111336-69-7Relevant academic research and scientific papers
Cycloadditions of aryl-substituted 1,2,4-triazines with 2-cyclopropylidene-1,3-dimethylimidazolidine - Zwitterions as discrete intermediates
Ernd, Michael,Heuschmann, Manfred,Zipse, Hendrik
, p. 1491 - 1518 (2007/10/03)
Cycloadditions of 2-cyclopropylidene-1,3-dimethylimidazolidine (1), a strong, electron-rich C-nucleophile, with a variety of aryl-substituted 1,2,4-triazines occur at temperatures between -100 and +100°, depending on the substitution pattern. At low tempe
ELECTRONIC SPECTRA OF asym-TRIAZINYL GROUPS
Shkurko, O. P.,Gogin, L. L.,Baram, S. G.,Mamaev, V. P.
, p. 216 - 221 (2007/10/02)
The induction, resonance, and Hammett constants of 3-, 5-, and 6-asym-triazinyl groups were calculated from the data of 1H, 13C, 19F NMR spectra of isomeric aminophenyl-, hydroxyphenyl-, phenyl-, and fluorophenyl-asym-triazines.
