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Deoxygenative Borylation of Secondary and Tertiary Alcohols
Two different approaches for the deoxygenative radical borylation of secondary and tertiary alcohols are presented. These transformations either proceed through a metal‐free silyl‐radical‐mediated pathway or utilize visible‐light photoredox catalysis. Readily available xanthates or methyl oxalates a...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6772128/ https://www.ncbi.nlm.nih.gov/pubmed/31050141 http://dx.doi.org/10.1002/anie.201904028 |
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author | Friese, Florian W. Studer, Armido |
author_facet | Friese, Florian W. Studer, Armido |
author_sort | Friese, Florian W. |
collection | PubMed |
description | Two different approaches for the deoxygenative radical borylation of secondary and tertiary alcohols are presented. These transformations either proceed through a metal‐free silyl‐radical‐mediated pathway or utilize visible‐light photoredox catalysis. Readily available xanthates or methyl oxalates are used as radical precursors. The reactions show broad substrate scope and high functional‐group tolerance, and are conducted under mild and practical conditions. |
format | Online Article Text |
id | pubmed-6772128 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-67721282019-10-07 Deoxygenative Borylation of Secondary and Tertiary Alcohols Friese, Florian W. Studer, Armido Angew Chem Int Ed Engl Communications Two different approaches for the deoxygenative radical borylation of secondary and tertiary alcohols are presented. These transformations either proceed through a metal‐free silyl‐radical‐mediated pathway or utilize visible‐light photoredox catalysis. Readily available xanthates or methyl oxalates are used as radical precursors. The reactions show broad substrate scope and high functional‐group tolerance, and are conducted under mild and practical conditions. John Wiley and Sons Inc. 2019-06-05 2019-07-08 /pmc/articles/PMC6772128/ /pubmed/31050141 http://dx.doi.org/10.1002/anie.201904028 Text en © 2019 The Authors. Published by Wiley-VCH Verlag GmbH & Co. KGaA. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made. |
spellingShingle | Communications Friese, Florian W. Studer, Armido Deoxygenative Borylation of Secondary and Tertiary Alcohols |
title | Deoxygenative Borylation of Secondary and Tertiary Alcohols |
title_full | Deoxygenative Borylation of Secondary and Tertiary Alcohols |
title_fullStr | Deoxygenative Borylation of Secondary and Tertiary Alcohols |
title_full_unstemmed | Deoxygenative Borylation of Secondary and Tertiary Alcohols |
title_short | Deoxygenative Borylation of Secondary and Tertiary Alcohols |
title_sort | deoxygenative borylation of secondary and tertiary alcohols |
topic | Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6772128/ https://www.ncbi.nlm.nih.gov/pubmed/31050141 http://dx.doi.org/10.1002/anie.201904028 |
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