AZOCOUPLING REACTIONS OF ENAMINOCARBONYL DERIVATIVES OF 1,2,3,4-TETRAHYDROISOQUINOLINE WITH DIAZONIUM SALTS

Authors

  • Н. Н. Полыгалова Perm State Pharmaceutical Academy, Perm 614990
  • А. Г. Михайловский Perm State Pharmaceutical Academy, Perm 614990
  • М. И. Вахрин Perm State Pharmaceutical Academy, Perm 614990

DOI:

https://doi.org/10.1007/7822

Keywords:

azo compounds, diazonium salts, secondary and tertiary enamines, 1, 2, 3, 4-tetrahydroisoquinolines, azohydrazone tautomerization

Abstract

It has been shown that enamino amide and enamino ketone derivatives of 1,2,3,4-tetrahydroisoquinoline react with diazonium salts to form azo compounds. Depending on the enamine structure they can exist just as azo dyes or as azohydrazone tautomers.

How to Cite
Polygalova, N. N.; MIkhailovskii, A. G.; Vakhrin, M. I.  Chem. Heterocycl. Compd. 2006, 42, 1200. [Khim. Geterotsikl. Soedin. 2006, 1382.]

For this article in the English edition see DOI 10.1007/s10593-006-0226-8


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Published

2023-05-22

Issue

No. 9 (2006)

Section

Original Papers