Electron transfer-induced reduction of organic halides with amines

dc.citation.epage	5585	en_US
dc.citation.spage	5582	en_US
dc.citation.volume	54	en_US
dc.contributor.author	Fukuyama, Takahide	en_US
dc.contributor.author	Fujita, Yuki	en_US
dc.contributor.author	Miyoshi, Hayato	en_US
dc.contributor.author	Ryu, Ilhyong	en_US
dc.contributor.author	Kao, Shih-Chieh	en_US
dc.contributor.author	Wu, Yen-Ku	en_US
dc.contributor.department	應用化學系	zh_TW
dc.contributor.department	Department of Applied Chemistry	en_US
dc.date.accessioned	2018-08-21T05:53:42Z
dc.date.available	2018-08-21T05:53:42Z
dc.date.issued	2018-06-04	en_US
dc.description.abstract	Reduction 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.identifier.doi	10.1039/c8cc02445f	en_US
dc.identifier.issn	1359-7345	en_US
dc.identifier.journal	CHEMICAL COMMUNICATIONS	en_US
dc.identifier.uri	http://dx.doi.org/10.1039/c8cc02445f	en_US
dc.identifier.uri	https://ir.lib.nycu.edu.tw/handle/11536/145051
dc.identifier.wosnumber	WOS:000433510000018	en_US
dc.language.iso	en_US	en_US
dc.title	Electron transfer-induced reduction of organic halides with amines	en_US
dc.type	Article	en_US

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