{"id":11,"date":"2021-08-16T14:41:00","date_gmt":"2021-08-16T05:41:00","guid":{"rendered":"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group-test\/?page_id=11"},"modified":"2025-07-28T16:24:44","modified_gmt":"2025-07-28T07:24:44","slug":"publications","status":"publish","type":"page","link":"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"<h2>Original Papers<\/h2>\n<h4>&lt;2025&gt;<\/h4>\n<p>42. Effects of Countercations in Dianionic Dibenzosilepinyl Salts on the Structure and Hyperconjugative Antiaromaticity<\/p>\n<p>Kana Kobayashi, Takuya Kuwabara*<\/p>\n<p><em>Organometallics<\/em>\u00a0<strong>2025<\/strong>, <em>44<\/em>, 1483-1490.<\/p>\n<p>DOI: <a href=\"https:\/\/pubs.acs.org\/doi\/full\/10.1021\/acs.organomet.5c00149\">10.1021\/acs.organomet.5c00149<\/a><\/p>\n<p>41. Gram-scale Synthesis of Dibenzo[<em>a<\/em>,<em>e<\/em>]pentalenes from Trialkyl(phenylethynyl)silanes via Organosodium Intermediates<\/p>\n<p>Ayane Sato, Takuya Kuwabara*<\/p>\n<p><em>J. Org. Chem.<\/em> <strong>2025<\/strong>, <em>90<\/em>, 9258-9262.<\/p>\n<p>DOI: <a title=\"DOI URL\" href=\"https:\/\/doi.org\/10.1021\/acs.joc.5c00458\">10.1021\/acs.joc.5c00458<\/a><\/p>\n<p>Preprint ver.: <em>ChemRxiv<\/em>.<strong> 2025<\/strong><\/p>\n<p>DOI: 10.26434\/chemrxiv-2025-8dmvw-v2<\/p>\n<p>40. Synthesis of a dilithiobutadiene bearing extremely bulky silyl substituents and its reactivity toward functionalized silanes<\/p>\n<p>Katharina Munster, Shunsuke Kudo, Takuya Kuwabara, Eriko Shimamura, Shunsuke Furukawa, Yusuke Yoshida, Shintaro Ishida, Takeaki Iwamoto, Kazuki Tanifuji, Yasuhiro Ohki, Mao Minoura, Masaichi Saito*<\/p>\n<p><em>Dalton Trans<\/em>. <strong>2025<\/strong>, <em>54<\/em>, 4030-4038.<\/p>\n<p>DOI: <a class=\"text--small\" title=\"Link to landing page via DOI\" href=\"https:\/\/doi.org\/10.1039\/D4DT03537B\">10.1039\/D4DT03537B<\/a><\/p>\n<h4>&lt;2024&gt;<\/h4>\n<p>39. 5,10-Diiododibenzo[a,e]pentalene<\/p>\n<p>Natsumi Ohara, Chinatsu Ogiwara, Takuya Kuwabara*<\/p>\n<p><em>Molbank<\/em> <strong>2024<\/strong>, <em>2024<\/em>, M1937.<\/p>\n<p>DOI: <a href=\"https:\/\/doi.org\/10.3390\/M1937\">10.3390\/M1937<\/a><\/p>\n<p>38. 9,10-Bis(5<em>H<\/em>-dibenzo[<em>b<\/em>,<em>f<\/em>]azepino)anthracene<\/p>\n<p>Himeko Kawaguchi, Takuya Kuwabara<\/p>\n<p><em>Molbank<\/em> <strong>2024<\/strong>, <em>2024<\/em>, M1917.<\/p>\n<p>DOI: <a href=\"https:\/\/www.mdpi.com\/1422-8599\/2024\/4\/M1917#\">10.3390\/M1917<\/a><\/p>\n<p>&nbsp;<\/p>\n<p>37. Arylboronic Acid Pinacol Esters as Stable Boron Sources for<br \/>\nDihydrodibenzoborepin Derivatives and a Dibenzoborole<\/p>\n<p>Himeko Kawaguchi, Kotomi Fuse, Nanoka Maeda, Takuya Kuwabara<\/p>\n<p><em>Molecules<\/em> <strong>2024<\/strong>, <em>29<\/em>, 4024.<\/p>\n<p><a href=\"https:\/\/www.mdpi.com\/1420-3049\/29\/17\/4024\">DOI: 10.3390\/molecules29174024<\/a><\/p>\n<p>preprint ver.: <em>Preprints<\/em> <strong>2024<\/strong>, 2024071789. (DOI: <a href=\"https:\/\/www.preprints.org\/manuscript\/202407.1789\/v1\">10.20944\/preprints202407.1789.v1<\/a>)<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-401\" src=\"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2024\/08\/Molecules_ArBpin_GA.tif_-300x195.jpg\" alt=\"\" width=\"431\" height=\"281\" srcset=\"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2024\/08\/Molecules_ArBpin_GA.tif_-300x195.jpg 300w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2024\/08\/Molecules_ArBpin_GA.tif_-768x500.jpg 768w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2024\/08\/Molecules_ArBpin_GA.tif_-24x16.jpg 24w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2024\/08\/Molecules_ArBpin_GA.tif_-36x23.jpg 36w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2024\/08\/Molecules_ArBpin_GA.tif_-48x31.jpg 48w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2024\/08\/Molecules_ArBpin_GA.tif_.jpg 953w\" sizes=\"auto, (max-width: 431px) 100vw, 431px\" \/><\/p>\n<p>36. Lithium Salt of 2,5-Bis(trimethylsilyl)stannolyl Anion: Synthesis, Structure, and Nonaromatic Character<\/p>\n<p>Kohei Kitamura, Youichi Ishii, Takuya Kuwabara<\/p>\n<p><em>Inorganics<\/em> <strong>2024<\/strong>, <em>12<\/em>, 92.