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
Source: 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
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