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Palladium-Catalyzed Cascade Arylation of Vinylogous Esters Enabled by Tris(1-adamantyl)phosphine

dc.citation.epage9290en_US
dc.citation.issue23en_US
dc.citation.spage9286en_US
dc.citation.volume21en_US
dc.citation.woscount0en_US
dc.contributor.authorYang, Yi-Chien_US
dc.contributor.authorLin, Yi-Chingen_US
dc.contributor.authorWu, Yen-Kuen_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.date.accessioned2020-01-02T00:04:19Z
dc.date.available2020-01-02T00:04:19Z
dc.date.issued2019-12-06en_US
dc.description.abstractDescribed is a method for the transformation of a cyclic vinylogous ester to the corresponding polyarylated product. We found a catalytic system comprising palladium diacetate and tris(1-adamantyl)phosphine is quite effective in promoting a set of controlled cascade arylations. As a result, a range of novel (hetero)aryl-containing scaffolds was synthesized with a high level of efficiency.en_US
dc.identifier.doi10.1021/acs.orglett.9b03071en_US
dc.identifier.issn1523-7060en_US
dc.identifier.journalORGANIC LETTERSen_US
dc.identifier.urihttp://dx.doi.org/10.1021/acs.orglett.9b03071en_US
dc.identifier.urihttps://ir.lib.nycu.edu.tw/handle/11536/153368
dc.identifier.wosnumberWOS:000502163300002en_US
dc.language.isoen_USen_US
dc.titlePalladium-Catalyzed Cascade Arylation of Vinylogous Esters Enabled by Tris(1-adamantyl)phosphineen_US
dc.typeArticleen_US

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