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1.2.4- Triazole - from

Fig. 6.3 CycUc voltammogram (1st cycle) of sterling silver (92.5% Ag, 7.5% Cu) in 0.5M NaCH3COO, pH 4, v = lOmV/s copper and silver oxidation peaks, indicating surface passivation in presence of Ata (3-amino,1,2,4-triazole) (from [304])... Fig. 6.3 CycUc voltammogram (1st cycle) of sterling silver (92.5% Ag, 7.5% Cu) in 0.5M NaCH3COO, pH 4, v = lOmV/s copper and silver oxidation peaks, indicating surface passivation in presence of Ata (3-amino,1,2,4-triazole) (from [304])...
Ruccia and co-workers187, 188 also succeeded in obtaining some 1,2,4-triazoles from 3-amino-l,2,4-oxadiazoles by the series of reactions shown in Eq. (71). Isolation of the intermediate (99) could also be bypassed by heating 98 directly with the p-toluidine at 120°-170°. [Pg.106]

Fig. 9.6 Formation and degradation of 1,2,4-triazole from photocataiytic degradation of tnadimefon. A Triadinefon, O 1,2,4-Triazole. Fig. 9.6 Formation and degradation of 1,2,4-triazole from photocataiytic degradation of tnadimefon. A Triadinefon, O 1,2,4-Triazole.
The one-pot, three-component synthesis of 1,2,4-triazoles from primary amines, acyl hydrazines and dimethoxy-A(-A(-dimethylmethanamine [84] was utilized for the preparation of compounds 235 (Scheme 41), which were evaluated for their anticonvulsant and neurotoxic properties [85]. The anticonvulsant activity was measured in mice by the maximal electroshock test (MES) and the neurotoxicity in mice by the rotarod neurotoxicity test (Tox). The majority of the compounds... [Pg.276]

Insensitivity to photolysis is suggested by the formation of 1,2,4-triazoles from some other heterocycles. However, mesoionic 4-aryl-l-phenyl-l,2,4-triazolin-3-ones (44) are decomposed on photolysis as in Scheme 12 (72CC498) triazolinethiones lose sulfur only <70AJC631>. [Pg.744]

Other examples of the same type include the regioselective synthesis of 1-substituted 1,2,4-triazoles from either 4-aminotriazole (1) [Eq. (70)]... [Pg.157]


See other pages where 1.2.4- Triazole - from is mentioned: [Pg.512]    [Pg.566]    [Pg.566]    [Pg.715]    [Pg.716]    [Pg.716]    [Pg.716]    [Pg.717]    [Pg.742]    [Pg.826]    [Pg.864]    [Pg.897]    [Pg.153]    [Pg.191]    [Pg.512]    [Pg.566]    [Pg.566]    [Pg.715]    [Pg.716]    [Pg.716]    [Pg.716]    [Pg.717]    [Pg.742]    [Pg.826]    [Pg.864]    [Pg.897]    [Pg.63]    [Pg.749]    [Pg.512]    [Pg.566]    [Pg.566]    [Pg.715]    [Pg.716]    [Pg.716]    [Pg.716]    [Pg.717]    [Pg.742]    [Pg.864]    [Pg.897]    [Pg.395]   


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1,2,3-Triazoles, computed stability formation from 1,2,4-triazine 4-oxides

1.2.3- Triazoles from azides

1.2.3- Triazoles, from -cycloaddition

1.2.3- Triazoles, synthesis from oximes

1.2.4- Triazole - from 3-amino

1.2.4- Triazole - from amidrazones

1.2.4- Triazole - from carbodiimides

1.2.4- Triazole - from dioxide

1.2.4- Triazoles 3,5-diamino- from

1.2.4- Triazoles 3,5-diaryl— from

1.2.4- Triazoles 3-amino— from

1.2.4- Triazoles 3-hydrazino- from

1.2.4- Triazoles 3-hydroxymethyl- from

1.2.4- Triazoles 4-hydroxy- from

1.2.4- Triazoles 5-amino-3-mercapto- from

1.2.4- Triazoles formation from 1,2,4-triazines

1.2.4- Triazoles ring synthesis from hydrazine derivatives

1.2.4- Triazoles, 3-mercapto- from

8-Azapurines 1,2,3-triazoles from

Amidines, from triazoles

Benzyl triazoles from

Dipolar cycloadditions 1,2,3-triazoles from

Indole from 1-phenyl-1,2,4-triazole

Syntheses from Triazoles

Tetrazoles from azido-1,2,3-triazoles

Triazole from click chemistry reaction

Triazoles carbenes from

Triazoles from Pyrimidine Derivatives

Triazoles, from rearrangement

Triazoles, from rearrangement 1,2,4-oxadiazoles

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