Results 241 to 250 of about 52,437 (280)

Combating oxi-inflamm-aging: Passerini adducts tethered with 1,2,3-triazoles for enhanced antioxidant defense and 5-LOX inhibition. [PDF]

RSC Med Chem
Ayoup MS, Rashwan MM, Soliman SM, Ghareeb DA, Ashraf S, Ismail MMF, Tageldin GN, Sonousi A, Awad LF.   +8 more
europepmc   +1 more source

Fe₃O₄@HA-Cu(OAc)₂ nanocomposite as a nanomagnetic water-compatible catalyst for efficient synthesis of 1,2,3-triazoles in water. [PDF]

Sci Rep
Arjmandzadeh B, Jafari AA.
europepmc   +1 more source

In vitro and in silico evaluation of synthetic compounds derived from bi-triazoles against asexual and sexual forms of Plasmodium falciparum. [PDF]

Malar J
do Nascimento Martinez L, da Silva MA, Fialho SN, Almeida ML, Dos Santos Ferreira A, de Jesus Gouveia A, do Nascimento WDSP, Dos Santos APA, Rossi NRDLP, de Medeiros JF, Araújo NF, de Santana QLO, Kaiser CR, Ferreira SB, da Silva Araujo M, Teles CBG.   +15 more
europepmc   +1 more source

Tandem Cu(I)-Catalyzed Dipolar Cycloaddition-C-H Activation for the In-Flow Synthesis of <i>N</i>-Pyridyl-5-amino-1,2,3-triazole-4-carboxylates. [PDF]

Org Lett
Donato E, Mayorquín-Torres MC, Puglisi A, Benaglia M, Adamo MFA, Stevens CV.   +5 more
europepmc   +1 more source

Supramolecular assembly properties of a mixed-sequence recognition-encoded melamine oligomer.

Org Biomol Chem
Dhiman M, Smith JT, Hunter CA.
europepmc   +1 more source

Elucidating structural and molecular requirements of somatostatin subtype-4 agonist bound complexes using quantum mechanics approaches.

Org Biomol Chem
Slater O, Kontoyianni M.
europepmc   +1 more source

Some of the next articles are maybe not open access.

Related searches:

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
Mehrnoosh Hashemzadeh, Lee Peyton, S Gallagher   +2 more
openaire   +3 more sources

Phototautomerism of triazolo-triazole scaffold

Journal of Molecular Structure, 2020
It is shown that 4-methyl-7-(4-hydroxyphenyl)-[1,2,4]-triazolo[3,2-c][1,2,4]triazole exhibits a rich photoinduced protolytic behavior: Förster cycle shows that the protonated nitrogen of the triazolo-triazole ring is a weak photoacid, with ?pKa?-3; furthermore, at moderately basic pH its deprotonated monoanion exhibits a long distance water mediated ...
Capobianco A., Di Donato M., Caruso T., Centore R., Lapini A., Manfredi C., Velardo A., Volino S., Peluso A.   +8 more
openaire   +6 more sources

Silylated Tetrazoles and Triazoles

Zeitschrift für anorganische und allgemeine Chemie, 2009
Abstract1‐Dimethysilyltetrazole (1) has been prepared from 1H‐tetrazole and chlorodimethylsilane in the presence of 2,6‐lutidine, bis(1‐tetrazolyl)dimethylsilane (2) from the reaction of 1H‐tetrazole, dimethyldichlorosilane and triethylamine and 5‐(trimethylsilylamino)‐1H‐tetrazole (3) from 5‐amino‐tetrazole monohydrate and hexamethyldisilazane.
Gronde, Ingo, Mitzel, Norbert W.
openaire   +2 more sources

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.
Péter Dvortsák, László Pongó, Jozsef Reiter   +2 more
openaire   +2 more sources