Please use this identifier to cite or link to this item: http://hdl.handle.net/10397/30625
Title: Highly enantioslective synthesis of multisubstituted polyfunctional dihydropyrrole via an organocatalytic tandem Michael/cyclization sequence
Authors: Zhang, G
Zhang, Y
Jiang, X
Yan, W
Wang, R
Issue Date: 2011
Publisher: American Chemical Society
Source: Organic letters, 2011, v. 13, no. 15, p. 3806-3809 How to cite?
Journal: Organic letters 
Abstract: A unique approach to asymmetric synthesis of various optically pure multisubstituted 2,3-dihydropyrroles catalyzed by a novel rosin-derived tertiary amine-thiourea via a tandem Michael/cyclization sequence with high yield (up to 97%) and good to excellent enantioselectivities (up to 97% ee) is present. This strategy provides an efficient and convenient method to access enantioenrich nitrogen heterocycles.
URI: http://hdl.handle.net/10397/30625
ISSN: 1523-7060
EISSN: 1523-7052
DOI: 10.1021/ol201299u
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