Microwave synthesis and antifungal evaluations of some chalcones and their derived diaryl-cyclohexenones.
J Environ Sci Health B
; 45(6): 524-30, 2010 Aug.
Article
em En
| MEDLINE
| ID: mdl-20574873
ABSTRACT
Microwave irradiation (MWI) of acetophenones and substituted benzaldehydes in water resulted in a "green-chemistry" procedure for the preparation of chalcones (1-14), through base catalyzed Claisen-Schmidt condensation reaction, in good yields. Further 3,5-diaryl-6-carbethoxy-2-cyclohexen-1-ones (1a-14a) were prepared through base catalyzed cyclocondensation of above chalcones with ethylacetoacetate using MWI as the energy source and silica as support. Out of fourteen cyclohexenones, ten (1a, 4a, 5a, 6a, 7a, 9a, 10a, 11a, 12a and 13a) are reported for the first time in literature. The synthesized compounds were characterized using various spectroscopic techniques, viz. ((1)H NMR and IR) and screened for their antifungal activity in vitro against Sclerotium rolfsii and Rhizoctonia solani by poisoned food technique. The compounds tested were found to be active against R. solani whereas against S. rolfsii, moderate activity was observed, as evident from LC(50) values. The most potent compounds against R. solani were 1-(4-Fluoro-phenyl)-3-phenyl-propenone (13) and 1,3-Diphenyl-propenone (14) having LC(50) values of 2.36 and 2.49 mg L(- 1) respectively (LC(50) of Hexaconazole = 1.12 mg L(- 1)) and against S. rolfsii 3-(4-Fluoro-phenyl)-5-(3-nitro-phenyl)-6-carbethoxy-2-cyclohexen-1-one (12a) was most active having LC(50) value of 285 mg L(- 1)compared to Hexaconazole (LC(50) = 1.27 mg L(- 1)).
Texto completo:
1
Bases de dados:
MEDLINE
Assunto principal:
Basidiomycota
/
Chalconas
/
Antifúngicos
Idioma:
En
Revista:
J Environ Sci Health B
Ano de publicação:
2010
Tipo de documento:
Article
País de afiliação:
Índia