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硅烷/丁醇钾(HSiR/KO Bu)介导反应的机理研究

Mechanistic Aspects of Hydrosilane/Potassium -Butoxide (HSiR/KO Bu)-Mediated Reactions.

作者信息

Jenkins Ian D, Krenske Elizabeth H

机构信息

Griffith Institute for Drug Discovery, Griffith University, Nathan, QLD 4111, Australia.

School of Chemistry and Molecular Biosciences, The University of Queensland, Brisbane, QLD 4072, Australia.

出版信息

ACS Omega. 2020 Mar 23;5(13):7053-7058. doi: 10.1021/acsomega.0c00366. eCollection 2020 Apr 7.

Abstract

The hydrosilane/potassium -butoxide reagent system has attracted significant attention over the last 5 years since the discovery of its ability to silylate heteroarene C-H bonds. Numerous useful HSiR/KO Bu-mediated transformations are now known, including silylation of sp, sp, and sp C-H bonds, reductive cleavage of C-O, C-S, and C-N bonds, reduction of polycyclic arenes, and hydrosilylation and polymerization of styrenes. This mini-review surveys the rich diversity of reaction mechanisms, both ionic and free radical and including hydride transfer, H atom transfer, and electron transfer, that have been uncovered during recent studies on the HSiR/KO Bu reagent system. Several mechanistic phenomena that remain to be explained are also highlighted.

摘要

自发现氢硅烷/丁醇钾试剂体系能够硅烷化杂芳烃C-H键以来,在过去5年中该体系已引起了广泛关注。目前已知许多有用的HSiR/KO Bu介导的转化反应,包括 sp、sp 和 sp C-H 键的硅烷化、C-O、C-S 和 C-N 键的还原裂解、多环芳烃的还原以及苯乙烯的硅氢化和聚合反应。本综述概述了近期关于HSiR/KO Bu试剂体系的研究中所揭示的丰富多样的反应机理,包括离子型和自由基型,以及氢化物转移、H原子转移和电子转移等。同时也强调了一些有待解释的机理现象。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0055/7143413/6f9364c17137/ao0c00366_0001.jpg

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