Molecules 2000, 5(3), 580-582; doi:10.3390/50300580
Article

The Importance of Keto-Enol Forms of Arylpropanoids Acting as Antifungal Compounds

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Published: 22 March 2000
This is an open access article distributed under the Creative Commons Attribution License which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
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 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(3):580-582.

Chicago/Turabian Style

Giannini, 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.

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