Synthesis and properties of enaminoketohydrazides of the 1,2,3,4-tetrahydroisoquinoline series

Authors

  • А. Г. Михайловский Institute of Technical Chemistry, Urals Branch, Russian Academy of Sciences, Perm 614000
  • M. O. Декапpилевич N. D. Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Moscow 117913

Abstract

It has been established that the reaction of 2,3-dioxopyrrolo[2,1-a]isoquinolines with hydrazine occurs at the lactam carbonyl with fission of the pyrroledione ring and the formation of enaminoketohydrazides, the structure of which was confirmed by X-ray crystallographic and spectral data on these compounds and their derivatives (hydrazones).

How to Cite
Mikhailovskii, A. G.; Dekaprilevich, M. O. Chem. Heterocycl. Compd. 1998, 34, 957. [Khim. Geterotsikl. Soedin. 1998, 34, 1111.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF02311333

Published

1998-08-25

Issue

No. 8 (1998)

Section

Original Papers