Issue 11, 2015

Metal-free TBAI-catalyzed arylsulfonylation of activated alkenes with sulfonylhydrazides

Abstract

An efficient metal-free oxidative arylsulfonylation of α,β-unsaturated imides with sulfonylhydrazides leading to isoquinoline-1,3(2H,4H)-dione derivatives has been developed. The procedure involves the generation of sulfonyl radicals via cleavage of the S–N bond of sulfonylhydrazides with sulfonylation and C–H functionalization. The protocol uses the economical and environmentally friendly TBAI–TBHP catalytic system, and the corresponding isoquinoline-1,3(2H,4H)-diones with various functional groups were obtained in moderate to good yields.

Graphical abstract: Metal-free TBAI-catalyzed arylsulfonylation of activated alkenes with sulfonylhydrazides

Supplementary files

Article information

Article type
Paper
Submitted
03 Aug 2014
Accepted
22 Jan 2015
First published
22 Jan 2015

Org. Biomol. Chem., 2015,13, 3308-3313

Author version available

Metal-free TBAI-catalyzed arylsulfonylation of activated alkenes with sulfonylhydrazides

W. Yu, P. Hu, Y. Fan, C. Yu, X. Yan, X. Li and X. Xu, Org. Biomol. Chem., 2015, 13, 3308 DOI: 10.1039/C4OB01651C

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