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Please use this identifier to cite or link to this item: https://doi.org/10.1021/ja201627h
DC FieldValue
dc.titleEnantioselective bromoaminocyclization using amino-thiocarbamate catalysts
dc.contributor.authorZhou, L.
dc.contributor.authorChen, J.
dc.contributor.authorTan, C.K.
dc.contributor.authorYeung, Y.-Y.
dc.date.accessioned2014-06-23T05:38:31Z
dc.date.available2014-06-23T05:38:31Z
dc.date.issued2011-06-22
dc.identifier.citationZhou, L., Chen, J., Tan, C.K., Yeung, Y.-Y. (2011-06-22). Enantioselective bromoaminocyclization using amino-thiocarbamate catalysts. Journal of the American Chemical Society 133 (24) : 9164-9167. ScholarBank@NUS Repository. https://doi.org/10.1021/ja201627h
dc.identifier.issn00027863
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/76096
dc.description.abstractA facile and efficient enantioselective bromoaminocyclization of unsaturated sulfonamides has been developed using an amino-thiocarbamate catalyst. A range of enantioenriched pyrrolidines were prepared with up to 99% yield and 99% ee. The corresponding lactams could be obtained through oxidation of the pyrrolidines. © 2011 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ja201627h
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/ja201627h
dc.description.sourcetitleJournal of the American Chemical Society
dc.description.volume133
dc.description.issue24
dc.description.page9164-9167
dc.description.codenJACSA
dc.identifier.isiut000291915100008
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