{"id":221,"date":"2020-12-31T14:27:05","date_gmt":"2020-12-31T05:27:05","guid":{"rendered":"https:\/\/mitsudo.net\/?page_id=221"},"modified":"2026-03-26T11:35:21","modified_gmt":"2026-03-26T02:35:21","slug":"list_of_publications","status":"publish","type":"page","link":"https:\/\/mitsudo.net\/en\/list_of_publications\/","title":{"rendered":"List of Publications"},"content":{"rendered":"

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Preprints<\/h2>\r\n

(1) Synthesis of Boranils by Iodide-Mediated Demethylative Borylation and Their Properties<\/strong>
Koichi Mitsudo,* Ryo Magata, Eisuke Sato, Tomoya Nakamura, Atsushi Wakamiya, and Seiji Suga*
ChemRxiv<\/em> 2026.
<\/strong>DOI: 10.26434\/chemrxiv.15000608\/v2<\/a><\/p>\r\n

Original Papers<\/h2>\r\n

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(110) Electrochemical Synthesis of Benzo[b]Phosphole Oxides via Dehydrogenative Annulation Using 1,4-Diazabicyclo[2.2.2]Octane as a Mediator<\/strong>
Koichi Mitsudo,* Sakura Kinjo, Yasuyuki Okumura, Eisuke Sato, Riki Kato, Yuta Nishina, Seiji Suga*
ChemElectroChem<\/em> 2026<\/strong>, in press.<\/p>\r\n

(109) Side-Chain Engineering of Oligothiophene-Extended Triphenylamines for Stable Radical Cations with NIR-II to NIR-III Absorption<\/strong>
Masafumi Yano,* Koji Yamashita, Minori Yano, Yoshitsugu Komai, Yuki Arikata, Koichi Mitsudo, Yukiyasu Kashiwagi
Org. Electron.<\/em>\u00a0<\/span>2026<\/strong>,\u00a0<\/span>154<\/em>, 107415.<\/span>
DOI: 10.1016\/j.orgel.2026.107415
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(108) Redox-Controlled Near-Infrared-to-Near-Infrared Optical Switching in TPA dimers<\/strong>
Masafumi Yano,* Kaito Nakazawa, Sentaro Yamada, Yuta Yamamoto, Tetsuo Yajima, Koichi Mitsudo, Yukiyasu Kashiwagi
Phys. Chem. Chem. Phys.<\/em> 2026<\/strong>, 28<\/em>, 5640\u20135644.
DOI: 10.1039\/D5CP04771D<\/a>
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(107) Crystal Structure of Tris[4-(3,4-dimethoxythiophen-2-yl)phenyl]amine<\/strong>
Masafumi Yano,* Yukiyasu Kashiwagi, Koki Oishi, Minori Yano, Koichi Mitsudo
Acta Crystallogr., Sect. E<\/em> 2026<\/strong>, 82<\/em>,\u00a0148\u2013151.
DOI: 10.1107\/S2056989026000058<\/a><\/p>\r\n

(106) Synthesis of Thienoacenes by Electrochemical Double C\u2013S Cyclization Using a Halogen Mediator<\/strong>
Koichi Mitsudo,* Takuya Nagahara, Nozomi Kataura, Yuka Okamura, Toki Yonezawa, Yuri Tachibana, Nolan Soulie, Keisuke Shigemori, Eisuke Sato, Hiroki Mandai, Seiji Suga*
Commun. Chem.<\/em> 2025<\/strong>, 8<\/em>, 366.
DOI: 10.1038\/s42004-025-01748-z<\/a>
<\/em>(Originally posted on ChemRxiv<\/em> 2024<\/strong>. <\/em>DOI: 10.26434\/chemrxiv-2024-hnc81<\/a>)<\/p>\r\n

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(105) Bioinspired Electrochemical Cyclization toward the Divergent Synthesis of Mavacurane- and Akuammiline-Type Alkaloid<\/strong>
Eisuke Sato,* Tomohiro Nakahama, Yuika Nomura, Koichi Mitsudo, and Seiji Suga*
Org. Lett.<\/em> 2025<\/strong>, 27<\/em>, 11818\u201311823.
DOI: 10.1021\/acs.orglett.5c03645<\/a>
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(104) Synthesis of N<\/em>,O<\/em>-Bidentate Difluoroboron Complexes via Iodide-Promoted Demethylative Borylation<\/strong>
Koichi Mitsudo,* Naoto Maekawa, Ryo Magata, Eisuke Sato, Tomoya Nakamura, Atsushi Wakamiya, Seiji Suga*
Org. Lett.<\/em> 2025<\/strong>, 27, 10636\u201310641.
(Published as part of\u00a0<\/span>Organic Letters<\/i>\u00a0<\/span>special issue<\/a>\u00a0\u201c\u03c0-Conjugated Molecules and Materials\u201d.<\/span>)
DOI: 10.1021\/acs.orglett.5c02613<\/a>
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(103) Electrochemical Generation of Sulfonamidyl Radicals via Anodic Oxidation of Hydrogen Bonding Complexes: Applications to Electrosynthesis of Benzosultams<\/strong>
Yasuyuki Okumura, Eisuke Sato, Koichi Mitsudo,* Seiji Suga*
JACS Au<\/em> 2025<\/strong>, 5<\/em>, 3974\u20133981.
DOI: 10.1021\/jacsau.5c00619<\/a>
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(102) Transformation of \u03b1,\u03b2-Unsaturated Aldehydes with a Small Amount of Electricity: Cyanosilylation, Isomerization, and Nucleophilic Addition<\/strong>
Mayu Fujii, Nanaho Ueno, Koichi Mitsudo, Eisuke Sato,* Seiji Suga*
Org. Lett.<\/em> 2025<\/strong>, 27, 6953\u20136958.
DOI: 10.1021\/acs.orglett.5c01790<\/a>
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(101) Cyanomethylation of Aldehydes on an Electrochemical Microflow System and Utility of Machine Learning-Assisted Examination of the Reaction Conditions<\/strong>
Eisuke Sato,* Akine Tani, Tomoyuki Miyao, Shumpei Kunimoto, Shinobu Takizawa, Koichi Mitsudo, Seiji Suga*
Chem. Eur. J.<\/em> 2025<\/strong>, 31<\/em>, e202501257.
DOI: 10.1002\/chem.202501257<\/a>
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(100) Electrogenerated Lewis Acid-Catalyzed Claisen Rearrangement of Allyl Aryl Ethers<\/strong>
Yuta Niki, Koichi Mitsudo, Eisuke Sato,* Seiji Suga*
Org. Lett.<\/em> 2024<\/strong>, 26<\/em>, 11111\u201311116.
DOI: 10.1021\/acs.orglett.4c03928<\/a>
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(99) N<\/em>-Phenylphenothiazine Radical Cation with Extended \u03c0-Systems: Enhanced Heat Resistance of Triarylamine Radical Cations as Near-Infrared Absorbing Dyes<\/strong>
Masafumi Yano,* Minami Ueda, Tatsuo Yajima, Koichi Mitsudo, Yukiyasu Kashiwagi
Colorants<\/em> 2024<\/strong>, 3<\/em>, 350\u2013359.
DOI: 10.3390\/colorants3040024<\/a><\/p>\r\n

