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dc.contributor.authorHO, TLen_US
dc.contributor.authorYANG, PFen_US
dc.date.accessioned2014-12-08T15:03:34Z-
dc.date.available2014-12-08T15:03:34Z-
dc.date.issued1995-01-02en_US
dc.identifier.issn0040-4020en_US
dc.identifier.urihttp://dx.doi.org/10.1016/0040-4020(94)00942-Nen_US
dc.identifier.urihttp://hdl.handle.net/11536/2108-
dc.description.abstractPhenolic sesquiterpenes including sesquichamaenol, 6-(2-hydroxy-4-methylphenyl)-2-methyl-3-beptanone, and curcuphenol methyl ether have been obtained from oxidative cleavage of bicyclic precursors by treatment with acidic hydrogen peroxide in a process which probably parallels a biogenetic step A ketone intermediate for curcudiol has also been acquired in the same manner.en_US
dc.language.isoen_USen_US
dc.titleSYNTHESIS OF PHENOLIC SESQUITERPENES VIA OXIDATIVE CLEAVAGE OF BENZOCYCLOALKENOLSen_US
dc.typeArticleen_US
dc.identifier.doi10.1016/0040-4020(94)00942-Nen_US
dc.identifier.journalTETRAHEDRONen_US
dc.citation.volume51en_US
dc.citation.issue1en_US
dc.citation.spage181en_US
dc.citation.epage192en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:A1995QB13700018-
dc.citation.woscount16-
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