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Cu-Catalyzed Carbocyclization for General Synthesis of <i>N</i>-Containing Heterocyclics Enabled by BrCF<sub>2</sub>COOEt as a C1 Source

Xiaofang Song, Lijing Zhang, Xing‐Guo Zhang, Hai‐Yong Tu

2024The Journal of Organic Chemistry15 citationsDOI

Abstract

A practical and efficient copper-catalyzed carbocyclization of 2-functionalized anilines with ethyl bromodifluoroacetate has been developed. Ethyl bromodifluoroacetate is employed as the C1 source via quadruple cleavage in this transformation. This reaction can afford a variety of N -containing heterocyclics with satisfactory yields and excellent functional group compatibility.

Topics & Concepts

ChemistryCatalysisCombinatorial chemistryCompatibility (geochemistry)CopperOrganic chemistryChemical engineeringEngineeringFluorine in Organic ChemistryCatalytic C–H Functionalization MethodsCyclopropane Reaction Mechanisms
Cu-Catalyzed Carbocyclization for General Synthesis of <i>N</i>-Containing Heterocyclics Enabled by BrCF<sub>2</sub>COOEt as a C1 Source | Litcius