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|Title:||Enantioselective organocatalytic Michael-hemiketalization catalyzed by a trans-bifunctional indane thiourea catalyst||Authors:||Gao, Y.
|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|
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