-
specificity for the
cytochrome P450 than
imidazoles,
thereby making them more
potent than the
imidazoles. Some
imidazole derivatives show
effects on insects...
- The Debus–Radziszewski
imidazole synthesis is a multi-component
reaction used for the
synthesis of
imidazoles from a 1,2-dicarbonyl, an aldehyde, and ammonia...
- the Van
Leusen reaction is
particularly useful to form
oxazoles and
imidazoles. The
reaction mechanism consists of the
initial deprotonation of TosMIC...
-
Imidazoline is a
class of
heterocycles formally derived from
imidazoles by the
reduction of one of the two
double bonds.
Three isomers are known, 2-imidazolines...
- ring
containing two or
three nitrogen atoms. The
imidazole antifungals contain a 1,3-diazole (
imidazole) ring (two
nitrogen atoms),
whereas the triazole...
-
Imidazole alkaloids are a
group of
alkaloids whose basic structure contains the
imidazole ring system. In nature,
imidazole alkaloids are
found both as...
-
particularly important (e.g. baby products, "no more tears"
shampoos etc.).
Imidazoles can be
prepared from
dehydrogenation of imidazolines. As a structural...
- burning, itching,
redness (erythema), and one
outbreak of a
pruritic rash.
Imidazoles devoid of the
nitro group no
longer have any
antiprotozoal activity, however...
-
aromatic organic compound that
consists of two
rings (pyrimidine and
imidazole)
fused together. It is water-soluble.
Purine also
gives its name to the...
- PMID 26730217. Reedijk,R. (1969). "Pyrazoles and
imidazoles as ligands. II.
Coordination compounds of N-methyl
imidazole with
metal perchlorates and tetrafluoroborates"...
