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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 | 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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