Abstract
Products of reaction between bicyclo[2.2.1]hept-5-ene-endo-endo-2,3-dicarboxylic anhydride (endic anhydride) and cyclic amines were obtained. By an example of one of amido acids a conformational analysis was performed and character of hydrogen bonds was studied using quantum-chemical calculations by PM3 procedure. endo-3-(4-Antipyrylcarbomoyl)-bicyclo[2.2.1]hept-5-ene-endo-2-carboxylic acid with a secondary amide group was converted into the corresponding carboximide which was epoxidized by performic acid.
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