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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...

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Detalles Bibliográficos
Autores principales: Friese, Florian W., Studer, Armido
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Royal Society of Chemistry 2019
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.
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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
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