<\/p>\n<p>DOI: <a href=\"https:\/\/doi.org\/10.3390\/inorganics12030092\">10.3390\/inorganics12030092<\/a><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-364\" src=\"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2024\/03\/36_GA-300x179.png\" alt=\"\" width=\"300\" height=\"179\" srcset=\"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2024\/03\/36_GA-300x179.png 300w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2024\/03\/36_GA-1024x610.png 1024w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2024\/03\/36_GA-768x458.png 768w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2024\/03\/36_GA-24x14.png 24w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2024\/03\/36_GA-36x21.png 36w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2024\/03\/36_GA-48x29.png 48w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2024\/03\/36_GA.png 1262w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<h4>&lt;2023&gt;<\/h4>\n<p>35. Retro-Vinylidene Rearrangements of P- and S-Substituted Ruthenium Vinylidene Complexes<br \/>\nTakahiro Iwamoto, Kyoka Saito, Takuya Mitsubo, Takuya Kuwabara, Youichi Ishii<br \/>\n<em>Organometallics<\/em> <strong>2023<\/strong>, <em>42<\/em>, 167\u2013173.<br \/>\nDOI: <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.organomet.2c00552\">10.1021\/acs.organomet.2c00552<\/a><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-288\" src=\"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2023\/01\/TOC-300x168.jpg\" alt=\"\" width=\"300\" height=\"168\" srcset=\"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2023\/01\/TOC-300x168.jpg 300w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2023\/01\/TOC-24x13.jpg 24w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2023\/01\/TOC-36x20.jpg 36w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2023\/01\/TOC-48x27.jpg 48w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2023\/01\/TOC.jpg 630w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>34.\u00a0<em>Exo-<\/em>\u00a0and\u00a0<em>endo<\/em>-Isomers of Plumbylenes Supported by 1,3-Diethers of Calix[4]arene<\/p>\n<p>Ryunosuke Kuriki, Youichi Ishii, Takuya Kuwabara*<\/p>\n<p><em>Eur. J. Inorg. Chem.<\/em>\u00a0<strong>2023<\/strong>,\u00a0<em>26<\/em>, e202200655.<\/p>\n<p><em>Selected as EurJIC Talents<\/em><\/p>\n<p>DOI:\u00a0<a href=\"https:\/\/onlinelibrary.wiley.com\/share\/author\/X6ITQXXDZ6TENWG3MDH7?target=10.1002\/ejic.202200655\">10.1002\/ejic.202200655<\/a><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-265\" src=\"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/12\/PbCalix-300x194.jpg\" alt=\"\" width=\"300\" height=\"194\" srcset=\"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/12\/PbCalix-300x194.jpg 300w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/12\/PbCalix-24x16.jpg 24w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/12\/PbCalix-36x23.jpg 36w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/12\/PbCalix-48x31.jpg 48w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/12\/PbCalix.jpg 520w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<h4>&lt;2022&gt;<\/h4>\n<p>33. Inorganic salt-assisted assembly of anionic \u03c0-conjugated rings enabling <sup>7<\/sup>Li NMR-based evaluation of antiaromaticity<\/p>\n<p>Shotaro Ito, Youichi Ishii, Takuya Kuwabara*<\/p>\n<p><em>Dalton Trans.<\/em> <strong>2022<\/strong>, <em>51<\/em>, 16397\u201316402.<\/p>\n<p>DOI: <a class=\"text--small\" title=\"Link to landing page via DOI\" href=\"https:\/\/doi.org\/10.1039\/D2DT02649J\">10.1039\/D2DT02649J<\/a><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-239\" src=\"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/10\/TOC_2-300x163.jpg\" alt=\"\" width=\"300\" height=\"163\" srcset=\"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/10\/TOC_2-300x163.jpg 300w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/10\/TOC_2-24x13.jpg 24w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/10\/TOC_2-36x20.jpg 36w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/10\/TOC_2-48x26.jpg 48w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/10\/TOC_2.jpg 310w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>32. Perfluorocycloparaphenylenes<\/p>\n<p>Hiroki Shudo, Motonobu Kuwayama, Masafumi Shimasaki, Taishi Nishihara, Youhei Takeda, Takuya Kuwabara, Akiko Yagi, Yasutomo Segawa,* Kenichiro Itami*<\/p>\n<p><em>Nat. Commun.