SYNTHETIC STUDIES TOWARDS FAVELINE METHYL-ETHER

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DC Field	Value	Language
dc.contributor.author	HO, TL	en_US
dc.contributor.author	CHEN, CK	en_US
dc.date.accessioned	2014-12-08T15:03:22Z	-
dc.date.available	2014-12-08T15:03:22Z	-
dc.date.issued	1995-05-15	en_US
dc.identifier.issn	0040-4020	en_US
dc.identifier.uri	http://dx.doi.org/10.1016/0040-4020(95)00240-9	en_US
dc.identifier.uri	http://hdl.handle.net/11536/1917	-
dc.description.abstract	A convergent approach to faveline methyl ether based on Claisen rearrangement is delineated Thus the benzylic and allylic alcohol substrate was assembled by a Grignard reaction, and the rearrangement product was oxidized and cyclized. Double bond isomers of faveline methyl ether were obtained.	en_US
dc.language.iso	en_US	en_US
dc.title	SYNTHETIC STUDIES TOWARDS FAVELINE METHYL-ETHER	en_US
dc.type	Article	en_US
dc.identifier.doi	10.1016/0040-4020(95)00240-9	en_US
dc.identifier.journal	TETRAHEDRON	en_US
dc.citation.volume	51	en_US
dc.citation.issue	20	en_US
dc.citation.spage	5819	en_US
dc.citation.epage	5824	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:A1995QY11200010	-
dc.citation.woscount	4	-
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