Extension de la reaction de Wittig: Condensation “d'ylures enolates” sur les cetones aliphatiques |
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Authors: | C Broquet |
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Institution: | C.N.R.S., Groupe de Recherche no 12, 2 rue H. Dunant, 94320 Thiais, France |
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Abstract: | The enolate ylide Ph3P+C?C(Ph)O?Li+ obtained by the reaction of HMPT-Li with the benzoylmethylenetriphenylphosphorane Ph3PCHCOPh reacts with aliphatic ketones, in contrast to its precursor. This condensation makes it possible to prepare β,γ-unsaturated ketones, of type RCHC(R′)CH2COPh, instead of the α,β isomer usually obtained in a Wittig reaction. |
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