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

ACS Omega

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

Published: April 2020

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.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC7143413PMC
http://dx.doi.org/10.1021/acsomega.0c00366DOI Listing

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

ACS Omega

April 2020

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

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.

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