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dc.contributor.authorHo, TLen_US
dc.contributor.authorChein, RJen_US
dc.date.accessioned2014-12-08T15:17:01Z-
dc.date.available2014-12-08T15:17:01Z-
dc.date.issued2006-04-01en_US
dc.identifier.issn0009-4536en_US
dc.identifier.urihttp://hdl.handle.net/11536/12452-
dc.description.abstractFluorinated 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.isoen_USen_US
dc.subjectRitter reactionen_US
dc.subject4,5-dihydrooxazoleen_US
dc.titleRitter reaction of 1-aryl-1-fluoro-2-haloethanesen_US
dc.typeArticleen_US
dc.identifier.journalJOURNAL OF THE CHINESE CHEMICAL SOCIETYen_US
dc.citation.volume53en_US
dc.citation.issue2en_US
dc.citation.spage429en_US
dc.citation.epage430en_US
dc.contributor.department應用化學系zh_TW
dc.contributor.departmentDepartment of Applied Chemistryen_US
dc.identifier.wosnumberWOS:000237261100024-
dc.citation.woscount1-
Appears in Collections:Articles


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