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|    Message 54,448 of 55,615    |
|    Peter Jason to All    |
|    Enolate synthesis question.    |
|    29 Sep 18 11:12:45    |
      From: pj@jostle.com              In a crossed Claisen reaction between esters, one       of which has no alpha-hydrogens, can this latter       be used as solvent for the reaction for dissolving       NaEhoxide, KEthoxide etc.              For the synthesis of a malonic ester from       DiEthylCarbonate and Ethyl Hexanoate (to give       BuRtMalonic Ester), is a trace of EhOH absolutly       necessary?              --- SoupGate-Win32 v1.05        * Origin: you cannot sedate... all the things you hate (1:229/2)    |
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