| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5268635 | Tetrahedron Letters | 2010 | 4 Pages |
Abstract
The tetraenic macrolide antibiotic natamycin and the pentaenic macrolide flavofungin gave monoadducts on Diels-Alder reaction with 4-phenyl-1,2,4-triazoline-3,5-dione. The regioselectivity of the reaction as well as the conformation of the products was studied using theoretical calculations.
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Authors
Zsolt Fejes, Attila Mándi, István Komáromi, László Majoros, Gyula Batta, Pál Herczegh,