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.
E. G. Mckenna and B. J. Walker, J. Chem. Soc., Chem. Commun., 1989, 568 DOI: 10.1039/C39890000568
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