30252-14-3Relevant academic research and scientific papers
AMIDOACETONE ENOLATE ANIONS: ALKYLATION AND MICHAEL REACTION
Hoye, Thomas R.,Duff, Steven R.,King, Rita S.
, p. 3433 - 3436 (2007/10/02)
The lithyum enolate derived from benzamidoacetone (1) can be regiospecifically alkylated at C(1) and stereospecifically added in conjugate fashion to cyclohexenone without resorting to protection of free NH.Comparison is made with alkylations of methyl hippurate.
