Please use this identifier to cite or link to this item: https://doi.org/10.1039/c1ob05477e
Title: Chiral indane skeleton based thiourea catalyzed highly stereoselective cascade Michael-enolation-cyclization reaction
Authors: Ren, Q.
Gao, Y.
Wang, J. 
Issue Date: 21-Jul-2011
Citation: Ren, Q., Gao, Y., Wang, J. (2011-07-21). Chiral indane skeleton based thiourea catalyzed highly stereoselective cascade Michael-enolation-cyclization reaction. Organic and Biomolecular Chemistry 9 (14) : 5297-5302. ScholarBank@NUS Repository. https://doi.org/10.1039/c1ob05477e
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). © The Royal Society of Chemistry 2011.
Source Title: Organic and Biomolecular Chemistry
URI: http://scholarbank.nus.edu.sg/handle/10635/75750
ISSN: 14770520
DOI: 10.1039/c1ob05477e
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