dc.contributor.authorChew, Renta Jonathan
dc.contributor.authorHuang, Yinhua
dc.contributor.authorLi, Yongxin
dc.contributor.authorPullarkat, Sumod A.
dc.contributor.authorLeung, Pak-Hing
dc.date.accessioned2014-04-09T07:42:11Z
dc.date.available2014-04-09T07:42:11Z
dc.date.copyright2013en_US
dc.date.issued2013
dc.identifier.citationChew, R. J., Huang, Y., Li, Y., Pullarkat, S. A., & Leung, P. H. (2013). Enantioselective addition of diphenylphosphine to 3-methyl-4-nitro-5-alkenylisoxazoles. Advanced Synthesis & Catalysis, 355(7), 1403-1408.en_US
dc.identifier.issn1615-4150en_US
dc.identifier.urihttp://hdl.handle.net/10220/19200
dc.description.abstractAn enantioselective Michael addition reaction of diphenylphosphine to substituted alkenylisoxazoles has been developed. The reaction proceeds efficiently under mild conditions with high yields (up to 99%) and moderate to excellent enantioselectivities (up to 92%) thus providing a hitherto unavailable direct access to a library of chiral tertiary phosphine-functionalized isoxazoles.en_US
dc.language.isoenen_US
dc.relation.ispartofseriesAdvanced Synthesis & Catalysisen_US
dc.rights© 2013 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.en_US
dc.subjectDRNTU::Science::Chemistry::Organic chemistry
dc.titleEnantioselective addition of diphenylphosphine to 3-methyl-4-nitro-5-alkenylisoxazolesen_US
dc.typeJournal Article
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen_US
dc.identifier.doihttp://dx.doi.org/10.1002/adsc.201300164


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