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

Abstract

Diene condensation of N-substituted 2,3-dichlorobicyclo [2.2.1] hept-5-ene-2,3-dicarboxylic acid imides with hexachlorocyclopentadiene proceeds regioselectively through the double bond of dienophile, resulting in the corresponding polychlorinatedcyclic adducts with endo configuration.

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.…”