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Selective trifluorination of alkyl aryl sulfides using IF5
Ayuba, Shinichi
Hiramatsu, Chiharu
Fukuhara, Tsuyoshi
Hara, Shoji
?, ??
Location: http://www.elsevier.com/wps/find/journaldescription.cws_home/942/description#description
http://hdl.handle.net/2115/560
Tetrahedron. 60(50), 2004, 11445-11541
http://dx.doi.org/10.1016/j.tet.2004.09.076

In the reaction of IF5 with alkyl aryl sulfides in heptane under reflux conditions, the arylthio group migrated once and three fluorine atoms were selectively introduced on the alkyl chain. In order to find the reason why the reaction stopped at the trifluorination step, we examined the oxidation potentials of the starting material, a reaction intermediate, and the product, and the time course of the reactions.

Belongs to: Hokkaido University Collection of Scholarly and Academic Papers

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Selective trifluorination of alkyl aryl sulfides using IF5
Id. 5707262
Idioma inglés
Titulo Selective trifluorination of alkyl aryl sulfides using IF5
Autor(es) Ayuba, Shinichi
Hiramatsu, Chiharu
Fukuhara, Tsuyoshi
Hara, Shoji
?, ??
Location http://www.elsevier.com/wps/find/journaldescription.cws_home/942/description#description
http://hdl.handle.net/2115/560
Tetrahedron. 60(50), 2004, 11445-11541
http://dx.doi.org/10.1016/j.tet.2004.09.076
Versión 1.0
Estado Final
Descripción In the reaction of IF5 with alkyl aryl sulfides in heptane under reflux conditions, the arylthio group migrated once and three fluorine atoms were selectively introduced on the alkyl chain. In order to find the reason why the reaction stopped at the trifluorination step, we examined the oxidation potentials of the starting material, a reaction intermediate, and the product, and the time course of the reactions.
Tipo 84063 bytes
application/pdf
Palabras clave Halogenation
Tipo de recurso article (author version)
Tipo de Interactividad Expositivo
Nivel de Interactividad muy bajo
Audiencia Estudiante
Profesor
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Estructura Atomic
Coste no
Copyright
Formatos 84063 bytes
application/pdf
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Fecha de contribución 25-oct-2007
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