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(98) SN<\/sub>Ar Hexafluoroisopropoxylation of Electron-rich Aryl Fluoride with a Catalytic Electrical Input
<\/strong>Eisuke Sato,* Tomohiro Nakahama, Koichi Mitsudo, Seiji Suga*
Chem. Lett.<\/em>\u00a0<\/span>2024<\/strong>,\u00a0<\/span>53<\/em>, upae196,<\/span>
DOI:\u00a0<\/span>10.1093\/chemle\/upae196<\/a>
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(97) Electrocatalytic Hydrogenation of Pyridines and Other Nitrogen-Containing Aromatic Compounds<\/strong>
Naoki Shida*, Yugo Shimizu, Akizumi Yonezawa, Juri Harada, Yuka Furutani, Yusuke Muto, Ryo Kurihara, Junko N. Kondo, Eisuke Sato, Koichi Mitsudo, Seiji Suga, Shoji Iguchi, Kazuhide Kamiya, and Mahito Atobe*<\/span>
J. Am. Chem. Soc.<\/em>\u00a0<\/span>2024<\/strong>, 146<\/em>, 30212\u201330221.<\/span>
DOI:\u00a0<\/span>10.1021\/jacs.4c09107<\/a>
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(96) Electrocatalytic Hydrogenation of Cyanoarenes, Nitroarenes, Quinolines, and Pyridines under Mild Conditions with a Proton-Exchange Membrane Reactor<\/strong>
Koichi Mitsudo,* Atsushi Osaki, Haruka Inoue, Eisuke Sato, Naoki Shida, Mahito Atobe, Seiji Suga*
Beilstein J. Org. Chem.<\/em> 2024<\/strong>, 20<\/em>, 1560\u20131571.
DOI: 10.3762\/bjoc.20.139<\/a>
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(95) Sequential Paired Electrochemical Transformation of Styrene Oxide via Anodic Meinwald Rearrangement and Cathodic Nitromethylation in an Electrochemical Flow Reactor with Catalytic Electrical Input<\/strong>
Eisuke Sato,* Kanon Nagamine, Chika Sasaki, Shumpei Kunimoto, Koichi Mitsudo, Seiji Suga*
Synthesis<\/em> 2024<\/strong>, 56<\/em>, 2507\u20132512.
DOI: 10.1055\/a-2309-6737<\/a>
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(94) [1,2]-Retro-Brook Rearrangement Induced by Electrochemical Reduction of Silyl Enolates<\/strong>
Ban Kinoshita, Saki Maejima, Yuta Niki, Koichi Mitsudo, Seiji Suga, Hideki Yorimitsu*
Bull. Chem. Soc. Jpn.<\/em> 2024<\/strong>, 97<\/em>, uoae038.
DOI: 10.1093\/bulcsj\/uoae038<\/a>
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(93) Synthesis and properties of thieno[3,2-b]thiophene appended triarylamine radical cations: Near-infrared absorbing dye with absorption beyond 1400\u202fnm<\/strong>
Masafumi Yano,* Kazushi Ueda, Yuto Shimizu, Yuki Arikata, Misaki Nakai, Tatsuo Yajima, Koichi Mitsudo, Yukiyasu Kashiwagi
Dyes Pigm.<\/em> 2024<\/strong>, 222<\/em>, 111916.
DOI: 10.1016\/j.dyepig.2023.111916<\/a>
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(92)\u00a0Alkynylation of Aldehydes Initiated by Cathodic Reduction<\/strong>
Eisuke Sato,* Mayu Fujii, Koichi Mitsudo, Seiji Suga*
ChemElectroChem<\/em> 2023<\/strong>, e202300499.
DOI: 10.1002\/celc.202300499<\/a>
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(91) Electrochemical Synthesis of Dibenzothiophene S,S-Dioxides from Biaryl Sulfonyl Hydrazides<\/strong>
Yasuyuki Okumura, Eisuke Sato, Koichi Mitsudo,* Seiji Suga*
Electrochemistry<\/em> 2023<\/strong>, 91<\/em>, 112007.
DOI: 10.5796\/electrochemistry.23-67078<\/a>
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(90) Cathodic N\u2013O Bond Cleavage of N<\/em>-Alkoxy Amide<\/strong>
Eisuke Sato,* Sayaka Ogita, Koichi Mitsudo, Seiji Suga*
Electrochemistry<\/em> 2023<\/strong>, 91<\/em>, 112005.
DOI: 10.5796\/electrochemistry.23-67079<\/a>
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(89) Anodic Dehydrogenative Aromatization of Tetrahydrocarbazoles Leading to Carbazoles<\/strong>
Eisuke Sato*, Ayaka Yukiue, Koichi Mitsudo, Seiji Suga*
Org. Lett.<\/em> 2023<\/strong>, 25<\/em>, 5339\u20135344.
DOI: 10.1021\/acs.orglett.3c01914<\/a>
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(88) Electrochemical Synthesis of Sultone Derivatives via Dehydrogenative C\u2013O Bond Formation<\/strong>
Koichi Mitsudo,* Yasuyuki Okumura, Kotaro Yohena, Yuji Kurimoto, Eisuke Sato, Seiji Suga*
Org. Lett.<\/em> 2023<\/strong>,\u00a025<\/em>, 3476\u20133481.
DOI: 10.1021\/acs.orglett.3c01062<\/a>
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(87) Electrochemical Cross-Coupling Reactions between Arylboronic Esters and Aryllithiums Using NaBr as a Halogen Mediator<\/strong>
Koichi Mitsudo,* Keisuke Shigemori , Taro Shibata , Hiroki Mandai , Eisuke Sato , Seiji Suga*
Synthesis<\/em> 2023<\/strong>, 55<\/em>, 2999\u20133004.
DOI: 10.1055\/a-2034-9821<\/a>
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(86) Electrochemical Carbon-Ferrier Rearrangement Using a Microflow Reactor and Machine Learning-Assisted Exploration of Suitable Conditions<\/strong>
Eisuke Sato,* Gaku Tachiwaki, Mayu Fujii, Koichi Mitsudo, Takashi Washio, Shinobu Takizawa, Seiji Suga*
Org. Process Res. Dev.<\/em> 2024<\/strong>, 28<\/em>, 1422\u20131429.
DOI: 10.1021\/acs.oprd.2c00267<\/a>
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(85) Electrochemical Synthesis of Dibenzothiophenes via Intramolecular C\u2013S Cyclization with a Halogen Mediator<\/strong>
Koichi Mitsudo,* Yuri Tachibana, Eisuke Sato, Seiji Suga*
Org. Lett.<\/em> 2022<\/strong>, 24<\/em>, 8547\u20138552.
DOI: 10.1021\/acs.orglett.2c03574<\/a>
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(84) A Facile Access to Spirooxindoles by Halogen-Mediated Electrochemical Semi-pinacol Rearrangement<\/strong>
Eisuke Sato,* Sae Kangawa, Koichi Mitsudo, Seiji Suga*
Chem. Lett.<\/em> 2022<\/strong>, 51<\/em>, 1067\u20131069.
DOI: 10.1246\/cl.220368<\/a>
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(83) Electrochemical Hydrogenation of Enones Using a Proton-Exchange Membrane Reactor: Selectivity and Utility<\/strong>
Koichi Mitsudo, Haruka Inoue, Yuta Niki, Eisuke Sato, Seiji Suga*
Beilstein J. Org. Chem.<\/em> 2022<\/strong>, 18<\/em>, 1055\u20131061.
DOI: 10.3762\/bjoc.18.107<\/a>
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(82) Substituent Control of Near-Infrared Absorption of Triphenylamine Radical Cation<\/strong>
Masafumi Yano,* Mai Sasaoka, Kohei Tamada, Misaki Nakai, Tatsuo Yajima, Koichi Mitsudo, Yukiyasu Kashiwagi
Colorants<\/em> 2022<\/strong>, 1<\/em>, 354\u2013362
DOI: 10.3390\/colorants1030021<\/a><\/p>\r\n

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(81) An Efficient Protocol for Selective Silylation of Hydroxy Group Using N<\/em>,O<\/em>-Bis(tert<\/em>-butyldimethylsilyl)acetamide and N<\/em>,N<\/em>-Dimethyl-4-aminopyridine N<\/em>-Oxide<\/strong>
Hiroki Mandai,* Yuichiro Matsuura, Fatin Mahfuzah Binti Johari, Koichi Mitsudo, Seiji Suga*
Chem. Lett.<\/em> 2022<\/strong>, 51, 953\u2013956.
DOI: 10.1246\/cl.220281<\/a>
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(80) Near-Infrared Absorbing Molecule Based on Triphenylamine-Radical Cation with Extended Homoaryl \u03c0-System<\/strong>
Masafumi Yano,* Kohei Tamada, Misaki Nakai, Koichi Mitsudo, Yukiyasu Kashiwagi
Colorants<\/em> 2022<\/strong>, 1<\/em>, 226\u2013235.
DOI: 10.3390\/colorants1020014<\/a>
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(79) Electro-oxidative Trimerization of 1,2-Dimethoxybenzene: Reductive Workup Strategy and Alternating Current Electrolysis to Peel off the Precipitated Radical Cation Ion Pair<\/strong>
Eisuke Sato, Yuta Niki, Koichi Mitsudo, Seiji Suga*
Chem. Lett.<\/em> 2022<\/strong>, 51<\/em>, 629\u2013632.
DOI: 10.1246\/cl.220112<\/a>
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(78) Near-Infrared Absorption of a Benzothiophene-Appended Triphenylamine Radical Cation: a Novel Molecular Design of NIR-II Dye
<\/strong>Masafumi Yano,* Yoshinori Inada, Yuki Hayashi, Misaki Nakai, Koichi Mitsudo, Yukiyasu Kashiwagi
<\/strong>Dyes Pigm.<\/em> 2022<\/strong>, 197<\/em>, 109929.
DOI: 10.1016\/j.dyepig.2021.109929<\/a>
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(77) Application of an Electrochemical Microflow Reactor for Cyanosilylation: Machine Learning-Assisted Exploration of Suitable Reaction Conditions for Semi-Large Scale Synthesis<\/strong>
Eisuke Sato, Mayu Fujii, Hiroki Tanaka, Koichi Mitsudo, Masaru Kondo, Shinobu Takizawa, Hiroaki Sasai, Takeshi Washio, Kazunori Ishikawa, Seiji Suga*
J. Org. Chem.<\/em> 2021<\/strong>, 86<\/em>, 16035\u201316044.
DOI: 10.1021\/acs.joc.1c01242<\/a>
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(76) Synthesis, Optical and Electrochemical Properties of 4,4′-Bibenzo[c<\/em>]thiophene Derivatives<\/strong>
Kotaro Obayashi, Keiichi Imato, Satoshi Aoyama, Toshiaki Enoki, Seiji Akiyama, Mio Ishida, Seiji Suga, Koichi Mitsudo, Yousuke Ooyama*
RSC Adv.<\/em> 2021<\/strong>, 11<\/em>, 18870\u201318880
DOI: 10.1039\/D1RA01189H\u00a0<\/a>
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(75) Cu-Catalyzed Dehydrogenative C\u2013O Cyclization for the Synthesis of Furan-Fused Thienoacenes<\/strong>
Koichi Mitsudo,* Yoshiaki Kobashi, Kaito Nakata, Yuji Kurimoto, Eisuke Sato, Hiroki Mandai, Seiji Suga*
Org. Lett.<\/em> 2021<\/strong>, 23<\/em>, 4322\u20134326.
DOI: 10.1021\/acs.orglett.1c01256<\/a><\/p>\r\n

