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Copper-catalyzed yne-allylic substitutions: concept and recent developments

Shuang Yang, Xinqiang Fang

2024Beilstein Journal of Organic Chemistry17 citationsDOIOpen Access PDF

Abstract

The catalytic (asymmetric) allylation and propargylation have been established as powerful strategies allowing access to enantioenriched α-chiral alkenes and alkynes. In this context, combining allylic and propargylic substitutions offers new opportunities to expand the scope of transition metal-catalyzed substitution reactions. Since its discovery in 2022, copper-catalyzed yne-allylic substitution has undergone rapid development and significant progress has been made using the key copper vinyl allenylidene intermediates. This review summarizes the developments and illustrates the influences of copper salt, ligand, and substitution pattern of the substrate on the regioselectivity and stereoselectivity.

Topics & Concepts

Allylic rearrangementChemistryStereoselectivityRegioselectivityCatalysisCopperCombinatorial chemistryContext (archaeology)Substitution (logic)Substitution reactionLigand (biochemistry)Organic chemistryComputer scienceBiochemistryPaleontologyReceptorProgramming languageBiologyCatalytic C–H Functionalization MethodsCatalytic Alkyne ReactionsAsymmetric Synthesis and Catalysis
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