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Photoredox-catalyzed fluorodifluoroacetylation of alkenes with FSOCFCOMe and EtN·3HF
Photoredox-catalyzed three-component fluorodifluoroacetylation of aromatic alkenes is reported, which features a wide substrate scope and functional group tolerance. An advantage of the reaction is the use of a nucleophilic fluoride source and a general difluoroacetylation reagent for the fluorodifl...
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Published in: | Organic & biomolecular chemistry 2022-05, Vol.2 (18), p.3726-373 |
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Main Authors: | , , , |
Format: | Article |
Language: | |
Online Access: | Get full text |
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Summary: | Photoredox-catalyzed three-component fluorodifluoroacetylation of aromatic alkenes is reported, which features a wide substrate scope and functional group tolerance. An advantage of the reaction is the use of a nucleophilic fluoride source and a general difluoroacetylation reagent for the fluorodifluoroacetylation of alkenes.
Photoredox-catalyzed fluorodifluoroacetylation of alkenes with FSO
2
CF
2
CO
2
Me and Et
3
N·3HF is disclosed. A range of the aromatic alkenes were transformed to the corresponding γ-fluorinated α,α-difluoroacetates in high yields with high regioselectivities. |
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ISSN: | 1477-0520 1477-0539 |
DOI: | 10.1039/d2ob00488g |