《Bioactive 1,2,3-Triazoles: An Account on their Synthesis, Structural Diversity and Biological Applications》 was written by da S. M. Forezi, Luana; Lima, Carolina G. S.; Amaral, Adriane A. P.; Ferreira, Patricia G.; de Souza, Maria Cecilia B. V.; Cunha, Anna C.; de C. da Silva, Fernando; Ferreira, Vitor F.. COA of Formula: C2H3N3This research focused ontriazole structural diversity biol active mol; biological activity; cycloaddition; diazocompounds; heterocycles; synthetic methods. The article conveys some information:
The triazole heterocycle is a privileged scaffold in medicinal chem., since its structure is present in a large number of biol. active mols., including several drugs currently in the market. Due to their vast applications, a wide variety of methods are described for their preparation, such as the 1,3-dipolar cycloaddition and processes involving diazo compounds and diazo transfer reactions. Considering the significant number of contributions from our research group to this chem. in recent decades, in this account we discuss both the development of new methods for the synthesis of 1,2,3-triazoles and the preparation of new triazole-functionalized biol. active mols. using classical approaches. In the part of experimental materials, we found many familiar compounds, such as 1H-1,2,3-Triazole(cas: 288-36-8COA of Formula: C2H3N3)
1H-1,2,3-Triazole(cas: 288-36-8) belongs to triazoles. Triazoles are an important group of nitrogen-containing five-membered heterocyclic scaffolds. Triazoles are core structures of several drugs and pharmaceutical agents. Triazole derivatives possess antimicrobial, antiparasitic, antidiabetic, analgesic, and anti-inflammatory properties COA of Formula: C2H3N3
Referemce:
1,2,3-Triazole – Wikipedia,
Triazoles – an overview | ScienceDirect Topics