<\/em> <strong>2022<\/strong>, <em>13<\/em>, 3713.<\/p>\n<p>DOI: <a class=\"underline mat-body-1 ng-star-inserted\" href=\"https:\/\/doi.org\/10.1038\/s41467-022-31530-x\" target=\"_blank\" rel=\"noopener noreferrer\">10.1038\/s41467-022-31530-x<\/a><\/p>\n<p>PrePrint version: DOI: <a href=\"https:\/\/chemrxiv.org\/engage\/chemrxiv\/article-details\/616fccbaa3d2c9f67edce1cb\">10.33774\/chemrxiv-2021-7kd63<\/a><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-medium wp-image-217\" src=\"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/07\/F10CPP-300x177.jpg\" alt=\"\" width=\"300\" height=\"177\" srcset=\"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/07\/F10CPP-300x177.jpg 300w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/07\/F10CPP-768x452.jpg 768w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/07\/F10CPP-24x14.jpg 24w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/07\/F10CPP-36x21.jpg 36w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/07\/F10CPP-48x28.jpg 48w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/07\/F10CPP.jpg 972w\" sizes=\"auto, (max-width: 300px) 100vw, 300px\" \/><\/p>\n<p>31. Weakly Bound Dimer of a Diaryloxygermylene Derived from a<br \/>\n<em><sup>t<\/sup><\/em>BuPh<sub>2<\/sub>Si-Substituted 2,2&#8242;-Methylenediphenol<\/p>\n<p>Ryo Yamazaki, Ryunosuke Kuriki, Asuka Sugihara, Youichi Ishii and Takuya Kuwabara*<\/p>\n<p><em>Crystals<\/em> <strong>2022<\/strong>, <em>12<\/em>, 605.<\/p>\n<p>DOI: <a href=\"https:\/\/www.mdpi.com\/2073-4352\/12\/5\/605\/htm\">10.3390\/cryst12050605<\/a><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-195\" src=\"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2022Crystals_GA-300x84.jpg\" alt=\"\" width=\"536\" height=\"150\" srcset=\"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2022Crystals_GA-300x84.jpg 300w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2022Crystals_GA-1024x285.jpg 1024w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2022Crystals_GA-768x214.jpg 768w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2022Crystals_GA-24x7.jpg 24w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2022Crystals_GA-36x10.jpg 36w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2022Crystals_GA-48x13.jpg 48w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2022Crystals_GA.jpg 1106w\" sizes=\"auto, (max-width: 536px) 100vw, 536px\" \/><\/p>\n<p>30. Experimental Observation of \u03b2-Carbon Elimination from Alkenylrhodium Complexes through Exchange Reactions of the Alkenyl Unit<\/p>\n<p>Takahiro Iwamoto, Koushi Shibuya, Tomoyuki Takakuwa, Takuya Kuwabara, Youichi Ishii*<\/p>\n<p><em>Organometallics<\/em> <strong>2022<\/strong>, 41, 182\u2013186.<\/p>\n<p>DOI: <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.organomet.1c00695\">10.1021\/acs.organomet.1c00695<\/a><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-197\" src=\"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2021_OM_TOC-300x91.png\" alt=\"\" width=\"538\" height=\"163\" srcset=\"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2021_OM_TOC-300x91.png 300w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2021_OM_TOC-24x7.png 24w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2021_OM_TOC-36x11.png 36w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2021_OM_TOC-48x15.png 48w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2021_OM_TOC.png 478w\" sizes=\"auto, (max-width: 538px) 100vw, 538px\" \/><\/p>\n<h4>&lt;2021&gt;<\/h4>\n<p>29. A new strategy for hyperconjugative antiaromatic compounds utilizing negative charges: a dibenzo[<em>b<\/em>,<em>f<\/em>]silepinyl dianion<\/p>\n<p>Shotaro Ito, Youichi Ishii, Kazuya Ishimura, Takuya Kuwabara*<\/p>\n<p><em>Chem. Commun.<\/em> <strong>2021<\/strong>, <em>57<\/em>, 11330\u201311333.