SYNTHESIS OF PYRIDIN-2(1H)-ONES BY THE INTRAMOLECULAR CYCLIZATION OF AMIDES OF β-ENAMINO KETONES

Authors

  • Д. С. Гончаров F. M. Dostoevsky Omsk State University, Omsk 644077
  • А. С. Костюченко F. M. Dostoevsky Omsk State University, Omsk 644077
  • А. С. Фисюк F. M. Dostoevsky Omsk State University, Omsk 644077

DOI:

https://doi.org/10.1007/6637

Keywords:

amide, β-enamino ketone, pyridin-2(1H)-ones, intramolecular cyclization

Abstract

It has been shown that intramolecular cyclization of N-(1-methyl-3-oxobut-1-en-1-yl)phenyl- and -tosylacetamides in basic media lead to 3-phenyl- and 3-tosyl-substituted 4,6-dimethylpyridin-2(1H)-ones.

How to Cite
Goncharov, D. S.; Kostuchenko, A. S.; Fisyuk, A. S. Chem. Heterocycl. Compd. 2009, 45, 793. [Khim. Geterotsikl. Soedin. 2009, 1005.]

For this article in the English edition see DOI 10.1007/s10593-009-0358-8


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Published

2022-02-28

Issue

No. 7 (2009)

Section

Original Papers