Results 41 to 50 of about 25,084 (189)
Synthesis of New Bis-1,2,4-Triazole Derivatives
A series of new 1,2/1,3-bis[o-(N-methylidenamino-3-aryl-5-phenyl-4H-1,2,4-triazole-4-yl)phenoxy]ethane/propane derivatives 4 were prepared in good yields bytreatment of 4-amino-3-aryl-5-phenyl-4H-1,2,4-triazoles 2 with certain bis-aldehydes 1.Compounds 4
Hakan Bektas, Olcay Bekircan
doaj +1 more source
Studies on Potential Pesticides Part-XII [PDF]
Fifteen N/sup 1/-(4-Nitrophenoxyacetyl)N/sup 4/-aryl/cryclohexyl-3-thiosemicarbazide, eleven 3-(4-Nitrophenoxymethyl)-4-aryl/cyclohexyl-5-mercapto1,2,4-triazoles and four 2-Arylamino-5-(4-Nitrophenoxymethyl)-1,3,4-oxadiazole derivatives were prepared and
Misra, Hemant K., Sen, Anil K.
core +2 more sources
Several fluoro phenyl triazoles were synthesized using click chemistry between fluoro phenyl azides and phenyl acetylene. Under ultrasound irradiation, this synthetic procedure was performed with Cu (I) in the presence of 1,10-phenanthroline.
Elisa Leyva +3 more
doaj +1 more source
Syntheses of 1, 2, 4 Triazole Derivatives and their Biological Activity [PDF]
Cyclisation of [4‐(4‐oxo‐2‐phenyl‐4H‐quinazolin‐3‐yl)‐phenoxy]‐acetic acid‐N′‐(substituted phenyl)‐thiosemicarbazides with sodium metal in 99.0 % ethanol gave 3‐[4‐(4‐substituted phenyl‐5‐thioxo‐4,5‐dihydro‐1H‐1,2,4 triazol‐3‐ylmethoxy)‐ phenyl]‐2‐phenyl‐3H‐quinazolin‐4‐one .
Freddy H. Havaldar, Abhay R. Patil
openaire +2 more sources
Analysis of natural and anthropogenic factors aff ecting the ability of Lepidium sativum L. to adapt to the toxicity of triazole xenobiotics [PDF]
The eff ects of natural factors (temperatures +34°C and +20°C) and anthropogenic xenobiotics (1,2,4-TriH; 1-(CH3 SO2 )-1H-1,2,4-Tri; 4-(PhSO2 )-4H-1,2,4-Tri; 4-(TolSO2 )-4H-1,2,4-Tri) on watercress Lepidium sativum L. was studied.
Isaichkin, Vadim A. +2 more
doaj +1 more source
Synthesis and characterization of some novel 1,2,4-triazoles, 1,3,4-thiadiazoles and Schiff\u27s bases incorporating imidazole moiety as potential antimicrobial agents [PDF]
(1,4,5-Triphenylimidazol-2-yl-thio)butyric acid hydrazide (3) was obtained via alkylation of 1,4,5-triphenylimidazol-2-thiol (1) with ethylbromobutyrate, followed by addition of hydrazine hydrate. Treatment of acid hydrazide 3 with carbon disulfide in an
ADEEB AL-SHEIKH ALI +4 more
core +3 more sources
This study describes the synthesis and antioxidant activity of new 1,4-disubstituted 1,2,3-triazoles. These compounds were generated semi-synthetically using the Cu(I)-catalysed azide-alkyne cycloaddition (CuAAC) reaction between ethyl 2-azidoacetate and
JOSEFA A. DA CUNHA LIMA +6 more
doaj +1 more source
Introduction. Modern medicine is faced with the resistance of Candida spp. to antimycotics, due to changes in the expression and structure of the ERG11 gene, the molecular target of triazoles.
Yuri V. Nesvizhsky +9 more
doaj +1 more source
Con el objetivo de determinar la efectividad de cinco fungicidas en el combate del rocío azucarado del sorgo causado por Sphacelia sorghi McRae, se llevó a cabo un experimento en el campo experimental del Centro Nacional de Investigaciones Agropecuarias ...
Héctor Mena +4 more
doaj +1 more source
Mycobacterium Tuberculosis Cytochromes (MTB CYP121) and its Molecular interaction with (E)-N’-benzylideneisonicotinohydrazide Inhibitors [PDF]
Mycobacterium tuberculosis is a leading cause of infectious disease in the world today. The present anti-tuberculosis drugs have side-effects primarily liver damage and other adverse reactions like nausea, anorexia and vomiting.
SaniUba and AdamuUzairu, Adeniji Elijah Shola
core +2 more sources

