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 language | English |
|---|---|
| Pages (from-to) | 2383-2385 |
| Number of pages | 3 |
| Journal | Bulletin of the Academy of Sciences of the USSR Division of Chemical Science |
| Volume | 33 |
| Issue number | 11 |
| DOIs | |
| Publication status | Published - 1 Nov 1984 |
| Externally published | Yes |
ASJC Scopus subject areas
- Chemistry(all)
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Cite this
Prikhod'ko, T. A., Vasilevskii, S. F., & Shvartsberg, M. S. (1984). Cyclizaticn of 3-formyl-2-acetylenylindole oximes. Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 33(11), 2383-2385. https://doi.org/10.1007/BF00948858