urabe, Y. Nakagawa, K. Mukai, K. Fukushima, N. Aoki, H. Itoh,&nbsp;M. Nagatomo, M. Inoue, &#8220;Total synthesis and biological evaluation of 19-hydroxysarmentogenin-3-O-a-L-rhamnoside, trewianin, and their aglycons,&#8221;&nbsp;<strong><em>J. Org. Chem.<\/em><\/strong>&nbsp;<strong>2018<\/strong>,&nbsp;<em>83<\/em>, 13888\u201313910.<br><br><img loading=\"lazy\" decoding=\"async\" width=\"500\" height=\"234\" class=\"wp-image-110\" style=\"width: 600px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/22.gif\" alt=\"\"><br><br>DOI:&nbsp;<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.joc.8b02219\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/acs.joc.8b02219<\/a><br><br><\/li>\n\n\n\n<li>M. Koshimizu,&nbsp;M. Nagatomo, M. Inoue, &#8220;Construction of a pentacyclic ring system of isoryanodane diterpenoids by SmI<sub>2<\/sub>-mediated transannular cyclization,&#8221;&nbsp;<strong><em>Tetrahedron.<\/em><\/strong>&nbsp;<strong>2018<\/strong>,&nbsp;<em>74<\/em>, 3384\u20133390.<br><br><img loading=\"lazy\" decoding=\"async\" width=\"2560\" height=\"463\" class=\"wp-image-111\" style=\"width: 800px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/21-scaled.jpg\" alt=\"\" srcset=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/21-scaled.jpg 2560w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/21-300x54.jpg 300w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/21-1024x185.jpg 1024w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/21-768x139.jpg 768w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/21-1536x278.jpg 1536w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/21-2048x370.jpg 2048w\" sizes=\"(max-width: 2560px) 100vw, 2560px\" \/><br><br>DOI:&nbsp;<a href=\"http:\/\/doi.org\/10.1016\/j.tet.2018.03.061\" target=\"_blank\" rel=\"noreferrer noopener\">10.1016\/j.tet.2018.03.061<\/a><br><br><\/li>\n\n\n\n<li>H. Fujino,&nbsp;M. Nagatomo, A. Paudel, S. Panthee, H. Hamamoto, K. Sekimizu, M. Inoue, &#8220;Unified Total Synthesis of Polyoxin J, L, and Their Fluorinated Analogues on the Basis of Decarbonylative Radical Coupling Reactions,&#8221;&nbsp;<strong><em>Angew. Chem. Int. Ed.<\/em><\/strong>&nbsp;<strong>2017<\/strong>,&nbsp;<em>56<\/em>, 11865\u201311869.<br><br><img loading=\"lazy\" decoding=\"async\" width=\"500\" height=\"378\" class=\"wp-image-112\" style=\"width: 500px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/20.png\" alt=\"\" srcset=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/20.png 500w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/20-300x227.png 300w\" sizes=\"(max-width: 500px) 100vw, 500px\" \/><br><br>DOI:&nbsp;<a href=\"http:\/\/doi.org\/10.1002\/anie.201706671\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/anie.201706671<\/a><br><br><\/li>\n\n\n\n<li>K. Masuda, M. Tanigawa,&nbsp;M. Nagatomo, D. Urabe, M. Inoue, &#8220;Construction of carbocycles initiated by Cu-catalyzed radical reaction of Cl<sub>2<\/sub>C(CN)<sub>2<\/sub>,&#8221;&nbsp;<strong><em>Tetrahedron<\/em><\/strong>&nbsp;<strong>2017<\/strong>,&nbsp;<em>73<\/em>, 3596\u20133605.<br><br><img loading=\"lazy\" decoding=\"async\" width=\"589\" height=\"120\" class=\"wp-image-113\" style=\"width: 700px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/19.jpg\" alt=\"\" srcset=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/19.jpg 589w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/19-300x61.jpg 300w\" sizes=\"(max-width: 589px) 100vw, 589px\" \/><br><br>DOI:&nbsp;<a href=\"http:\/\/doi.org\/10.1016\/j.tet.2017.03.063\">10.1016\/j.tet.2017.03.063<\/a><br><br><\/li>\n\n\n\n<li>T. Kawamata,&nbsp;M. Nagatomo, M. Inoue, &#8220;Total Synthesis of Zaragozic Acid C: Implementation of Photochemical C(sp3)-H Acylation,&#8221;&nbsp;<strong><em>J. Am. Chem. Soc.<\/em><\/strong>&nbsp;<strong>2017<\/strong>,&nbsp;<em>139<\/em>, 1814\u20131817.