934814-05-8Relevant academic research and scientific papers
Synthesis of 1,2,4-Triazine Compounds via Two Distinct One-Pot Domino Protocols
Liu, Yafeng,Guo, Xin,Tang, Dong,Wang, Jing,Wu, Ping,Han, Jianwei,Chen, Baohua
supporting information, p. 1222 - 1226 (2017/09/02)
1,2,4-Triazine compounds were synthesized via two coupled domino strategies employing simple and readily available arylacetaldehydes/arylethyl alcohols as starting materials. The reactions proceed smoothly in one pot with the advantages of high functional
Synthesis of 1,2,4-triazine derivatives via [4 + 2] domino annulation reactions in one pot
Tang, Dong,Wang, Jing,Wu, Ping,Guo, Xin,Li, Ji-Hui,Yang, Sen,Chen, Bao-Hua
, p. 12514 - 12518 (2016/02/18)
Simple and efficient [4 + 2] domino annulation reactions have been developed for the synthesis of 1,2,4-triazine derivatives. The strategies exhibit high performance with moderate to high yields, using easily available materials including ketones, aldehyd
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
