Please use this identifier to cite or link to this item: 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
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