Autor: |
Guimarães, Eduardo F. S., Graça, Gabriela A. P., Diogo, Emilay B. T., Almeida, Renata G., Pereira, Daiane B., Araujo, Maria H., da Silva, Caren D. G., Gatto, Claudia C., Ramos, Victor F. S., Menna‐Barreto, Rubem F. S., Jardim, Guilherme A. M., da Silva Júnior, Eufrânio N. |
Zdroj: |
Chemistry - An Asian Journal; 12/16/2024, Vol. 19 Issue 24, p1-6, 6p |
Abstrakt: |
An eco‐friendly electrochemical halogenation of 2‐amino‐1,4‐naphthoquinones has been developed. The new mild and energy efficient methodology comprises sustainable features like oxidant free and double role of the halogen source as electrolyte, originating twenty‐six amino‐halogenated naphthoquinoidal derivatives in good yields under mild conditions. This novel methodology permitted access to new potent trypanocidal prototypes, where six compounds were more active than benznidazole, the current market drug used in the treatment of Chagas Disease. [ABSTRACT FROM AUTHOR] |
Databáze: |
Complementary Index |
Externí odkaz: |
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