<\/p>\n<p>DOI: <a class=\"text--small\" title=\"Link to landing page via DOI\" href=\"https:\/\/doi.org\/10.1039\/D1CC04434F\">10.1039\/D1CC04434F<\/a><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-196\" src=\"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2021_CC_TOC-300x150.png\" alt=\"\" width=\"542\" height=\"271\" srcset=\"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2021_CC_TOC-300x150.png 300w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2021_CC_TOC-24x12.png 24w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2021_CC_TOC-36x18.png 36w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2021_CC_TOC-48x24.png 48w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2021_CC_TOC.png 302w\" sizes=\"auto, (max-width: 542px) 100vw, 542px\" \/><\/p>\n<h4>&lt;2020&gt;<\/h4>\n<p dir=\"ltr\">28. Selective Double CH Activation at a Methylene Carbon in Methylenediphenol Derivatives to Generate Carbene-Bridged Dinuclear Iridium Complexes<\/p>\n<p dir=\"ltr\">Takuya Kuwabara, Takuya Toriumi, Mika Suzuki, and Youichi Ishii*<\/p>\n<p dir=\"ltr\"><em>Organometallics<\/em> <strong>2020<\/strong>, <em>39<\/em>, 4500\u20134509.<\/p>\n<p dir=\"ltr\">DOI:<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.organomet.0c00595\">10.1021\/acs.organomet.0c00595<\/a><\/p>\n<p dir=\"ltr\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-198\" src=\"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2020_OM_TOC_300-300x168.png\" alt=\"\" width=\"392\" height=\"220\" srcset=\"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2020_OM_TOC_300-300x168.png 300w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2020_OM_TOC_300-768x429.png 768w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2020_OM_TOC_300-24x13.png 24w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2020_OM_TOC_300-36x20.png 36w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2020_OM_TOC_300-48x27.png 48w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2020_OM_TOC_300.png 1004w\" sizes=\"auto, (max-width: 392px) 100vw, 392px\" \/><img loading=\"lazy\" decoding=\"async\" class=\" wp-image-77\" src=\"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2021\/09\/Cover_DoublCH-226x300.jpg\" alt=\"\" width=\"173\" height=\"230\" srcset=\"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2021\/09\/Cover_DoublCH-226x300.jpg 226w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2021\/09\/Cover_DoublCH-771x1024.jpg 771w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2021\/09\/Cover_DoublCH-768x1020.jpg 768w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2021\/09\/Cover_DoublCH-1156x1536.jpg 1156w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2021\/09\/Cover_DoublCH-1542x2048.jpg 1542w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2021\/09\/Cover_DoublCH-scaled.jpg 1927w\" sizes=\"auto, (max-width: 173px) 100vw, 173px\" \/><\/p>\n<p dir=\"ltr\">Selected as the cover picture of issue 24.<\/p>\n<p>27. Synthesis and Structures of Diaryloxystannylenes and -plumbylenes embedded in 1,3-Diethers of Thiacalix[4]arene<\/p>\n<p>Ryunosuke Kuriki, Takuya Kuwabara,* and Youichi Ishii*<\/p>\n<p><em>Dalton Trans<\/em>. <strong>2020<\/strong>, <em>49<\/em>, 12234\u201312241.<\/p>\n<p>DOI:<a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2020\/dt\/d0dt02496a#!divAbstract\">10.1039\/D0DT02496A<\/a><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-201\" src=\"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2020_Dalton_TOC-300x74.png\" alt=\"\" width=\"567\" height=\"140\" srcset=\"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2020_Dalton_TOC-300x74.png 300w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2020_Dalton_TOC-1024x253.png 1024w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2020_Dalton_TOC-768x190.png 768w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2020_Dalton_TOC-1536x379.png 1536w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2020_Dalton_TOC-2048x506.png 2048w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2020_Dalton_TOC-24x6.png 24w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2020_Dalton_TOC-36x9.png 36w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2020_Dalton_TOC-48x12.png 48w\" sizes=\"auto, (max-width: 567px) 100vw, 567px\" \/><\/p>\n<p dir=\"ltr\">26. A Tin Analogue of the Cycloheptatrienyl Anion: Synthesis, Structure, and Further Reduction to Form a Dianionic Species<\/p>\n<p dir=\"ltr\">Shotaro Ito, Takuya Kuwabara,* and Youichi Ishii*<\/p>\n<p dir=\"ltr\"><em>Organometallics<\/em> <strong>2020<\/strong>, <em>39<\/em>, 640\u2013644.