Lacasse catalyzed-synthesis of 4,4′-biphenyldiamine from P-chloroaniline. Evaluation of antifungal and antioxidant activities

2Citations
Citations of this article
5Readers
Mendeley users who have this article in their library.

Abstract

Laccase is a copper-containing oxidase that catalyzes reduction of molecular oxygen to water and the oxidation of a phenolic compound. In this paper, laccase was utilized to synthesize 4,4′-Biphenyldiamine using p-chloroaniline as substrate by means of a coupling reaction. The synthesized compound, 4,4′-Biphenyldiamine, presented low antifungal activity against the phytopathogenic fungus Botrytis cinerea, however the antioxidant ability, measurement by ORAC-PGR method, was higher than substrate. This work corresponds to the first report of synthesis 4,4′-Biphenyldiamine, from p-chloroaniline in a lacasse-catalyzed reaction.

Cite

CITATION STYLE

APA

Campos, A. M., Mendoza, L., Vasquez, J., Melo, R., Salas, J., & Cotoras, M. (2016). Lacasse catalyzed-synthesis of 4,4′-biphenyldiamine from P-chloroaniline. Evaluation of antifungal and antioxidant activities. Journal of the Chilean Chemical Society, 61(3), 3031–3033. https://doi.org/10.4067/S0717-97072016000300004

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free