119927-91-2Relevant academic research and scientific papers
Oxygenophilic Organoaluminum-Mediated Conjugate Addition of Alkyllithium and Grignard Reagents to Quinone Monoketals and Quinol Ethers. The Directing Effect of a Methoxy Group on the 1,4-Addition Process
Stern, Alan J.,Rohde, Jeffrey J.,Swenton, John S.
, p. 4413 - 4419 (2007/10/02)
Complexation of quinone monoketals and quinol ethers with methylaluminum bis(2,6-di-tert-butyl-4-methylphenoxide), the MAD reagent, followed by addition of organolithium or Grignard reagents gives products from 1,4-addition of the organometallic reagent t
Oxygenophilic Organoaluminium-promoted 1,4-Addition of Organolithium Reagents to Quinone Monoacetals
Stern, Alan J.,Swenton, John S.
, p. 1255 - 1256 (2007/10/02)
Complexation of quinone monoacetals with methylaluminium bis-(2,6-di-t-butyl-4-methylphenoxide), followed by addition of organolithium reagents, gives products from 1,4-addition of the organolithium reagent to the quinone monoacetal.