<\/p>\n<p dir=\"ltr\">DOI:<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.organomet.0c00042\">10.1021\/acs.organomet.0c00042<\/a><\/p>\n<p dir=\"ltr\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone wp-image-205\" src=\"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2020_OM_StannepinylAnion-300x68.png\" alt=\"\" width=\"582\" height=\"132\" srcset=\"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2020_OM_StannepinylAnion-300x68.png 300w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2020_OM_StannepinylAnion-768x175.png 768w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2020_OM_StannepinylAnion-24x5.png 24w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2020_OM_StannepinylAnion-36x8.png 36w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2020_OM_StannepinylAnion-48x11.png 48w, https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-content\/uploads\/sites\/32\/2022\/05\/2020_OM_StannepinylAnion.png 802w\" sizes=\"auto, (max-width: 582px) 100vw, 582px\" \/><\/p>\n<p dir=\"ltr\">25. Ruthenium Vinylidene Complexes Generated by Selective 1,2-Migration of P- and S- Substituents: Synthesis, Structures, and Dichromism Arising from an Intermolecular CH\u2026O Hydrogen Bond<\/p>\n<p dir=\"ltr\">Takuya Kuwabara, Yutaka Aoki, Kousuke Sakajiri, Kazuki Deguchi, ShuheiTakamori, Ai Hamano, Keiko Takano, Hirohiko Houjou and Youichi Ishii*<\/p>\n<p dir=\"ltr\"><em>Organometallics<\/em> <strong>2020<\/strong>, <em>39<\/em>, 711\u2013718.<\/p>\n<p dir=\"ltr\">DOI:<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.organomet.9b00856\">10.1021\/acs.organomet.9b00856<\/a><\/p>\n<h4 dir=\"ltr\">&lt;2019&gt;<\/h4>\n<p dir=\"ltr\">24. Inverted Sandwich Rh Complex Bearing a Plumbole Ligand and Its Catalytic Activity<\/p>\n<p dir=\"ltr\">Masaichi Saito, Marisa Nakada, Takuya Kuwabara, Ryota Owada, Shunsuke Furukawa, Radhika Narayanan, Ninori Abe, Masahiko Hada, Ken Tanaka, Yoshihiko Yamamoto<\/p>\n<p dir=\"ltr\"><em>Organometallics<\/em> <strong>2019<\/strong>, <em>38<\/em>, 3099\u20133103.<\/p>\n<p dir=\"ltr\">DOI:<a title=\"DOI URL\" href=\"https:\/\/doi.org\/10.1021\/acs.organomet.9b00339\">10.1021\/acs.organomet.9b00339<\/a><\/p>\n<p dir=\"ltr\">23. Synthesis of Phosphaphenalenium Salts via P\u2013C Reductive Elimination at a Ru(II) Center and Their Fluorescence Properties<\/p>\n<p dir=\"ltr\">Takahiro Kato, Takuya Kuwabara, Yasunori Minami, Tamejiro Hiyama, and Youichi Ishii*<\/p>\n<p dir=\"ltr\"><em>Bull. Chem. Soc. Jpn.<\/em> <strong>2019<\/strong>, <em>92<\/em>, 1131\u20131141.<\/p>\n<p dir=\"ltr\">DOI:<a href=\"https:\/\/www.journal.csj.jp\/doi\/abs\/10.1246\/bcsj.20190090\">10.1246\/bcsj.20190090<\/a><\/p>\n<p dir=\"ltr\">22. Molybdenum-Mediated Vinylidene Rearrangement of Internal Acylalkynes and Sulfonylalkynes<\/p>\n<p dir=\"ltr\">Takuya Kuwabara, Kousuke Sakajiri, Yousuke Oyama, Shintaro Kodama , and Youichi Ishii*<\/p>\n<p dir=\"ltr\"><em>Organometallics<\/em> <strong>2019<\/strong>, <em>38<\/em>, 1560\u20131566.<\/p>\n<p dir=\"ltr\">DOI:<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.organomet.9b00019\">10.1021\/acs.organomet.9b00019<\/a><\/p>\n<h4 dir=\"ltr\">&lt;2018&gt;<\/h4>\n<p dir=\"ltr\">21. Ring Slippage and Dissociation of Pentamethylcyclopentadienyl Ligand in an (\u03b7<sup>5<\/sup>-Cp*)Ir Complex with a \u03ba<sup>3<\/sup>&#8211;<em>O<\/em>,<em>C<\/em>,<em>O<\/em> Tridentate Calix[4]arene Ligand under Mild Conditions<\/p>\n<p dir=\"ltr\">Takuya Kuwabara, Ryogen Tezuka, Mikiya Ishikawa, Takuya Yamazaki, Shintaro Kodama and Youichi Ishii*<\/p>\n<p dir=\"ltr\"><em>Organometallics<\/em> <strong>2018<\/strong>, <em>37<\/em>, 1829\u20131832.<\/p>\n<p dir=\"ltr\">DOI:<a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.organomet.8b00257\">10.1021\/acs.organomet.8b00257<\/a><\/p>\n<p dir=\"ltr\">20. Dinuclear Nickel Complexes Doubly Bridged by Hydrogencyanamido Ligands: Synthesis, Structures and Magnetic Properties<\/p>\n<p dir=\"ltr\">Takuya Kuwabara, Natsumi Shiga, Shintaro Kodama, Hirohiko Sato, Hirohiko Houjou and Youichi Ishii*<\/p>\n<p dir=\"ltr\"><em>Eur. J. Inorg. Chem.<\/em> <strong>2018<\/strong>, 3413\u20133417.