Issue 57, 2016

Consecutive visible-light photoredox decarboxylative couplings of adipic acid active esters with alkynyl sulfones leading to cyclic compounds

Abstract

Novel and efficient consecutive photoredox decarboxylative couplings of adipic acid active esters (bis(1,3-dioxoisoindolin-2-yl)-substituted hexanedioates) with substituted 1-(2-arylethynylsulfonyl)benzenes have been developed under visible-light photocatalysis. The successive photoredox decarboxylative C–C bond formation at room temperature afforded the corresponding cyclic compounds in good yields with tolerance of some functional groups.

Graphical abstract: Consecutive visible-light photoredox decarboxylative couplings of adipic acid active esters with alkynyl sulfones leading to cyclic compounds

Supplementary files

Article information

Article type
Communication
Submitted
25 May 2016
Accepted
20 Jun 2016
First published
20 Jun 2016

Chem. Commun., 2016,52, 8862-8864

Author version available

Consecutive visible-light photoredox decarboxylative couplings of adipic acid active esters with alkynyl sulfones leading to cyclic compounds

J. Li, H. Tian, M. Jiang, H. Yang, Y. Zhao and H. Fu, Chem. Commun., 2016, 52, 8862 DOI: 10.1039/C6CC04386K

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