Highly efficient synthesis of chiral quaternary 3-aminooxindoles promoted by zinc(ii) chloride via Et2Zn-catalysed addition of Grignard reagents to isaltin-derived N-tert-butanesulfinyl ketimines†
Guangling Bian,Zhongxiang Chen,Xiaohan Xia,Mi Zhou,Caiyan Cui
RSC Advances Pub Date : 08/03/2017 00:00:00 , DOI:10.1039/C7RA07692D
Abstract

A highly efficient and practical approach to chiral quaternary 3-aminooxindoles was developed via Et2Zn catalyzed diastereoselective addition of Grignard reagents to isaltin-derived N-tert-butanesulfinyl ketimines giving good to excellent yields and diastereoselectivities with broad substrates and reagent scopes promoted by zinc(II) chloride.

Graphical abstract: Highly efficient synthesis of chiral quaternary 3-aminooxindoles promoted by zinc(ii) chloride via Et2Zn-catalysed addition of Grignard reagents to isaltin-derived N-tert-butanesulfinyl ketimines