Metal-free TBAI-catalyzed arylsulfonylation of activated alkenes with sulfonylhydrazides. Issue 11 (3rd February 2015)

• Record Type: Journal Article
• Authors: Yu, Wubin; Hu, Peizhu; Fan, Yuanyuan; Yu, Congyao; Yan, Xinhuan; Li, Xiaoqing; Xu, Xiangsheng
• Is Part Of: Organic & biomolecular chemistry. Volume 13:Issue 11(2015)
• Page Start: 3308
• Page End: 3313
• Publication Date: 2015-02-03
• Subjects: Chemistry, Organic -- Periodicals; Bioorganic chemistry -- Periodicals; Chemistry, Physical organic -- Periodicals; 547
• DOI: 10.1039/c4ob01651c
• Languages: English
• ISSNs: 1477-0520

Abstract

Abstract : An efficient approach to isoquinoline-1, 3(2 H, 4 H )-dione derivatives through metal-free oxidative arylsulfonylation of α, β-unsaturated imides with sulfonylhydrazides is developed. Abstract : An efficient metal-free oxidative arylsulfonylation of α, β-unsaturated imides with sulfonylhydrazides leading to isoquinoline-1, 3(2 H, 4 H )-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(2 H, 4 H )-diones with various functional groups were obtained in moderate to good yields.