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Please use this identifier to cite or link to this item: https://doi.org/10.1021/ol200840e
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dc.titleAminothiocarbamate-catalyzed asymmetric bromolactonization of 1,2-disubstituted olefinic acids
dc.contributor.authorTan, C.K.
dc.contributor.authorZhou, L.
dc.contributor.authorYeung, Y.-Y.
dc.date.accessioned2014-10-16T08:20:08Z
dc.date.available2014-10-16T08:20:08Z
dc.date.issued2011-05-20
dc.identifier.citationTan, C.K., Zhou, L., Yeung, Y.-Y. (2011-05-20). Aminothiocarbamate-catalyzed asymmetric bromolactonization of 1,2-disubstituted olefinic acids. Organic Letters 13 (10) : 2738-2741. ScholarBank@NUS Repository. https://doi.org/10.1021/ol200840e
dc.identifier.issn15237060
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/93077
dc.description.abstractAn efficient and enantioselective bromolactonization of 1,2-disubstituted olefinic acids using an amino-thiocarbamate catalyst has been developed, resulting in the formation of δ-lactones containing two chiral centers with up to 99% yield, 95% ee. © 2011 American Chemical Society.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ol200840e
dc.sourceScopus
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1021/ol200840e
dc.description.sourcetitleOrganic Letters
dc.description.volume13
dc.description.issue10
dc.description.page2738-2741
dc.identifier.isiut000290465800058
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