178685-60-4Relevant academic research and scientific papers
Addition reactions of cyclic s-trans-enaminones with Grignard reagents
Shawe, Thomas T.,Hansen, Darren B.,Peet, Kelly Ann,Prokopowicz, Anthony S.,Robinson, Patrice M.,Cannon, Annatina,Dougherty, Kathleen E.,Ross, Andrew A.,Landino, Linda M.
, p. 1547 - 1556 (2007/10/03)
Addition of Grignard reagents to s-transenaminones derived from 1,3-cycloalkanediones are described. In dichloromethane, addition of phenylmagnesium bromide gave 3-phenyl substituted cycloalkenones. Alkylmagnesium halides underwent multiple addition reactions, giving mixtures of the 3-alkylcycloalkenones and 1,3-dialkyl-3-(dialkylamino)cyclohexenes. In tetrahydrofuran, only the 3-alkylcycloalkenone was obtained.
