A method for transesterification of the ester groups in dialkylaziridine dicarboxylates by electrophilic activation of the carbonyl group in the presence of magnesium acetate with the preservation of the aziridine ring was developed and the use of modified aziridine dicarboxylates in the synthesis of sterically hindered derivatives of fullerenes C-60, 2',5'-disubstituted fulleropyrrolidines, was demonstrated.

Original languageEnglish
Pages (from-to)875-880
Number of pages6
JournalChemistry of Heterocyclic Compounds
Volume56
Issue number7
DOIs
StatePublished - Jul 2020

    Scopus subject areas

  • Chemistry(all)
  • Organic Chemistry

    Research areas

  • 1,3-dipolar cycloaddition, aziridines, electrophilic activation, fullerenes, stereodirected synthesis, transesterification, OXAZOLIDINES, AZOMETHINE YLIDES, AZIRIDINES, STRUCTURAL DIVERSITY, CYCLOADDITION, INHIBITION, STEREOSELECTIVE-SYNTHESIS

ID: 62157471