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https://hdl.handle.net/10356/103835
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DC Field | Value | Language |
---|---|---|
dc.contributor.author | Bates, Roderick Wayland | en |
dc.contributor.author | Lim, Chia Juan | en |
dc.contributor.author | Collier, Steven J. | en |
dc.contributor.author | Sukumaran, Joly | en |
dc.date.accessioned | 2015-06-10T08:48:48Z | en |
dc.date.accessioned | 2019-12-06T21:21:18Z | - |
dc.date.available | 2015-06-10T08:48:48Z | en |
dc.date.available | 2019-12-06T21:21:18Z | - |
dc.date.copyright | 2015 | en |
dc.date.issued | 2015 | en |
dc.identifier.citation | Bates, 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.issn | 2193-5807 | en |
dc.identifier.uri | https://hdl.handle.net/10356/103835 | - |
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.iso | en | en |
dc.relation.ispartofseries | Asian journal of organic chemistry | en |
dc.rights | © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim. | en |
dc.subject | DRNTU::Science::Chemistry::Organic chemistry | en |
dc.title | Synthesis of (−)-deoxynupharidine by allenic hydroxylamine cyclisation | en |
dc.type | Journal Article | en |
dc.contributor.school | School of Physical and Mathematical Sciences | en |
dc.identifier.doi | 10.1002/ajoc.201500094 | en |
item.fulltext | No Fulltext | - |
item.grantfulltext | none | - |
Appears in Collections: | SPMS Journal Articles |
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