107006-48-4Relevant academic research and scientific papers
Chemoselective cyclizations of divinyl ketones to cyclohexenones mediated by Lewis acid and base
Magomedov, Nabi A.,Ruggiero, Piero L.,Tang, Yuchen
, p. 3373 - 3375 (2004)
(Chemical Equation Presented) Chemoselective cyclizations of divinyl ketones to cyclohexenones mediated by a sterically demanding Lewis acid and an amine base have been accomplished under mild reaction conditions. The extension of this methodology to the
γ-ALKYLATION OF α'-(PHENYLSULFONYL)-α,β-UNSATURATED KETONES: THE TRIANION IMPERATIVE
Lansbury, Peter T.,Spagnuolo, Ciro J.,Grimm, Erich L.
, p. 2725 - 2726 (2007/10/02)
γ-alkylation of the title compounds with primary alkyl iodides is possible only when both α'-protons are first ionized with excess lithium diisopropylamide.