<br><br>(Highlighted in&nbsp;<a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0036-1590102\" target=\"_blank\" rel=\"noreferrer noopener\"><strong><em>Synfacts<\/em><\/strong>&nbsp;<strong>2017<\/strong>,&nbsp;<em>13<\/em>, 0337.&nbsp;<\/a>and selected as its Cover Picture)<br><br><img loading=\"lazy\" decoding=\"async\" width=\"5209\" height=\"2907\" class=\"wp-image-114\" style=\"width: 600px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/18.png\" alt=\"\" srcset=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/18.png 5209w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/18-300x167.png 300w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/18-1024x571.png 1024w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/18-768x429.png 768w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/18-1536x857.png 1536w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/18-2048x1143.png 2048w\" sizes=\"(max-width: 5209px) 100vw, 5209px\" \/><br><br>DOI:&nbsp;<a href=\"http:\/\/doi.org\/10.1021\/jacs.6b13263\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/jacs.6b13263<\/a><br><br><\/li>\n\n\n\n<li>K. Masuda,&nbsp;M. Nagatomo, M. Inoue, &#8220;Direct assembly of multiply oxygenated carbon chains by decarbonylative radical-radical coupling reactions,&#8221;&nbsp;<strong><em>Nature Chem.<\/em><\/strong>&nbsp;<strong>2017<\/strong>,&nbsp;<em>9<\/em>, 207\u2013212.<br><br>(Highlighted in&nbsp;<a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0036-1590266\" target=\"_blank\" rel=\"noreferrer noopener\"><strong><em>Synfacts<\/em><\/strong>&nbsp;<strong>2017<\/strong>,&nbsp;<em>13<\/em>, 0534.&nbsp;<\/a>)<br>(Associated Link:&nbsp;<a href=\"http:\/\/www.nature.com\/nchem\/journal\/v9\/n3\/full\/nchem.2734.html\" target=\"_blank\" rel=\"noreferrer noopener\">News and Views &#8211; &#8220;Organic chemistry: A radical step forward&#8221;<\/a>)<br><br><img loading=\"lazy\" decoding=\"async\" width=\"1092\" height=\"481\" class=\"wp-image-115\" style=\"width: 600px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/17.jpg\" alt=\"\" srcset=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/17.jpg 1092w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/17-300x132.jpg 300w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/17-1024x451.jpg 1024w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/17-768x338.jpg 768w\" sizes=\"(max-width: 1092px) 100vw, 1092px\" \/><br><br>DOI:&nbsp;<a href=\"http:\/\/doi.org\/10.1038\/nchem.2639\" target=\"_blank\" rel=\"noreferrer noopener\">10.1038\/nchem.2639<\/a><br><br><\/li>\n\n\n\n<li>S. Matsumura, Y. Matsui,&nbsp;M. Nagatomo, M. Inoue, &#8220;Stereoselective construction of&nbsp;<em>anti<\/em>&#8211; and&nbsp;<em>syn<\/em>-1,2-diol structures via decarbonylative radical coupling of \u03b1-alkoxyacyl tellurides,&#8221;&nbsp;<strong><em>Tetrahedron<\/em><\/strong>&nbsp;<strong>2016<\/strong>,&nbsp;<em>72<\/em>, 4859\u20134866.<br><br><img loading=\"lazy\" decoding=\"async\" width=\"589\" height=\"146\" class=\"wp-image-116\" style=\"width: 700px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/16.jpg\" alt=\"\" srcset=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/16.jpg 589w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/16-300x74.jpg 300w\" sizes=\"(max-width: 589px) 100vw, 589px\" \/><br><br>DOI:&nbsp;<a href=\"http:\/\/doi.org\/10.1016\/j.tet.2016.06.056\" target=\"_blank\" rel=\"noreferrer noopener\">10.1016\/j.tet.2016.06.056<\/a><br><br><\/li>\n\n\n\n<li>D. Kamimura,&nbsp;M. Nagatomo, D. Urabe, M. Inoue, &#8220;Expanding the scope of Et<sub>3<\/sub>B\/O<sub>2<\/sub>-mediated coupling reactions of O,Te-acetal,&#8221;&nbsp;<strong><em>Tetrahedron<\/em><\/strong>&nbsp;<strong>2016<\/strong>,&nbsp;<em>72<\/em>, 7839\u20137848.