Issue 29, 2022

Excited-state palladium-catalysed reductive alkylation of imines: scope and mechanism

Abstract

Palladium catalysis induced by visible-light irradiation is a promising tool for promoting unusual chemical transformations. We describe the development of excited-state palladium-catalyzed reductive alkylation of imines with alkyl bromides. The new methodology shows broad functional group tolerance and can additionally be applied in the direct three-component reaction of aldehydes, anilines, and alkyl bromides to give the alkyl amines under mild reaction conditions. Time-resolved photoluminescence experiments allowed the determination of the excited-state reaction kinetics and indicate that the reaction is proceeding via the inner-sphere electron transfer mechanism.

Graphical abstract: Excited-state palladium-catalysed reductive alkylation of imines: scope and mechanism

Supplementary files

Article information

Article type
Edge Article
Submitted
26 Apr 2022
Accepted
01 Jul 2022
First published
07 Jul 2022
This article is Open Access

All publication charges for this article have been paid for by the Royal Society of Chemistry
Creative Commons BY-NC license

Chem. Sci., 2022,13, 8583-8589

Excited-state palladium-catalysed reductive alkylation of imines: scope and mechanism

R. Kancherla, K. Muralirajan and M. Rueping, Chem. Sci., 2022, 13, 8583 DOI: 10.1039/D2SC02363F

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