Direct synthesis of 5-arylethynyl-1,2,4-triazines via direct CH-functionalization

An efficient synthetic approach towards 5-arylethynyl-1,2,4-triazines via direct C-H-functionalization of 5-H-1,2,4-triazines in reaction with lithium acetylenes is reported

The synthesis of 6-phenoxyphenylamino-2,2'-bipyridines as new fluorophores

New alpha-arylamino-substituted 2,2'-bipyridine type ligands are prepared. © 2019 Author(s)

Asymmetrically Functionalized 1,3-Di(2-pyridyl)benzenes: Synthesis and Photophysical Studies

A convenient synthetic approach to asymmetrically functionalized 1,3-di(2-pyridyl)benzenes starting from 3-(3-bromophenyl)-1,2,4-triazines using sequential aza-Diels–Alder reactions and Stille cross-coupling is reported. Photophysical properties of the obtained compounds are studied. © 2021, The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.This work was supported by Russian Science Foundation (Grant № 19-73-10144) and Grants Council of the President of the Russian Federation (no. NSh-2700.2020.3). No other sources of funding were involved

Synthesis of 2-Phenyl-2-(5-Phenyl-2,2'-Bipyridin-6-yl)-Acetonitrile by «1,2,4-Triazine» Method with Using Autoclave

This work was supported by the Russian Science Foundation (Ref. № 18-73-00301)

The Synthesis of 6-Phenoxyphenylamino-2,2'-Bipyridines as New Fluorophores

This work was supported by the Russian Science Foundation (Ref. № 18-73-10119)