-
formula C2H3N3.
Triazoles exhibit substantial isomerism,
depending on the
positioning of the
nitrogen atoms within the ring. Many
triazoles are versatile...
-
cycloadditions favor 1,4-disubstituted
triazoles,
Ruthenium catalyzed cycloaddition favor 1,5-disubstituted
triazoles. This
chemistry was
expanded by Zhu...
-
formula C2H3N3,
called triazoles,
which have a five-membered ring of two
carbon atoms and
three nitrogen atoms. 1,2,4-
Triazole and its
derivatives find...
-
contain a 1,3-diazole (imidazole) ring (two
nitrogen atoms),
whereas the
triazole antifungals have a ring with
three nitrogen atoms.
Bifonazole Butoconazole...
-
azoles is the
triazoles,
which includes fluconazole, itraconazole, and voriconazole. The
difference between the
imidazoles and the
triazoles involves the...
- oral
treatment of
systemic fungal infections, in the
early 1980s. Later,
triazoles fluconazole and itraconazole, with a
broader spectrum of
antifungal activity...
-
azides and
terminal alkynes are
united to
afford 1,4-regioisomers of 1,2,3-
triazoles as sole
products (substitution at
positions 1' and 4' as
shown above)...
-
another activated alkene)
reacts with azides,
giving triazoles as a product. However,
these product triazoles are not
aromatic as they are in the
CuAAC or SPAAC...
- 3-Amino-1,2,4-
triazole (3-AT) is a
heterocyclic organic compound that
consists of a 1,2,4-
triazole substituted with an
amino group. 3-AT is a competitive...
- 1,1'-Azobis-1,2,3-
triazole is a
moderately explosive but
comparatively stable chemical compound[citation needed]
which contains a long
continuous chain...
