Please use this identifier to cite or link to this item: https://hdl.handle.net/10356/103835
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dc.contributor.authorBates, Roderick Waylanden
dc.contributor.authorLim, Chia Juanen
dc.contributor.authorCollier, Steven J.en
dc.contributor.authorSukumaran, Jolyen
dc.date.accessioned2015-06-10T08:48:48Zen
dc.date.accessioned2019-12-06T21:21:18Z-
dc.date.available2015-06-10T08:48:48Zen
dc.date.available2019-12-06T21:21:18Z-
dc.date.copyright2015en
dc.date.issued2015en
dc.identifier.citationBates, R. W., Lim, C. J., Collier, S. J., & Sukumaran, J. (2015). Synthesis of (−)-deoxynupharidine by allenic hydroxylamine cyclisation. Asian journal of organic chemistry, 4(7), 652-658.en
dc.identifier.issn2193-5807en
dc.identifier.urihttps://hdl.handle.net/10356/103835-
dc.identifier.urihttp://hdl.handle.net/10220/25855en
dc.description.abstract(−)-Deoxynupharidine has been synthesised via an intermediate that can also be used for other Nuphar alkaloids. Significant steps include the optimised enzymatic resolution of an allenic alcohol, highly diastereoselective silver-catalysed cyclisation of an allenic hydroxylamine, selective cross-metathesis, diastereoselective intramolecular reductive amination, and stereoelectronically controlled enolate alkylation.en
dc.language.isoenen
dc.relation.ispartofseriesAsian journal of organic chemistryen
dc.rights© 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.en
dc.subjectDRNTU::Science::Chemistry::Organic chemistryen
dc.titleSynthesis of (−)-deoxynupharidine by allenic hydroxylamine cyclisationen
dc.typeJournal Articleen
dc.contributor.schoolSchool of Physical and Mathematical Sciencesen
dc.identifier.doihttp://dx.doi.org/10.1002/ajoc.201500094en
item.grantfulltextnone-
item.fulltextNo Fulltext-
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