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dc.contributor.authorHo, TLen_US
dc.contributor.authorChang, MHen_US
dc.date.accessioned2014-12-08T15:46:13Z-
dc.date.available2014-12-08T15:46:13Z-
dc.date.issued1999-09-07en_US
dc.identifier.issn0300-922Xen_US
dc.identifier.urihttp://dx.doi.org/10.1039/a904068den_US
dc.identifier.urihttp://hdl.handle.net/11536/31092-
dc.description.abstractA dihydroisobenzofuran (13) was obtained from beta-ionone in 10 steps via an intramolecular Diels-Alder reaction. On further oxidation, reductive ring opening and decarboxylation, cuparene and herbertene were synthesized.en_US
dc.language.isoen_USen_US
dc.titleSynthesis of cuparene and herbertene via a common intermediateen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/a904068den_US
dc.identifier.journalJOURNAL OF THE CHEMICAL SOCIETY-PERKIN TRANSACTIONS 1en_US
dc.citation.volumeen_US
dc.citation.issue17en_US
dc.citation.spage2479en_US
dc.citation.epage2482en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000082423200014-
dc.citation.woscount22-
Appears in Collections:Articles


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