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(74) Electrosynthesis of Phosphacycles via Dehydrogenative C\u2013P Bond Formation Using DABCO as a Mediator
<\/strong>Yuji Kurimoto, Jun Yamashita, Koichi Mitsudo,* Eisuke Sato, Seiji Suga*
Org. Lett.<\/em> 2021<\/strong>, 23<\/em>, 3120\u20133124.
DOI: 10.1021\/acs.orglett.1c00807<\/a>
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(73) Acylative Desymmetrization of Glycerol Derivatives by Chiral DMAP Derivatives
<\/strong>Hiroki Mandai,* Kosuke Ashihara, Koichi Mitsudo, Seiji Suga*
Heterocycles<\/em> 2021<\/strong>, 102<\/em>, 1083\u20131090.
DOI: 10.3987\/COM-21-14433<\/a>
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(72) Kinetic Resolution of Tertiary Alcohols by Chiral DMAP Derivatives: Enantioselective Access to 3-Hydroxy-3-Substituted 2-Oxindoles<\/strong>
Hiroki Mandai,* Ryuhei Shiomoto, Kazuki Fujii, Koichi Mitsudo, Seiji Suga*
Org. Lett.<\/em> 2021<\/strong>, 23<\/em>, 1169\u20131174.
DOI: 10.1021\/acs.orglett.0c03956<\/a>
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(71) Acylative Desymmetrization of Cyclic meso<\/em>-1,3-Diols by Chiral DMAP Derivatives<\/strong>
Hiroki Mandai,* Tsubasa Hironaka, Koichi Mitsudo, Seiji Suga*
Chem. Lett.<\/em> 2021<\/strong>, 50<\/em>, 471\u2013474.
DOI: 10.1246\/cl.200809<\/a>
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(70) Synthesis of 9-Substituted Fluorenols and Heteroring-fused Analogues by Intramolecular C\u2013H Functionalization
<\/strong>Yuji Kurimoto, Koichi Mitsudo,* Seiji Suga*
Chem. Lett.<\/em> 2021<\/strong>, 50<\/em>, 378\u2013381.
DOI: 10.1246\/cl.200807<\/a>
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(69) Integrated Synthesis of Thienyl Thioethers and Thieno[3,2-b<\/em>]thiophenes via Benzothiophen-3(2H<\/em>)-ones<\/strong>
Koichi Mitsudo,* Nanae Habara, Yoshiaki Kobashi, Yuji Kurimoto, Hiroki Mandai, Seiji Suga*
Synlett<\/em> 2020<\/strong>, 31<\/em>, 1947\u20131952.
DOI: 10.1055\/s-0040-1707280<\/a>
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(68) Crystal structure of tris[4-(naphthalen-1-yl)phenyl]amine
<\/strong>Masafumi Yano,* Yukiyasu Kashiwagi, Yoshinori Inada, Yuki Hayashi, Koichi Mitsudo, Koji Kubono
Acta Crystallogr., Sect. E<\/em> 2020<\/strong>, 76<\/em>, 1649\u20131652.<\/span>
DOI: 10.1107\/S2056989020012529<\/a><\/span><\/p>\r\n

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(67) Photo- and Redox-Active Benzofuran-Appended Triphenylamine and Near-Infrared Absorption of Its Radical Cation<\/strong>
Masafumi Yano,* Yoshinori Inada, Yuki Hayashi, Tatsuo Yajima, Koichi Mitsudo, Yukiyasu Kashiwagi
Chem. Lett.<\/em> 2020<\/strong>, 49<\/em>, 685\u2013688.
DOI: 10.1246\/cl.200161<\/a>
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(66) Electrochemical Synthesis of Thienoacene Derivatives: Transition Metal-Free Dehydrogenative C\u2013S Coupling Promoted by a Halogen Mediator<\/strong>
Koichi Mitsudo,* Ren Matsuo, Toki Yonezawa, Haruka Inoue, Hiroki Mandai, Seiji Suga*
Angew. Chem., Int. Ed.<\/em> 2020<\/strong>, 59<\/em>, 7803\u20137807.
DOI: 10.1002\/anie.202001149<\/a>
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(65) 1,10-Phenanthroline- or Electron-Promoted Cyanation of Aryl Iodides<\/strong>
Koichi Mitsudo,* Kazuki Yoshioka, Takayuki Hirata, Hiroki Mandai, Koji Midorikawa, Seiji Suga*
Synlett<\/em> 2019<\/strong>, 30<\/em>, 1209\u20131214.
DOI: 10.1055\/s-0037-1611793<\/a>
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(64) Iodide-Mediated or Iodide-Catalyzed Demethylation and Friedel\u2013Crafts C\u2013H Borylative Cyclization Leading to Thiophene-Fused 1,2-Oxaborine Derivatives<\/strong>
Keisuke Shigemori, Momoka Watanabe, Julie Kong, Koichi Mitsudo,* Atsushi Wakamiya, Hiroki Mandai, Seiji Suga*
Org. Lett.<\/em> 2019<\/strong>, 21<\/em>, 2171\u20132175.
DOI: 10.1021\/acs.orglett.9b00485<\/a>
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(63) Enantioselective Acyl Migration Reactions of Furanyl Carbonates with Chiral DMAP Derivatives<\/strong>
Kazuki Fujii, Koichi Mitsudo, Hiroki Mandai,* Toshinobu Korenaga, Seiji Suga*
Chem. Eur. J.<\/em> 2019<\/strong>, 25<\/em>, 2208\u20132212.
DOI: 10.1002\/chem.201806050<\/a>
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(62) Synthesis and Properties of Dithieno-Fused 1,4-Azaborine Derivatives<\/strong>
Koichi Mitsudo,* Keisuke Shigemori, Hiroki Mandai, Atsushi Wakamiya, Seiji Suga*
Org. Lett.<\/em> 2018<\/strong>, 20<\/em>, 7336\u20137340.
DOI: 10.1021\/acs.orglett.8b03316<\/a>
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(61) Enantioselective Desymmetrization of 1,3-Diols by a Chiral DMAP Derivative<\/strong>
Hiroki Mandai,* Kosuke Ashihara, Koichi Mitsudo, Seiji Suga*
Chem. Lett.<\/em> 2018<\/strong>, 47<\/em>, 1360\u20131363.
DOI: 10.1246\/cl.180697<\/a>
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(60) Dynamic Kinetic Resolution of Azlactones by a Chiral N<\/em>,N<\/em>-Dimethyl-4-aminopyridine Derivative Containing a 1,1\u02b9-Binaphthyl Unit: Importance of Amide Groups<\/strong>
Hiroki Mandai,* Kohei Hongo, Takuma Fujiwara, Kazuki Fujii, Koichi Mitsudo, Seiji Suga*
Org. Lett.<\/em> 2018<\/strong>, 20<\/em>, 4811\u20134814.
DOI: 10.1021\/acs.orglett.8b01960<\/a>
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(59) Cu\/Fe\/O=PPh3<\/sub>-Catalyzed Etherification for the Synthesis of Aryl 3-Benzo[b<\/em>]thienyl Ethers<\/strong>
Koichi Mitsudo,* Takuya Asada, Tomohiro Inada, Yuji Kurimoto, Hiroki Mandai, Seiji Suga*
Chem. Lett.<\/em> 2018<\/strong>, 47<\/em>, 1044\u20131047.
DOI: 10.1246\/cl.180425<\/a>
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(58) Efficient Synthesis and Properties of [1]Benzothieno[3,2-b<\/em>]thieno[2,3-d<\/em>]furans and [1]Benzothieno[3,2-b<\/em>]thieno[2,3-d<\/em>]thiophenes<\/strong>
Yuji Kurimoto, Koichi Mitsudo,* Hiroki Mandai, Atsushi Wakamiya, Yasujiro Murata, Hiroki Mori, Yasushi Nishihara, Seiji Suga*
Asian J. Org. Chem.<\/em> 2018<\/strong>, 7<\/em>, 1635\u20131641.
DOI: 10.1002\/ajoc.201800270<\/a>
Selected as a Cover Feature (DOI: 10.1002\/ajoc.201800442<\/a>)
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(57) Stereoselective Nucleophilic Additions to Cyclic N<\/em>-Acyliminium Ions Using the Indirect Cation Pool Method: Elucidation of Stereoselectivity by Spectroscopic Conformational Analysis and DFT Calculations<\/strong>
Koichi Mitsudo, Junya Yamamoto, Tomoya Akagi, Atsuhiro Yamashita, Masahiro Haisa, Kazuki Yoshioka, Hiroki Mandai, Koji Ueoka, Christian Hempel, Jun-ichi Yoshida, Seiji Suga*
Beilstein J. Org. Chem.<\/em> 2018<\/strong>, 14<\/em>, 1192\u20131202.
DOI: 10.3762\/bjoc.14.100<\/a>
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(56) Regioselective DMAD-Insertion Reaction of Silyl Dienol Ether of \u03b3-Pyrone under Catalyst- and Heating-free Conditions<\/strong>
Ichiro Hayakawa,* Yuji Yamanaka, Koichi Mitsudo, Hiromi Ota, Akira Sakakura*
Heterocycles<\/em> 2017<\/strong>, 94<\/em>, 2299\u20132306.
DOI: 10.3987\/COM-17-13820<\/a>
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(55) Desymmetrization of meso-1,2-Diols by a Chiral N<\/em>,N<\/em>-4-Dimethylaminopyridine Derivative Containing a 1,1′-Binaphthyl Unit: Importance of the Hydroxy Groups<\/strong>
Hiroki Mandai,* Hiroshi Yasuhara, Kazuki Fujii, Yukihito Shimomura, Koichi Mitsudo, Seiji Suga*
J. Org. Chem.<\/em> 2017<\/strong>, 82<\/em>, 6846\u20136856.
DOI: 10.1021\/acs.joc.7b00992<\/a>
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(54) Synthesis of 3-Benzo[b<\/em>]thienyl 3-Thienyl Ether via an Addition\u2013Elimination Reaction and Its Transformation to an Oxygen-Fused Dithiophene Skeleton: Synthesis and Properties of Benzodithienofuran and Its \u03c0-Extended Derivatives<\/strong>
Koichi Mitsudo,* Yuji Kurimoto, Hiroki Mandai, Seiji Suga*
Org. Lett.<\/em> 2017<\/strong>, 19<\/em>, 2821\u20132824.
DOI: 10.1021\/acs.orglett.7b00969<\/a>
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(53) Rh-Catalyzed Dehydrogenative Cyclization Leading to Benzosilolothiophene Derivatives via Si\u2013H\/C\u2013H Bond Cleavage<\/strong>
Koichi Mitsudo,* Seiichi Tanaka, Ryota Isobuchi, Tomohiro Inada, Hiroki Mandai, Toshinobu Korenaga, Atsushi Wakamiya, Yasujiro Murata, Seiji Suga*
Org. Lett.<\/em> 2017<\/strong>, 19<\/em>, 2564\u20132567.
DOI: 10.1021\/acs.orglett.7b00878<\/a>
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(52) Hydrogen Bonding-Assisted Enhancement of the Reaction Rate and Selectivity in the Kinetic Resolution of d,l-1,2-Diols with Chiral Nucleophilic Catalysts<\/strong>
Kazuki Fujii, Koichi Mitsudo, Hiroki Mandai,* Seiji Suga*
Adv. Synth. Catal.<\/em> 2017<\/strong>, 359<\/em>, 2778\u20132788.
DOI: 10.1002\/adsc.201700057<\/a>
\"ads2017\"<\/p>\r\n

