24744-57-8Relevant academic research and scientific papers
A Simple and Efficient Procedure for the Preparation of p-Quinols by Hypervalent Iodine Oxidation of Phenols and Phenol Tripropylsilyl Ethers
McKillop, Alexander,McLaren, Lee,Taylor, Richard J. K.
, p. 2047 - 2048 (2007/10/02)
Oxidation of para-substituted phenols with benzene (BTIB) in aqueous acetonitrile at 0 deg C gives p-quinols in moderate to good yields; higher yields are obtained when tripropylsilyl ethers of phenols are used.
ADDITION OF FUNCTIONALIZED ORGANOLITHIUM REAGENTS TO p-BENZOQUINONES AND CYCLOHEXADIENONES: SYNTHESIS OF FUNCTIONALIZED CYCLOHEXADIENONES, DIENOLS AND DIENEDIOLS
Fischer, Alfred,Henderson, George Narayanan
, p. 131 - 134 (2007/10/02)
Low temperature addition of functionalized alkyllithium reagents to p-benzoquinones produces 4-alkyl-4-hydroxycyclohexa-2,5-dienones, and reaction of excess of the reagents with quinones yields 1,4-dialkylcyclohexa-2,5-diene-1,4-diols.With 4-acetoxy-, 4-h
