Synthesis, Structure, and Biological Activity of Products of Reactions of 3,4-Dioxohexane-1,6-dioic Acid Esters with 2-Aminophenol
- Autores: Mukovoz P.1, Slepukhin P.2,3, Danilova E.4, Aysuvakova O.1, Glinushkin A.1
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Afiliações:
- All-Russian Research Institute of Phytopathology
- Postovskii Institute of Organic Synthesis, Ural Branch
- Ural Federal University
- Ivanovo State University of Chemistry and Technology
- Edição: Volume 88, Nº 7 (2018)
- Páginas: 1363-1368
- Seção: Article
- URL: https://journals.rcsi.science/1070-3632/article/view/222301
- DOI: https://doi.org/10.1134/S1070363218070022
- ID: 222301
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Resumo
Bioactive derivatives of 1,4-benzoxazine have been prepared via reactions of 3,4-dioxohexane-1,6- dioic (ketipic) acid esters with 2-aminophenol. (2'Z)-2,2'-(2-Hydroxy-2H-1,4-benzoxazin-2-yl-3-ilidene)diacetic acid esters or (2Z)-[2-oxo-2H-1,4-benzoxazin-3(4H)-ylidene]acetic acid esters can be formed depending on the conditions. The structures of the products of dialkyl ketipate esters reactions with 2-aminophenol were determined by means of X-ray diffraction. It has been demonstrated that the prepared compounds exhibit antimycotic activity against test cultures of plant pathogenic fungi (Fusauium sp., Alternarium sp., and Bipolaris soraciniana).
Sobre autores
P. Mukovoz
All-Russian Research Institute of Phytopathology
Autor responsável pela correspondência
Email: mpp27@mail.ru
Rússia, ul. Institut 5, Bolshie Vyazemy, 143050
P. Slepukhin
Postovskii Institute of Organic Synthesis, Ural Branch; Ural Federal University
Email: mpp27@mail.ru
Rússia, Yekaterinburg; Yekaterinburg
E. Danilova
Ivanovo State University of Chemistry and Technology
Email: mpp27@mail.ru
Rússia, Ivanovo
O. Aysuvakova
All-Russian Research Institute of Phytopathology
Email: mpp27@mail.ru
Rússia, ul. Institut 5, Bolshie Vyazemy, 143050
A. Glinushkin
All-Russian Research Institute of Phytopathology
Email: mpp27@mail.ru
Rússia, ul. Institut 5, Bolshie Vyazemy, 143050