Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/103844
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dc.contributor.authorZong, Lilien
dc.contributor.authorBan, Xuen
dc.contributor.authorKee, Choon Weeen
dc.contributor.authorTan, Choon-Hongen
dc.date.accessioned2015-01-15T08:16:41Zen
dc.date.accessioned2019-12-06T21:21:28Z-
dc.date.available2015-01-15T08:16:41Zen
dc.date.available2019-12-06T21:21:28Z-
dc.date.copyright2014en
dc.date.issued2014en
dc.identifier.citationg, L., Ban, X., Kee, C. W., & Tan, C.-H. (2014). Catalytic enantioselective alkylation of sulfenate anions to chiral heterocyclic sulfoxides using halogenated pentanidium salts. Angewandte chemie international edition, 53(44), 11849-11853.en
dc.identifier.issn1433-7851en
dc.identifier.urihttps://hdl.handle.net/10356/103844-
dc.description.abstractWe report halogenated pentanidiums as phase-transfer catalysts for the asymmetric alkylation of sulfenate anions to various sulfoxides with high enantioselectivities (up to 99 % ee) and yields (up to 99 %). This approach gives access to enantioenriched heterocyclic sulfoxides that might not be compatible with strong oxidants or organometallic reagents. Computational studies have revealed that the multiple noncovalent interactions such as halogen bonds and nonclassical hydrogen bonds are involved.en
dc.language.isoenen
dc.relation.ispartofseriesAngewandte chemie international editionen
dc.rights© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.en
dc.subjectDRNTU::Science::Chemistry::Physical chemistry::Catalysisen
dc.titleCatalytic enantioselective alkylation of sulfenate anions to chiral heterocyclic sulfoxides using halogenated pentanidium saltsen
dc.typeJournal Articleen
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen
dc.identifier.doi10.1002/anie.201407512en
item.grantfulltextnone-
item.fulltextNo Fulltext-
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