Synthesis and antifungal activity of halogenated aromatic bis-γ-lactones analogous to avenaciolide

• Autor(a) principal: Castelo-Branco, Pedro A.
• Data de Publicação: 2011
• Outros Autores: Rubinger, Mayura M. M., Alves, Leandro de C., Liberto, Natalia A., Nepel, Thayane C. M., Catrinck, Mariana, Guilardi, Silvana, Silvério, Hudson A., Zambolim, Laércio, Piló-Veloso, Dorila, F. Neto, Wilson P.
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: LOCUS Repositório Institucional da UFV
• Texto Completo: http://dx.doi.org/10.1590/S0100-40422012000500016; http://www.locus.ufv.br/handle/123456789/18057
• topic: Avenaciolide analogues; Absolute structural determination; Antifungal activity

Here we describe the total syntheses and characterization by elemental analyses, infrared and NMR spectroscopy of three new compounds analogous to avenaciolide, a bis-γ-lactone isolated from Aspergillus avenaceus that possesses antifungal activity, where the octyl group of the natural product was replaced by aromatic groups containing chlorine and fluorine atoms. The effects of the avenaciolide, the novel compounds and their synthetic precursors on mycelia development and conidia germination of Colletotrichum gloeosporioides and Fusarium solani were evaluated in vitro. The title compounds were almost as active as avenaciolide. The absolute structures of the chlorinated analogs were determined by X-ray diffraction analysis.