Abstract:A mild and efficient procedure is described for the synthesis of amine-substituted diazoacetoacetates by the addition of ethyl 3-(tertbutyldimethylsilanoxy)-2-diazobut-3-enoate to aldimines catalysed by MgI 2 etherate (MgI 2 •(OEt 2 ) n ) in MeCN. The reaction produces good to excellent yield at room temperature.
Chemoselective reduction of β-enamino esters with NaBH(OAc)3 promoted by MgI2 etherate affords the corresponding β-amino esters in excellent yields in a short time under mild conditions.
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