<\/p>\n<p dir=\"ltr\">DOI:<a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/ejic.201800457\">10.1002\/ejic.201800457<\/a><\/p>\n<p dir=\"ltr\">19. P\u2013C reductive elimination in Ru(II) complexes to convert triarylphosphine ligands into five- or six-membered phosphacycles<\/p>\n<p dir=\"ltr\">Takuya Kuwabara, Takahiro Kato, Kouichi Takano, Shintaro Kodama, Yuuka Manabe, Noriko Tsuchida, Keiko Takano, Yasunori Minami, Tamejiro Hiyama and Youichi Ishii*<\/p>\n<p dir=\"ltr\"><em>Chem. Commun.<\/em> <strong>2018<\/strong>, <em>54<\/em>, 5357\u20135360.<\/p>\n<p dir=\"ltr\">DOI:<a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2018\/cc\/c8cc02539h#!divAbstract\">10.1039\/C8CC02539H<\/a><\/p>\n<p dir=\"ltr\">18. Activation of a Carbon-Carbon Bond in Internal Alkynes: Vinylidene Rearrangement of Disubstituted Alkynes at an Ir Complex<\/p>\n<p dir=\"ltr\">Takuya Kuwabara, Shuhei Takamori, Satoshi Kishi, Takahiro Watanabe, Yousuke Ikeda, Shintaro Kodama, Yasunori Minami, Tamejiro Hiyama, Youichi Ishii*<\/p>\n<p dir=\"ltr\"><em>Synlett<\/em>\u00a0<strong>2018<\/strong>, <em>29<\/em>, 727\u2013730.<\/p>\n<p dir=\"ltr\">DOI:<a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0036-1591511\">10.1055\/s-0036-1591511<\/a><\/p>\n<h4 dir=\"ltr\">&lt;2017&gt;<\/h4>\n<p dir=\"ltr\">17. Reactions of Dilithium Dibenzopentalenides with Cr(CO)<sub>3<\/sub>(CH<sub>3<\/sub>CN)<sub>3<\/sub>: Unexpected Formation of A Cubic Tetramer of An Anionic Hydrodibenzopentalenyl Complex<\/p>\n<p dir=\"ltr\">Takuya Kuwabara, Nobuaki Kurokawa, Masaichi Saito*<\/p>\n<p dir=\"ltr\"><em>ChemPlusChem<\/em> <strong>2017<\/strong>, <em>82<\/em>, 1039\u20131042.<\/p>\n<p dir=\"ltr\">DOI:<a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/full\/10.1002\/cplu.201700043\">org\/10.1002\/cplu.201700043<\/a><\/p>\n<p dir=\"ltr\">16. Synthesis and reactivity of a ruthenocene-type complex bearing an aromatic \u03c0-ligand with the heaviest group 14 element<\/p>\n<p dir=\"ltr\">Marisa Nakada, Takuya Kuwabara, Shunsuke Furukawa, Masahiko Hada, Mao Minoura, Masaichi Saito<\/p>\n<p dir=\"ltr\"><em>Chem. Sci.<\/em> <strong>2017<\/strong>, <em>8<\/em>, 3092\u20133097.<\/p>\n<p dir=\"ltr\">DOI:<a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2017\/sc\/c6sc04843a\">10.1039\/C6SC04843A<\/a><\/p>\n<h4 dir=\"ltr\">&lt;2016&gt;<\/h4>\n<p dir=\"ltr\">15. (\u03b7<sup>4<\/sup>-Butadiene)Sn(0) Complexes: A New Approach for Zero-valent p-Block Elements Utilizing a Butadiene as a 4\u03c0-Electron Donor<\/p>\n<p dir=\"ltr\">Takuya Kuwabara, Marisa Nakada, Jumpei Hamada, Jing-dong Guo, Shigeru Nagase, Masaichi Saito<\/p>\n<p dir=\"ltr\"><em>J. Am. Chem. Soc<\/em>. <strong>2016<\/strong>, <em>138<\/em>, 11378\u201311382.<\/p>\n<p dir=\"ltr\">DOI:<a title=\"DOI URL\" href=\"https:\/\/doi.org\/10.1021\/jacs.6b07304\">10.1021\/jacs.6b07304<\/a><\/p>\n<p dir=\"ltr\">Highlighted in <a href=\"https:\/\/www.chemistryviews.org\/details\/news\/9745121\/New_Type_of_Zero-Valent_Tin_Compound.html\">Chemistry Views<\/a>\u3001\u57fc\u7389\u5927\u5b66\u30d7\u30ec\u30b9\u30ea\u30ea\u30fc\u30b9<\/p>\n<h4 dir=\"ltr\">&lt;2015&gt;<\/h4>\n<p dir=\"ltr\">14. Synthesis of a Stannole Dianion Complex Bearing a \u03bc-\u03b7<sup>1<\/sup>;\u03b7<sup>1<\/sup>-Coordination Mode: Different Electronic State of Stannole Dianion Ligands Depending on Their Hapticity<\/p>\n<p dir=\"ltr\">Takuya Kuwabara, Masaichi Saito<\/p>\n<p dir=\"ltr\"><em>Organometallics<\/em> <strong>2015<\/strong>, <em>34<\/em>, 4202\u20134204.<\/p>\n<p dir=\"ltr\">DOI:<a title=\"DOI URL\" href=\"https:\/\/doi.org\/10.1021\/acs.organomet.5b00614\">10.1021\/acs.organomet.5b00614<\/a><\/p>\n<p dir=\"ltr\">13. Diverse Coordination Modes in Tin Analogues of Cyclopentadienyl Anion Depending on the Substituents on the Tin Atom<\/p>\n<p dir=\"ltr\">Takuya Kuwabara, Marisa Nakada, Jing-Dong Guo, Shigeru Nagase, Masaichi Saito<\/p>\n<p dir=\"ltr\"><em>Dalton Trans<\/em>. <strong>2015<\/strong>, <em>44<\/em>, 16266\u201316271.