Derivados 1,2,3-triazol

métodos de síntese e atividade antibacteriana

Authors

  • Guilheane Gonçalves Barbosa Exército Brasileiro, Instituto Militar de Engenharia. Rio de Janeiro, RJ, Brasil.
  • Alcino Palermo de Aguiar Exército Brasileiro, Instituto Militar de Engenharia. Rio de Janeiro, RJ, Brasil.

Keywords:

Triazole, Antibacterial, Cycloaddition, Bioactivity

Abstract

The administration of antimicrobials in cases of infectious diseases is inevitable, but their excessive and indiscriminate use has been influencing bacterial resistance. This health scenario constitutes an extensive threat to the sick population and in need of therapeutic treatment, which makes it necessary for the scientific community to engage in research and development of new prototypes with potential pharmacological properties. The 1,2,3-triazole heterocycle constitutes a nucleus that can be found in the structure of different bioactive compounds. Although there are different synthesis procedures for obtaining these derivatives, the most usual method is 1,3-dipolar cycloaddition of azides to alkynes, employing the use of copper as a reaction catalyst. This review presents the main synthesis strategies for obtaining 1,2,3-triazole derivatives, as well as results associated with their antibacterial property.

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Published

2020-10-01

How to Cite

Barbosa, G. G., & Aguiar , A. P. de. (2020). Derivados 1,2,3-triazol: métodos de síntese e atividade antibacteriana. Revista Militar De Ciência E Tecnologia, 37(4), 38–57. Retrieved from https://ebrevistas.eb.mil.br/CT/article/view/8569