Diphenylphosphinoyl chloride as a chlorinating agent - The selective double activation of 1,2-diols

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dc.contributor.authorFox, David J.en
dc.contributor.authorPedersen, Daniel Sejeren
dc.contributor.authorPetersen, Asger B.en
dc.contributor.authorWarren, Stuarten
dc.contributor.schoolSchool of Chemistry and Physics : Chemistryen
dc.date.issued2006en
dc.description© The Royal Society of Chemistry 2006en
dc.description.abstractTreatment of 1,2-diols with diphenylphosphinoyl chloride in pyridine produces beta-chloroethyl phosphinates which react with complete control of stereochemistry to give epoxides and azido-alcohols, useful intermediates in cyclopropane synthesis.en
dc.description.statementofresponsibilityDavid J. Fox, Daniel Sejer Pedersen, Asger B. Petersen and Stuart Warrenen
dc.identifier.citationOrganic and Biomolecular Chemistry , 2006; 4 (16):3117-3119en
dc.identifier.doi10.1039/b606881ben
dc.identifier.issn1477-0520en
dc.identifier.urihttp://hdl.handle.net/2440/47526
dc.publisherRoyal Society Chemistryen
dc.titleDiphenylphosphinoyl chloride as a chlorinating agent - The selective double activation of 1,2-diolsen
dc.typeJournal articleen

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