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|Title:||Guanidine-catalyzed enantioselective desymmetrization of meso-aziridines||Authors:||Zhang, Y.
|Issue Date:||7-Apr-2011||Citation:||Zhang, 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||Abstract:||An 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.||Source Title:||Chemical Communications||URI:||http://scholarbank.nus.edu.sg/handle/10635/76272||ISSN:||13597345||DOI:||10.1039/c0cc05840h|
|Appears in Collections:||Staff Publications|
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