Synthesis and properties of azoles and their derivatives XXXVIII. [2+3]-cycloaddition of C,C,N-triphenyl and <i>Z</i>-C,N-diphenyl nitrone to <i>n</i>-dec-1-ene in the light of semiempirical AM-1 calculations

Authors

  • B. Таборски Institute of Organic Chemistry and Technology, Technical University, Krakow 31-155
  • А. Бараньски Institute of Organic Chemistry and Technology, Technical University, Krakow 31-155

Abstract

The activation parameters of the [2+3]-cycloaddition of C,C,N-triphenyl nitrone and Z-C,N-diphenyl nitrone to n-dec-1-ene were calculated by the AM-1 method. It was shown that the paths leading to the respective isoxazolidines containing an octyl group at the C-5 position of the heterocyclic ring are preferred.

How to Cite
Taborski, V.; Baranski, A. Chem. Heterocycl. Compd. 1998, 34, 1032. [Khim. Geterotsikl. Soedin. 1998, 34, 1204.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF02251547

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Published

1998-09-25

Issue

No. 9 (1998)

Section

Original Papers