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pubmed-article:12735775pubmed:dateCreated2003-5-8lld:pubmed
pubmed-article:12735775pubmed:abstractText[reaction: see text] Electrophilic activation of hydrogen peroxide can be achieved in acidic alcohol solvents without the need for a metal catalyst. This concept is illustrated by the epoxidation of alkenes with H(2)O(2) employing phenol as a solvent. It is proposed that intermolecular hydrogen bonding between H(2)O(2) and phenol activates H(2)O(2) for oxygen-atom transfer. In this interaction, the role of phenol is purely catalytic.lld:pubmed
pubmed-article:12735775pubmed:languageenglld:pubmed
pubmed-article:12735775pubmed:journalhttp://linkedlifedata.com/r...lld:pubmed
pubmed-article:12735775pubmed:statusPubMed-not-MEDLINElld:pubmed
pubmed-article:12735775pubmed:monthMaylld:pubmed
pubmed-article:12735775pubmed:issn1523-7060lld:pubmed
pubmed-article:12735775pubmed:authorpubmed-author:De VosDirk...lld:pubmed
pubmed-article:12735775pubmed:authorpubmed-author:JacobsPierre...lld:pubmed
pubmed-article:12735775pubmed:authorpubmed-author:WahlenJoosJlld:pubmed
pubmed-article:12735775pubmed:issnTypePrintlld:pubmed
pubmed-article:12735775pubmed:day15lld:pubmed
pubmed-article:12735775pubmed:volume5lld:pubmed
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pubmed-article:12735775pubmed:pagination1777-80lld:pubmed
pubmed-article:12735775pubmed:year2003lld:pubmed
pubmed-article:12735775pubmed:articleTitleActivation of hydrogen peroxide through hydrogen-bonding interaction with acidic alcohols: epoxidation of alkenes in phenol.lld:pubmed
pubmed-article:12735775pubmed:affiliationDepartment of Interphase Chemistry, Centre for Surface Chemistry and Catalysis, Katholieke Universiteit Leuven, Kasteelpark Arenberg 23, B-3001 Heverlee, Belgium.lld:pubmed
pubmed-article:12735775pubmed:publicationTypeJournal Articlelld:pubmed