Please use this identifier to cite or link to this item: https://doi.org/10.1039/c0cc05840h
Title: Guanidine-catalyzed enantioselective desymmetrization of meso-aziridines
Authors: Zhang, Y.
Kee, C.W.
Lee, R.
Fu, X. 
Soh, J.Y.-T.
Loh, E.M.F.
Huang, K.-W.
Tan, C.-H. 
Issue Date: 7-Apr-2011
Source: 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
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