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Please use this identifier to cite or link to this item: https://doi.org/10.1002/anie.201304107
DC FieldValue
dc.titleCatalytic, enantioselective, and highly chemoselective bromocyclization of olefinic dicarbonyl compounds
dc.contributor.authorZhao, Y.
dc.contributor.authorJiang, X.
dc.contributor.authorYeung, Y.-Y.
dc.date.accessioned2014-06-23T05:33:36Z
dc.date.available2014-06-23T05:33:36Z
dc.date.issued2013-08-12
dc.identifier.citationZhao, Y., Jiang, X., Yeung, Y.-Y. (2013-08-12). Catalytic, enantioselective, and highly chemoselective bromocyclization of olefinic dicarbonyl compounds. Angewandte Chemie - International Edition 52 (33) : 8597-8601. ScholarBank@NUS Repository. https://doi.org/10.1002/anie.201304107
dc.identifier.issn14337851
dc.identifier.urihttp://scholarbank.nus.edu.sg/handle/10635/75701
dc.description.abstractOverriding preferences: An amine-thiocarbamate catalyst can mediate the facile, efficient, and highly enantioselective bromocyclization of olefinic 1,3-dicarbonyl compounds. In the presence of the bifunctional catalyst, the bromination occurs chemoselectively at the olefinic moiety rather than at the carbon atom in the α-position to the carbonyl units. Copyright © 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
dc.description.urihttp://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1002/anie.201304107
dc.sourceScopus
dc.subjectasymmetric catalysis
dc.subjectchemoselectivity
dc.subjectcyclization
dc.subjectfurans
dc.subjectLewis bases
dc.typeArticle
dc.contributor.departmentCHEMISTRY
dc.description.doi10.1002/anie.201304107
dc.description.sourcetitleAngewandte Chemie - International Edition
dc.description.volume52
dc.description.issue33
dc.description.page8597-8601
dc.description.codenACIEF
dc.identifier.isiut000322835700023
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