HETEROCYCLIC ANALOGS OF PLEIADENE. 73. INTRAMOLECULAR CYCLIZATION OF CINNAMOYL- AND <i>o</i>-CHLOROBENZOYLPERIMIDINES

Authors

  • И. В. Боровлев Stavropol State University, Stavropol 35500
  • О. П. Демидов Stavropol State University, Stavropol 35500
  • А. Ф. Пожарский Rostov State University, Rostov-on-Don 344090

Keywords:

acylperimidines, perimidine, intramolecular cyclization

Abstract

We have carried out the intramolecular cyclization of the anions of 4(9)- and 6(7)-cinnamoylperimidines and also of 4(9)-o-chlorobenzoylperimidine. These partially hydrogenated pyrido- and quino[1,2,3-cd]perimidines were obtained for the first time. Their 1H NMR spectroscopic features are discussed.

How to Cite
Borovlev, I. V.; Demidov, O. P.; Pozharskii, A. F. Chem. Heterocycl. Compd. 2002, 38, 1091. [Khim. Geterotsikl. Soedin. 2002, 1247.]

For this article in the English edition, see DOI https://doi.org/10.1023/A:1021209416136

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Published

2002-09-25

Issue

No. 9 (2002)

Section

Original Papers