Results 61 to 70 of about 45,356 (184)

Visible-Light-Induced Oxyalkylation of 1,2,4-Triazine-3,5(2H, 4H)‑diones with Ethers via Oxidative Cross-Dehydrogenative Coupling

open access: yes
An efficient and convenient method to synthesize 6-oxyalkylated 1,2,4-triazine-3,5­(2H, 4H)-diones has been developed via visible-light-induced cross-dehydrogenative coupling reaction between 1,2,4-triazine-3,5­(2H, 4H)-diones and ethers with a wide ...
Jiquan Zhao (4432000)   +5 more
core   +1 more source

Corn response to biological products and a nitrification inhibitor

open access: yesAgrosystems, Geosciences &Environment, Volume 9, Issue 2, June 2026.
Abstract Atmospheric nitrogen (N2) is converted into ammonia (NH3), a form that plants can use, through biological nitrogen (N) fixation by various microorganisms and bacterial genera. This study assessed the field performance of three biological N‐fixing products, or biostimulants (BS), including Gluconacetobacter diazotrophicus (BS1), Klebsiella ...
Rose M. Paul   +3 more
wiley   +1 more source

2-Phenyl-7-(4-pyridylmethylamino)-1,2,4-triazolo[1,5-a][1,3,5]triazin-5(4H)-oneFused heterocyclic systems with s-triazine ring. Part 17. For part 16, see Dolzhenko et al. (2011).

open access: yesActa Crystallographica Section E, 2011
In the title compound, C16H13N7O, the 1,2,4-triazolo[1,5-a][1,3,5]triazine heterocyclic system is essentially planar (r.m.s. deviation = 0.0375 Å).
Lip Lin Koh   +4 more
doaj   +1 more source

Synthesis, spectral characterization and antihaemostatic activity of 1,2,4-triazoles incorporating 1,2,4-triazine rings

open access: yes, 2006
A simple and high yielding method for the integration of a 1,2,4-triazole ring with 1,2,4-triazine-5-one (4a-j) has been developed starting from 3-arylsydnones (1a-d).
Sudha, Belgur S., Kamble, Ravindra R.
core   +1 more source

Reactions of 3-phenyl-1,2,4-triazine with some C-nucleophiles [PDF]

open access: yes, 2013
Dimedone is added at C(5) of 3-phenyl-1,2,4-triazine to give stable dihydro derivative. Its reaction with 1-aryl-3-methylpyrazol-5- ones proceeds with fragmentation affording 1,1,2,2-tetrakispyrazolylethane and amidrazone derivatives.
Ermakova, O. S.   +11 more
core   +1 more source

Targeting colorectal cancer with pyrazolo[4,3-e][1,2,4]triazine and pyrazolo[4,3-e]tetrazolo[1,5-b][1,2,4]triazine sulfonamides: comprehensive in vitro evaluation

open access: yesScientific Reports
Colorectal cancer (CRC) remains a major global health challenge, ranking as the third most common malignancy and the second leading cause of cancer-related mortality worldwide. This study aimed to evaluate a novel series of pyrazolo[4,3-e][1,2,4]triazine
Mateusz Kciuk   +6 more
doaj   +1 more source

Synthesis, Characterization, and BSA-Binding Studies of Novel Sulfonated Zinc-Triazine Complexes

open access: yesBioinorganic Chemistry and Applications, 2018
Four Zn(II) complexes containing a pyridyl triazine core (L1 = 3-(2-pyridyl)-5,6-di(2-furyl)-1,2,4-triazine-5′,5″-disulfonic acid disodium salt and L2 = 3-(2-pyridyl)-5,6-diphenyl-1,2,4-triazine-4′,4″-disulfonic acid sodium salt) were synthesized, and ...
Nalin Abeydeera   +2 more
doaj   +1 more source

Efficient Routes to Pyrazolo[3,4-e][1,2,4]triazines and a New Ring System: [1,2,4]Triazino[5,6-d][1,2,3]triazines

open access: yesMolecules, 2010
Arylhydrazonomalononitriles 1a,b react with phenylhydrazine to yield amidrazones 2a,b that cyclize to give 2-aryl-5-phenylhydrazono-2,5-dihydro-[1,2,4]-triazine-6-carbonitriles 5a,b upon reaction with dimethylformamide dimethylacetal (DMFDMA).
Hamad Mohamed Al-Matar   +3 more
doaj   +1 more source

Síntese de materiais orgânicos funcionais derivados do heterociclo 1,2,4-oxadiazol [PDF]

open access: yes, 2008
TCC (graduação) - Universidade Federal de Santa Catarina. Centro de Ciências Físicas e Matemáticas. Curso de Química.Este trabalho tem como objetivo geral a síntese de moléculas simétricas curvadas contendo o heterociclo 1,2,4 oxadiazol, bem como o ...
FERREIRA, Marli
core  

S‐Doped Carbon Nitride Thin Films From a Triazole Precursor

open access: yesCarbon Innovation, Volume 1, Issue 1, Page 78-85, June 2026.
Sulfur‐functionalized carbon nitride thin films are synthesized via low‐temperature chemical vapor deposition using a triazole‐derived precursor. Tunable sulfur incorporation modulates electronic and optical properties and enables efficient visible‐light photocatalysis with high conversion and selectivity.
Yen‐Han Wang   +3 more
wiley   +1 more source

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