Decarboxylative Borylation of Stabilized and Activated Carbon Radicals.
borylation
imidoyl chloride
inert radicals
photoredox reaction
Journal
Angewandte Chemie (International ed. in English)
ISSN: 1521-3773
Titre abrégé: Angew Chem Int Ed Engl
Pays: Germany
ID NLM: 0370543
Informations de publication
Date de publication:
01 Dec 2020
01 Dec 2020
Historique:
received:
08
06
2020
revised:
27
07
2020
pubmed:
26
8
2020
medline:
26
8
2020
entrez:
26
8
2020
Statut:
ppublish
Résumé
Redox-active esters (RAEs) as active radical precursors have been extensively studied for C-B bond formations. However, the analogous transformations of stabilized radicals from the corresponding acid precursors remain challenging owing to the strong preference towards single-electron oxidation to the stable carbocations. This work describes a general strategy for rapid access to various aliphatic and aromatic boronic esters by mild photoinduced decarboxylative borylation. Both aryl and alkyl radicals could be generated from the leaving group-assisted N-hydroxybenzimidoyl chloride esters, even α-CF
Identifiants
pubmed: 32840957
doi: 10.1002/anie.202008138
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
21875-21879Subventions
Organisme : National Natural Science Foundation of China
ID : 21772085, 21971107
Organisme : Fundamental Research Funds for the Central Universities
ID : 020514380220, 020514913412, 020514380131
Organisme : National Natural Science Foundation of China
ID : 21772085, 21971107, 22071101
Informations de copyright
© 2020 Wiley-VCH GmbH.
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