<\/p>\n<p dir=\"ltr\">DOI:<a class=\"text--small\" title=\"Link to landing page via DOI\" href=\"https:\/\/doi.org\/10.1039\/C5DT02202A\">10.1039\/C5DT02202A<\/a><\/p>\n<p dir=\"ltr\">Selected as the front inside cover\u3001Highlighted in A News Paper (\u65e5\u520a\u5de5\u696d\u65b0\u805e)\u3001<br \/>\nChem-Station <a href=\"https:\/\/www.chem-station.com\/blog\/2015\/10\/cpsn.html\">\u7b2c 4 \u56de\u30b9\u30dd\u30c3\u30c8\u30e9\u30a4\u30c8\u30ea\u30b5\u30fc\u30c1<\/a>\u3001\u57fc\u7389\u5927\u5b66\u30d7\u30ec\u30b9\u30ea\u30ea\u30fc\u30b9<\/p>\n<p dir=\"ltr\">12. Curved Oligophenylenes as Donors in Shape-Persistent Donor-Acceptor Macrocycles with Solvatofluorochromic Properties<\/p>\n<p dir=\"ltr\">Takuya Kuwabara, Jun Orii, Yasutomo Segawa, Kenichiro Itami<\/p>\n<p dir=\"ltr\"><em>Angew. Chem. Int. Ed.<\/em> <strong>2015<\/strong>, <em>54<\/em>, 9646\u20139649.<\/p>\n<p dir=\"ltr\">DOI:<a class=\"epub-doi\" href=\"https:\/\/doi.org\/10.1002\/anie.201503397\" aria-label=\"Digital Object Identifier\">10.1002\/anie.201503397<\/a><\/p>\n<p dir=\"ltr\">Highlighted in ACS Central Science (DOI: <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acscentsci.5b00339\">10.1021\/acscentsci.5b00339<\/a>)<\/p>\n<p dir=\"ltr\">11. Palladium-free Synthesis of [10]Cycloparaphenylene<\/p>\n<p dir=\"ltr\">Yasutomo Segawa, Takuya Kuwabara, Katsuma Matsui, Satoru Kawai, Kenichiro Itami<\/p>\n<p dir=\"ltr\"><em>Tetrahedron<\/em>\u00a0<strong>2015<\/strong>, <em>26\u201327<\/em>, 4500\u20134503.<\/p>\n<p dir=\"ltr\">DOI:<a class=\"doi\" title=\"Persistent link using digital object identifier\" href=\"https:\/\/doi.org\/10.1016\/j.tet.2015.02.066\" target=\"_blank\" rel=\"noreferrer noopener\" aria-label=\"Persistent link using digital object identifier\">10.1016\/j.tet.2015.02.066<\/a><\/p>\n<p dir=\"ltr\">10. A Reversible Two-electron Redox System Involving a Divalent Lead Species<\/p>\n<p dir=\"ltr\">Masaichi Saito, Marisa Nakada, Takuya Kuwabara, Mao Minoura<\/p>\n<p dir=\"ltr\"><em>Chem. Commun.<\/em> <strong>2015<\/strong>, <em>51<\/em>, 4674\u20134676.<\/p>\n<p dir=\"ltr\">DOI:<a class=\"text--small\" title=\"Link to landing page via DOI\" href=\"https:\/\/doi.org\/10.1039\/C4CC09856K\">10.1039\/C4CC09856K<\/a><\/p>\n<h4 dir=\"ltr\">&lt;2014&gt;<\/h4>\n<p dir=\"ltr\">9. Synthesis, Structures and Electronic Properties of Triple- and Double-Decker Ruthenocenes Incorporated by A Metallole Dianion Ligand<\/p>\n<p dir=\"ltr\">Takuya Kuwabara, Jing-Dong Guo, Shigeru Nagase, Takahiro Sasamori, Norihiro Tokitoh, Masaichi Saito<\/p>\n<p dir=\"ltr\"><em>J. Am. Chem. Soc.<\/em> <strong>2014<\/strong>, <em>136<\/em>, 13059\u201313064.<\/p>\n<p dir=\"ltr\">DOI:<a title=\"DOI URL\" href=\"https:\/\/doi.org\/10.1021\/ja507330p\">10.1021\/ja507330p<\/a><\/p>\n<p dir=\"ltr\">\u57fc\u7389\u5927\u5b66\u30d7\u30ec\u30b9\u30ea\u30ea\u30fc\u30b9<\/p>\n<p dir=\"ltr\">8. Enhancement of Stannylene Character in Stannole Dianion Equivalents Evidenced by NMR, M\u00f6ssbauer Spectroscopies and Theoretical Studies of Newly Synthesized Silyl-substituted Dilithiostannoles<\/p>\n<p dir=\"ltr\">Takuya Kuwabara, Jing-Dong Guo, Shigeru Nagase, Mao Minoura, Rolfe H. Herber, Masaichi Saito<\/p>\n<p dir=\"ltr\"><em>Organometallics<\/em> <strong>2014<\/strong>, <em>33<\/em>, 2910\u20132913.<\/p>\n<p dir=\"ltr\">DOI:<a title=\"DOI URL\" href=\"https:\/\/doi.org\/10.1021\/om5003717\">10.1021\/om5003717<\/a><\/p>\n<p dir=\"ltr\">7. Facile Synthesis of Dibenzopentalene Dianions and Their Application as New \u03c0- extended Ligands<\/p>\n<p dir=\"ltr\">Takuya Kuwabara, Kazuya Ishimura, Takahiro Sasamori, Norihiro Tokitoh, Masaichi Saito<\/p>\n<p dir=\"ltr\"><em>Chem. Eur. J.<\/em> <strong>2014<\/strong>, <em>20<\/em>, 7571\u20137575.<\/p>\n<p dir=\"ltr\">DOI:<a class=\"epub-doi\" href=\"https:\/\/doi.org\/10.1002\/chem.201402304\" aria-label=\"Digital Object Identifier\">10.1002\/chem.201402304<\/a><\/p>\n<p dir=\"ltr\">6. Diversity of the Structures in a Distannene Complex and its Reduction to Generate Six-membered Ti<sub>2<\/sub>Sn<sub>4<\/sub> Ring Complex<\/p>\n<p dir=\"ltr\">Takuya Kuwabara, Jing-Dong Guo, Shigeru Nagase, Masaichi Saito<\/p>\n<p dir=\"ltr\"><em>Angew. Chem. Int. Ed.<\/em> <strong>2014<\/strong>, <em>53<\/em>, 434\u2013438.<\/p>\n<p dir=\"ltr\">DOI:<a class=\"epub-doi\" href=\"https:\/\/doi.org\/10.1002\/anie.201308565\" aria-label=\"Digital Object Identifier\">10.1002\/anie.201308565<\/a><\/p>\n<h4 dir=\"ltr\">&lt;2013&gt;<\/h4>\n<p dir=\"ltr\">6. Unexpected Formation of Ru<sub>2<\/sub>Sn<sub>2<\/sub> Bicyclic Four-Membered Ring Complexes with Butterfly and Inverse-Sandwich Structures<\/p>\n<p dir=\"ltr\">Takuya Kuwabara, Masaichi Saito, Jing-Dong Guo, Shigeru Nagase<\/p>\n<p dir=\"ltr\"><em>Inorg. Chem.