-
common example of dienone–phenol
rearrangement is 4,4-disubstituted
cyclohexadienone [de]
converting into a
stable 3,4-disubstituted
phenol in presence...
-
Phenol exhibits keto-enol
tautomerism with its
unstable keto
tautomer cyclohexadienone, but the
effect is
nearly negligible. The
equilibrium constant for...
- Type II, the
racemization of
optically active biphenyls, the type A
cyclohexadienone rearrangement, the type B
cyclohexenone rearrangement, the di-π-methane...
- 2-cyclohexenone
oxime to
aniline under acidic conditions. The
isomerization of
cyclohexadienones gives the
aromatic tautomer phenol.
Isomerization of 1,4-naphthalenediol...
- phenols, as well as
alcohols and
thiols to the
corresponding cyclohexadienones. The
cyclohexadienones, also
referred to in the
literature as Chinolether, cleave...
-
Eigenschaften von (Phenylseleno)cyclohexenonen und
deren Überführung in
Cyclohexadienone".
Chemische Berichte (in German). 111 (5): 1944–1957. doi:10.1002/cber...
-
classic example of this
reaction is the
conversion of p-cresol to a
cyclohexadienone (with the aid of
aluminium chloride as a
catalyst and tetrachloromethane...
- be
described as a
carbenium ion or with an
iminocyclohexadiene or
cyclohexadienone partial structure. The
central carbon atom in the dyes is therefore...
-
trifluoroperacetic acid or
hydrogen peroxide gives 2,3,4,5,6,6-hexamethyl-2,4-
cyclohexadienone:) It has also been used as a
solvent for 3He-NMR spectroscopy. Just...
- the
conversion of
hexamethylbenzene to 2,3,4,5,6,6-hexamethyl-2,4-
cyclohexadienone: In
addition to
simple oxidation of
aromatic rings to form carbonyl...