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(51) An Intramolecular Nucleophile-Catalyzed Aldol-Lactonization (NCAL) Reaction of S<\/em>-Aryl-(E<\/em>)-6-oxohex-2-enethioate with N<\/em>,N<\/em>-4-Dimethylaminopyridine N<\/em>-Oxide<\/strong>
Hiroki Mandai,* Keita Shimowaki, Kohei Hongo, Koichi Mitsudo, Seiji Suga*
Heterocycles<\/em> 2017<\/strong>, 94<\/em>, 492\u2013502.
DOI: 10.3987\/COM-16-13614<\/a>
\"Heterocycles2017\"<\/p>\r\n

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(50) Facile Synthesis of Naphthothiophenone Derivatives and Anthradithiophenedione via Friedel\u2013Crafts Acylation and Their Fundamental Properties<\/strong>
Koichi Mitsudo,* Takashi Murakami, Takuya Shibasaki, Tomohiro Inada, Hiroki Mandai, Hiromi Ota, Seiji Suga*
Synlett<\/em> 2016<\/strong>, 27<\/em>, 2327\u20132332.
DOI: 10.1055\/s-0035-1562470<\/a>
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(49) Kinetic Resolution of Secondary Carbinols by a Chiral N,N-4-Dimethylaminopyridine Derivative Containing a 1,1\u2032-Binaphthyl Unit: Hydrogen Bonding Affects Catalytic Activity and Enantioselectivity<\/strong>
Kazuki Fujii, Koichi Mitsudo, Hiroki Mandai,* Seiji Suga*
Bull. Chem. Soc. Jpn.<\/em> 2016<\/strong>, 89<\/em>, 1081\u20131092.
DOI: 10.1246\/bcsj.20160135<\/a><\/p>\r\n

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(48) Enantioselective Acyl Transfer Catalysis by a Combination of Common Catalytic Motifs and Electrostatic Interactions<\/strong>
Hiroki Mandai,* Kazuki Fujii, Hiroshi Yasuhara, Kenko Abe, Koichi Mitsudo, Toshinobu Korenaga, Seiji Suga*
Nat. Commun.<\/em> 2016<\/strong>, 7<\/em>, 11297.
DOI: 10.1038\/ncomms11297<\/a><\/p>\r\n

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(47) Facile Synthesis of 1,4-Bis(diaryl)-1,3-butadiynes Bearing Two Amino Moieties by Electrochemical Reaction Site Switching, and Their Solvatochromic Fluorescence<\/strong>
Natsuyo Kamimoto, Nariaki Nakamura, Akina Tsutsumi, Hiroki Mandai, Koichi Mitsudo,* Atsushi Wakamiya, Yasujiro Murata, Jun-ya Hasegawa, Seiji Suga*
Asian J. Org. Chem.<\/em> 2016<\/strong>, 5<\/em>, 373\u2013379.
DOI: 10.1002\/ajoc.201500502<\/a>
Selected as an Inside Cover<\/p>\r\n

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(46) Bacteriogenic Iron Oxide as an Effective Catalyst for Baeyer\u2013Villiger Oxidation with Molecular Oxygen and Benzaldehyde<\/strong>
Kyoko Mandai, Minae Hanata, Koichi Mitsudo, Hiroki Mandai, Seiji Suga,* Hideki Hashimoto, Jun Takada
Tetrahedron<\/em> 2015<\/strong>, 71<\/em>, 9403\u20139407.
DOI: 10.1016\/j.tet.2015.10.057<\/a><\/p>\r\n

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(45) Synthesis and Properties of Ethene-Bridged Terthiophenes<\/strong>
Koichi Mitsudo,* Hidehiko Sato, Arata Yamasaki, Natsuyo Kamimoto, Jun Goto, Hiroki Mandai, Seiji Suga*
Org. Lett.<\/em> 2015<\/strong>, 17<\/em>, 4858\u20134861.
DOI: 10.1021\/acs.orglett.5b02417<\/a><\/p>\r\n

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(44) Enantioselective Steglich Rearrangement of Oxindole Derivatives by Easily Accessible Chiral N,N-4-(Dimethylamino)pyridine Derivatives<\/strong>
Hiroki Mandai,* Takuma Fujiwara, Katsuaki Noda, Kazuki Fujii, Koichi Mitsudo, Toshinobu Korenaga, Seiji Suga*
Org. Lett.<\/em> 2015<\/strong>, 17<\/em>, 4436\u20134439.
DOI: 10.1021\/acs.orglett.5b02089<\/a><\/p>\r\n

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(43) Palladium-Catalyzed Domino C\u2013H\/N\u2013H Functionalization: An Efficient Approach to Nitrogen-Bridged Heteroacenes<\/strong>
Natsuyo Kamimoto, Dieter Schollmeyer, Koichi Mitsudo, Seiji Suga, Siegfried R. Waldvogel*
Chem. – Eur. J.<\/em> 2015<\/strong>, 21<\/em>, 8257\u20138261.
DOI: 10.1002\/chem.201500897<\/a><\/p>\r\n

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(42) An Efficient Petasis Boronic-Mannich Reaction of Chiral Lactol Derivatives Prepared from D-Araboascorbic Acid<\/strong>
Hiroki Mandai,* Hiroshi Yamada, Keita Shimowaki, Koichi Mitsudo, Seiji Suga*
Synthesis<\/em> 2014<\/strong>, 46<\/em>, 2672\u20132681.
DOI: 10.1055\/s-0034-1378900<\/a><\/p>\r\n

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(41) Synthetic (+)-Terrein Suppresses Interleukin-6\/soluble Intereleukin-6 Receptor Induced-secretion of Vascular Endothelial Growth Factor in Human Gingival Fibroblasts<\/strong>
Hiroki Mandai,* Kazuhiro Omori, Daisuke Yamamoto, Toki Tsumura, Kyouta Murota, Satoshi Yamamoto, Koichi Mitsudo, Soichiro Ibaragi, Akira Sasaki, Hiroshi Maeda, Shogo Takashiba, Seiji Suga*
Bioorg. Med. Chem.<\/em> 2014<\/strong>, 22<\/em>, 5338\u20135344.
DOI: 10.1016\/j.bmc.2014.07.047<\/a><\/p>\r\n

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(40) Remarkable Enhancement of the Rate of the Intramolecular Morita-Baylis-Hillman Reaction by the Combination of a Nucleophilic Catalyst and 1,3-Diphenyl-2-thiourea<\/strong>
Hiroki Mandai,* Keita Shimowaki, Koichi Mitsudo, Seiji Suga*
Asian J. Org. Chem.<\/em> 2014<\/strong>, 3<\/em>, 437\u2013441.
DOI: 10.1002\/ajoc.201402001<\/a><\/p>\r\n

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(39) Electro-reductive Halogen\u2013Deuterium Exchange and Methylation of Aryl Halides in Acetonitrile<\/strong>
Koichi Mitsudo,* Takahiro Okada, Shuichi Shimohara, Hiroki Mandai, Seiji Suga*
Electrochemistry<\/em> 2013<\/strong>, 81<\/em>, 362\u2013364.
DOI: 10.5796\/electrochemistry.81.362<\/a><\/p>\r\n

