Abstract
1. Iodine atoms in any position of the pyrrole ring are capable of being replaced by acetylenic groups under the conditions of palladium complex and copper catalysis. We accomplished the acetylenic condensation of a number of α- and β-iodopyrroles. 2. The alkaline cleavage of the thus-synthesized tertiary pyrrolylacetylenic alcohols leads to ethynylpyrroles.
| Original language | English |
|---|---|
| Pages (from-to) | 1346-1350 |
| Number of pages | 5 |
| Journal | Bulletin of the Academy of Sciences of the USSR Division of Chemical Science |
| Volume | 29 |
| Issue number | 8 |
| DOIs | |
| Publication status | Published - 1 Aug 1980 |
| Externally published | Yes |
ASJC Scopus subject areas
- Chemistry(all)
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Cite this
Vasilevskii, S. F., Sundukova, T. A., Shvartsberg, M. S., & Kotlyarevskii, I. L. (1980). Synthesis of acetylenyl-N-methylpyrroles. Bulletin of the Academy of Sciences of the USSR Division of Chemical Science, 29(8), 1346-1350. https://doi.org/10.1007/BF00950586