A novel photoinduced ring opening and isomerization of adamantane-2-spiro isoxazolines using MO(CO)(6)

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DC Field	Value	Language
dc.contributor.author	Senthilvelan, Annamalai	en_US
dc.contributor.author	Lee, Gene-Hsiang	en_US
dc.contributor.author	Chung, Wen-Sheng	en_US
dc.date.accessioned	2014-12-08T15:15:38Z	-
dc.date.available	2014-12-08T15:15:38Z	-
dc.date.issued	2006-10-02	en_US
dc.identifier.issn	0040-4039	en_US
dc.identifier.uri	http://dx.doi.org/10.1016/j.tetlet.2006.07.156	en_US
dc.identifier.uri	http://hdl.handle.net/11536/11687	-
dc.description.abstract	The MO(Co)(6)-mediated photoinduced ring-opening reactions of adamantane isoxazolines involve novel rearrangement that provide enaminoketones as major products and beta-hydroxy ketones as minor ones; in contrast, only beta-hydroxy ketones and alpha,beta-unsaturated ketones were obtained under thermal condition. (c) 2006 Elsevier Ltd. All rights reserved.	en_US
dc.language.iso	en_US	en_US
dc.subject	adamantane isoxazolines	en_US
dc.subject	photorearrangement	en_US
dc.subject	isomerization	en_US
dc.subject	enaminoketones	en_US
dc.title	A novel photoinduced ring opening and isomerization of adamantane-2-spiro isoxazolines using MO(CO)(6)	en_US
dc.type	Article	en_US
dc.identifier.doi	10.1016/j.tetlet.2006.07.156	en_US
dc.identifier.journal	TETRAHEDRON LETTERS	en_US
dc.citation.volume	47	en_US
dc.citation.issue	40	en_US
dc.citation.spage	7179	en_US
dc.citation.epage	7183	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:000240887000013	-
dc.citation.woscount	9	-
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