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(38) Recyclable Palladium Catalyst in PEG\/CH3<\/sub>CN Biphasic System for Electro-oxidative Wacker-type Reaction<\/strong>
Koichi Mitsudo,* Satoshi Fukunaga, Tomoya Fujita, Hiroki Mandai, Seiji Suga, Hideo Tanaka*
Electrochemistry<\/em> 2013<\/strong>, 81<\/em>, 347\u2013349.
DOI: 10.5796\/electrochemistry.81.347<\/a><\/p>\r\n

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(37) Synthesis of Hexa(furan-2-yl)benzenes and Their \u03c0-Extended Derivatives
<\/strong>Koichi Mitsudo,* Jyunji Harada, Yo Tanaka, Hiroki Mandai, Chie Nishioka, Hideo Tanaka, Atsushi Wakamiya, Yasujiro Murata, Seiji Suga*
J. Org. Chem.<\/em> 2013<\/strong>, 78<\/em>, 2763\u20132768.
DOI: 10.1021\/jo302652r<\/a>
Highlighted in SYNFACTS. Swager, T. M.; Belger, C. Synfacts<\/em> 2013, 9<\/em>, 0615.<\/p>\r\n

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(36) Kinetic Resolution of Secondary Alcohols by Chiral DMAP Derivatives Prepared by the Ugi Multicomponent Reaction<\/strong>
Hiroki Mandai,* Shunsuke Irie, Masaru Akehi, Kazunobu Yuri, Masaaki Yoden, Koichi Mitsudo, Seiji Suga*
Heterocycles<\/em> 2013<\/strong>, 87<\/em>, 329\u2013340.
DOI: 10.3987\/COM-12-12624<\/a><\/p>\r\n

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(35) Electro-reductive Cyclization of Aryl Halides Promoted by Fluorene Derivatives<\/strong>
Koichi Mitsudo,* Yumiko Nakagawa, Jun-ichi Mizukawa, Hideo Tanaka, Ryoichi Akaba, Takahiro Okada, Seiji Suga*
Electrochim. Acta<\/em> 2012<\/strong>, 82<\/em>, 444\u2013449.
DOI: 10.1016\/j.electacta.2012.03.130<\/a><\/p>\r\n

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(34) Site-selective Sequential Coupling Reactions Controlled by \u201cElectrochemical Reaction Site Switching\u201d: a Straightforward Approach to 1,4-Bis(diaryl)buta-1,3-diynes<\/strong>
Koichi Mitsudo,* Natsuyo Kamimoto, Hiroki Murakami, Hiroki Mandai, Atsushi Wakamiya, Yasujiro Murata, Seiji Suga*
Org. Biomol. Chem.<\/em> 2012<\/strong>, 10<\/em>, 9562\u20139569.
DOI: 10.1039\/C2OB26567B<\/a><\/p>\r\n

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(33) Kinetic Resolution of Secondary Alcohols by the Combination of a Chiral Br\u00f8nsted Acid, DABCO, and Acetyl Chloride<\/strong>
Hiroki Mandai,* Kyouta Murota, Koichi Mitsudo, Seiji Suga*
Org. Lett.<\/em> 2012<\/strong>, 14<\/em>, 3486\u20133489.
DOI: 10.1021\/ol301373x<\/a><\/p>\r\n

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(32) Synthesis of Nitrogen-Bridged Terthiophenes by Tandem Buchwald\u2013Hartwig Coupling and Their Properties<\/strong>
Koichi Mitsudo,* Shuichi Shimohara, Jun Mizoguchi, Hiroki Mandai, Seiji Suga*
Org. Lett.<\/em> 2012<\/strong>, 14<\/em>, 2702\u20132705.
DOI: 10.1021\/ol300887t<\/a><\/p>\r\n

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(31) Synthetic Studies of DMAP Derivatives by Diastereoselective Ugi Reaction<\/strong>
Hiroki Mandai,* Shunsuke Irie, Koichi Mitsudo, Seiji Suga*
Molecules<\/em> 2011<\/strong>, 16<\/em>, 8815\u20138832.
DOI: 10.3390\/molecules16108815<\/a><\/p>\r\n

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(30) Kumada-Tamao-Corriu Coupling Using N-Heterocyclic Carbene Ligands Bearing Pyridyl Group and Ethylenedioxyl Moiety<\/strong>
Koichi Mitsudo,* Yuta Doi, Syunsuke Sakamoto, Hiroki Murakami, Hiroki Mandai, Seiji Suga*
Chem. Lett.<\/em> 2011<\/strong>, 40<\/em>, 936\u2013938.
DOI: 10.1246\/cl.2011.936<\/a><\/p>\r\n

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(29) Electrochemical Generation of Silver Acetylides from Terminal Alkynes with a Ag Anode and Integration into Sequential Pd-Catalysed Coupling with Arylboronic Acids<\/strong>
Koichi Mitsudo,* Takuya Shiraga, Jun-ichi Mizukawa, Seiji Suga, Hideo Tanaka*
Chem. Commun.<\/em> 2010<\/strong>, 46<\/em>, 9256\u20139258.
DOI: 10.1039\/C0CC02633F<\/a><\/p>\r\n

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(28) Synthesis and Oxidative Polymerization of Dialkyl Fluorene-9,9-dicarboxylates<\/strong>
Yanying Zhang, Song Tu, Koichi Mitsudo, Hideo Tanaka,* Shunzo Suematsu, Kenji Machida, Daisuke Horii, Shuichi Ishimoto, Kenji Tamamitsu
Tetrahedron Lett.<\/em> 2009<\/strong>, 50<\/em>, 6057\u20136059.
DOI: 10.1016\/j.tetlet.2009.08.052<\/a><\/p>\r\n

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(27) Pd\/TEMPO-Catalyzed Electrooxidative Synthesis of Biaryls from Arylboronic Acids or Arylboronic Esters<\/strong>
Koichi Mitsudo,* Takuya Shiraga, Daisuke Kagen, Deqing Shi, James Y. Becker, Hideo Tanaka*
Tetrahedron<\/em> 2009<\/strong>, 65<\/em>, 8384\u20138388.
DOI: 10.1016\/j.tet.2009.08.004<\/a><\/p>\r\n

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(26) Preparation of a Cationic Bisoxazolinic Nickel Pincer Catalyst and Its Applications to Michael Addition and Mizoroki\u2013Heck Reaction<\/strong>
Koichi Mitsudo,* Tatsuhiko Imura, Takashi Yamaguchi, Hideo Tanaka*
Tetrahedron Lett.<\/em> 2008<\/strong>, 49<\/em>, 7287\u20137289.
DOI: 10.1016\/j.tetlet.2008.10.029<\/a><\/p>\r\n

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(25) Pd\/TEMPO Double-mediatory Electrooxidative Wacker-type Cyclizations<\/strong>
Koichi Mitsudo,* Toru Ishii, Hideo Tanaka*
Electrochemistry<\/em> 2008<\/strong>, 76<\/em>, 859\u2013861.
DOI: 10.5796\/electrochemistry.76.859<\/a><\/p>\r\n

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(24) Electrooxidative Homo-coupling of Arylboronic Acids Catalyzed by Electrogenerated Cationic Palladium Catalysts<\/strong>
Koichi Mitsudo,* Takuya Shiraga, Hideo Tanaka*
Tetrahedron Lett.<\/em> 2008<\/strong>, 49<\/em>, 6593\u20136595.
DOI: 10.1016\/j.tetlet.2008.09.022<\/a><\/p>\r\n

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(23) RhCl3<\/sub>\/Amine-Catalyzed [2 + 2 + 2] Cyclization of Alkynes<\/strong>
Kenta Yoshida, Ichiro Morimoto, Koichi Mitsudo,* Hideo Tanaka*
Tetrahedron<\/em> 2008<\/strong>, 64<\/em>, 5800\u20135807.
DOI: 10.1016\/j.tet.2008.03.079<\/a><\/p>\r\n

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(22) Facile Synthetic Procedure for and Electrochemical Properties of Hexa(2-thienyl)benzenes Directed towards Electroactive Materials<\/strong>
Kenta Yoshida, Ichiro Morimoto, Koichi Mitsudo,* Hideo Tanaka*
Tetrahedron Lett.<\/em> 2008<\/strong>, 49<\/em>, 2363\u20132365.
DOI: 10.1016\/j.tetlet.2008.02.069<\/a><\/p>\r\n

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(21) Anionic WS-TEMPO-mediatory Electrooxidation of Alcohols in Water: Halide-free Oxidation Directed towards a Totally Closed System<\/strong>
Koichi Mitsudo, Hiroki Kumagai, Fumiko Takabatake, Jun Kubota, Hideo Tanaka*
Tetrahedron Lett.<\/em> 2007<\/strong>, 48<\/em>, 8994\u20138997.
DOI: 10.1016\/j.tetlet.2007.10.088<\/a><\/p>\r\n

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(20) RhCl3<\/sub>\/Amine-catalyzed Cyclotrimerization of Alkynes<\/strong>
Kenta Yoshida, Ichiro Morimoto, Koichi Mitsudo, Hideo Tanaka*
Chem. Lett.<\/em> 2007<\/strong>, 36<\/em>, 998\u2013999.
DOI: 10.1246\/cl.2007.998<\/a><\/p>\r\n

