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ID 60783
著者
Mitsudo, Koichi Division of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University ORCID Kaken ID publons researchmap
Matsuo, Ren Division of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University
Yonezawa, Toki Division of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University
Inoue, Haruka Division of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University
Mandai, Hiroki Department of Medical Technology, Gifu University of Medical Science ORCID Kaken ID publons researchmap
Suga, Seiji Division of Applied Chemistry, Graduate School of Natural Science and Technology, Okayama University ORCID Kaken ID researchmap
抄録
The first electrochemical dehydrogenative C−S bond formation leading to thienoacene derivatives is described. Several thienoacene derivatives were synthesized by dehydrogenative C−H/S−H coupling. The addition of nBu4NBr, which catalytically promoted the reaction as a halogen mediator, was essential.
キーワード
cross-coupling
cyclization
electrochemistry
heterocycles
synthetic methods
備考
This is the peer reviewed version of the following article: Mitsudo Koichi et. al. Electrochemical Synthesis of Thienoacene Derivatives: Transition‐Metal‐Free Dehydrogenative C−S Coupling Promoted by a Halogen Mediator. Angewandte Chemie International Edition 59(20) 7803-7807(2020), which has been published in final form at https://doi.org/10.1002/anie.202001149. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Use of Self-Archived Versions
This fulltext is available in Feb. 2021.
発行日
2020-02-20
出版物タイトル
Angewandte Chemie International Edition
59巻
20号
出版者
Wiley
開始ページ
7803
終了ページ
7807
ISSN
1433-7851
NCID
AA11614189
資料タイプ
学術雑誌論文
言語
English
OAI-PMH Set
岡山大学
論文のバージョン
author
PubMed ID
DOI
Web of Science KeyUT
関連URL
isVersionOf https://doi.org/10.1002/anie.202001149
助成機関名
日本学術振興会
助成番号
JP19K05477
JP19K05478
JP18H04455