The reaction of amidoximes with carboxylic acids or their esters under high-pressure conditions
- Authors: Baikov S.V.1, Stashina G.A.2, Chernoburova E.I.2, Krylov V.B.2, Zavarzin I.V.2, Kofanov E.R.3
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Affiliations:
- K. D. Ushinsky Yaroslavl State Pedagogical University
- N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
- Yaroslavl State Technical University
- Issue: Vol 68, No 2 (2019)
- Pages: 347-350
- Section: Full Articles
- URL: https://ogarev-online.ru/1066-5285/article/view/243252
- DOI: https://doi.org/10.1007/s11172-019-2391-9
- ID: 243252
Cite item
Abstract
3,5-Disubstituted 1,2,4-oxadiazoles were synthesized by the reaction of amidoximes with carboxylic acids or their esters under high-pressure conditions (10 kbar). The reaction proceeds without the use of other reagents or catalysts. Both aliphatic and aromatic carboxylic acids undergo this reaction. The obtained 1,2,4-oxadiazoles possess high fungicidal activity.
About the authors
S. V. Baikov
K. D. Ushinsky Yaroslavl State Pedagogical University
Email: zavi@ioc.ac.ru
Russian Federation, 108 ul. Respublikanskaya, Yaroslavl, 150000
G. A. Stashina
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: zavi@ioc.ac.ru
Russian Federation, 47 Leninskii prosp., Moscow, 119991
E. I. Chernoburova
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: zavi@ioc.ac.ru
Russian Federation, 47 Leninskii prosp., Moscow, 119991
V. B. Krylov
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Email: zavi@ioc.ac.ru
Russian Federation, 47 Leninskii prosp., Moscow, 119991
I. V. Zavarzin
N. D. Zelinsky Institute of Organic Chemistry, Russian Academy of Sciences
Author for correspondence.
Email: zavi@ioc.ac.ru
Russian Federation, 47 Leninskii prosp., Moscow, 119991
E. R. Kofanov
Yaroslavl State Technical University
Email: zavi@ioc.ac.ru
Russian Federation, 88 Moskovskii prosp., Yaroslavl, 150023
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