Issue 24, 2024

Palladium-catalyzed enantioselective arylation of trichloro- or tri-/difluoroacetaldimine precursors

Abstract

A palladium-catalyzed asymmetric α-arylation of N-carbamoyl imine precursors containing CCl3, CF3 and CF2H is presented. This protocol provides facile access to a series of chiral α-aryl trichloroethylamines bearing various functional groups, with moderate to high yields (40–82% yield) and high enantioselectivity (80–99% ee).

Graphical abstract: Palladium-catalyzed enantioselective arylation of trichloro- or tri-/difluoroacetaldimine precursors

Supplementary files

Article information

Article type
Communication
Submitted
05 Jan 2024
Accepted
22 Feb 2024
First published
23 Feb 2024

Chem. Commun., 2024,60, 3303-3306

Palladium-catalyzed enantioselective arylation of trichloro- or tri-/difluoroacetaldimine precursors

J. Wei, Z. Du, X. Wang, C. Ji, L. Li and Y. You, Chem. Commun., 2024, 60, 3303 DOI: 10.1039/D4CC00022F

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