Stereochimie comparative de bromation,dans l'ether,d'enolates lithique et potassique,d'ethers d'enol methyliques et d'enols en serie 4-t.butyl 1-benzoyl cyclohexane et en serie β-phenyl butyrophenone |
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Authors: | M Bettahar M Charpentier-Morize |
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Institution: | G.R. 12, C.N.R.S., 2 à 8 Rue Henri Dunant, 94320 Thiais, France |
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Abstract: | The steric course of bromination of cyclic and acyclic metal enolates in ether, independent of the nature of the metal (lithium or potassium), is identical to that of enols but very different from that of methyl enol ethers. The stereochemical results are compatible with the previously postulated six-centre cyclic halogenation mechanisms of enols |
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