The hydrosilane/potassium tert-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 HSiR3/KOtBu-mediated transformations are now known, including silylation of sp, sp2, and sp3 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 HSiR3/KOtBu reagent system. Several mechanistic phenomena that remain to be explained are also highlighted.
CITATION STYLE
Jenkins, I. D., & Krenske, E. H. (2020, April 7). Mechanistic Aspects of Hydrosilane/Potassium tert-Butoxide (HSiR3/KO tBu)-Mediated Reactions. ACS Omega. American Chemical Society. https://doi.org/10.1021/acsomega.0c00366
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