Synthesis of N-substituted imides of 2,3-dichlorobicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic Acid

FUNGICIDAL PROPERTIES OF N-(p-CARBOXYPHENYL)IMIDE-2,3-DICHLOROBICYCLO-[2.2.1]HEPT-5-EN-2,3-DICARBOXYLIC ACID

“…The compounds of the bicycle-[2.2.1]hept-and [2.2.2]oct-5-ene series are known to have a wide spectrum of biological and physiological action [4][5][6][7][8][9]12] and, accordingly, our works [4,6,8,10,11,13], devoted to the study of the reaction of diene synthesis of N-aryldichloromaleinimides with cyclopentadiene (CPD), have shown that the obtained compounds are included in the sphere of action of these compounds.…”

Synthesis of New Halogen-Containing Norbornene Adducts Based on N-Substituted Imides of 2,3-Dichlorbicyclo [2.2.1] Hept-5-ene-2,3- Dicarboxylic Acids and Hexachlorocyclopentadiene

“…Previously, we investigated the diene condensation of N-substituted imidates of dichloromaleic acid with cyclopentadiene and 1,3cyclohexadiene, leading to the formation of bicyclic adducts. The structure and properties of the synthesized compounds were studied, as well as certain patterns of reactions [15][16][17][18][19][20].…”