<\/em> <strong>2013<\/strong>, <em>52<\/em>, 3585\u20133587.<\/p>\n<p dir=\"ltr\">DOI:<a title=\"DOI URL\" href=\"https:\/\/doi.org\/10.1021\/ic302782n\">10.1021\/ic302782n<\/a><\/p>\n<h4 dir=\"ltr\">&lt;2011&gt;<\/h4>\n<p dir=\"ltr\">4. Synthesis of a Novel Lithocene that has Aromatic-like Nature with Non-aromatic Rings<\/p>\n<p dir=\"ltr\">Masaichi Saito, Takuya Kuwabara, Kazuya Ishimura, Shigeru Nagase<\/p>\n<p dir=\"ltr\"><em>Chem. Asian. J.<\/em> <strong>2011<\/strong>, <em>6<\/em>, 2907\u20132910.<\/p>\n<p dir=\"ltr\">DOI:<a class=\"id-link\" href=\"https:\/\/doi.org\/10.1002\/asia.201100619\" target=\"_blank\" rel=\"noopener\" data-ga-category=\"full_text\" data-ga-action=\"DOI\">10.1002\/asia.201100619<\/a><\/p>\n<p dir=\"ltr\">3. 1,1&#8242;-Di-tert-butyl-2,2&#8242;,3,3&#8242;,4,4&#8242;,5,5&#8242;-octaethyl-1,1&#8242;-bistannole<\/p>\n<p dir=\"ltr\">Takuya Kuwabara, Masaichi Saito<\/p>\n<p dir=\"ltr\"><em>Acta Cryst.<\/em> <strong>2011<\/strong>, <em>E67<\/em>, m949.<\/p>\n<p dir=\"ltr\">DOI<a title=\"Open URL link\" href=\"https:\/\/doi.org\/10.1107\/S1600536811022951\">10.1107\/S1600536811022951<\/a><\/p>\n<h4 dir=\"ltr\">&lt;2010&gt;<\/h4>\n<p dir=\"ltr\">2. Synthesis, Structure and Reaction of Tetraethyldilithiostannole<\/p>\n<p dir=\"ltr\">Masaichi Saito, Takuya Kuwabara, Chika Kambayashi, Michikazu Yoshioka, Kazuya Ishimura, Shigeru Nagase<\/p>\n<p dir=\"ltr\"><em>Chem. Lett.<\/em> <strong>2010<\/strong>, <em>39<\/em>, 700\u2013701.<\/p>\n<p dir=\"ltr\">DOI: <a href=\"https:\/\/doi.org\/10.1246\/cl.2010.700\">10.1246\/cl.2010.700<\/a><\/p>\n<p dir=\"ltr\">Selected as Editor\u2019s Choice<\/p>\n<p dir=\"ltr\">1. Synthesis and Structures of Lithium Salts of Stannole Anions<\/p>\n<p dir=\"ltr\">Masaichi Saito, Takuya Kuwabara, Kazuya Ishimura, Shigeru Nagase<\/p>\n<p dir=\"ltr\"><em>Bull. Chem. Soc. Jpn.<\/em> <strong>2010<\/strong>, <em>83<\/em>, 825\u2013827.<\/p>\n<p dir=\"ltr\">DOI: <a href=\"https:\/\/doi.org\/10.1246\/bcsj.20100057\">10.1246\/bcsj.20100057<\/a><\/p>\n<h2>Books and Reviews<\/h2>\n<p>1. Review de Debut &#8220;\u74b0\u3072\u305a\u307f\u3092\u3082\u3064\u4e09\u914d\u4f4d\u30ea\u30f3\u5316\u5408\u7269\u306e\u89e6\u5a92\u958b\u767a&#8221;<\/p>\n<p>\u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a\u8a8c, 2018, 76, 1100\u20131101.<\/p>\n<p>DOI: <a class=\"bluelink-style\" href=\"https:\/\/doi.org\/10.5059\/yukigoseikyokaishi.76.1100\">org\/10.5059\/yukigoseikyokaishi.76.1100<\/a><\/p>\n<p>2. Siloles, Germoles, Stannoles, and Plumboles<\/p>\n<p>Takuya Kuwabara, Masaichi Saito<\/p>\n<p><em>Comprehensive Heterocyclic Chemistry IV (Fourth Edition)<\/em><\/p>\n<p><strong>2022<\/strong>, <em>3<\/em>, 798\u2013832.<\/p>\n<p>DOI: <a class=\"nova-legacy-e-link nova-legacy-e-link--color-inherit nova-legacy-e-link--theme-decorated\" href=\"http:\/\/dx.doi.org\/10.1016\/B978-0-12-409547-2.14789-4\" target=\"_blank\" rel=\"noopener\">10.1016\/B978-0-12-409547-2.14789-4<\/a><\/p>\n<div dir=\"ltr\"><\/div>\n<div dir=\"ltr\"><\/div>\n","protected":false},"excerpt":{"rendered":"<p>Original Papers &lt;2025&gt; 42. Effects of Countercations in Dianionic Dibenzosilepinyl Salts on the Structur &hellip; <a href=\"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/publications\/\">\u7d9a\u304d\u3092\u8aad\u3080 <span class=\"meta-nav\">&rarr;<\/span><\/a><\/p>\n","protected":false},"author":43,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-11","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-json\/wp\/v2\/pages\/11","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-json\/wp\/v2\/users\/43"}],"replies":[{"embeddable":true,"href":"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-json\/wp\/v2\/comments?post=11"}],"version-history":[{"count":69,"href":"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-json\/wp\/v2\/pages\/11\/revisions"}],"predecessor-version":[{"id":461,"href":"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-json\/wp\/v2\/pages\/11\/revisions\/461"}],"wp:attachment":[{"href":"https:\/\/www-p.sci.ocha.ac.jp\/kuwabara-group\/wp-json\/wp\/v2\/media?parent=11"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}