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Regioselective copper-catalyzed direct arylation of benzodithiophene-S,S-tetraoxide†
D. P. Khambhati,K. A. N. Sachinthani,A. L. Rheingold,T. L. Nelson
Chemical Communications Pub Date : 04/10/2017 00:00:00 , DOI:10.1039/C7CC01781B
Abstract

An efficient copper-catalyzed direct arylation reaction for the regioselective functionalization of benzodithiophene-S,S-tetraoxide has been developed. The method demonstrates a broad scope with isolated yields ranging from good to excellent. Furthermore, the reaction specificity for aryl iodides over the unreactive aryl bromides provide a opportunity to generate a new donor–acceptor–donor triad.

Graphical abstract: Regioselective copper-catalyzed direct arylation of benzodithiophene-S,S-tetraoxide
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