The influence of substitution in the quinoxaline nucleus on 1,3-dipolar cycloaddition reactions

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5 Citations (Scopus)

Abstract

The reaction mechanism of 1,3-dipolar cycloadditions of both symmetric and unsymmetric benzo-condensed diazines with a nitrilimine dipole, to give two different mono- and bis-cycloadducts, in tetrahydrofuran (THF) solution, was studied by DFT calculatio ns. The results obtained show that each 1,3-dipolar cycloaddition reaction always proceeds by a two steps mechanism, in which the first intermediate shows only one covalent bond between the beta carbon of the nitrilimine and the aromatic nitrogen of the diazine molecule. The structure and energy content of the two transition states of the two cycloaddition steps, in the case of the unsymmetric benzo-condensed diazine, nicely explains why the product of the bis-cycloaddi tions is exclusively observed and why the product of a mono-cycloaddition is not isolated for the symmetric reaction pathway.
Original languageEnglish
Pages (from-to)116-122
Number of pages7
JournalComputational and Theoretical Chemistry
Volume1013
Publication statusPublished - 2013

All Science Journal Classification (ASJC) codes

  • Biochemistry
  • Condensed Matter Physics
  • Physical and Theoretical Chemistry

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