Cyclizaticn of 3-formyl-2-acetylenylindole oximes

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

Research output: Contribution to journalArticle

6 Citations (Scopus)

Abstract

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
Volume33
Issue number11
DOIs
Publication statusPublished - 1 Nov 1984
Externally publishedYes

Fingerprint

Carbolines
Oximes
Oxides
1-methylindole
pyridine

ASJC Scopus subject areas

  • Chemistry(all)

Cite this

Cyclizaticn of 3-formyl-2-acetylenylindole oximes. / Prikhod'ko, T. A.; Vasilevskii, S. F.; Shvartsberg, M. S.

In: Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, Vol. 33, No. 11, 01.11.1984, p. 2383-2385.

Research output: Contribution to journalArticle

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