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dc.contributor.authorHo, TLen_US
dc.contributor.authorChein, RJen_US
dc.date.accessioned2019-04-02T05:59:34Z-
dc.date.available2019-04-02T05:59:34Z-
dc.date.issued1996-05-21en_US
dc.identifier.issn1359-7345en_US
dc.identifier.urihttp://dx.doi.org/10.1039/cc9960001147en_US
dc.identifier.urihttp://hdl.handle.net/11536/149193-
dc.description.abstractFurodysinin is synthesised by elaboration of (1R, 2R)-(+)-limonene oxide; key reactions include a tandem Claisen rearrangement-ene reaction and trapping of a conjugate adduct of an enone providing a bicyclic precursor of the sesquiterpene.en_US
dc.language.isoen_USen_US
dc.titleSynthesis of (-)-furodysinin from (+)-limoneneen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/cc9960001147en_US
dc.identifier.journalCHEMICAL COMMUNICATIONSen_US
dc.citation.spage1147en_US
dc.citation.epage1147en_US
dc.contributor.department應用數學系zh_TW
dc.contributor.departmentDepartment of Applied Mathematicsen_US
dc.identifier.wosnumberWOS:A1996UN96900029en_US
dc.citation.woscount5en_US
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