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.
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CITATION STYLE
Kancherla, R., Muralirajan, K., & Rueping, M. (2022). Excited-state palladium-catalysed reductive alkylation of imines: scope and mechanism. Chemical Science, 13(29), 8583–8589. https://doi.org/10.1039/d2sc02363f
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