EPOXIDATION OF ISOLATED DOUBLE BONDS WITH 30% HYDROGEN PEROXIDE CATALYZED BY PERTUNGSTATE SALTS

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dc.contributor.authorJ.Prandi, H.B.Kagan
dc.date.accessioned2012-11-09T09:05:11Z
dc.date.accessioned2025-02-17T13:59:35Z
dc.date.available2012-11-09T09:05:11Z
dc.date.issued2012-11-09
dc.descriptionA practical procedure for the epoxidation of alkenes is described. The reaction is performed between 30 and 5O“C in 1,2-dichloroethane with 30% hydrogen peroxide and acatalytic amount of a quaternary phosphonium or ammonium pertungstate. Allylic alcohols are very reactive and require lower temperatures for their epoxidation.en_US
dc.description.abstractA practical procedure for the epoxidation of alkenes is described. The reaction is performed between 30 and 5O“C in 1,2-dichloroethane with 30% hydrogen peroxide and acatalytic amount of a quaternary phosphonium or ammonium pertungstate. Allylic alcohols are very reactive and require lower temperatures for their epoxidation.en_US
dc.identifier.urihttps://dl.ftveti.edu.et/handle/123456789/3977
dc.language.isoenen_US
dc.subjectEPOXIDATION OF ISOLATED DOUBLE BONDS WITH 30% HYDROGEN PEROXIDE CATALYZED BY PERTUNGSTATE SALTSen_US
dc.titleEPOXIDATION OF ISOLATED DOUBLE BONDS WITH 30% HYDROGEN PEROXIDE CATALYZED BY PERTUNGSTATE SALTSen_US
dc.typeArticleen_US

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