Issue 11, 2015

A highly diastereoselective Friedel–Crafts reaction of indoles with isatin-derived N-sulfinyl ketimines towards the efficient synthesis of chiral tetrasubstituted 3-indolyl-3-aminooxindoles

Abstract

A Lewis acid promoted highly diastereoselective asymmetric Friedel–Crafts alkylation of indoles with isatin-derived N-tert-butanesulfinyl ketimines is described. The reaction can be accomplished with ease in the presence of a catalytic amount of Bi(OTf)3, providing a series of 3-indolyl-3-aminooxindoles in excellent diastereoselectivities (up to 98% de) and yields (up to 99%).

Graphical abstract: A highly diastereoselective Friedel–Crafts reaction of indoles with isatin-derived N-sulfinyl ketimines towards the efficient synthesis of chiral tetrasubstituted 3-indolyl-3-aminooxindoles

Supplementary files

Article information

Article type
Paper
Submitted
13 Jan 2015
Accepted
29 Jan 2015
First published
29 Jan 2015

Org. Biomol. Chem., 2015,13, 3363-3370

A highly diastereoselective Friedel–Crafts reaction of indoles with isatin-derived N-sulfinyl ketimines towards the efficient synthesis of chiral tetrasubstituted 3-indolyl-3-aminooxindoles

J. Chen, W. Chen, Y. Li and M. Xu, Org. Biomol. Chem., 2015, 13, 3363 DOI: 10.1039/C5OB00063G

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