REACTION OF VICINAL THIENO[2,3-<i>b</i>]PYRIDINE AMINOAMIDES WITH LAWESSON'S REAGENT

Authors

  • В. М. Редькин Kuban State Technological University
  • Т. А. Строганова Kuban State Technological University
  • В. К. Василин Kuban State Technological University
  • Г. Д. Крапивин Kuban State Technological University

DOI:

https://doi.org/10.1007/892

Keywords:

3-aminothieno[2, 3-b]pyridinecarboxamides, diazaphosphinines, Lawesson's reagent, thionation

Abstract

The reaction of vicinal thieno[2,3-b]pyridine aminoamides with Lawesson's reagent gave new condensed diazaphosphinine derivatives. The structure of the substituent at the amide nitrogen atom and the reagent ratio were found to affect the direction of this reaction.

Authors: V. M. Red'kin, T. A. Stroganova, V. K. Vasilin, and G. D. Krapivin

English Translation in Chemistry of Heterocyclic Compounds, 2012, 48 (11), pp 1701-1709

http://link.springer.com/article/10.1007/s10593-013-1196-2

Downloads

Published

2013-08-27

Issue

No. 11 (2012)

Section

Original Papers