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Please use this identifier to cite or link to this item: https://doi.org/10.1021/ja104168q
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dc.titleFacile, efficient, and catalyst-free electrophilic aminoalkoxylation of olefins: Scope and application
dc.contributor.authorZhou, L.
dc.contributor.authorTan, C.K.
dc.contributor.authorZhou, J.
dc.contributor.authorYeung, Y.-Y.
dc.date.accessioned2014-06-23T05:39:25Z
dc.date.available2014-06-23T05:39:25Z
dc.date.issued2010-08-04
dc.identifier.citationZhou, L., Tan, C.K., Zhou, J., Yeung, Y.-Y. (2010-08-04). Facile, efficient, and catalyst-free electrophilic aminoalkoxylation of olefins: Scope and application. Journal of the American Chemical Society 132 (30) : 10245-10247. ScholarBank@NUS Repository. https://doi.org/10.1021/ja104168q
dc.identifier.issn00027863
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/76169
dc.description.abstractA new one-pot electrophilic aminoalkoxylation reaction using olefin, cyclic ether, amine, and N-bromosuccinimide has been developed. The olefinic substrates and the cyclic ether partners can be flexibly varied to produce a range of amino ether derivatives. This novel protocol has been applied in the facile and efficient synthesis of biologically active morpholine compounds. © 2010 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ja104168q
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/ja104168q
dc.description.sourcetitleJournal of the American Chemical Society
dc.description.volume132
dc.description.issue30
dc.description.page10245-10247
dc.description.codenJACSA
dc.identifier.isiut000280456100013
Appears in Collections:Staff Publications

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