Results 91 to 100 of about 26,240 (223)

Amidrazones in the Synthesis of 1H‐1,2,4‐Triazoles. [PDF]

ChemInform, 2006
AbstractChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.
Ahmed M. Nour El-Din, Moshen A.-M. Gomaa, Magda S. Fahmi, Ashraf A. Aly   +3 more
openaire   +2 more sources

Regioselective alkylation of 1,2,4-triazole using ionic liquids under microwave conditions

Green Processing and Synthesis, 2016
1-Substituted 1,2,4-triazole derivatives present in a large number of compounds and display a variety of bioactivities such as antibiotic, anti-inflammatory, anti-diabetic, antipsychotic, and anticancer.
Kaur Ramandeep, Kumar Bhupinder, Dwivedi Ashish Ranjan, Kumar Vinod   +3 more
doaj   +1 more source

C-Glycosyl 1,2,4-triazoles: Synthesis of the 3-β-d-glucopyranosyl-1,5-disubstituted and 5-β-d-glucopyranosyl-1,3-disubstituted variants [PDF]

, 2018
K
Páhi, András, Somsák, László, Szabó, Erzsébet Katalin   +2 more
core   +1 more source

Heterogeneous Electrocatalytic CO2 Reduction by Supported Molecular Catalysts Well Dispersed on Electrode Surface

ChemElectroChem, EarlyView.
This mini review overviews the most recent advances (2020–2024) in heterogeneous electrocatalytic CO2R by well‐dispersed molecular catalysts on electrode surface, mainly focusing on the impacts of efficient molecule‐level dispersion and rational catalyst‐support interactions on electronic properties, multi‐electron transfer kinetics, and overall ...
Ke Ma, Shiyu Zhang, Weixuan Nie
wiley   +1 more source

Regioselectivity in the Thermal Rearrangement of Unsymmetrical 4-Methyl-4H-1,2,4-triazoles to 1-Methyl-1H-1,2,4-triazoles [PDF]

Molecules, 2001
The rearrangement of 4-methyl-3,5-diaryl-4H-1,2,4-triazoles to the corresponding 1-methyl-3,5-diaryl-1H-1,2,4-triazoles showed regioselectivity comparable to that observed for the alkylation of 3,5-diaryl-1H-1,2,4-triazoles. This lends support to a proposed mechanism for the rearrangement that involves consecutive nucleophilic displacements steps.
Gautun, Odd Reidar, Carlsen, Per Henning
openaire   +4 more sources

catena-Poly[[triaqua­zinc(II)]-μ-1H-1,2,4-triazole-3,5-dicarboxyl­ato] [PDF]

, 2008
In the title compound, [Zn(C4HN3O4)(H2O)3]n, each ZnII atom adopts a distorted octa­hedral coordination geometry, being surrounded by one chelating and one monodentate 1H-1,2,4-triazole-3,5-dicarboxyl­ate ligand and three water mol­ecules.
Cheng, Lin, Sun, Yan-Yan, Zhang, Gong, Zhang, Ya-Wen   +3 more
core   +3 more sources

Advances in Mechanochemical Methods for One‐Pot Multistep Organic Synthesis

Chemistry – A European Journal, Accepted Article.
Mechanochemical synthesis has emerged as a powerful and more sustainable alternative to conventional solution‐based methods, offering advantages such as no or only minimal solvent use, reduced reaction times, and simplified operational conditions.
Michael Schnürch, Nina Biedermann
wiley   +1 more source

The study of antimicrobial activity of 2-((4-R-3-(morpholinomethylene)-4H-1,2,4-triazole-5-yl)thio)acetic acid salts

Zaporožskij Medicinskij Žurnal, 2016
The purpose of the work was to study the antimicrobial activity of 2-((4-R-3-(morfolinomethylene)-4H-1,2,4-triazole-5-yl)thio) acetic acid salts by "hanging drop" and “serial dilution” methods in broth (limiting concentration option) and establish some ...
R. О. Shcherbyna, O. I. Panasenko, Ye. G. Knysh, H. A. Fotina, E. V. Vashchyk, T. I. Fotina   +5 more
doaj   +1 more source

Two reaction routes for the preparation of aromatic polyoxadiazoles and polytriazoles: Syntheses and properties [PDF]

, 1994
Two reaction routes for the preparation of aromatic poly-1,3,4-oxadiazoles and poly-1,2,4-triazoles are studied and their influence on the physical properties, i.e., inherent viscosity, glass transition, degradation temperature, and film integrity of the
Boom, J.P., Boom, J.P., Hensema, E.R., Hensema, E.R., Mulder, M.H.V., Smolders, C.A., Smolders, C.A.   +6 more
core   +2 more sources

Development of Water‐Soluble 3‐Nitro‐2‐Pyridinesulfenate for Disulfide Bond Formation of Peptide Under Aqueous Conditions

Chemistry – A European Journal, EarlyView.
Highly water‐soluble Npy‐sulfenate functions as an efficient oxidizing agent for the formation of disulfide bonds in thiol‐containing peptides. The Npy‐sulfenate can be used to form a disulfide bond with a thiol‐containing peptide produced by thiol‐additive‐free NCL, thereby facilitating the one‐pot synthesis of adrenomedullin.
Akihiro Taguchi, Megumi Sakata, Ryusei Yamamoto, Hayate Shida, Saeka Kuraishi, Sho Konno, Kentaro Takayama, Atsuhiko Taniguchi, Yoshio Hayashi   +8 more
wiley   +1 more source