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Please use this identifier to cite or link to this item: https://doi.org/10.1021/ja311202e
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dc.titleC2-symmetric cyclic selenium-catalyzed enantioselective bromoaminocyclization
dc.contributor.authorChen, F.
dc.contributor.authorTan, C.K.
dc.contributor.authorYeung, Y.-Y.
dc.date.accessioned2014-10-16T08:21:48Z
dc.date.available2014-10-16T08:21:48Z
dc.date.issued2013-01-30
dc.identifier.citationChen, F., Tan, C.K., Yeung, Y.-Y. (2013-01-30). C2-symmetric cyclic selenium-catalyzed enantioselective bromoaminocyclization. Journal of the American Chemical Society 135 (4) : 1232-1235. ScholarBank@NUS Repository. https://doi.org/10.1021/ja311202e
dc.identifier.issn00027863
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/93221
dc.description.abstractA catalytic asymmetric bromocyclization of trisubstituted olefinic amides that uses a C2-symmetric mannitol-derived cyclic selenium catalyst and a stoichiometric amount of N-bromophthalimide is reported. The resulting enantioenriched pyrrolidine products, which contain two stereogenic centers, can undergo rearrangement to yield 2,3-disubstituted piperidines with excellent diastereoselectivity and enantiospecificity. © 2013 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ja311202e
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/ja311202e
dc.description.sourcetitleJournal of the American Chemical Society
dc.description.volume135
dc.description.issue4
dc.description.page1232-1235
dc.description.codenJACSA
dc.identifier.isiut000314492500016
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