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dc.contributor.authorChang, Wong-Jinen_US
dc.contributor.authorKulkarni, Manohar V.en_US
dc.contributor.authorSun, Chung-Mingen_US
dc.date.accessioned2019-04-03T06:36:37Z-
dc.date.available2019-04-03T06:36:37Z-
dc.date.issued2015-01-01en_US
dc.identifier.issn2046-2069en_US
dc.identifier.urihttp://dx.doi.org/10.1039/c5ra18763jen_US
dc.identifier.urihttp://hdl.handle.net/11536/129446-
dc.description.abstractA one-pot multi component reaction of selenoureas, which are in situ generated from L-amino esters and isoselenocyanates, with alpha-bromoketone under ultrasonication. Selenourea and alpha-bromoketones formed 2-iminoselenazoles through a Hantzsch selenazole-type reaction. The steric effect of the alpha-substituted bromoketones on the rate of the tandem reaction was studied to understand the reaction mechanism by isolating the key reaction intermediate, 2-iminoselenol.en_US
dc.language.isoen_USen_US
dc.titleRegioselective one-pot three component synthesis of chiral 2-iminoselenazolines under sonicationen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c5ra18763jen_US
dc.identifier.journalRSC ADVANCESen_US
dc.citation.volume5en_US
dc.citation.issue118en_US
dc.citation.spage97113en_US
dc.citation.epage97120en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000365220100004en_US
dc.citation.woscount1en_US
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