<br><br><img loading=\"lazy\" decoding=\"async\" width=\"589\" height=\"110\" class=\"wp-image-117\" style=\"width: 700px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/15.jpg\" alt=\"\" srcset=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/15.jpg 589w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/15-300x56.jpg 300w\" sizes=\"(max-width: 589px) 100vw, 589px\" \/><br><br>DOI:&nbsp;<a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040402016302769\" target=\"_blank\" rel=\"noreferrer noopener\">10.1016\/j.tet.2016.04.023<\/a><br><br><\/li>\n\n\n\n<li>K. Masuda,&nbsp;M. Nagatomo, M. Inoue, &#8220;Chemical Conversion of Ryanodol to Ryanodine,&#8221;&nbsp;<strong><em>Chem. Pharm. Bull.<\/em><\/strong>&nbsp;<strong>2016<\/strong>,&nbsp;<em>64<\/em>, 874\u2013879.<br><br><img loading=\"lazy\" decoding=\"async\" width=\"421\" height=\"142\" class=\"wp-image-118\" style=\"width: 600px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/14.png\" alt=\"\" srcset=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/14.png 421w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/14-300x101.png 300w\" sizes=\"(max-width: 421px) 100vw, 421px\" \/><br><br>DOI:&nbsp;<a href=\"http:\/\/doi.org\/10.1248\/cpb.c16-00214\" target=\"_blank\" rel=\"noreferrer noopener\">10.1248\/cpb.c16-00214<\/a><br><br><\/li>\n\n\n\n<li>M. Koshimizu,&nbsp;M. Nagatomo, M. Inoue, &#8220;Unified Total Synthesis of 3-<em>epi<\/em>-Ryanodol, Cinnzeylanol, Cinncassiols A and B, and Structural Revision of Natural Ryanodol and Cinnacasol,&#8221;&nbsp;<strong><em>Angew. Chem. Int. Ed.<\/em><\/strong>&nbsp;<strong>2016<\/strong>,&nbsp;<em>55<\/em>, 2493\u20132497.<br><br><img loading=\"lazy\" decoding=\"async\" width=\"447\" height=\"326\" class=\"wp-image-119\" style=\"width: 500px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/13.jpg\" alt=\"\" srcset=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/13.jpg 447w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/13-300x219.jpg 300w\" sizes=\"(max-width: 447px) 100vw, 447px\" \/><br><br>DOI:&nbsp;<a href=\"http:\/\/dx.doi.org\/10.1002\/anie.201511116\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/anie.201511116<\/a><br><br><\/li>\n\n\n\n<li>K. Masuda, M. Koshimizu,&nbsp;M. Nagatomo, M. Inoue, &#8220;Asymmetric Total Synthesis of (+)-Ryanodol and (+)-Ryanodine,&#8221;&nbsp;<strong><em>Chem. Eur. J.<\/em><\/strong>&nbsp;<strong>2016<\/strong>,&nbsp;<em>22<\/em>, 230\u2013236.<br><br><img loading=\"lazy\" decoding=\"async\" width=\"521\" height=\"158\" class=\"wp-image-120\" style=\"width: 600px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/12.jpg\" alt=\"\" srcset=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/12.jpg 521w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/12-300x91.jpg 300w\" sizes=\"(max-width: 521px) 100vw, 521px\" \/><br><br>DOI:&nbsp;<a href=\"http:\/\/dx.doi.org\/10.1002\/chem.201503641\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/chem.201503641<\/a><br><br><\/li>\n\n\n\n<li>M. Nagatomo, K. Hagiwara, K. Masuda, M. Koshimizu, T. Kawamata, Y. Matsui, D. Urabe, M. Inoue, &#8221; Symmetry-Driven Strategy for the Assembly of the Core Tetracycle of (+)-Ryanodine: Synthetic Utility of a Cobalt-Catalyzed Olefin Oxidation and \u03b1-Alkoxy Bridgehead Radical Reaction,&#8221;&nbsp;<strong><em>Chem. Eur. J.<\/em><\/strong>&nbsp;<strong>2016<\/strong>,&nbsp;<em>22<\/em>, 222\u2013229.<br><br><img loading=\"lazy\" decoding=\"async\" width=\"521\" height=\"158\" class=\"wp-image-122\" style=\"width: 600px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/11.jpg\" alt=\"\" srcset=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/11.jpg 521w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/11-300x91.jpg 300w\" sizes=\"(max-width: 521px) 100vw, 521px\" \/><br><br>DOI:&nbsp;<a href=\"http:\/\/dx.doi.org\/10.1002\/chem.201503640\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/chem.201503640<\/a><br><br><\/li>\n\n\n\n<li>M. Nagatomo, D. Kamimura, Y. Matsui, K. Masuda, M. Inoue, &#8220;Et<sub>3<\/sub>B-Mediated Two- and Three-Component Coupling Reactions via Radical Decarbonylation of \u03b1-Alkoxyacyl Tellurides: Single-Step Construction of Densely Oxygenated Carboskeletons,&#8221;&nbsp;<strong><em>Chem. Sci.