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dc.contributor.authorHo, TLen_US
dc.contributor.authorChen, CKen_US
dc.date.accessioned2014-12-08T15:17:35Z-
dc.date.available2014-12-08T15:17:35Z-
dc.date.issued2006en_US
dc.identifier.issn0018-019Xen_US
dc.identifier.urihttp://hdl.handle.net/11536/12762-
dc.identifier.urihttp://dx.doi.org/10.1002/hlca.200690003en_US
dc.description.abstractTangutorine (1) in the racemic form has been assembled from tryptamine and aldehyde 3. The synthetic design was based on uncovering a hidden symmetry in the nontryptamine portion of the norketone 2. A five-step process with an overall yield of 7% was developed in which 2 was transformed into the target molecule via a Vilsineier-Haack reaction and two reduction steps.en_US
dc.language.isoen_USen_US
dc.titleSynthesis of tangutorineen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/hlca.200690003en_US
dc.identifier.journalHELVETICA CHIMICA ACTAen_US
dc.citation.volume89en_US
dc.citation.issue1en_US
dc.citation.spage122en_US
dc.citation.epage126en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000234988100013-
dc.citation.woscount12-
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