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

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Chemistry of Heterocyclic Compounds Aims and scope

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).

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Authors
  1. A. G. Mikhailovskii
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  2. M. O. Dekaprilevich
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Additional information

Institute of Technical Chemistry, Urals Branch, Russian Academy of Sciences, Perm 614000, Russia. N. D. Zelinskii Institute of Organic Chemistry, Russian Academy of Sciences, Moscow 117913, Russia. Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 8, pp. 1111–1117, August, 1998.

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Mikhailovskii, A.G., Dekaprilevich, M.O. Synthesis and properties of enaminoketohydrazides of the 1,2,3,4-tetrahydroisoquinoline series. Chem Heterocycl Compd 34, 957–963 (1998). https://doi.org/10.1007/BF02311333

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  • DOI: https://doi.org/10.1007/BF02311333

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