Please use this identifier to cite or link to this item: https://scholarbank.nus.edu.sg/handle/10635/93299
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.
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/10635/93299
ISSN: 16154150
Appears in Collections:Staff Publications

Show full item record
Files in This Item:
There are no files associated with this item.

SCOPUSTM   
Citations

80
checked on Feb 26, 2018

WEB OF SCIENCETM
Citations

83
checked on Jul 17, 2019

Page view(s)

47
checked on Nov 30, 2019

Google ScholarTM

Check


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.