Total synthesis of (+)-beta-himachalene

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DC Field	Value	Language
dc.contributor.author	Ho, TL	en_US
dc.contributor.author	Chein, RJ	en_US
dc.date.accessioned	2014-12-08T15:17:44Z	-
dc.date.available	2014-12-08T15:17:44Z	-
dc.date.issued	2006	en_US
dc.identifier.issn	0018-019X	en_US
dc.identifier.uri	http://hdl.handle.net/11536/12886	-
dc.identifier.uri	http://dx.doi.org/10.1002/hlca.200690025	en_US
dc.description.abstract	An enantioselective synthesis of (+)-beta-himachalene (2) was accomplished starting from (1S,2R)-1,2-epoxy-p-menth-8-ene (3) in 15 or 16 steps with an overall yield of ca. 6% (Schemes 3, 5, and 6). Key transformations include an Ireland Claisen rearrangement, a Corey oxidative cyclization, and a ring expansion.	en_US
dc.language.iso	en_US	en_US
dc.title	Total synthesis of (+)-beta-himachalene	en_US
dc.type	Article	en_US
dc.identifier.doi	10.1002/hlca.200690025	en_US
dc.identifier.journal	HELVETICA CHIMICA ACTA	en_US
dc.citation.volume	89	en_US
dc.citation.issue	2	en_US
dc.citation.spage	231	en_US
dc.citation.epage	239	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:000235742400006	-
dc.citation.woscount	6	-
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