Results 311 to 320 of about 67,290 (378)
Some of the next articles are maybe not open access.
Antimalarials. 3. 1,2,4-Triazines
Journal of Medicinal Chemistry, 1976The syntheses of a number of substituted 1,2,4-triazines as potential antimalarials are described. The structural requirements for antimalarial activity are discussed with reference to the substituents of a phenyl group in the 6 position and amino groups at the 3 and 5 positions.
L C, March +4 more
openaire +2 more sources
Methods of Synthesis for the Azolo[1,2,4]Triazines
Chemistry of Heterocyclic Compounds, 2020E. Voinkov +5 more
semanticscholar +1 more source
Rubber Chemistry and Technology, 1966
Abstract Three technically feasible routes have now been established for preparation of linear perfluoroalkylene triazine polymers. The most advanced route is based on addition polymerization of long chain fluorocarbon dinitriles and diamidines, followed by acylation and cyclodehydration to triazine polymer.
openaire +1 more source
Abstract Three technically feasible routes have now been established for preparation of linear perfluoroalkylene triazine polymers. The most advanced route is based on addition polymerization of long chain fluorocarbon dinitriles and diamidines, followed by acylation and cyclodehydration to triazine polymer.
openaire +1 more source
2001
[290-38-0] C3H3N3 (MW 81.09) InChI = 1S/C3H3N3/c1-2-5-6-3-4-1/h1-3H InChIKey = FYADHXFMURLYQI-UHFFFAOYSA-N (electron-deficient heteroaromatic azadiene capable of participation in inverse electron demand Diels–Alder reactions with electron-rich dienophiles1) Alternate Names: as-triazine; α-triazine; isotriazine ...
Dale L. Boger, Minsheng Zhang
openaire +1 more source
[290-38-0] C3H3N3 (MW 81.09) InChI = 1S/C3H3N3/c1-2-5-6-3-4-1/h1-3H InChIKey = FYADHXFMURLYQI-UHFFFAOYSA-N (electron-deficient heteroaromatic azadiene capable of participation in inverse electron demand Diels–Alder reactions with electron-rich dienophiles1) Alternate Names: as-triazine; α-triazine; isotriazine ...
Dale L. Boger, Minsheng Zhang
openaire +1 more source
1976
Publisher Summary This chapter provides a comprehensive review of developments in 1,2,3-triazine chemistry from 1960 to the beginning of 1974. There are relatively few methods available for the preparation of condensed 1,2,3-triazines. The most commonly employed procedure is diazotization of a suitably ortho-substituted aniline or aminosubstituted ...
Ryszard J. Kobylecki, Alexander Mckillop
openaire +1 more source
Publisher Summary This chapter provides a comprehensive review of developments in 1,2,3-triazine chemistry from 1960 to the beginning of 1974. There are relatively few methods available for the preparation of condensed 1,2,3-triazines. The most commonly employed procedure is diazotization of a suitably ortho-substituted aniline or aminosubstituted ...
Ryszard J. Kobylecki, Alexander Mckillop
openaire +1 more source
Triazines. XXII. Fluoro-s-triazines
Journal of the American Chemical Society, 1959Ehrenfried Kober, Christoph Grundmann
openaire +1 more source
Biologically active azolo-1,2,4-triazines and azolopyrimidines
Russian chemical bulletin, 2018V. Rusinov, V. Charushin, O. Chupakhin
semanticscholar +1 more source
Triazine-based condensing reagents
Biopolymers, 2000The synthesis, properties, and application of condensing reagents derived from 1,3,5-triazines are described. The mechanism of activation of carboxylic function, structure of reactive intermediates, and mechanism of acylation of nucleophiles are presented.
openaire +2 more sources
Gold-Catalyzed Regiodivergent [2 + 2 + 2]-Cycloadditions of Allenes with Triazines.
Organic Letters, 2017Shiyong Peng, Shengyu Cao, Jiangtao Sun
semanticscholar +1 more source

