Please use this identifier to cite or link to this item: https://doi.org/10.1039/c0cc05840h
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dc.titleGuanidine-catalyzed enantioselective desymmetrization of meso-aziridines
dc.contributor.authorZhang, Y.
dc.contributor.authorKee, C.W.
dc.contributor.authorLee, R.
dc.contributor.authorFu, X.
dc.contributor.authorSoh, J.Y.-T.
dc.contributor.authorLoh, E.M.F.
dc.contributor.authorHuang, K.-W.
dc.contributor.authorTan, C.-H.
dc.date.accessioned2014-06-23T05:40:43Z
dc.date.available2014-06-23T05:40:43Z
dc.date.issued2011-04-07
dc.identifier.citationZhang, Y., Kee, C.W., Lee, R., Fu, X., Soh, J.Y.-T., Loh, E.M.F., Huang, K.-W., Tan, C.-H. (2011-04-07). Guanidine-catalyzed enantioselective desymmetrization of meso-aziridines. Chemical Communications 47 (13) : 3897-3899. ScholarBank@NUS Repository. https://doi.org/10.1039/c0cc05840h
dc.identifier.issn13597345
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/76272
dc.description.abstractAn amino-indanol derived chiral guanidine was developed as an efficient Brønsted base catalyst for the desymmetrization of meso-aziridines with both thiols and carbamodithioic acids as nucleophiles, which provided 1,2-difunctionalized ring-opened products in high yields and enantioselectivities. © The Royal Society of Chemistry.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c0cc05840h
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1039/c0cc05840h
dc.description.sourcetitleChemical Communications
dc.description.volume47
dc.description.issue13
dc.description.page3897-3899
dc.description.codenCHCOF
dc.identifier.isiut000288386600058
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