Please use this identifier to cite or link to this item: https://doi.org/10.1039/b810905m
Title: Tandem conjugate addition-elimination reaction promoted by chiral pyrrolidinyl sulfonamide (CPS)
Authors: Xu, J.
Fu, X. 
Low, R.
Goh, Y.-P.
Jiang, Z. 
Tan, C.-H. 
Issue Date: 2008
Citation: Xu, J., Fu, X., Low, R., Goh, Y.-P., Jiang, Z., Tan, C.-H. (2008). Tandem conjugate addition-elimination reaction promoted by chiral pyrrolidinyl sulfonamide (CPS). Chemical Communications (43) : 5526-5528. ScholarBank@NUS Repository. https://doi.org/10.1039/b810905m
Abstract: Chiral pyrrolidinyl sulfonamides have been found to promote the conjugate addition-elimination reaction between activated allylic bromides and 1,3-dicarbonyl compounds with high enantioselectivities and the highly functionalised products can be used to generate a variety of interesting enantiomerically pure compounds via simple transformations. © The Royal Society of Chemistry.
Source Title: Chemical Communications
URI: http://scholarbank.nus.edu.sg/handle/10635/77212
ISSN: 13597345
DOI: 10.1039/b810905m
Appears in Collections:Staff Publications

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