| Literature DB >> 34514474 |
Biligma D Tsyrenova1, Victor N Khrustalev2,3, Valentine G Nenajdenko1.
Abstract
An efficient synthesis of 2-pyridine derived 4-azido-1,2,3-triazoles was elaborated using the corresponding dichlorodiazadienes as precursors. The reaction of the prepared 2-azine substituted diazadienes with sodium azide permits the preparation of target triazoles isolated in up to 92% yield. Subsequent thermal cyclization was studied. Elimination of molecular nitrogen promoted the cyclization of nitrene at the azine nitrogen. As a result, a family of 2H-[1,2,3]triazolo[4',5':3,4]pyrazolo[1,5-a]pyridin-5-ium-4-ides was prepared. The synthesized compounds are members of a new heterocyclic system. Moreover, these compounds are new attractive blue light emitting molecules.Entities:
Year: 2021 PMID: 34514474 DOI: 10.1039/d1ob01084k
Source DB: PubMed Journal: Org Biomol Chem ISSN: 1477-0520 Impact factor: 3.876