EFFECT OF SUBSTITUENTS IN THE CUMULENE AND ARYL FRAGMENTS OF AROYLKETENES ON THE STEREOSELECTIVITY OF DIELS-ALDER HETEROREACTION WITH MONO-, BI-, AND POLYCYCLIC TERPENOIDS CONTAINING A CARBONYL GROUP

Authors

  • Д. Д. Некрасов Perm State University
  • А. С. Обухова Perm State University
  • Н. Ю. Лисовенко Perm State University
  • А. Е. Рубцов Perm State University

DOI:

https://doi.org/10.1007/2943

Keywords:

aroylketenes, (R)-, (S)-spiro-1, 3-dioxin-4-ones, terpenoids, (4 2) cycloaddition

Abstract

Stereoisomeric adducts, substituted (R)-, (S)-spiro[6-aryldioxin-4-ones] have been obtained by thermolysis of 5-arylfuran-2,3-diones in the presence of menthone and allobetulone.

How to Cite
Nekrasov, D. D.; Obukhova, A. S.; Lisovenko, N. Yu.; Roobtsov, A. E. Chem. Heterocycl. Compd. 2010, 46, 413. [Khim. Geterotsikl. Soedin. 2010, 522.]

For this article in the English edition see DOI 10.1007/s10593-010-0525-y

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Published

2016-01-13

Issue

No. 4 (2010)

Section

Original Papers