REACTION OF ENAMINES AND AZAENAMINES CONTAINING A THIOAMIDE GROUP WITH DIMETHYL ACETYLENEDICARBOXYLATE

Authors

  • Н. П. Бельская Ural Federal University named after the First President of Russia B. N. Yeltsin
  • К. И. Луговик Ural Federal University named after the First President of Russia B. N. Yeltsin
  • А. Д. Ивина Ural Federal University named after the First President of Russia B. N. Yeltsin
  • В. А. Бакулев Ural Federal University named after the First President of Russia B. N. Yeltsin
  • Дж. Фан State Key Laboratory of Elemento-organic Chemistry, Nankai University

DOI:

https://doi.org/10.1007/1755

Keywords:

azaenamines, dimethyl acetylenedicarboxylate, enamines, thiazolidinones, thiopyrans, cycloaddition, cyclocondensation

Abstract

The reaction between enamines and azaenamines containing a thioamide group and dimethyl acetylenedicarboxylate was studied under various conditions. It was shown that exchanging one of the carbon atoms in the structure of the investigated compounds for a nitrogen atom significantly affected the reactivity. Functionalized thiopyrans and thiazolidinones were obtained during this investigation.

How to Cite
Belskaya, N. P.; Lugovik, K. I.; Ivina, A. D.; Bakulev, V. A.; Fan, Z. J. Chem. Heterocycl. Compd. 2014, 50, 888. [Khim. Geterotsikl. Soedin. 2014, 962.]

For this article in the English edition see DOI 10.1007/s10593-014-1543-y

Author Biography

Н. П. Бельская, Ural Federal University named after the First President of Russia B. N. Yeltsin

Наталия Павловна Бельская

professor of organic synthesis technology department

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Published

2014-07-06

Issue

No. 6 (2014)

Section

Original Papers