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(19) Electrochemical Generation of Cationic Pd Catalysts and Application to Pd\/TEMPO Double-Mediatory Electrooxidative Wacker-type Reactions<\/strong>
Koichi Mitsudo,* Takashi Kaide, Eriko Nakamoto, Kenta Yoshida, Hideo Tanaka*
J. Am. Chem. Soc.<\/em> 2007<\/strong>, 129<\/em>, 2246\u20132247.
DOI: 10.1021\/ja069043r<\/a><\/p>\r\n

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(18) Electropolymerization of 9,9-Dialkyl-substituted Fluorenes with Long Alkyl Chains and Redox Responses of the Resulted Electroactive Films for Electrochemical Capacitor Materials<\/strong>
Shunzo Suematsu,* Koichi Mitsudo, Fumiaki Katagiri, Hideo Tanaka*
Electrochemistry<\/em>\u00a02007<\/strong>, 75<\/em>, 54\u201357.
DOI: 10.5796\/electrochemistry.75.54<\/a><\/p>\r\n

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(17) Selectively Substituted Thiophenes and Indoles by a Tandem Palladium Catalyzed Multicomponent Reaction<\/strong>
Koichi Mitsudo, Praew Thansandote, Thorsten Wilhelm, Brian Mariampillai, Mark Lautens*<\/strong>
Org. Lett.<\/em> 2006<\/strong>, 8<\/em>, 3939\u20133942.
DOI: 10.1021\/ol061373t<\/a><\/p>\r\n

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(16) Synthesis of 2\u2032,3\u2032-Dideoxynucleosides via C\u2013S Bond Cleavage: N-Glycosylation of 2,3-Dideoxy-1-[(2-pyridylmethyl)thio]glycoside<\/strong>
Koichi Mitsudo, Wataru Matsuda, Seiji Miyahara, Hideo Tanaka*
Tetrahedron Lett.<\/em> 2006<\/strong>, 47<\/em>, 5147\u20135150.
DOI: 10.1016\/j.tetlet.2006.05.060<\/a><\/p>\r\n

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(15) Water-soluble N-Oxyl Compounds-mediated Electrooxidation of Alcohols in Water: a Prominent Access to a Totally Closed System.<\/strong>
Jun Kubota, Yusuke Shimizu, Koichi Mitsudo, Hideo Tanaka*
Tetrahedron Lett.<\/em> 2005<\/strong>, 46<\/em>, 8975\u20138979.
DOI: 10.1016\/j.tetlet.2005.10.114<\/a><\/p>\r\n

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(14) Electrooxidative Glycosylation through C\u2013S Bond Cleavage of 1-Arylthio-2,3-dideoxyglycosides. Synthesis of 2′,3′-Dideoxynucleosides<\/strong>
Koichi Mitsudo, Takashi Kawaguchi, Seiji Miyahara, Wataru Matsuda, Manabu Kuroboshi, Hideo Tanaka*
Org. Lett.<\/em> 2005<\/strong>, 7<\/em>, 4649\u20134652.
DOI: 10.1021\/ol051776d<\/a><\/p>\r\n

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(13) Catalytic Intermolecular Pauson\u2013Khand-type Reaction: Strong Directing Effect of Pyridylsilyl and Pyrimidylsilyl Groups and Isolation of Ru Complexes Relevant to Catalytic Reaction<\/strong>
Kenichiro Itami,* Koichi Mitsudo, Kazuyoshi Fujita, Youichi Ohashi, Jun-ichi Yoshida*
J. Am. Chem. Soc.<\/em> 2004<\/strong>, 126<\/em>, 11058\u201311066.
DOI: 10.1021\/ja047484+<\/a><\/p>\r\n

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(12) A Pyridylsilyl Group Expands the Scope of Catalytic Intermolecular Pauson-Khand Reactions<\/strong>
Kenichiro Itami,* Koichi Mitsudo, Jun-ichi Yoshida*
Angew. Chem., Int. Ed.<\/em> 2002<\/strong>, 41<\/em>, 3481\u20133484.
DOI: 10.1002\/1521-3773(20020916)41:18<3481::AID-ANIE3481>3.0.CO;2-X<\/a><\/p>\r\n

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(11) Metal-Catalyzed Hydrosilylation of Alkenes and Alkynes Using Dimethyl(pyridyl)silane<\/strong>
Kenichiro Itami, Koichi Mitsudo, Akira Nishino, Jun-ichi Yoshida*
J. Org. Chem.<\/em> 2002<\/strong>, 67<\/em>, 2645\u20132652.
DOI: 10.1021\/jo0163389<\/a><\/p>\r\n

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(10) Unusual Metal-Dependent Acceleration and Deceleration in the Metal-Catalyzed Hydrosilylation of Olefin Using Pyridyldimethylsilanes<\/strong>
Kenichiro Itami, Koichi Mitsudo, Akira Nishino, Jun-ichi Yoshida*
Chem. Lett.<\/em> 2001<\/strong>, 30<\/em>, 1088\u20131089.
DOI: 10.1246\/cl.2001.1088<\/a><\/p>\r\n

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(9) Diversity-Oriented Synthesis of Multisubstituted Olefins through the Sequential Integration of Palladium-Catalyzed Cross-Coupling Reactions. 2-Pyridyldimethyl(vinyl)silane as a Versatile Platform for Olefin Synthesis<\/strong>
Kenichiro Itami, Toshiki Nokami, Yoji Ishimura, Koichi Mitsudo, Toshiyuki Kamei, Jun-ichi Yoshida*
J. Am. Chem. Soc.<\/em> 2001<\/strong>, 123<\/em>, 11577\u201311585.
DOI: 10.1021\/ja016790+<\/a><\/p>\r\n

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(8) Directed Intermolecular Carbomagnesation Across Vinylsilanes: 2-PyMe2Si Group as a Removable Directing Group<\/strong>
Kenichiro Itami, Koichi Mitsudo, Jun-ichi Yoshida*
Angew. Chem., Int. Ed.<\/em> 2001<\/strong>, 40<\/em>, 2337\u20132339.
DOI: 10.1002\/1521-3773(20010618)40:12<2337::AID-ANIE2337>3.0.CO;2-Q<\/a><\/p>\r\n

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(7) Pyridyl Group Assisted Deprotonation of a Methyl Group on Silicon: Complex Induced Proximity Effect and Novel Hydroxymethylation<\/strong>
Kenichiro Itami, Toshiyuki Kamei, Koichi Mitsudo, Toshiki Nokami, Jun-ichi Yoshida*
J. Org. Chem.<\/em> 2001<\/strong>, 66<\/em>, 3970\u20133976.
DOI: 10.1021\/jo015528g<\/a><\/p>\r\n

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(6) Highly Efficient Carbopalladation Across Vinylsilane: Dual Role of the 2-PyMe2Si Group as a Directing Group and as a Phase Tag<\/strong>
Kenichiro Itami, Koichi Mitsudo, Toshiyuki Kamei, Tooru Koike, Toshiki Nokami, Jun-ichi Yoshida*
J. Am. Chem. Soc.<\/em> 2000<\/strong>, 122<\/em>, 12013\u201312014.
DOI: 10.1021\/ja002582q<\/a><\/p>\r\n

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(5) Oxidation of 2-Pyridyldimethylsilyl Group to Hydroxyl Group by H2O2\/KF. Implication of Fluoride Ion Accelerated 2-Pyridyl-Silyl Bond Cleavage<\/strong>
Kenichiro Itami, Koichi Mitsudo, Jun-ichi Yoshida*
J. Org. Chem.<\/em> 1999<\/strong>, 64<\/em>, 8709\u20138714.
DOI: 10.1021\/jo990740u<\/a><\/p>\r\n

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(4) Optical Resolution and Epimerization of Fluorosilane Having an Optically Active Amino Group: A New, Convenient Access to Optically Active Silicon Compounds<\/strong>
Atsushi Kawachi, Hirofumi Maeda, Koichi Mitsudo, Kohei Tamao*
Organometallics<\/em> 1999<\/strong>, 18<\/em>, 4530\u20134533.
DOI: 10.1021\/om9904394<\/a><\/p>\r\n

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(3) (2-Pyridyldimethylsilyl)methyl Lithium as a Novel Hydroxymethylating Reagent<\/strong>
Kenichiro Itami, Koichi Mitsudo, Jun-ichi Yoshida*
Tetrahedron Lett.<\/em> 1999<\/strong>, 40<\/em>, 5537\u20135540.
DOI: 10.1016\/S0040-4039(99)01028-X<\/a><\/p>\r\n

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(2) Facile Generation of \u03b1-Silyl Carbanion of Trimethylsilyl Group Assisted by Intramolecular Pyridyl Group Coordination<\/strong>
Kenichiro Itami, Koichi Mitsudo, Jun-ichi Yoshida*
Tetrahedron Lett.<\/em> 1999<\/strong>, 40<\/em>, 5533\u20135536.
DOI: 10.1016\/S0040-4039(99)01027-8<\/a><\/p>\r\n

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(1) 2-Pyridylsilyl Group as a Multifunctional “Phase Tag” for Solution Phase Synthesis<\/strong>
Jun-ichi Yoshida,* Kenichiro Itami, Koichi Mitsudo, Seiji Suga
Tetrahedron Lett.<\/em> 1999<\/strong>, 40<\/em>, 3403\u20133406.
DOI: 10.1016\/S0040-4039(99)00474-8<\/a><\/p>\r\n

