NEW SYNTHESIS OF THE DIHYDROINDOLIZINOQUINOLINE SYSTEM BY INTRAMOLECULAR CYCLIZATION OF SULFUR YLIDE

Authors

  • Ф. З. Галин Institute of Organic Chemistry, Ufa Scientific Center of the Russian Academy of Sciences (RAN), Ufa 450054
  • С. Н. Лакеев Institute of Organic Chemistry, Ufa Scientific Center of the Russian Academy of Sciences (RAN), Ufa 450054
  • И. З. Муллагалин Institute of Organic Chemistry, Ufa Scientific Center of the Russian Academy of Sciences (RAN), Ufa 450054
  • И. О. Майданова Institute of Organic Chemistry, Ufa Scientific Center of the Russian Academy of Sciences (RAN), Ufa 450054

DOI:

https://doi.org/10.1007/8425

Keywords:

keto-stabilized sulfur ylide, 6-methylthio-8, 9-dihydroindolizino[1, 2-b]quinoline-7, 11-dione, intramolecular cyclization

Abstract

An efficient method is proposed for obtaining the  dihydroindolizinoquinoline system by intramolecular cyclization of keto-stabilized sulfonium ylide obtained from  β-alanine and quinoline-2,3-dicarboxylic acid anhydride.

How to Cite
Galin, F. Z.; Lakeev, S. N.; Myllagalin, I. Z.; Maydanova, I. O.  Chem. Heterocycl. Compd. 2004, 40, 1564. [Khim. Geterotsikl. Soedin. 2004, 1813.]

For this article in the English edition, see DOI 10.1007/s10593-005-0100-0

 

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Published

2023-12-13

Issue

No. 12 (2004)

Section

Original Papers