Please use this identifier to cite or link to this item: https://doi.org/10.1002/adsc.200700326
Title: Chiral bicyclic guanidine as a versatile brønsted base catalyst for the enantioselective michael reactions of dithiomalonates and β-keto thioesters
Authors: Ye, W.
Jiang, Z. 
Zhao, Y. 
Goh, S.L.M.
Leow, D.
Soh, Y.-T.
Tan, C.-H. 
Keywords: Asymmetric catalysis
Dithiomalonates
Guanidines
Michael addition
Organic catalysis
Issue Date: Nov-2007
Citation: Ye, W., Jiang, Z., Zhao, Y., Goh, S.L.M., Leow, D., Soh, Y.-T., Tan, C.-H. (2007-11). Chiral bicyclic guanidine as a versatile brønsted base catalyst for the enantioselective michael reactions of dithiomalonates and β-keto thioesters. Advanced Synthesis and Catalysis 349 (16) : 2454-2458. ScholarBank@NUS Repository. https://doi.org/10.1002/adsc.200700326
Abstract: A chiral bicyclic guanidine was developed as a versatile Brønsted base catalyst for the enantioselective Michael reactions of dithiomalonates and β-keto thioesters using a range of acceptors including maleimides, cyclic enones, furanone and acyclic 1,4-dicarbonylbutenes. © 2007 Wiley-VCH Verlag GmbH & Co. KGaA.
Source Title: Advanced Synthesis and Catalysis
URI: http://scholarbank.nus.edu.sg/handle/10635/75744
ISSN: 16154150
DOI: 10.1002/adsc.200700326
Appears in Collections:Staff Publications

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