One-pot formation of aza-enolates from secondary amines and condensation to esters and alkyl bromides
作者:Alice Chevalley、Jean-Pierre Férézou
DOI:10.1016/j.tet.2012.04.105
日期:2012.7
Starting from commercial secondary amines, a one-pot procedure allows a direct access to enaminones through a one-pot deprotonation/oxidation/in situ re-deprotonation/acylation sequence without intermediate isolation of the intermediate Schiff base or its corresponding enamine tautomer. An alternative one-pot sequence involving a similar oxidation step followed by one or two alkylation steps yields