<\/em><\/strong>&nbsp;<strong>2015<\/strong>,&nbsp;<em>6<\/em>, 2765\u20132769.<br><br><img loading=\"lazy\" decoding=\"async\" width=\"375\" height=\"103\" class=\"wp-image-123\" style=\"width: 600px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/10.gif\" alt=\"\"><br><br>DOI:&nbsp;<a href=\"http:\/\/dx.doi.org\/10.1039\/C5SC00457H\" target=\"_blank\" rel=\"noreferrer noopener\">10.1039\/C5SC00457H<\/a><br><br><\/li>\n\n\n\n<li>S. Yoshioka,&nbsp;M. Nagatomo, M. Inoue, &#8220;Application of Two Direct C(sp<sup>3<\/sup>)-H Functionalizations for Total Synthesis of (+)-Lactacystin,&#8221;&nbsp;<strong><em>Org. Lett.<\/em><\/strong>&nbsp;<strong>2015<\/strong>,&nbsp;<em>17<\/em>, 90\u201393.<br><br><img loading=\"lazy\" decoding=\"async\" width=\"500\" height=\"117\" class=\"wp-image-124\" style=\"width: 600px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/9.gif\" alt=\"\"><br><br>DOI:&nbsp;<a href=\"http:\/\/dx.doi.org\/10.1021\/ol503291s\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/ol503291s<\/a><br><br><\/li>\n\n\n\n<li>M. Nagatomo, H. Nishiyama, H. Fujino, M. Inoue, &#8220;Decarbonylative Radical Coupling of \u03b1-Aminoacyl Tellurides: Single-Step Preparation of \u03b3-Amino and \u03b1,\u03b2-Diamino Acids and Rapid Synthesis of Gabapentin and Manzacidin A,&#8221;&nbsp;<strong><em>Angew. Chem. Int. Ed.<\/em><\/strong>&nbsp;<strong>2015<\/strong>,&nbsp;<em>54<\/em>, 1537\u20131541.<br><br>(Selected as Hot Paper)<br><br><img loading=\"lazy\" decoding=\"async\" width=\"500\" height=\"123\" class=\"wp-image-125\" style=\"width: 600px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/8.gif\" alt=\"\"><br><br>DOI:&nbsp;<a href=\"http:\/\/dx.doi.org\/10.1002\/anie.201410186\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/anie.201410186<\/a><br><br><\/li>\n\n\n\n<li>M. Nagatomo, S. Yoshioka, M. Inoue, &#8220;Enantioselective Radical Alkynylation of C(sp<sup>3<\/sup>)-H Bonds Using Sulfoximine as a Traceless Chiral Auxiliary,&#8221;&nbsp;<strong><em>Chem. Asian. J.<\/em><\/strong>&nbsp;<strong>2015<\/strong>,&nbsp;<em>10<\/em>, 120\u2013123.<br><br><img loading=\"lazy\" decoding=\"async\" width=\"410\" height=\"140\" class=\"wp-image-126\" style=\"width: 500px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/7.gif\" alt=\"\"><br><br>DOI:&nbsp;<a href=\"http:\/\/dx.doi.org\/10.1002\/asia.201402983\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/asia.201402983<\/a><br><br><\/li>\n\n\n\n<li>Y. Amaoka,&nbsp;M. Nagatomo, M. Watanabe, K. Tao, S. Kamijo, M. Inoue, &#8220;Photochemically Induced Radical Alkenylation of C(sp<sup>3<\/sup>)-H Bonds,&#8221;&nbsp;<strong><em>Chem. Sci.<\/em><\/strong>&nbsp;<strong>2014<\/strong>,&nbsp;<em>5<\/em>, 4339\u20134345.<br><br><img loading=\"lazy\" decoding=\"async\" width=\"371\" height=\"189\" class=\"wp-image-128\" style=\"width: 500px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/6.gif\" alt=\"\"><br><br>DOI:&nbsp;<a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2014\/sc\/c4sc01631a\" target=\"_blank\" rel=\"noreferrer noopener\">10.1039\/C4SC01631A<\/a><br><br><\/li>\n\n\n\n<li>M. Nagatomo, M. Koshimizu, K. Masuda, T. Tabuchi, D. Urabe, M. Inoue &#8220;Total Synthesis of Ryanodol,&#8221;&nbsp;<strong><em>J. Am. Chem. Soc.<\/em><\/strong>&nbsp;<strong>2014<\/strong>,&nbsp;<em>136<\/em>, 5916\u20135919.