Metallaphotoredox Perfluoroalkylation of Organobromides

Ruppert–Prakash type reagents (TMSCF3, TMSC2F5, and TMSC3F7) are readily available, air-stable, and easy-to-handle fluoroalkyl sources. Herein, we describe a mild, copper-catalyzed cross-coupling of these fluoroalkyl nucleophiles with aryl and alkyl bromides to produce a diverse array of trifluorome...

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Veröffentlicht in:Journal of the American Chemical Society 2020-11, Vol.142 (46), p.19480-19486
Hauptverfasser: Zhao, Xiangbo, MacMillan, David W. C
Format: Artikel
Sprache:eng
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Zusammenfassung:Ruppert–Prakash type reagents (TMSCF3, TMSC2F5, and TMSC3F7) are readily available, air-stable, and easy-to-handle fluoroalkyl sources. Herein, we describe a mild, copper-catalyzed cross-coupling of these fluoroalkyl nucleophiles with aryl and alkyl bromides to produce a diverse array of trifluoromethyl, pentafluoroethyl, and heptafluoropropyl adducts. This light-mediated transformation proceeds via a silyl-radical-mediated halogen atom abstraction pathway, which enables perfluoroalkylation of a broad range of organobromides of variable steric and electronic demand. The utility of the method is demonstrated through the late-stage functionalization of several drug analogues.
ISSN:0002-7863
1520-5126
DOI:10.1021/jacs.0c09977