Ritter reaction of 1-aryl-1-fluoro-2-haloethanes

完整後設資料紀錄

DC 欄位	值	語言
dc.contributor.author	Ho, TL	en_US
dc.contributor.author	Chein, RJ	en_US
dc.date.accessioned	2014-12-08T15:17:01Z	-
dc.date.available	2014-12-08T15:17:01Z	-
dc.date.issued	2006-04-01	en_US
dc.identifier.issn	0009-4536	en_US
dc.identifier.uri	http://hdl.handle.net/11536/12452	-
dc.description.abstract	Fluorinated phenethyl bromides 1, 2, and 3, prove to be totally inert under Ritter reaction conditions in the presence of either SnCl4 or AgNO3, due to the strong deactivation by the gem-difluoro unit. Subjecting 2-bromo-1-fluoro-1-phenylethane to SnCl4 in MeCN at elevated temperatures led to formation of 2-methyl-4-phenyl-4,5-dihydrooxazole.	en_US
dc.language.iso	en_US	en_US
dc.subject	Ritter reaction	en_US
dc.subject	4,5-dihydrooxazole	en_US
dc.title	Ritter reaction of 1-aryl-1-fluoro-2-haloethanes	en_US
dc.type	Article	en_US
dc.identifier.journal	JOURNAL OF THE CHINESE CHEMICAL SOCIETY	en_US
dc.citation.volume	53	en_US
dc.citation.issue	2	en_US
dc.citation.spage	429	en_US
dc.citation.epage	430	en_US
dc.contributor.department	應用化學系	zh_TW
dc.contributor.department	Department of Applied Chemistry	en_US
dc.identifier.wosnumber	WOS:000237261100024	-
dc.citation.woscount	1	-
顯示於類別：	期刊論文