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https://doi.org/10.1039/c2ob25327e
| Title: | A highly enantioselective approach towards 2-substituted 3-bromopyrrolidines | Authors: | Chen, J. Zhou, L. Yeung, Y.-Y. |
Issue Date: | 21-May-2012 | Citation: | Chen, J., Zhou, L., Yeung, Y.-Y. (2012-05-21). A highly enantioselective approach towards 2-substituted 3-bromopyrrolidines. Organic and Biomolecular Chemistry 10 (19) : 3808-3811. ScholarBank@NUS Repository. https://doi.org/10.1039/c2ob25327e | Abstract: | A facile and highly enantioselective approach towards 2-substituted 3-bromopyrrolidines has been developed. The process involves an amino-thiocarbamate catalyzed bromoaminocyclization of 1,2-disubstituted olefinic amides. The pyrrolidine products could readily be converted into other useful building blocks including a dihydropyrrole and a 2-substituted pyrrolidine. © 2012 The Royal Society of Chemistry. | Source Title: | Organic and Biomolecular Chemistry | URI: | http://scholarbank.nus.edu.sg/handle/10635/75428 | ISSN: | 14770520 | DOI: | 10.1039/c2ob25327e |
| Appears in Collections: | Staff Publications |
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