Results 11 to 20 of about 8,177 (163)

Triazines, Tetrazines, and Fused Ring Polyaza Systems

open access: yes, 2012
The review covers work published in the calendar year 2011. Novel reaction chemistry and new ring synthetic methods for 1,2,3-triazines, 1,2,4-triazines, 1,3,5-triazines, tetrazines, and purines are reviewed.
Prokhorov, Anton M.   +3 more
core   +1 more source

One-Pot Acid-Catalyzed Ring-Opening/Cyclization/Oxidation of Aziridines with N-Tosylhydrazones: Access to 1,2,4-Triazines

open access: yes, 2017
A new, three-step, telescoped reaction sequence for the regioselective conversion of N-tosyl hydrazones and aziridines to 3,6-disubstituted and 3,5,6-trisubstituted 1,2,4-triazines is described. The process involves an efficient nucleophilic ring opening
Lorène Crespin   +14 more
core   +1 more source

Synthesis of U reido-s-triazines [PDF]

open access: yes, 1968
Ureido-s-triazines were prepared by the reaction of melamines with ureas. When amines were mixed in this reaction mixture,substituted ureido-s-trazines were obtained.
NISHIKAWA, Akihumi   +7 more
core   +1 more source

Synthesis and pharmacological evaluation of new fluorine substituted pyrimido[1,2-b][1,2,4]triazines and [1,3,5]-triazino-[1,2-b][1,2,4]triazines derived as CDK2 potential inhibitors [PDF]

open access: yes, 2020
New fluorine-substituted polyfunctional pyrimido-[1,2-b]-[1,2,4]triazines and [1,3,5]-triazino[1,2-b]-[1,2,4]triazines were synthesized via the reaction between 3-amino-6-(2-aminophenyl)-1,2,4-triazin-5(2H)-one with polyfunctional oxygen/sulfur/nitrogen ...
Alotaibi, Fatimah, Bakhotmah, Dina
core   +1 more source

Cycloadditions of Noncomplementary Substituted 1,2,3-Triazines

open access: yes, 2015
: The scope of the [4 + 2] cycloaddition reactions of substituted 1,2,3-triazines, bearing noncomple-mentary substitution with electron-withdrawing groups at C4 and/or C6, is described. The studies define key electronic and steric effects of substituents
Dale L. Boger (1306542)   +9 more
core   +1 more source

Impact of Solvent and Protonation State on Rotational Barriers in [s]-Triazines

open access: yes
Amine-substituted [s]-triazines display hindered rotation around the triazine-N bond. While this barrier, ΔG‡, has been measured to be between 15.1 and 17.7 kcal/mol for neutral triazines, the impacts that solvent and protonation state have not been ...
Hongjun Pan (1718257)   +2 more
core   +1 more source

Isomeric triazines exhibit unique profiles of bioorthogonal reactivity [PDF]

open access: yes, 2019
Expanding the scope of bioorthogonal reactivity requires access to new and mutually compatible reagents. We report here that 1,2,4-triazines can be tuned to exhibit unique reaction profiles with biocompatible strained alkenes and alkynes.
Long, Zane G   +16 more
core   +1 more source

Crosslinking of Polyolefins in the Presence of New s-Triazines

open access: yes, 1975
In the crosslinking of polyolefins (such as polyethylene, ethylene-propylene copolymers, and ethylene-(vinyl acetate) copolymers), multiply unsaturated s-triazines (such as triallylcyanurate (TAC), 2-alkylamino-4,6-diallyloxy-s-triazines, and the bridged
R. Wiedenmann, H. Ahne, W. Kleeberg
core   +1 more source

Nucleophilic Aromatic Substitution of 5Bromo-1,2,3-triazines with Phenols

open access: yes, 2022
Nucleophilic aromatic substitution (SNAr) reaction in classic textbook is a stepwise mechanism, and few examples of concerted reactions have been reported.
Shanshan Li   +17 more
core   +1 more source

On 1 ,3,5-Triazines. Part--II : Synthesis of 2,4-Dithio-3,5- Diaryl-6-Phenylimino-Hexahydro-1,3,5-Triazines and 2,6- Dithio-3, 5-Diaryl-4-Phenylimino-Hexahydro-1,3,5-Triazines

open access: yes, 1982
Department of Chemistry, Nagpur University, Nagpnr-440 010 Manuscript received 2 May 7981, revised 17 December 1981, accepted 2 February 1982 New synthetic procedures are reported for the preparation of 2,4-dithio-3,5- diaryl-6-phenylimino-hexahydro-1 ...
(Miss) MANIK W. AMBBKAR   +3 more
core   +1 more source

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