O-Acylation of ketoximes of the furan and thiophene series in the liquid-solid body system under interphase catalysts conditions

Authors

  • Э. Абеле Latvian Institute of Organic Synthesis, Riga LV-1006
  • Ю. Попелис Latvian Institute of Organic Synthesis, Riga LV-1006
  • М. Гаварc Latvian Institute of Organic Synthesis, Riga LV-1006
  • А. Гаухмaн Latvian Institute of Organic Synthesis, Riga LV-1006
  • M. Шиманска Latvian Institute of Organic Synthesis, Riga LV-1006
  • Э. Лукевиц Latvian Institute of Organic Synthesis, Riga LV-1006

Abstract

The acylation of 2-furanyl- and 2-thienylalkylketoximes by acyl chlorides in a two-phase catalytic system (solid K2CO3-C6H6-18-crown-6) at room temperature leads to a selective formation of the corresponding O-acetylketoximes in the form of a mixture of E- and Z-isomers.

How to Cite
Abele, É.; Popelis, Yu.; Gavars, M.; Gaukhman, A.; Shimanska, M.; Lukevits, É. Chem. Heterocycl. Compd. 1994, 30, 762. [Khim. Geterotsikl. Soedin. 1994, 867.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01169629

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Published

1994-07-25

Issue

No. 7 (1994)

Section

Original Papers