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Mechanistic Aspects of Hydrosilane/Potassium tert-Butoxide (HSiR(3)/KO(t)Bu)-Mediated Reactions
[Image: see text] 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 HSiR(3)/KO(t)Bu-mediated transformations are now known, including silylation of sp,...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
American Chemical Society
2020
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Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7143413/ https://www.ncbi.nlm.nih.gov/pubmed/32280845 http://dx.doi.org/10.1021/acsomega.0c00366 |
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author | Jenkins, Ian D. Krenske, Elizabeth H. |
author_facet | Jenkins, Ian D. Krenske, Elizabeth H. |
author_sort | Jenkins, Ian D. |
collection | PubMed |
description | [Image: see text] 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 HSiR(3)/KO(t)Bu-mediated transformations are now known, including silylation of sp, sp(2), and sp(3) 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(3)/KO(t)Bu reagent system. Several mechanistic phenomena that remain to be explained are also highlighted. |
format | Online Article Text |
id | pubmed-7143413 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | American Chemical Society |
record_format | MEDLINE/PubMed |
spelling | pubmed-71434132020-04-10 Mechanistic Aspects of Hydrosilane/Potassium tert-Butoxide (HSiR(3)/KO(t)Bu)-Mediated Reactions Jenkins, Ian D. Krenske, Elizabeth H. ACS Omega [Image: see text] 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 HSiR(3)/KO(t)Bu-mediated transformations are now known, including silylation of sp, sp(2), and sp(3) 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(3)/KO(t)Bu reagent system. Several mechanistic phenomena that remain to be explained are also highlighted. American Chemical Society 2020-03-23 /pmc/articles/PMC7143413/ /pubmed/32280845 http://dx.doi.org/10.1021/acsomega.0c00366 Text en Copyright © 2020 American Chemical Society This is an open access article published under an ACS AuthorChoice License (http://pubs.acs.org/page/policy/authorchoice_termsofuse.html) , which permits copying and redistribution of the article or any adaptations for non-commercial purposes. |
spellingShingle | Jenkins, Ian D. Krenske, Elizabeth H. Mechanistic Aspects of Hydrosilane/Potassium tert-Butoxide (HSiR(3)/KO(t)Bu)-Mediated Reactions |
title | Mechanistic Aspects of Hydrosilane/Potassium tert-Butoxide (HSiR(3)/KO(t)Bu)-Mediated
Reactions |
title_full | Mechanistic Aspects of Hydrosilane/Potassium tert-Butoxide (HSiR(3)/KO(t)Bu)-Mediated
Reactions |
title_fullStr | Mechanistic Aspects of Hydrosilane/Potassium tert-Butoxide (HSiR(3)/KO(t)Bu)-Mediated
Reactions |
title_full_unstemmed | Mechanistic Aspects of Hydrosilane/Potassium tert-Butoxide (HSiR(3)/KO(t)Bu)-Mediated
Reactions |
title_short | Mechanistic Aspects of Hydrosilane/Potassium tert-Butoxide (HSiR(3)/KO(t)Bu)-Mediated
Reactions |
title_sort | mechanistic aspects of hydrosilane/potassium tert-butoxide (hsir(3)/ko(t)bu)-mediated
reactions |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7143413/ https://www.ncbi.nlm.nih.gov/pubmed/32280845 http://dx.doi.org/10.1021/acsomega.0c00366 |
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