Litcius/Paper detail

Catalytic Asymmetric Vinylogous and Bisvinylogous Propargylic Substitution

Hao-Dong Qian, Zhiheng Li, Shuang Deng, Chaochao Yao, Hua-Ming Xiang, Guang Xu, Zi-Qi Geng, Zihao Wang, Linfeng Chen, Chunrong Liu, Cuiju Zhu, Xiaotian Qi, Hao Xu

2022Journal of the American Chemical Society47 citationsDOI

Abstract

Distinct regio- and enantioselectivity control in copper-catalyzed vinylogous and bisvinylogous propargylic substitution has been accomplished by using a novel chiral N,N,P ligand. The developed method provides an efficient and selective approach to an array of highly enantioenriched alkynyl unsaturated carbonyl compounds. Salient features include excellent functional group tolerance and broad substrate scope. The synthetic utility of the developed method is further demonstrated by a gram-scale synthesis and by application to a range of transformations including enantioselective synthesis of unique challenging compounds.

Topics & Concepts

ChemistryEnantioselective synthesisCombinatorial chemistrySubstrate (aquarium)Functional groupCatalysisSubstitution (logic)Ligand (biochemistry)Scope (computer science)StereochemistryOrganic chemistryGeologyReceptorBiochemistryOceanographyComputer sciencePolymerProgramming languageCatalytic C–H Functionalization MethodsCatalytic Alkyne ReactionsAsymmetric Synthesis and Catalysis