Journal of the Chemical Society. Chemical communications p. 568 - 569 (1989)
Update date:2022-08-11
Topics:
McKenna, Eugene G.
Walker, Brian J.
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.
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