Regioselective one-pot three component synthesis of chiral 2-iminoselenazolines under sonication

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DC 欄位	值	語言
dc.contributor.author	Chang, Wong-Jin	en_US
dc.contributor.author	Kulkarni, Manohar V.	en_US
dc.contributor.author	Sun, Chung-Ming	en_US
dc.date.accessioned	2019-04-03T06:36:37Z	-
dc.date.available	2019-04-03T06:36:37Z	-
dc.date.issued	2015-01-01	en_US
dc.identifier.issn	2046-2069	en_US
dc.identifier.uri	http://dx.doi.org/10.1039/c5ra18763j	en_US
dc.identifier.uri	http://hdl.handle.net/11536/129446	-
dc.description.abstract	A 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.iso	en_US	en_US
dc.title	Regioselective one-pot three component synthesis of chiral 2-iminoselenazolines under sonication	en_US
dc.type	Article	en_US
dc.identifier.doi	10.1039/c5ra18763j	en_US
dc.identifier.journal	RSC ADVANCES	en_US
dc.citation.volume	5	en_US
dc.citation.issue	118	en_US
dc.citation.spage	97113	en_US
dc.citation.epage	97120	en_US
dc.contributor.department	應用化學系	zh_TW
dc.contributor.department	Department of Applied Chemistry	en_US
dc.identifier.wosnumber	WOS:000365220100004	en_US
dc.citation.woscount	1	en_US
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