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 |
Show full item record
Files in This Item:
There are no files associated with this item.
SCOPUSTM
Citations
90
checked on Oct 26, 2020
WEB OF SCIENCETM
Citations
87
checked on Oct 26, 2020
Page view(s)
94
checked on Oct 23, 2020
Google ScholarTM
Check
Altmetric
Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.