Cyclizaticn of 3-formyl-2-acetylenylindole oximes

T. A. Prikhod'ko, S. F. Vasilevskii, M. S. Shvartsberg

Research output: Contribution to journalArticlepeer-review

6 Citations (Scopus)


3-Formyl-2-acetylenyl-1-methylindole oximes readily undergo intramolecular heterocyclization with closure of a pyridine ring and formation of substituted γ-carboline N-oxides.

Original languageEnglish
Pages (from-to)2383-2385
Number of pages3
JournalBulletin of the Academy of Sciences of the USSR Division of Chemical Science
Issue number11
Publication statusPublished - 1 Nov 1984
Externally publishedYes

ASJC Scopus subject areas

  • Chemistry(all)

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