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dc.contributor.authorFukuyama, Takahideen_US
dc.contributor.authorRahman, Md Taifuren_US
dc.contributor.authorMashima, Hiroshien_US
dc.contributor.authorTakahashi, Hideoen_US
dc.contributor.authorRyu, Ilhyongen_US
dc.date.accessioned2018-08-21T05:54:27Z-
dc.date.available2018-08-21T05:54:27Z-
dc.date.issued2017-09-01en_US
dc.identifier.issn2052-4129en_US
dc.identifier.urihttp://dx.doi.org/10.1039/c7qo00331een_US
dc.identifier.urihttp://hdl.handle.net/11536/145962-
dc.description.abstractThe ionic liquids bearing an aromatic vinylic C-H moiety are not innocent during Pd-catalyzed crosscoupling reactions of aryl halides, since palladium-catalyzed direct C-H arylation of thiazolium and imidazolium ionic liquids competes.en_US
dc.language.isoen_USen_US
dc.titleIonic liquids are not innocent in Pd catalysis. C-H arylation of thiazolium and imidazolium ionic liquids with aryl halidesen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c7qo00331een_US
dc.identifier.journalORGANIC CHEMISTRY FRONTIERSen_US
dc.citation.volume4en_US
dc.citation.spage1863en_US
dc.citation.epage1866en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000408263400027en_US
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