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Please use this identifier to cite or link to this item: https://doi.org/10.1039/b810905m
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dc.titleTandem conjugate addition-elimination reaction promoted by chiral pyrrolidinyl sulfonamide (CPS)
dc.contributor.authorXu, J.
dc.contributor.authorFu, X.
dc.contributor.authorLow, R.
dc.contributor.authorGoh, Y.-P.
dc.contributor.authorJiang, Z.
dc.contributor.authorTan, C.-H.
dc.date.accessioned2014-06-23T05:52:15Z
dc.date.available2014-06-23T05:52:15Z
dc.date.issued2008
dc.identifier.citationXu, 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
dc.identifier.issn13597345
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/77212
dc.description.abstractChiral 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.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/b810905m
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1039/b810905m
dc.description.sourcetitleChemical Communications
dc.description.issue43
dc.description.page5526-5528
dc.description.codenCHCOF
dc.identifier.isiut000260775000015
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