REGIOSELECTIVE SYNTHESIS OF PYRIDIN-2-ONE DERIVATIVES BASED ON ETHYL(1-PHENYLETHYLIDENE)CYANOACETATE AND CYANOACETAMIDES

Authors

  • С. Р. Фефелова Luhansk Taras Shevchenko National University
  • Д. А. Красников Luhansk Taras Shevchenko National University
  • В. Д. Дяченко Luhansk Taras Shevchenko National University
  • А. Д. Дяченко Kyiv Taras Shevchenko National University

DOI:

https://doi.org/10.1007/1680

Keywords:

ethyl(1-phenylethylidene)cyanoacetate, cyanoacetamide, glutarimides, pyridin-2-ones, Michael addition

Abstract

Ethyl(1-phenylethylidene)cyanoacetate reacted with cyanoacetamides in alcohol solution of sodium ethoxide, forming various pyridin-2-ones. The cyclization direction of Michael adducts was affected by the nucleophilicity of cyanoacetamide used as a СН acid.

How to Cite
Fefelova, S. R.; Krasnikov, D. A.; Dyachenko, V. D.; Dyachenko, A. D. Chem. Heterocycl. Compd. 2014, 50, 1133. [Khim. Geterotsikl. Soedin. 2014, 1228.]

For this article in the English edition see DOI 10.1007/s10593-014-1573-5

Author Biographies

С. Р. Фефелова, Luhansk Taras Shevchenko National University

Светлана Романовна Фефелова

аспирант кафедры химии и биохимии

Д. А. Красников, Luhansk Taras Shevchenko National University

Денис Александрович Красников

к.х.н., доцент кафедры химии и биохимии

В. Д. Дяченко, Luhansk Taras Shevchenko National University

Владимир Данилович Дяченко

д.х.н., проф., завкафедры химии и биохимии

А. Д. Дяченко, Kyiv Taras Shevchenko National University

Александр Данилович Дяченко

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Published

2014-09-09

Issue

No. 8 (2014)

Section

Original Papers