AC_Int_ed_59_20.pdf 748 KB
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
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.
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.
Angewandte Chemie International Edition
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