Diverse natural and synthetic furan derivatives have shown biological activity. Here, we describe the preparation of benzyl and arylethyl β-furanamides with OH or OMe aryl substituents by an adapted sustainable method from a furoic acid using methyl chloroformate. Symmetric and asymmetric β,β'-furanamides have instead been prepared using azabenzotriazole based catalyst (HATU). The products have been evaluated for their antimicrobial properties on Gram positive and Gram negative bacteria. Just a minimal not-significant activity has been observed in some derivatives.

Hands-on synthesis of furanamides and evaluation of their antimicrobial activity / Mercogliano, Marcello; Iesce, Maria Rosaria; Alfieri, Maria Laura; Buommino, Elisabetta; Della Greca, Marina. - In: NATURAL PRODUCT RESEARCH. - ISSN 1478-6427. - 37:20(2023), pp. 3484-3491. [10.1080/14786419.2022.2087220]

Hands-on synthesis of furanamides and evaluation of their antimicrobial activity

Mercogliano, Marcello;Iesce, Maria Rosaria;Alfieri, Maria Laura;Buommino, Elisabetta
Penultimo
;
Della Greca, Marina
2023

Abstract

Diverse natural and synthetic furan derivatives have shown biological activity. Here, we describe the preparation of benzyl and arylethyl β-furanamides with OH or OMe aryl substituents by an adapted sustainable method from a furoic acid using methyl chloroformate. Symmetric and asymmetric β,β'-furanamides have instead been prepared using azabenzotriazole based catalyst (HATU). The products have been evaluated for their antimicrobial properties on Gram positive and Gram negative bacteria. Just a minimal not-significant activity has been observed in some derivatives.
2023
Hands-on synthesis of furanamides and evaluation of their antimicrobial activity / Mercogliano, Marcello; Iesce, Maria Rosaria; Alfieri, Maria Laura; Buommino, Elisabetta; Della Greca, Marina. - In: NATURAL PRODUCT RESEARCH. - ISSN 1478-6427. - 37:20(2023), pp. 3484-3491. [10.1080/14786419.2022.2087220]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/899222
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