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Reviews<\/h2>\r\n

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(R8) Electrochemical synthesis of heterocyclic compounds via carbon\u2013heteroatom bond formation: direct and indirect electrolysis
<\/strong>Yasuyuki Okumura, Eisuke Sato, Koichi Mitsudo,* Seiji Suga*
Chem. Lett.<\/em> 2024<\/strong>, 53<\/em>, upae146.
DOI: 10.1093\/chemle\/upae146<\/a><\/span><\/p>\r\n

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(R7) Electrochemical Coupling Reactions Using Non-Transition Metal Mediators: Recent Advances<\/strong>
Koichi Mitsudo,* Yasuyuki Okumura, Eisuke Sato, Seiji Suga*
Eur. J. Org. Chem.<\/em> 2023<\/strong>, e202300835.
DOI: 10.1002\/ejoc.202300835<\/a><\/p>\r\n

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(R6) Electro-oxidative Coupling Reactions Leading to \u03c0-Conjugated Compounds<\/strong>
Koichi Mitsudo*
Chem. Rec.<\/em> 2021<\/strong>, 21<\/em>, 2269\u20132276.
<\/span>DOI: 10.1002\/tcr.202100033<\/a><\/span><\/p>\r\n

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(R5) 2.9 Electrochemical Organic Synthesis via Radical Species in Free Radicals: Fundamentals and Applications in Organic Synthesis 2<\/strong>
Koichi Mitsudo and Seiji Suga
Science Synth.<\/em> 2020<\/strong>, 5.
DOI: 10.1055\/sos-SD-233-00170<\/a><\/p>\r\n

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(R4) <\/span>Miniaturization and Combinatorial Approach in Organic Electrochemistry
<\/b>Koichi Mitsudo, Yuji Kurimoto, Kazuki Yoshioka, Seiji Suga*
Chem. Rev.<\/i> 2018<\/b>, 118<\/i>, 5985\u20135999.
DOI: 10.1021\/acs.chemrev.7b00532<\/span><\/a><\/p>\r\n

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(R3) <\/span>Combinatorial electrochemistry for organic synthesis
<\/b>Koichi Mitsudo, Yuji Kurimoto, Kazuki Yoshioka, Seiji Suga*
Curr. Opin. Electrochem.<\/i> 2018<\/b>, 8<\/i>, 8\u201313.
DOI: 10.1016\/j.coelec.2017.10.026<\/span><\/a><\/p>\r\n

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(R2) <\/span>Design of Redox-Mediatory Systems for Electro-organic Synthesis
<\/b>Hideo Tanaka,* Manabu Kuroboshi, Koichi Mitsudo
Electrochemistry<\/i> 2009<\/b>, 77<\/i>, 1002\u20131009.
DOI: 10.5796\/electrochemistry.77.1002<\/span><\/a><\/p>\r\n

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(R1) <\/span>Pyridylsilyl Group-Driven Cross-Coupling Reactions
<\/b>Kenichiro Itami, Koichi Mitsudo, Toshiki Nokami, Toshiyuki Kamei, Tooru Koike, Jun-ichi Yoshida*
J. Organomet. Chem.<\/i> 2002<\/b>, 653<\/i>, 105\u2013113.
DOI: 10.1016\/S0022-328X(02)01173-7<\/span><\/a><\/p>\r\n

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\u65e5\u672c\u8a9e\u7dcf\u8aac\u3068\u7d39\u4ecb\u8a18\u4e8b<\/h2>\r\n

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(9) \u6a5f\u80fd\u6027\u5206\u5b50\u5408\u6210\u3092\u6307\u5411\u3057\u305f\u96fb\u6c17\u5316\u5b66\u7684\u306a\u70ad\u7d20-\u30d8\u30c6\u30ed\u539f\u5b50\u7d50\u5408\u5f62\u6210\u53cd\u5fdc<\/strong>
\u5149\u85e4\u8015\u4e00
\u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a\u8a8c 2025<\/strong>, 83<\/em>, 207\u2013217.<\/p>\r\n

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(8) \u6709\u6a5f\u96fb\u6c17\u5316\u5b66\u3068\u6709\u6a5f\u91d1\u5c5e\u5316\u5b66\u306b\u3088\u308b\u6709\u6a5f\u5408\u6210<\/strong>
\u5149\u85e4\u8015\u4e00
\u79d1\u5b66\u3068\u5de5\u696d 2022<\/strong>, 96<\/em>, 10\u201318.<\/p>\r\n

\r\n\r\n<\/p>\r\n

(7) \uff1c\u6700\u65b0\u306e\u30c8\u30d4\u30c3\u30af\u30b9\uff1e\u6709\u6a5f\u96fb\u89e3\u5408\u6210\u306e\u30eb\u30cd\u30b5\u30f3\u30b9\u2014\u96fb\u6c17\u3092\u4f7f\u3063\u305f\u70ad\u7d20\u30fc\u30d8\u30c6\u30ed\u539f\u5b50\u7d50\u5408\u5f62\u6210<\/strong>
\u5149\u85e4\u8015\u4e00\u30fb\u83c5\u8aa0\u6cbb
\u6708\u520a\u5316\u5b662020\u5e7410\u6708\u53f7<\/p>\r\n

\r\n\r\n<\/p>\r\n

(6) <\/strong>\u30de\u30a4\u30af\u30ed\u30d5\u30ed\u30fc\u96fb\u89e3\u5408\u6210\u306e\u7279\u9577\u3068\u6700\u65b0\u52d5\u5411
<\/strong>\u5149\u85e4\u8015\u4e00\u30fb\u5409\u5ca1\u548c\u7d00\u30fb\u83c5\u8aa0\u6cbb
\u6708\u520a\u30d5\u30a1\u30a4\u30f3\u30b1\u30df\u30ab\u30eb2018\u5e7412\u6708\u53f7<\/p>\r\n

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(5)<\/span> \u6709\u6a5f\u96fb\u89e3\u3068\u6709\u6a5f\u91d1\u5c5e\u306e\u5354\u594f\u7684\u30ec\u30c9\u30c3\u30af\u30b9\u5316\u5b66\u306b\u57fa\u3065\u304f\u5206\u5b50\u69cb\u7bc9
<\/strong>\u5149\u85e4\u8015\u4e00
\u5316\u5b66\u5de5\u696d<\/span> 2018\u5e74<\/span>11\u6708\u53f7<\/span><\/p>\r\n

\r\n\r\n<\/p>\r\n

(4) <\/span>\u96fb\u89e3\u767a\u751f\u30ab\u30c1\u30aa\u30f3\u6027\u30d1\u30e9\u30b8\u30a6\u30e0\u89e6\u5a92\u3092\u7528\u3044\u308b\u6709\u6a5f\u5408\u6210
<\/strong>\u5149\u85e4\u8015\u4e00\u30fb\u83c5\u8aa0\u6cbb
Electrochemistry<\/i> 2015<\/b>, 83<\/i>, 477\u2013482.<\/span><\/p>\r\n

\r\n\r\n<\/p>\r\n

(3) <\/span>\u96fb\u6c17\u5316\u5b66\u7684\u306a\u9178\u5316\u30d7\u30ed\u30bb\u30b9\u3092\u542b\u3080\u30ab\u30c3\u30d7\u30ea\u30f3\u30b0\u53cd\u5fdc\u306e\u958b\u767a\u3068\u62e1\u5f35\u03c0<\/span>\u96fb\u5b50\u7cfb\u5316\u5408\u7269\u5408\u6210\u3078\u306e\u5fdc\u7528<\/strong>
\u5149\u85e4\u8015\u4e00\u30fb\u7530\u4e2d\u79c0\u96c4\u30fb\u83c5\u8aa0\u6cbb
\u6709\u6a5f\u5408\u6210\u5316\u5b66\u5354\u4f1a\u8a8c<\/span> 2015<\/b>, 73<\/i>, 171\u2013180.<\/span><\/p>\r\n

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(2) <\/span>\uff1c\u6ce8\u76ee\u306e\u8ad6\u6587\uff1e\u30e1\u30bf\u30ce\u30fc\u30eb\u304b\u3089\u6c34\u7d20\u3092\u4f5c\u308b<\/strong>
\u5149\u85e4\u8015\u4e00
\u6708\u520a\u5316\u5b662013<\/span>\u5e748<\/span>\u6708\u53f7<\/p>\r\n

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(1) <\/span>\u6709\u6a5f\u91d1\u5c5e\u30cf\u30a4\u30e9\u30a4\u30c8 <\/span>\u300c\u30cf\u30ed\u30b2\u30f3\u5316\u30a2\u30ea\u30fc\u30eb\u306e\u89e6\u5a92\u7684\u30c8\u30ea\u30d5\u30eb\u30aa\u30ed\u30e1\u30c1\u30eb\u5316\u53cd\u5fdc\u300d<\/strong>
\u5149\u85e4\u8015\u4e00
Organometallic News<\/i> 2011<\/b> pp29<\/p>\r\n

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\u8457\u66f8<\/h2>\r\n

\r\n\r\n<\/p>\r\n

(2) Novel Electrolytic Processes<\/strong>
Koichi Mitsudo
Sustainable & Functional Redox Chemistry, Edited by Shinsuke Inagi, 2022 (RSC Book) Chapter 3 (\u5206\u62c5\u57f7\u7b46)<\/p>\r\n

