完整後設資料紀錄
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dc.contributor.authorTseng, Yi-Lunen_US
dc.contributor.authorLiang, Min-Chiehen_US
dc.contributor.authorChen, I-Chiaen_US
dc.contributor.authorWu, Yen-Kuen_US
dc.date.accessioned2018-08-21T05:53:23Z-
dc.date.available2018-08-21T05:53:23Z-
dc.date.issued2018-03-01en_US
dc.identifier.issn0936-5214en_US
dc.identifier.urihttp://dx.doi.org/10.1055/s-0036-1591739en_US
dc.identifier.urihttp://hdl.handle.net/11536/144627-
dc.description.abstractA concise approach to the total syntheses of racemic paniculidines B and C is described. The route features a combined Tamaru allylation/olefin cross-metathesis sequence for the regiocontrolled synthesis of prenylindole intermediates. In addition, we report a transformation of the prenylated indole into 2-methylcarbazole catalyzed by sulfonic acid-functionalized silica gel.en_US
dc.language.isoen_USen_US
dc.subjectprenylindolesen_US
dc.subjectTamaru allylationen_US
dc.subjectcross-metathesisen_US
dc.subjectcarbazolesen_US
dc.subjecttotal synthesisen_US
dc.subjectalkaloidsen_US
dc.titleA Combined Tamaru Allylation/Olefin Cross-Metathesis Approach for the Total Syntheses of (+/-)-Paniculidine B, (+/-)-Paniculidine C, and 2-Methylcarbazoleen_US
dc.typeArticleen_US
dc.identifier.doi10.1055/s-0036-1591739en_US
dc.identifier.journalSYNLETTen_US
dc.citation.volume29en_US
dc.citation.spage609en_US
dc.citation.epage612en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000426600100015en_US
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