Heterocylization of N-phenylamino-2-pyrrolidones

Authors

  • B. П. Жестков All-Russian Scientific Center for the Safety of Biologically Active Substances (VNTs BAV), Kupavna, Moscow Oblast, 142450
  • В. B. Дружинина All-Russian Scientific Center for the Safety of Biologically Active Substances (VNTs BAV), Kupavna, Moscow Oblast, 142450
  • А. B. Рудницких All-Russian Scientific Center for the Safety of Biologically Active Substances (VNTs BAV), Kupavna, Moscow Oblast, 142450

Abstract

Hetrocylization of N-phenylamino-2-pyrrolidones with solutions of phosgene takes place with the formation of dihydropyrrolo[2,3-b]indoles, which on acid cleavage give 2-oxotryptamines or their derivatives.

How to Cite
Zhestkov, V. P.; Druzhinina, V. V.; Rudnitskikh, A. V. Chem. Heterocycl. Compd. 1995, 31, 279. [Khim. Geterotsikl. Soedin. 1995, 325.]

For this article in the English edition, see DOI https://doi.org/10.1007/BF01373543

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Published

1995-03-25

Issue

No. 3 (1995)

Section

Original Papers