- bond is electron-poor.
Nitrosophenols and
naphthols isomerize to the
oxime quinone in solution, but reversibly;
nitrosophenol ethers typically dealkylate...
- The
Synthesis of o-
Nitrosophenols". J. Org. Chem. 32 (8): 2516–2520. doi:10.1021/jo01283a033. Cronheim, G. (1947). "o-
Nitrosophenols. II. New Substituted...
- by acid-catalyzed
condensation of
corresponding 5-(dialkylamino)-2-
nitrosophenols with 2-naphthol. The
yields are
generally moderate as no co-oxidant...
-
prepared by acid-catalyzed
condensation of
either 5-(dialkylamino)-2-
nitrosophenols with 1-naphthylamine, 3-(dialkylamino)phenols with N-alkylated...
-
aniline and
aniline hydrochloride, or by the
action of
aniline on para-
nitrosophenol or para-nitrosodiphenylamine. The
indulines are
prepared as mentioned...
- of the
structure of
mercury b- , lead- and
organotin derivatives of
nitrosophenols,
Nesmeyanov discovered the
phenomenon of metallotropy, that is, a special...
- "2-Substituted and 2,6-disubstituted 1,4-benzoquinone 4-oximes ("p-
nitrosophenols")". Aust. J. Chem. 22 (5): 935–970. doi:10.1071/CH9690935. Baldwin,...
- copper-catalyzed
reaction of
phenols and
hydroxylamine hydrochloride to give o-
nitrosophenols. This
reaction is
today known as the
Baudisch reaction.
Baudisch drowned...
- is unusual.
Simple synthetic analogues have been made
containing 2-
nitrosophenol itself.
These complexes adopt a
facial geometry owing to the binding...
