Synthesis of spiro analogs of lilolidine alkaloids

Authors

  • B. B. Кузнецов Russian University of National Friendship, Moscow 117198
  • A. P. Пальма Russian University of National Friendship, Moscow 117198
  • H. C. Простаков Russian University of National Friendship, Moscow 117198
  • А. В. Варламов Russian University of National Friendship, Moscow 117198

Abstract

The Friedel-Krafts intramolecular cyclization of N-chloroacetyl- and N-α-bromopropionyl-4-methylspiro[tetrahydroquinoline-2-cyclohexanes] was used to obtain 2-oxo-1,2,5,6-tetrahydro-4H-spiro[pyrrolo(3,2,1-i,j)quinoline-4,1′-cyclohexanes]— spiro analogs of lilolidine alkaloids.

How to Cite
Kuznetsov, V. V.; Pal'ma, A. R.; Prostakov, N. S.; Varlamov, A. V. Chem. Heterocycl. Compd. 1993, 29, 1296. [Khim. Geterotsikl. Soedin. 1993, 1504.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF00532028

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Published

1993-11-25

Issue

No. 11 (1993)

Section

Original Papers