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I know that if I treat a ketone like cyclohexanone with SiMe₃Cl I'll get a sylil enol ether.

Now is this process  quantitative?
Or in the solution I have some cyclohexanone and some silyl enol ether....    ??  Because in this case I also get the self condensation product in a crossed aldol condensation


(I think that with silyl enol ether the self condensation should be minimal because looking to wikipedia I've seen that in order to avoid a self condensation of an aldehyde I should convert  it  in a silyl enol ether! )

thanks