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dc.contributor.authorFukuyama, Takahideen_US
dc.contributor.authorFujita, Yukien_US
dc.contributor.authorMiyoshi, Hayatoen_US
dc.contributor.authorRyu, Ilhyongen_US
dc.contributor.authorKao, Shih-Chiehen_US
dc.contributor.authorWu, Yen-Kuen_US
dc.date.accessioned2018-08-21T05:53:42Z-
dc.date.available2018-08-21T05:53:42Z-
dc.date.issued2018-06-04en_US
dc.identifier.issn1359-7345en_US
dc.identifier.urihttp://dx.doi.org/10.1039/c8cc02445fen_US
dc.identifier.urihttp://hdl.handle.net/11536/145051-
dc.description.abstractReduction of a variety of organo halides was examined by using amines as a sacrificial hydrogen source. UV light-induced reduction of vinyl and aryl halides with triethylamine proceeded smoothly to give the corresponding reduced products. High temperature heating also caused the reduction and DABCO (1,4-diazabicyclo[2.2.2]octane) also served as a good reducing reagent.en_US
dc.language.isoen_USen_US
dc.titleElectron transfer-induced reduction of organic halides with aminesen_US
dc.typeArticleen_US
dc.identifier.doi10.1039/c8cc02445fen_US
dc.identifier.journalCHEMICAL COMMUNICATIONSen_US
dc.citation.volume54en_US
dc.citation.spage5582en_US
dc.citation.epage5585en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000433510000018en_US
Appears in Collections:Articles


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