Open AccessFUNGICIDAL PROPERTIES OF N-(p-CARBOXYPHENYL)IMIDE-2,3-DICHLOROBICYCLO-[2.2.1]HEPT-5-EN-2,3-DICARBOXYLIC ACID
Author(s) -
Ya. M. Nagiev
Publication year - 2021
Publication title -
azərbaycan kimya jurnalı/azerbajčan himiâ žurnaly
Language(s) - English
Resource type - Journals
eISSN - 2522-1841
pISSN - 0005-2531
DOI - 10.32737/0005-2531-2021-1-72-77
Subject(s) - imide , dicarboxylic acid , oxidizing agent , chemistry , cyclopentadiene , acetic acid , acetic anhydride , sulfate , organic chemistry , catalysis
As a result of the interaction of substituted aminobenzoic acids and dichloromaleic anhydride in glacial acetic acid, various N-substituted imides of dichloromaleic acid have been obtained. Based on the diene synthesis of cyclopentadiene and N-substituted imides of dichloromaleic acid, N-(orthometa- and para-carboxyphenyl)imides of 2,3-dichlorocyclo-[2.2.1]hept-5-ene-2,3-dicarboxylic acid have been syn¬thesized. The obtained imides have been tested as a potential effective complex biologically active drug. The results of multiple tests have demonstrated that these compounds possess, simultangonsly, high fungicidal and bactericidal activity against cotton verticillus wilt. So, for a concentration of 0.1%, the obtained compounds almost completely destroy the fungus verticillum dahliae, as well as thionic iron-oxidizing and sulfate-reducing aerobic bacteria VKM V-458 and VKM V-1388