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Dual gold/photoredox-catalyzed bis-arylative cyclization of chiral homopropargyl sulfonamides with diazonium salts: rapid access to enantioenriched 2,3-dihydropyrroles†
Ze-Shu Wang,Tong-De Tan,Cai-Ming Wang,Ding-Qiang Yuan,Te Zhang,Pengfei Zhu,Chunyin Zhu,Jin-Mei Zhou
Chemical Communications Pub Date : 05/24/2017 00:00:00 , DOI:10.1039/C7CC03262E
Abstract

A novel dual gold/photoredox-catalyzed bis-arylative cyclization of chiral homopropargyl sulfonamides with diazonium salts has been developed, allowing the facile synthesis of various enantioenriched 2,3-dihydropyrroles in generally moderate to good yields with excellent enantioselectivities under very mild conditions without using any strong oxidants. The reaction is proposed to undergo an AuI/AuIII redox cycle promoted by visible-light photoredox catalysis.

Graphical abstract: Dual gold/photoredox-catalyzed bis-arylative cyclization of chiral homopropargyl sulfonamides with diazonium salts: rapid access to enantioenriched 2,3-dihydropyrroles
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