Depending on the position of the substituent (α-phenyl) on the phenol ring (o-, m-, or p-substituted), different quinone methides can be generated. Each QM will have distinct reactivity due to the position of the phenyl group.
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2-Aziridinecarboxylic acid, 1-benzoyl-3-(2S)-1,4-dioxaspiro[4.5]dec-2-yl-, ethyl ester, (2R,3R)-
6-phenyl-4-(phenylthio)hex-2-ene
Benzene, 1-nitro-4-(1,1,2-trimethyl-2-nitrobutyl)-
3-(2,6-Dichlorophenyl)-6,7-dihydro-1,2-benzisoxazol-4(5H)-one
palladium acetate
threo-1-acetoxy-2-bromo-1-phenylpropane
2-azido-1-iodo-1-phenylcyclohexane
(hex-1-en-3-yloxy)(trimethyl)silane
2-Propenoic acid, 3-hydroxy-2,2-dimethylpropyl ester, (Z)-
C7H13NO
