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Expeditious diastereoselective construction of a thiochroman skeleton via a cinchona alkaloid-derived catalyst†
Chenggang Zhou,Yaojun Gao,Qiao Ren,Kun Zhang,Hansong Cheng,Wei Wang,Jian Wang
Organic & Biomolecular Chemistry Pub Date : 09/22/2011 00:00:00 , DOI:10.1039/C1OB06497E
Abstract

An example of diastereoselective and enantioselective synthesis of thiochroman derivatives through a sulfa-Michael–Michael cascade sequence is disclosed. This is a significant complement of the quinine-thiourea catalyzed sulfa-Michael–Michael cascade reaction. The densely functionalized target thiochromans were obtained in high diastereoselectivities, and with high to excellent enantioselectivities.

Graphical abstract: Expeditious diastereoselective construction of a thiochroman skeleton via a cinchona alkaloid-derived catalyst
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