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New avenues for C–B bond formation via radical intermediates
This perspective gives an overview on recent findings in the emerging area of C-radical borylation using diborons as radical trapping reagents. Aryl, vinyl and alkyl boronic esters can be accessed via such an approach under mild conditions. These processes are complementary to established transition...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Royal Society of Chemistry
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6977546/ https://www.ncbi.nlm.nih.gov/pubmed/32015798 http://dx.doi.org/10.1039/c9sc03765a |
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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 | This perspective gives an overview on recent findings in the emerging area of C-radical borylation using diborons as radical trapping reagents. Aryl, vinyl and alkyl boronic esters can be accessed via such an approach under mild conditions. These processes are complementary to established transition metal catalysed cross coupling reactions. Radical borylations can be conducted in the absence of a transition metal but some processes require transition metals as catalysts. It will be shown that various readily available C-radical precursors can be used to run these borylations. For a better understanding of the chemistry, mechanistic discussions are also presented and an outlook on this topic will be provided at the end of the article. |
format | Online Article Text |
id | pubmed-6977546 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Royal Society of Chemistry |
record_format | MEDLINE/PubMed |
spelling | pubmed-69775462020-02-03 New avenues for C–B bond formation via radical intermediates Friese, Florian W. Studer, Armido Chem Sci Chemistry This perspective gives an overview on recent findings in the emerging area of C-radical borylation using diborons as radical trapping reagents. Aryl, vinyl and alkyl boronic esters can be accessed via such an approach under mild conditions. These processes are complementary to established transition metal catalysed cross coupling reactions. Radical borylations can be conducted in the absence of a transition metal but some processes require transition metals as catalysts. It will be shown that various readily available C-radical precursors can be used to run these borylations. For a better understanding of the chemistry, mechanistic discussions are also presented and an outlook on this topic will be provided at the end of the article. Royal Society of Chemistry 2019-09-03 /pmc/articles/PMC6977546/ /pubmed/32015798 http://dx.doi.org/10.1039/c9sc03765a Text en This journal is © The Royal Society of Chemistry 2019 https://creativecommons.org/licenses/by-nc/3.0/This article is freely available. This article is licensed under a Creative Commons Attribution Non Commercial 3.0 Unported Licence (CC BY-NC 3.0) |
spellingShingle | Chemistry Friese, Florian W. Studer, Armido New avenues for C–B bond formation via radical intermediates |
title | New avenues for C–B bond formation via radical intermediates |
title_full | New avenues for C–B bond formation via radical intermediates |
title_fullStr | New avenues for C–B bond formation via radical intermediates |
title_full_unstemmed | New avenues for C–B bond formation via radical intermediates |
title_short | New avenues for C–B bond formation via radical intermediates |
title_sort | new avenues for c–b bond formation via radical intermediates |
topic | Chemistry |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6977546/ https://www.ncbi.nlm.nih.gov/pubmed/32015798 http://dx.doi.org/10.1039/c9sc03765a |
work_keys_str_mv | AT frieseflorianw newavenuesforcbbondformationviaradicalintermediates AT studerarmido newavenuesforcbbondformationviaradicalintermediates |