80476-97-7Relevant academic research and scientific papers
CONJUGATE REDUCTION OF QUINONE DERIVATIVES. A ROUTE TO PHENOL KETO-TAUTOMER EQUIVALENTS
Doty, Barbara J.,Morrow, Gary W.
, p. 6125 - 6128 (1990)
1,4-Addition of hydride to quinone monoketals 1 and p-quinol ethers 2, mediated by bis-(2,6-di-t-butyl-4-methylphenoxy)-methylaluminum (MAD), affords 4,4-substituted-2-cyclohexen-1-ones 3, which represent keto-tautomer equivalents of phenols.
