Enantioselective organocatalytic Michael-hemiketalization catalyzed by a trans-bifunctional indane thiourea catalyst

Please use this identifier to cite or link to this item: https://doi.org/10.1039/c1ob05404j

Title:	Enantioselective organocatalytic Michael-hemiketalization catalyzed by a trans-bifunctional indane thiourea catalyst
Authors:	Gao, Y. Ren, Q. Ang, S.-M. Wang, J.
Issue Date:	21-May-2011
Citation:	Gao, Y., Ren, Q., Ang, S.-M., Wang, J. (2011-05-21). Enantioselective organocatalytic Michael-hemiketalization catalyzed by a trans-bifunctional indane thiourea catalyst. Organic and Biomolecular Chemistry 9 (10) : 3691-3697. ScholarBank@NUS Repository. https://doi.org/10.1039/c1ob05404j
Abstract:	An efficient, convenient and enantioselective Michael-hemiketalization reaction has been developed for the synthesis of naphthoquinones. In this work, a novel trans-bifunctional indane thiourea catalyst has been reported to promote this process to afford high yields (up to 99%) and high to excellent enantiomeric excesses (90-98% ee). © 2011 The Royal Society of Chemistry.
Source Title:	Organic and Biomolecular Chemistry
URI:	http://scholarbank.nus.edu.sg/handle/10635/76106
ISSN:	14770520
DOI:	10.1039/c1ob05404j
Appears in Collections:	Staff Publications

There are no files associated with this item.

Check