REARRANGEMENT OF THE ADDUCTS OF α-(AMINOCARBONYL)ACETAMIDOXIMES WITH ACYLACETYLENES, LEADING TO 2-AMINOPYRROLE DERIVATIVES

Authors

  • Е. Е. Пивнева St. Petersburg State University
  • А. В. Галенко St. Petersburg State University
  • Д. В. Дарьин St. Petersburg State University
  • П. С. Лобанов St. Petersburg State University

DOI:

https://doi.org/10.1007/1160

Keywords:

2-aminopyrroles, O-vinylamidoximes, [3, 3] sigmatropic rearrangement

Abstract

The rearrangement and cyclization of O-vinylamidoximes, which are adducts of α-(aminocarbonyl)acetamidoximes with acetylenic ketones, leads to 2-acylaminopyrroles.

Authors: E. E. Pivneva, A. V. Galenko, D. V. Dar'in, and P. S. Lobanov.

English Translation in Chemistry of Heterocyclic Compounds, 2012, 48 (6), pp 875-880

http://link.springer.com/article/10.1007/s10593-012-1069-0

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Published

2013-11-14

Issue

No. 6 (2012)

Section

Original Papers