Heterocyclization reaction of propargyl acetate with β-dicarbonyl compounds

Authors

  • Ш. O. Баданян Institute of Organic Chemistry, Armenian National Academy of Sciences, Erevan 375091
  • Ж. А. Чобaнян Institute of Organic Chemistry, Armenian National Academy of Sciences, Erevan 375091
  • M. P. Тиpакян Institute of Organic Chemistry, Armenian National Academy of Sciences, Erevan 375091
  • А. O. Даниелян Institute of Organic Chemistry, Armenian National Academy of Sciences, Erevan 375091

Abstract

The regiochemistry of the reaction of propargyl acetate with CH acids in the presence of mercury(II) acetate in dimethylsulfoxide has been investigated. Derivatives of furan or unsaturated diketones were isolated depending on the nature of the 1,3-dicarbonyl and the possibility of reduction of the organomercury intermediate.

How to Cite
Badanyan, S. O.; Chobanyan, Z. A.; Tirakyan, M. R.; Danilelyan, A. O. Chem. Heterocycl. Compd. 1998, 34, 781. [Khim. Geterotsikl. Soedin. 1998, 34, 904.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF02251682

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Published

1998-07-25

Issue

No. 7 (1998)

Section

Original Papers