<br><br><img loading=\"lazy\" decoding=\"async\" width=\"1563\" height=\"349\" class=\"wp-image-127\" style=\"width: 700px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/5.jpg\" alt=\"\" srcset=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/5.jpg 1563w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/5-300x67.jpg 300w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/5-1024x229.jpg 1024w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/5-768x171.jpg 768w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/5-1536x343.jpg 1536w\" sizes=\"(max-width: 1563px) 100vw, 1563px\" \/><br><br>DOI:&nbsp;<a href=\"http:\/\/dx.doi.org\/10.1021\/ja502770n\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/ja502770n<\/a><br><br><\/li>\n\n\n\n<li>D. Kamimura, D. Urabe,&nbsp;M. Nagatomo, M. Inoue, &#8220;Et<sub>3<\/sub>B\u2010Mediated Radical-Polar Crossover Reaction for Single-Step Coupling of O,Te-Acetal, \u03b1,\u03b2-Unsaturated Ketones, and Aldehydes\/Ketones,&#8221;&nbsp;<strong><em>Org. Lett.<\/em><\/strong>&nbsp;<strong>2013<\/strong>,&nbsp;<em>15<\/em>, 5122\u20135125.<br><br><img loading=\"lazy\" decoding=\"async\" width=\"500\" height=\"137\" class=\"wp-image-129\" style=\"width: 600px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/4.gif\" alt=\"\"><br><br>DOI:&nbsp;<a href=\"http:\/\/dx.doi.org\/10.1021\/ol402563v\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/ol402563v<\/a><br><br><\/li>\n\n\n\n<li>Y. Amaoka,&nbsp;M. Nagatomo, M. Inoue, &#8220;Metal-Free Fluorination of C(sp<sup>3<\/sup>)-H Bonds Using a Catalytic N-Oxyl Radical,&#8221;&nbsp;<strong><em>Org. Lett.<\/em><\/strong>&nbsp;<strong>2013<\/strong>,&nbsp;<em>15<\/em>, 2160\u20132163.<br><br><img loading=\"lazy\" decoding=\"async\" width=\"375\" height=\"144\" class=\"wp-image-130\" style=\"width: 500px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/3.gif\" alt=\"\"><br><br>DOI:&nbsp;<a href=\"http:\/\/dx.doi.org\/10.1021\/ol4006757\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/ol4006757<\/a><br><br><\/li>\n\n\n\n<li>D. Urabe,&nbsp;M. Nagatomo, K. Hagiwara, K. Masuda, M. Inoue, &#8220;Symmetry-Driven Synthesis of 9-Demethyl-10,15-dideoxyryanodol,&#8221;&nbsp;<strong><em>Chem. Sci.<\/em><\/strong>&nbsp;<strong>2013<\/strong>,&nbsp;<em>4<\/em>, 1615\u20131619.<br><br><img loading=\"lazy\" decoding=\"async\" width=\"378\" height=\"103\" class=\"wp-image-131\" style=\"width: 600px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/2.gif\" alt=\"\"><br><br>DOI:&nbsp;<a href=\"http:\/\/dx.doi.org\/10.1039\/C3SC00023K\" target=\"_blank\" rel=\"noreferrer noopener\">10.1039\/C3SC00023K<\/a><br><br><\/li>\n\n\n\n<li>M. Nagatomo, T. Nakata, &#8220;Stereoselective Synthesis of Maitotoxin GHI-Ring System Having a 1,2-Diol Side Chain,&#8221;&nbsp;<strong><em>Heterocycles<\/em><\/strong>&nbsp;<strong>2008<\/strong>, 76, 1069\u20131074.<br>DOI:&nbsp;<a href=\"http:\/\/dx.doi.org\/10.3987\/COM-08-S(N)113\" target=\"_blank\" rel=\"noreferrer noopener\">10.3987\/COM-08-S(N)113<\/a><\/li>\n<\/ol>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"2\">\u7dcf\u8aac<\/h3>\n\n\n\n<ol reversed>\n<li>\u5f66\u6839\u60a0\u4eba\u3001\u9577\u53cb\u512a\u5178\u3001\u4e95\u4e0a\u5c06\u884c &#8220;\u8907\u96d1\u5206\u5b50\u69cb\u7bc9\u306e\u5358\u7d14\u5316\uff1a\u30ec\u30b8\u30cb\u30d5\u30a7\u30e9\u30c8\u30ad\u30b7\u30f3\u306e3\u3064\u306e\u5168\u5408\u6210\u7d4c\u8def\u306e\u78ba\u7acb\u201d <strong><em>\u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a\u8a8c<\/em><\/strong> <strong>2023<\/strong>, <em>81<\/em>, 1136\u20131149.<br><br><img loading=\"lazy\" decoding=\"async\" width=\"1993\" height=\"674\" class=\"wp-image-232\" style=\"width: 700px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2024\/01\/2023socj_RTX.png\" alt=\"\"><br><br>DOI:&nbsp;<a href=\"http:\/\/dx.doi.org\/10.5059\/yukigoseikyokaishi.81.1136\" target=\"_blank\" rel=\"noreferrer noopener\">10.5059\/yukigoseikyokaishi.81.1136<\/a><br><br><\/li>\n\n\n\n<li>H. Fujino,&nbsp;M. Nagatomo, M. Inoue, &#8220;Total Syntheses of Hikosamine and Hikizimycin,&#8221;&nbsp;<strong><em>J. Org. Chem.