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Please use this identifier to cite or link to this item: https://doi.org/10.1039/c2ob25327e
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dc.titleA highly enantioselective approach towards 2-substituted 3-bromopyrrolidines
dc.contributor.authorChen, J.
dc.contributor.authorZhou, L.
dc.contributor.authorYeung, Y.-Y.
dc.date.accessioned2014-06-23T05:30:14Z
dc.date.available2014-06-23T05:30:14Z
dc.date.issued2012-05-21
dc.identifier.citationChen, 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
dc.identifier.issn14770520
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/75428
dc.description.abstractA 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.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1039/c2ob25327e
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1039/c2ob25327e
dc.description.sourcetitleOrganic and Biomolecular Chemistry
dc.description.volume10
dc.description.issue19
dc.description.page3808-3811
dc.description.codenOBCRA
dc.identifier.isiut000303166500003
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