Issue 14, 2011

Chiral indane skeleton based thiourea catalyzed highly stereoselective cascade Michael–enolation–cyclization reaction

Abstract

An efficient asymmetric cascade reaction catalyzed by a chiral bifunctional indane amine–thiourea catalyst has been developed. From a broad substrate scope, chiral dihydro-2H-pyran complexes that contained two stereogenic centers were obtained in a one-pot manner in good to excellent yields (72–97%) and high to excellent stereoselectivities (92–97% ee).

Graphical abstract: Chiral indane skeleton based thiourea catalyzed highly stereoselective cascade Michael–enolation–cyclization reaction

Supplementary files

Article information

Article type
Paper
Submitted
26 Mar 2011
Accepted
20 Apr 2011
First published
21 Apr 2011

Org. Biomol. Chem., 2011,9, 5297-5302

Chiral indane skeleton based thiourea catalyzed highly stereoselective cascade Michael–enolation–cyclization reaction

Q. Ren, Y. Gao and J. Wang, Org. Biomol. Chem., 2011, 9, 5297 DOI: 10.1039/C1OB05477E

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