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Molecules 2000, 5(3), 580-582; doi:10.3390/50300580
Article
The Importance of Keto-Enol Forms of Arylpropanoids Acting as Antifungal Compounds
1
Universidad Nacional de San Luis. Facultad de Química, Bioquímica y Farmacia. Cátedra de Química General. Chacabuco y Pedernera. 5700 San Luis, Argentina
2
Universidad Nacional de Rosario. Facultad de Bioquímica y Farmacia. Cátedra de Farmacognosia. Rosario, Argentina
* Author to whom correspondence should be addressed.
Published: 22 March 2000
Abstract: We report here the importance of a keto-enol equilibrium of an arylpropanoid series acting as antifungal agents. An interesting relationship between ln MIC, ∆E enolization and net atomic charges was found. Two compounds were synthesized and their MIC evaluated in order to prove the above relationship.
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MDPI and ACS Style
Giannini, F.; Devia, C.; Rodríguez, A.; Enriz, R.; Suvire, F.; Baldoni, H.; Furlan, R.; Zacchino, S. The Importance of Keto-Enol Forms of Arylpropanoids Acting as Antifungal Compounds. Molecules 2000, 5, 580-582.
AMA StyleGiannini F, Devia C, Rodríguez A, Enriz R, Suvire F, Baldoni H, Furlan R, Zacchino S. The Importance of Keto-Enol Forms of Arylpropanoids Acting as Antifungal Compounds. Molecules. 2000; 5(3):580-582.
Chicago/Turabian StyleGiannini, F.; Devia, C.; Rodríguez, A.; Enriz, R.; Suvire, F.; Baldoni, H.; Furlan, R.; Zacchino, S. 2000. "The Importance of Keto-Enol Forms of Arylpropanoids Acting as Antifungal Compounds." Molecules 5, no. 3: 580-582.
Molecules
EISSN 1420-3049
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