Formation and alkylation of enolates fro
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Irving J. Borowitz; E.W.R. Casper; R.K. Crouch
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Article
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1971
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Elsevier Science
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French
β 237 KB
The reactions of4+aloacetophenones, further substituted bye -halo or phenyl groups, with triphewlphosphine lead to isolable enol tripheqlphosphonium halides. 2,3 Cyclic &-haloketones, as typified by H-bromocyclohexanone, give the ketophosphonium ha1ide.h We have foundthat