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(1) \u62e1\u5f35\u03c0\u96fb\u5b50\u7cfb\u5206\u5b50\u306e\u96fb\u89e3\u5408\u6210<\/strong>
\u83c5 \u8aa0\u6cbb\u30fb\u5149\u85e4\u8015\u4e00
\u6709\u6a5f\u96fb\u89e3\u5408\u6210\u306e\u65b0\u6f6e\u6d41 \u76e3\u4fee\uff1a\u6df5\u4e0a\u5bff\u96c4\u3001\u8de1\u90e8\u771f\u4eba\u3001\u7a32\u6728\u4fe1\u4ecb\u30002021\u5e74 (\u30b7\u30fc\u30a8\u30e0\u30b7\u30fc\u51fa\u7248) \u7b2c18\u7ae0\uff08\u5206\u62c5\u57f7\u7b46\uff09<\/p>\r\n

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\u7279\u8a31<\/h2>\r\n

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(9) <\/strong>\u7279\u958b<\/strong>2020-059687<\/strong>\u3000\u300c\u30b7\u30a2\u30ce\u57fa\u3092\u6709\u3059\u308b\u82b3\u9999\u65cf\u5316\u5408\u7269\u306e\u88fd\u9020\u65b9\u6cd5\u300d
<\/strong>\u51fa\u9858\u65e5\u30002018\u5e7410\u670812\u65e5\uff08\u65e5\u5b9d\u5316\u5b66\u3001\u5ca1\u5c71\u5927\u5b66\uff09\u7dd1\u5ddd\u6643\u4e8c\u3001\u83c5\u8aa0\u6cbb\u3001\u5149\u85e4\u8015\u4e00\u3001\u842c\u4ee3\u5927\u6a39
2020\u5e744\u670816\u65e5\u516c\u958b<\/p>\r\n

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(8) <\/strong>\u7279\u958b<\/strong>2013-107845<\/strong>\u3000\u300c\u30d5\u30eb\u30aa\u30ec\u30f3\u8a98\u5c0e\u4f53\u53ca\u3073\u305d\u306e\u88fd\u9020\u65b9\u6cd5\u300d
<\/strong>\u51fa\u9858\u65e5\u30002011\u5e7411\u670818\u65e5\uff08\u65e5\u672c\u30b1\u30df\u30b3\u30f3\u3001\u5ca1\u5c71\u5927\u5b66\uff09\u5800\u4e95\u5927\u8f14\u3001\u672b\u677e\u4fca\u9020\u3001\u7389\u5149\u8ce2\u6b21\u3001\u7530\u4e2d\u79c0\u96c4\u3001\u9ed2\u661f\u5b66\u3001\u5149\u85e4\u8015\u4e00
2013\u5e746\u67086\u65e5\u516c\u958b<\/p>\r\n

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(7) <\/strong>\u518d\u8868<\/strong>2012\/176820<\/strong>\u300c\u7e2e\u5408\u8907\u7d20\u74b0\u5316\u5408\u7269\u304a\u3088\u3073\u305d\u306e\u91cd\u5408\u4f53\u300d
<\/strong>\u51fa\u9858\u65e5\u30002012\u5e746\u670820\u65e5 \uff08\u5ca1\u5c71\u5927\u5b66\u3001\u30af\u30e9\u30ec\uff09\u83c5 \u8aa0\u6cbb\u3001\u5149\u85e4\u8015\u4e00\u3001\u938c\u7530\u6cf0\u8f14\u3001\u9db4\u7530\u7f8e\u6a39\u3001\u5409\u672c\u7d14\u4e00\u3001\u6749\u5ca1\u5c1a
2012\u5e7412\u670827\u65e5\u516c\u958b<\/p>\r\n

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(6) <\/strong>\u7279\u958b<\/strong>2013-02585<\/strong>\u300c\u67b6\u6a4b\u6027\u30b8\u30c1\u30a8\u30ce\u30d4\u30ed\u30fc\u30eb\u5316\u5408\u7269\u304a\u3088\u3073\u305d\u306e\u91cd\u5408\u4f53\u300d
<\/strong>\u51fa\u9858\u65e5\u30002012\u5e743\u67086\u65e5\uff08\u5ca1\u5c71\u5927\u5b66\u3001\u30af\u30e9\u30ec\uff09\u83c5 \u8aa0\u6cbb\u3001\u5149\u85e4\u8015\u4e00\u3001\u938c\u7530\u6cf0\u8f14\u3001\u9db4\u7530\u7f8e\u6a39\u3001\u5409\u672c\u7d14\u4e00\u3001\u6749\u5ca1\u5c1a
2013\u5e742\u67087\u65e5\u516c\u958b<\/p>\r\n

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(5) <\/strong>\u7279\u958b<\/strong>2009-245900<\/strong>\u300c\u96fb\u6975\u6d3b\u7269\u8cea\u53ca\u3073\u3053\u308c\u3092\u7528\u3044\u305f\u96fb\u6975\u300d
<\/strong>\u51fa\u9858\u65e5\u30002008\u5e743\u670831\u65e5\uff08\u65e5\u672c\u30b1\u30df\u30b3\u30f3\u3001\u5ca1\u5c71\u5927\u5b66\uff09\u672b\u677e\u4fca\u9020\u3001\u753a\u7530\u5065\u6cbb\u3001\u7389\u5149\u8ce2\u6b21\u3001\u7530\u4e2d\u79c0\u96c4\u3001\u5149\u85e4\u8015\u4e00
<\/u>2009\u5e7410\u670822\u65e5\u516c\u958b<\/p>\r\n

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(4) <\/strong>\u7279\u958b<\/strong>2008-084786<\/strong>\u300c\u96fb\u6975\u6d3b\u7269\u8cea\u53ca\u3073\u305d\u308c\u3092\u7528\u3044\u305f\u96fb\u6c17\u5316\u5b66\u7d20\u5b50\u300d
<\/strong>\u51fa\u9858\u65e5\u30002006\u5e749\u670828\u65e5\uff08\u5ca1\u5c71\u5927\u5b66\u3001\u65e5\u672c\u30b1\u30df\u30b3\u30f3\uff09\u7530\u4e2d\u79c0\u96c4\u3001\u5149\u85e4\u8015\u4e00\u3001\u672b\u677e\u4fca\u9020\u3001\u753a\u7530\u5065\u6cbb\u3001\u7389\u5149\u8ce2\u6b21\u3001\u5185\u79c0\u5247
2008\u5e744\u670810\u65e5\u516c\u958b<\/p>\r\n

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(3) <\/strong>\u7279\u958b<\/strong>2008-050281<\/strong>\u300c\u30d9\u30f3\u30bc\u30f3\u5316\u5408\u7269\u306e\u88fd\u9020\u65b9\u6cd5\u300d
<\/strong>\u51fa\u9858\u65e5\u30002006\u5e748\u670823\u65e5\uff08\u5ca1\u5c71\u5927\u5b66\u3001\u5927\u585a\u5316\u5b66\uff09\u7530\u4e2d\u79c0\u96c4\u3001\u5149\u85e4\u8015\u4e00\u3001\u5409\u7530\u5065\u592a
2008\u5e743\u67086\u65e5\u516c\u958b<\/p>\r\n

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(2) <\/strong>\u7279\u958b<\/strong>2006-249454<\/strong>\u300c\uff14\uff0d\u7f6e\u63db\u30a2\u30bc\u30c1\u30b8\u30ce\u30f3\u8a98\u5c0e\u4f53\u306e\u88fd\u9020\u6cd5\u300d
<\/strong>\u51fa\u9858\u65e5\u30002005\u5e743\u67088\u65e5\uff08\u5ca1\u5c71\u5927\u5b66\u3001\u5927\u585a\u5316\u5b66\uff09\u7530\u4e2d\u79c0\u96c4\u3001\u5149\u85e4\u8015\u4e00\u3001\u77f3\u98db\u597d\u898f\u3001\u7b39\u5ca1\u4e09\u5343\u96c4
2006\u5e749\u670821\u65e5\u516c\u958b<\/p>\r\n

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(1) <\/strong>\u7279\u958b<\/strong>2006-223345<\/strong>\u300c\uff30\uff23\uff22\u3092\u542b\u3080\u5ec3\u6cb9\u306e\u7121\u5bb3\u5316\u51e6\u7406\u6cd5\u300d
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Preprints (1) Synthesis of Boranils by Iodide-Mediated Demethylative Borylation and Their PropertiesKoichi Mitsudo,* Ryo Magata, Eisuke Sato, Tomoya Nakamura, Atsushi Wakamiya, and Seiji Suga*ChemRxiv […]<\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"_locale":"en_US","_original_post":"https:\/\/mitsudo.net\/?page_id=204","footnotes":""},"class_list":["post-221","page","type-page","status-publish","hentry","en-US"],"_links":{"self":[{"href":"https:\/\/mitsudo.net\/wp-json\/wp\/v2\/pages\/221","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/mitsudo.net\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/mitsudo.net\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/mitsudo.net\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/mitsudo.net\/wp-json\/wp\/v2\/comments?post=221"}],"version-history":[{"count":179,"href":"https:\/\/mitsudo.net\/wp-json\/wp\/v2\/pages\/221\/revisions"}],"predecessor-version":[{"id":2738,"href":"https:\/\/mitsudo.net\/wp-json\/wp\/v2\/pages\/221\/revisions\/2738"}],"wp:attachment":[{"href":"https:\/\/mitsudo.net\/wp-json\/wp\/v2\/media?parent=221"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}