<\/em><\/strong>&nbsp;<strong>2021<\/strong>,&nbsp;<em>86<\/em>, 16220\u201316230.<br><br>(Selected as the cover picture&nbsp;<a href=\"https:\/\/pubs.acs.org\/toc\/joceah\/86\/23\" target=\"_blank\" rel=\"noreferrer noopener\">link<\/a>)<br><br><img loading=\"lazy\" decoding=\"async\" width=\"601\" height=\"324\" class=\"wp-image-133\" style=\"width: 500px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/s5.png\" alt=\"\" srcset=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/s5.png 601w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/s5-300x162.png 300w\" sizes=\"(max-width: 601px) 100vw, 601px\" \/><br><br>DOI:&nbsp;<a href=\"http:\/\/doi.org\/10.1021\/acs.joc.1c01773\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/acs.joc.1c01773<\/a><br><br><\/li>\n\n\n\n<li>M. Nagatomo, M. Inoue, &#8220;Convergent Assembly of Highly Oxygenated Natural Products Enabled by Intermolecular Radical Reactions,&#8221;&nbsp;<strong><em>Acc. Chem. Res.<\/em><\/strong>&nbsp;<strong>2021<\/strong>,&nbsp;<em>54<\/em>, 595\u2013604.<br><br><img loading=\"lazy\" decoding=\"async\" width=\"1911\" height=\"634\" class=\"wp-image-134\" style=\"width: 700px;\" src=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/s4.jpg\" alt=\"\" srcset=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/s4.jpg 1911w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/s4-300x100.jpg 300w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/s4-1024x340.jpg 1024w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/s4-768x255.jpg 768w, https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2023\/11\/s4-1536x510.jpg 1536w\" sizes=\"(max-width: 1911px) 100vw, 1911px\" \/><br><br>DOI:&nbsp;<a href=\"http:\/\/doi.org\/10.1021\/acs.accounts.0c00792\" target=\"_blank\" rel=\"noreferrer noopener\">10.1021\/acs.accounts.0c00792<\/a><br><br><\/li>\n\n\n\n<li>\u9577\u53cb\u512a\u5178\u3001&#8221;\u9ad8\u9178\u5316\u5ea6\u5929\u7136\u7269\u306e\u5168\u5408\u6210\u6226\u7565\u306e\u958b\u767a\uff1a\u5149\u5316\u5b66\u7684C(sp<sup>3<\/sup>)-H\u5b98\u80fd\u5316\u3092\u5229\u7528\u3057\u305f\u30e9\u30af\u30bf\u30b7\u30b9\u30c1\u30f3\u53ca\u3073\u30b6\u30e9\u30b4\u30b8\u30f3\u9178C\u306e\u5168\u5408\u6210,&#8221;&nbsp;<strong><em>YAKUGAKU ZASSHI<\/em><\/strong>&nbsp;<strong>2019<\/strong>,&nbsp;<em>139<\/em>, 651\u2013661.<br>DOI:&nbsp;<a href=\"https:\/\/doi.org\/10.1248\/yakushi.18-00210\" target=\"_blank\" rel=\"noreferrer noopener\">10.1248\/yakushi.18-00210<\/a><br><\/li>\n\n\n\n<li>\u9577\u53cb\u512a\u5178\u3001&#8221;\u7aae\u3059\u308c\u3070\u901a\u305a\uff0d\u30ea\u30a2\u30ce\u30b8\u30f3\u5168\u5408\u6210\u304b\u3089\u306e\u5b66\u3073,&#8221;&nbsp;<strong><em>\u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a\u8a8c<\/em><\/strong>&nbsp;<strong>2018<\/strong>,&nbsp;<em>76<\/em>, 494\u2013497.<br>DOI:&nbsp;<a href=\"https:\/\/doi.org\/10.5059\/yukigoseikyokaishi.76.494\" target=\"_blank\" rel=\"noreferrer noopener\">10.5059\/yukigoseikyokaishi.76.494<\/a><br><\/li>\n\n\n\n<li>\u9577\u53cb\u512a\u5178, &#8220;\u30aa\u30ad\u30b5\u30b8\u30ea\u30b8\u30f3\u3092\u7528\u3044\u305f\u30b9\u30c1\u30ec\u30f3\u985e\u306e\u4e0d\u6589\u30a2\u30df\u30ce\u30d2\u30c9\u30ed\u30ad\u30b7\u30eb\u5316\u53cd\u5fdc,&#8221;&nbsp;<strong><em>\u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a\u8a8c<\/em><\/strong>&nbsp;<strong>2013<\/strong>,&nbsp;<em>71<\/em>, 944\u2013945.<br>DOI:&nbsp;<a href=\"http:\/\/dx.doi.org\/10.5059\/yukigoseikyokaishi.71.944\" target=\"_blank\" rel=\"noreferrer noopener\">10.5059\/yukigoseikyokaishi.71.944<\/a><\/li>\n<\/ol>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"3\"><strong>\u8457\u66f8<\/strong><strong><\/strong><\/h3>\n\n\n\n<ol reversed>\n<li>\u9577\u53cb\u512a\u5178 \u201d\u74b0\u5883\u304c\u79c1\u3092\u80b2\u307f\u3001\u79c1\u304c\u74b0\u5883\u3092\u5275\u308b,\u201d <strong><em>\u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a\u8a8c<\/em><\/strong> <strong>2025<\/strong>, <em>83<\/em>, 666\u2013669.