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Wittig reactions of ylide anions derived from stabilised ylides
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1989
Year
Cross-coupling ReactionNitrile-stabilised Ylide AnionsEngineeringAlkene MetathesisStabilised Triphenylphosphonium YlidesOrganic ChemistryOrganometallic CatalysisCatalysisReaction IntermediateChemistryReaction ProcessPhenyl SubstituentBiomolecular EngineeringWittig Reactions
Ester- and nitrile-stabilised ylide anions are more reactive than the corresponding ylides and react with aldehydes and ketones to give alkenes in good yields; the reactivity of stabilised triphenylphosphonium ylides is greatly increased by the replacement of one phenyl substituent.