Results 241 to 250 of about 37,042 (298)

Neutral chiral bidentate tellurium-triazoles for enantioselective non-covalent chalcogen-bonding catalysis. [PDF]

Nat Commun
Massold L, O'Brien J, Fengler K, Keuper AC, Hidalgo-León R, Trujillo C, García Mancheño O.   +6 more
europepmc   +1 more source

Formal Markovnikov Hydroazolation of Alkenes via Reductive Activation of Alkylthianthrenium Salts. [PDF]

J Am Chem Soc
Matthews AD, Lorenz JR, Wickens ZK.
europepmc   +1 more source

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Triazole antifungals: A review

Drugs of Today, 2015
Invasive fungal infections and systemic mycosis, whether from nosocomial infection or immunodeficiency, have been on an upward trend for numerous years. Despite advancements in antifungal medication, treatment in certain patients can still be difficult for reasons such as impaired organ function, limited administration routes or poor safety profiles of
L R, Peyton, S, Gallagher, M, Hashemzadeh   +2 more
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Mesoionic 1,2,3-Triazoles and 1,2,3-Triazole Carbenes

2014
Routine access to 1,2,3-triazoles through the copper-catalyzed azide-alkyne “click” cycloaddition reaction has promoted the rapid development of 1,2,3-triazolylidenes as ligands for transition metals. The organometallic complexes containing this kind of N-heterocyclic carbene ligands (NHCs) have shown to possess unique structural characteristics ...
Jesus M. Aizpurua, Maialen Sagartzazu-Aizpurua, Zaira Monasterio   +2 more
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On Triazoles. VI. The acylation of 5‐amino‐1,2,4‐triazoles

Journal of Heterocyclic Chemistry, 1987
AbstractThe isomeric and tautomeric structure of I and II type monoacylated 5‐amino‐1,2,4‐triazole derivatives was studied with the help of their ir, uv, pmr and cmr spectra as well as model compounds prepared for this purpose. It was stated that the structure of the I type ring‐acylated derivatives is 2o and those of their II type isomers is 5a.
József Reiter, László Pongó, Péter Dvortsák   +2 more
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Synthesis of Triazole Nucleoside Derivatives

Nucleosides, Nucleotides & Nucleic Acids, 2003
AbstractFor Abstract see ChemInform Abstract in Full Text.
Zicheng, Li, Shuhua, Chen, Ning, Jiang, Gang, Cui   +3 more
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QSAR Prediction of Aquatic Toxicity of Triazoles and Benzo-Triazoles

2011
Triazoles and benzo-triazoles (TAZ/BTAZ) are potentially hazardous chemicals that adversely affect humans and other non-target species, and are on the list of substances of very high concern (SVHC) in the European regulation of chemicals REACH. TAZ/BTAZ are synthetic molecules used in various industrial processes (to obtain pharmaceuticals and ...
CASSANI, STEFANO, D’Onofrio E., KOVARICH, SIMONA, PAPA, ESTER, ROY, PARTHA PRATIM, GRAMATICA, PAOLA   +5 more
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