<br>DOI: <a href=\"https:\/\/doi.org\/10.5059\/yukigoseikyokaishi.83.666\" target=\"_blank\" rel=\"noreferrer noopener\">10.5059\/yukigoseikyokaishi.83.666<\/a><br>PDF\u3078\u306e\u30ea\u30f3\u30af\u306f<a href=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2025\/07\/83_666.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">\u3053\u3061\u3089<\/a>\u3002<br><\/li>\n\n\n\n<li>\u9577\u53cb\u512a\u5178&nbsp;\u201c\u7db2\u7f85\u7684\u5168\u5408\u6210\u6226\u7565\u306e\u63a2\u6c42\u3000\u30d7\u30ea\u30d3\u30ec\u30c3\u30b8\u306a\u69cb\u9020\u306e\u62bd\u51fa\u3068\u69cb\u7bc9,\u201d\u3000&nbsp;<strong><em>\u5316\u5b66\u3068\u5de5\u696d \u98db\u7fd4\u3059\u308b\u82e5\u624b\u7814\u7a76\u8005<\/em><\/strong>, \u65e5\u672c\u5316\u5b66\u4f1a, pp 584\u2013585 (2023).<br><\/li>\n\n\n\n<li>M. Nagatomo, \u201cTotal Syntheses of Densely Oxygenated Natural Products by Radical-Based Decarbonylative Convergent Assembly,\u201d\u3000&nbsp;<strong><em>New Tide of Natural Product Chemistry<\/em><\/strong>, Springer, Singapore, pp 259\u2013273 (2023).<br>DOI:&nbsp;<a href=\"http:\/\/dx.doi.org\/10.1007\/978-981-99-1714-3_12\" target=\"_blank\" rel=\"noreferrer noopener\">10.1007\/978-981-99-1714-3_12<\/a><br><\/li>\n\n\n\n<li>Submitted by Y. Xue, A. Parsad, G. Dong, Checked by J. Han,&nbsp;M. Nagatomo, M. Inoue, &#8220;\u03b1-Arylation of Cyclopentanones by Palladium\/Enamine Cooperative Catalysis,&#8221;&nbsp;<strong><em>Org. Synth.<\/em><\/strong>&nbsp;<strong>2023<\/strong>,&nbsp;<em>100<\/em>, 99\u2013112.<br>DOI:&nbsp;<a href=\"http:\/\/dx.doi.org\/10.15227\/orgsyn.100.0099\" target=\"_blank\" rel=\"noreferrer noopener\">10.15227\/orgsyn.100.0099<\/a><br><\/li>\n\n\n\n<li>Submitted by M. Varghese, H. E. Caputo, R. Xiao, A. Balijepalli, A. Hamoud, M. W. Grinstaff, Checked by K. Oga,&nbsp;M. Nagatomo, M. Inoue, &#8220;Stereoselective [2+2] Cycloadditions: Synthesis of a Tri-O-Bn-D-Glucal-derived \u03b2-Lactam,&#8221;&nbsp;<strong><em>Org. Synth.<\/em><\/strong>&nbsp;<strong>2021<\/strong>,&nbsp;<em>98<\/em>, 491\u2013508.<br>DOI:&nbsp;<a href=\"http:\/\/dx.doi.org\/10.15227\/orgsyn.098.0491\" target=\"_blank\" rel=\"noreferrer noopener\">10.15227\/orgsyn.098.0491<\/a><br><\/li>\n\n\n\n<li>Submitted by Y. Chen, Q. Chen, L. Tan, L. Chen, X. Wang, Checked by Y. Komori,&nbsp;M. Nagatomo, M. Inoue, &#8220;Preparation of 1H-Indazole-3-carbonitrile,&#8221;&nbsp;<strong><em>Org. Synth.<\/em><\/strong>&nbsp;<strong>2020<\/strong>,&nbsp;<em>97<\/em>, 314\u2013326.<br>DOI:&nbsp;<a href=\"http:\/\/dx.doi.org\/10.15227\/orgsyn.097.0314\" target=\"_blank\" rel=\"noreferrer noopener\">10.15227\/orgsyn.097.0314<\/a><br><\/li>\n\n\n\n<li>Submitted by J. Klepp, W. Dillon, Y. Lin, P. Feng, B. W. Greatrex, Checked by Y. Imamura,&nbsp;M. Nagatomo, M. Inoue, &#8220;Preparation of (-)-Levoglucosenone from Cellulose Using Sulfuric Acid in Polyethylene Glycol,&#8221;&nbsp;<strong><em>Org. Synth.<\/em><\/strong>&nbsp;<strong>2020<\/strong>,&nbsp;<em>97<\/em>, 38\u201353.<br>DOI:&nbsp;<a href=\"http:\/\/dx.doi.org\/10.15227\/orgsyn.097.0038\" target=\"_blank\" rel=\"noreferrer noopener\">10.15227\/orgsyn.097.0038<\/a><br><\/li>\n\n\n\n<li>Submitted by Y. Kawashima, T. Furukawa, N. Chatani, M. Tobisu, Checked by T. Fukuda,&nbsp;M. Nagatomo, M. Inoue, &#8220;Nickel-Catalyzed Cross-Coupling of 2-Methoxynaphthalene with Methyl 4-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)benzoate,&#8221;&nbsp;<strong><em>Org. Synth.<\/em><\/strong>&nbsp;<strong>2019<\/strong>,&nbsp;<em>96<\/em>, 36\u201352.