Please use this identifier to cite or link to this item:
|Title:||Chiral bicyclic guanidine as a versatile brønsted base catalyst for the enantioselective michael reactions of dithiomalonates and β-keto thioesters||Authors:||Ye, W.
|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|
Show full item record
Files in This Item:
There are no files associated with this item.
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.