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dc.contributor.authorRaju, Selvamen_US
dc.contributor.authorHsiao, Huan-Changen_US
dc.contributor.authorThirupathi, Selvakumaren_US
dc.contributor.authorChen, Pei-Lingen_US
dc.contributor.authorChuang, Shih-Chingen_US
dc.date.accessioned2019-04-02T05:58:20Z-
dc.date.available2019-04-02T05:58:20Z-
dc.date.issued2019-02-19en_US
dc.identifier.issn1615-4150en_US
dc.identifier.urihttp://dx.doi.org/10.1002/adsc.201801352en_US
dc.identifier.urihttp://hdl.handle.net/11536/148934-
dc.description.abstractWe report the first example of Pd(II)-catalyzed highly step- and atom-economical benzofulvenation through free amine-directed ortho C-H bond activation of o-arylanilines. This paper presents a novel, simple, and efficient approach for the synthesis of benzofulvene derivatives from o-arylaniline substrates through C-H bond activation with two diarylacetylenes as an implicit benzofulvene unit. The reactivity of synthesized benzofulvenes toward oxidation was investigated, and they were shown to transform into phenanthridines, oxabenzofulvenes, and fluorescent polycyclics.en_US
dc.language.isoen_USen_US
dc.subjectbenzofulveneen_US
dc.subjectC-H bond activationen_US
dc.subjectdiphenylacetyleneen_US
dc.subjecto-arylanilineen_US
dc.subjectpalladiumen_US
dc.titlePalladium-Catalyzed Benzofulvenation of o-Arylanilines through C-H Bond Activation by Using Two Diarylacetylenes as an Implicit Benzofulveneen_US
dc.typeArticleen_US
dc.identifier.doi10.1002/adsc.201801352en_US
dc.identifier.journalADVANCED SYNTHESIS & CATALYSISen_US
dc.citation.volume361en_US
dc.citation.spage683en_US
dc.citation.epage689en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000459822800005en_US
dc.citation.woscount0en_US
Appears in Collections:Articles