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dc.contributor.authorHo, TLen_US
dc.contributor.authorChein, RJen_US
dc.date.accessioned2014-12-08T15:17:44Z-
dc.date.available2014-12-08T15:17:44Z-
dc.date.issued2006en_US
dc.identifier.issn0018-019Xen_US
dc.identifier.urihttp://hdl.handle.net/11536/12886-
dc.identifier.urihttp://dx.doi.org/10.1002/hlca.200690025en_US
dc.description.abstractAn 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.isoen_USen_US
dc.titleTotal synthesis of (+)-beta-himachaleneen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/hlca.200690025en_US
dc.identifier.journalHELVETICA CHIMICA ACTAen_US
dc.citation.volume89en_US
dc.citation.issue2en_US
dc.citation.spage231en_US
dc.citation.epage239en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000235742400006-
dc.citation.woscount6-
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