SYNTHESIS OF FUNCTIONALLY SUBSTITUTED PYRROLO[2,3-<i>g</i>]- AND PYRROLO[3,2-<i>f</i>]QUINOLINES FROM 5-AMINO-2-PHENYL- AND 5-AMINO-1-METHYL-2-PHENYLINDOLES

Authors

  • C. А. Ямашкин Mordovian State Pedagogical University, Saransk 430007
  • Г. А. Романова Mordovian State Pedagogical University, Saransk 430007
  • И. С. Романова Mordovian State Pedagogical University, Saransk 430007
  • М. А. Юровская Moscow M. V. Lomonosov State University, Moscow 119234

Keywords:

5-amino-2-phenylindole, 5-amino-1-methyl-2-phenylindole, acetoacetic ester, trifluoroacetoacetic ester, ethoxymethylenemalonic ester, functionally substituted pyrrolo[2,3-g]quinolines, functionally substituted pyrrolo[3,2-f]quinolines

Abstract

The behavior of 5-amino-2-phenyl- and 5-amino-1-methyl-2-phenylindoles in reactions with acetoacetic, trifluoroacetoacetic, and ethoxymethylenemalonic esters, leading to the preparation of pyrrolo[2,3-g]- and pyrrolo[3,2-f]quinolines with functional substituents has been studied.

How to Cite
Yamashkin, S. A.; Romanova, G. A.; Romanova, I. S.; Yurovskaya, M. A. Chem. Heterocycl. Compd. 2003, 39, 1188. [Khim. Geterotsikl. Soedin. 2003, 1354.]

For this article in the English edition, see DOI 10.1023/B:COHC.0000008264.35326.20

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Published

2003-09-25

Issue

No. 9 (2003)

Section

Original Papers