PROPERTIES OF 3,3-DIALKYL-3,4-DIHYDROISOQUINOLINE CYCLIC AZOMETHINES

Authors

  • О. В. Сурикова 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/10.1007/6231

Keywords:

3, 3-dialkyl-3, 4-dihydroisoquinolines, methyl ester and p-toluidide of iodoacetic acid, quaternary ammonium salts, dipolar [3 2] cycloaddition, reaction with potassium cyanide and malonodinitrile

Abstract

The reactions of 3,3-dialkyl-3,4-dihydroisoquinoline cyclic azomethines with the methyl ester and p‑toluidide of iodoacetic acid gave stable quaternary ammonium salts which were suitable dipoles for [3+2] cycloaddition reactions. Azomethines activated by iodomethylation react with potassium cyanide and malonodinitrile.

How to Cite
Surikova, O. V.; Mikhailovskii, A. G.; Vakhrin, M. I. Chem. Heterocycl. Compd. 2009, 45, 1473. [Khim. Geterotsikl. Soedin. 2010, 1828.]

For this article in the English edition see DOI 10.1007/s10593-010-0453-x

 

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Published

2021-03-26

Issue

No. 12 (2009)

Section

Original Papers