- In
organic chemistry,
imidic acids are
organic compounds with the
structure RC(−OH)=NR'. They are
tautomeric to non-tertiary
amides (RC(=O)−NHR') and isomeric...
-
organic compounds,
which can be
thought of as
esters formed between an
imidic acid (R−C(=NR′)OH) and an alcohol, with the
general formula R−C(=NR′)OR″...
-
imidic acid: H−N−C=O ⇌ N=C−O−H (e.g., the
latter is
encountered during nitrile hydrolysis reactions)
lactam – lactim, a
cyclic form of amide-
imidic acid...
-
Attack by
water converts 6 to
protonated imidic acid 7,
which undergoes loss of
proton to
arrive at the
imidic acid
tautomer of the
final amide. In an...
- to uridine,
uridine 5′-monophosphate is produced.
Uracil undergoes amide-
imidic acid
tautomeric shifts because any
nuclear instability the
molecule may...
-
developed for
specialized applications.
Amidogen Amino radical Amidicity Imidic acid
Metal amides "Amide
definition and
meaning -
Collins English Dictionary"...
- nonequivalent.
Examples include tautomerizations (keto-enol, lactam-lactim, amide-
imidic, enamine-imine, nitroso-oxime, ketene-ynol, etc) in
which one
isomer is...
-
useful γ-lactam
known as
Vince Lactam is obtained. A
lactim is a
cyclic imidic acid
compound characterized by an
endocyclic carbon-nitrogen
double bond...
-
common oxyacids that are
relatively easily prepared as pure substances.
Imidic acids are
created by
replacing =O with =NR in an oxyacid. An
oxyacid molecule...
-
peroxoimide acid
formed intermediately from benzonitrile. The
resulting imidic acid
tautomerizes to the benzamide. The
compound acts as a
strong oxidizing...
