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dc.contributor.authorChen, Shi-Yenen_US
dc.contributor.authorPao, Yu-Chiehen_US
dc.contributor.authorSahoo, Santosh K.en_US
dc.contributor.authorHuang, Wen-Chiaen_US
dc.contributor.authorLai, Yu-Yingen_US
dc.contributor.authorCheng, Yen-Juen_US
dc.date.accessioned2018-08-21T05:53:16Z-
dc.date.available2018-08-21T05:53:16Z-
dc.date.issued2018-02-11en_US
dc.identifier.issn1359-7345en_US
dc.identifier.urihttp://dx.doi.org/10.1039/c7cc08852cen_US
dc.identifier.urihttp://hdl.handle.net/11536/144477-
dc.description.abstractA series of new unsymmetrical benzotrichalcogenophenes (BTCs) were synthesized by the Pd-N-heterocyclic carbene catalyzed intramolecular C3-arylation of furan, thiophene, selenophene and tellurophene units. This is the first time that a C3-direct arylation of selenophene and tellurophene moieties has ever been demonstrated.en_US
dc.language.isoen_USen_US
dc.titleSynthesis of unsymmetrical benzotrichalcogenophenes by N-heterocyclic carbene-palladium-catalyzed intramolecular direct C3-arylation of chalcogenophenesen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c7cc08852cen_US
dc.identifier.journalCHEMICAL COMMUNICATIONSen_US
dc.citation.volume54en_US
dc.citation.spage1517en_US
dc.citation.epage1520en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000424224800028en_US
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