<br>DOI:&nbsp;<a href=\"http:\/\/dx.doi.org\/10.15227\/orgsyn.096.0036\" target=\"_blank\" rel=\"noreferrer noopener\">10.15227\/orgsyn.096.0036<\/a><br><\/li>\n\n\n\n<li>\u9577\u53cb\u512a\u5178, \u4e95\u4e0a\u5c06\u884c, \u201c\u30ea\u30a2\u30ce\u30c0\u30f3\u30b8\u30c6\u30eb\u30da\u30f3\u306e\u7d71\u4e00\u7684\u5168\u5408\u6210,\u201d\u3000&nbsp;<strong><em>\u5929\u7136\u6709\u6a5f\u5316\u5408\u7269\u306e\u5168\u5408\u6210\u3000\u72ec\u5275\u7684\u306a\u3082\u306e\u3065\u304f\u308a\u306e\u53cd\u5fdc\u3068\u6226\u7565(CSJ\u30ab\u30ec\u30f3\u30c8\u30ec\u30d3\u30e5\u30fc 27) (\u65e5\u672c\u5316\u5b66\u4f1a\u3000\u7de8)<\/em><\/strong>, \u5316\u5b66\u540c\u4eba, pp 103\u2013109 (2018).<\/li>\n<\/ol>\n\n\n\n<h3 class=\"wp-block-heading\" id=\"4\"><strong>\u4f9d\u983c\u89e3\u8aac\u8a18\u4e8b<\/strong><strong><\/strong><\/h3>\n\n\n\n<ol reversed>\n<li>\u9577\u53cb\u512a\u5178, \u4eca\u6751\u7950\u4eae, \u4e95\u4e0a\u5c06\u884c, &#8220;\u6297\u304c\u3093\u5264\u30bf\u30ad\u30bd\u30fc\u30eb\u306e\u5168\u5408\u6210\u2015\u2015\u30e9\u30b8\u30ab\u30eb\u53cd\u5fdc\u3092\u6d3b\u7528\u3057\u305f\u65b0\u3057\u3044\u5408\u6210\u6226\u7565\u3068\u305d\u306e\u5c55\u958b,&#8221;&nbsp;<strong><em>\u5316\u5b66<\/em><\/strong>&nbsp;<strong>2023<\/strong>,&nbsp;<em>78<\/em>&nbsp;(7), 33\u201337.<br>(<a href=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2024\/02\/7807kagaku_nagatomo.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">\u30ea\u30f3\u30af<\/a>)<br><\/li>\n\n\n\n<li>\u9577\u53cb\u512a\u5178\u3001&#8221;\u9ad8\u9178\u5316\u5ea6\u5929\u7136\u7269\u306e\u5168\u5408\u6210\u6226\u7565\u306e\u958b\u767a,&#8221;&nbsp;<strong><em>\u85ac\u4e8b\u65e5\u5831<\/em><\/strong>&nbsp;<strong>2018<\/strong>,&nbsp;<em>11995<\/em>, 21.<br><\/li>\n\n\n\n<li>\u4e95\u4e0a\u5c06\u884c\u3001&nbsp;\u9577\u53cb\u512a\u5178\u3001\u5360\u90e8\u5927\u4ecb\u3001&#8221;\u30e9\u30b8\u30ab\u30eb\u53cd\u5fdc\u3092\u57fa\u76e4\u3068\u3057\u305f\u9ad8\u9178\u5316\u5ea6\u5929\u7136\u7269\u306e\u53ce\u675f\u7684\u5408\u6210\u6226\u7565,&#8221;&nbsp;<strong><em>\u30d5\u30a1\u30eb\u30de\u30b7\u30a2<\/em><\/strong>&nbsp;<strong>2017<\/strong>,&nbsp;<em>53<\/em>(9), 860\u2013864.<br><\/li>\n\n\n\n<li>\u9577\u53cb\u512a\u5178, \u4e95\u4e0a\u5c06\u884c, &#8220;\u30ea\u30a2\u30ce\u30b8\u30f3\u985e\u306e\u7d71\u4e00\u7684\u5168\u5408\u6210-\u591a\u69d8\u6027\u3092\u5fd7\u5411\u3057\u305f\u5171\u901a\u4e2d\u9593\u4f53\u306e\u8a2d\u8a08\u6226\u7565,&#8221;&nbsp;<strong><em>\u5316\u5b66<\/em><\/strong>&nbsp;<strong>2016<\/strong>,&nbsp;<em>71<\/em>(4), 47\u201348.<br>(<a href=\"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-content\/uploads\/2024\/02\/kagaku2016.pdf\" target=\"_blank\" rel=\"noreferrer noopener\">\u30ea\u30f3\u30af<\/a>)<br><\/li>\n\n\n\n<li>T. Hoshikawa,&nbsp;M. Nagatomo, M. Inoue, \u201cPentafluorophenyl Isocyanate,\u201d&nbsp;<strong><em>e-EROS<\/em><\/strong>&nbsp;<strong>2013<\/strong>, RN01621.<br>DOI:&nbsp;<a href=\"http:\/\/dx.doi.org\/10.1002\/047084289X.rn01621\" target=\"_blank\" rel=\"noreferrer noopener\">10.1002\/047084289X.rn01621<\/a><\/li>\n<\/ol>\n","protected":false},"excerpt":{"rendered":"<p>\u7814\u7a76\u696d\u7e3e \u539f\u8457\u8ad6\u6587 \u7dcf\u8aac \u8457\u66f8 \u4f9d\u983c\u89e3\u8aac\u8a18\u4e8b<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"_links":{"self":[{"href":"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-json\/wp\/v2\/pages\/18"}],"collection":[{"href":"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-json\/wp\/v2\/comments?post=18"}],"version-history":[{"count":52,"href":"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-json\/wp\/v2\/pages\/18\/revisions"}],"predecessor-version":[{"id":894,"href":"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-json\/wp\/v2\/pages\/18\/revisions\/894"}],"wp:attachment":[{"href":"https:\/\/www.pharm.hokudai.ac.jp\/tengo_105\/wp-json\/wp\/v2\/media?parent=18"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}