Please use this identifier to cite or link to this item: https://doi.org/10.1021/ol5005609
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dc.titleN -bromosuccinimide-induced aminocyclization-aziridine ring-expansion cascade: An asymmetric and highly stereoselective approach toward the synthesis of azepane
dc.contributor.authorZhou, J.
dc.contributor.authorYeung, Y.-Y.
dc.date.accessioned2014-10-16T08:34:50Z
dc.date.available2014-10-16T08:34:50Z
dc.date.issued2014-04-18
dc.identifier.citationZhou, J., Yeung, Y.-Y. (2014-04-18). N -bromosuccinimide-induced aminocyclization-aziridine ring-expansion cascade: An asymmetric and highly stereoselective approach toward the synthesis of azepane. Organic Letters 16 (8) : 2134-2137. ScholarBank@NUS Repository. https://doi.org/10.1021/ol5005609
dc.identifier.issn15237052
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/94337
dc.description.abstractA novel N-bromosuccinimide induced aminocyclization-aziridine ring expansion cascade is reported. Substituted azepanes were isolated exclusively in good yields. The azepane products could be transformed into a number of functional molecules including piperidines, a bicyclic amine, and a bridgehead amide. © 2014 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ol5005609
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/ol5005609
dc.description.sourcetitleOrganic Letters
dc.description.volume16
dc.description.issue8
dc.description.page2134-2137
dc.description.codenORLEF
dc.identifier.isiut000334823600016
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