Synthesis of acetylenyl-N-methylpyrroles

S. F. Vasilevskii, T. A. Sundukova, M. S. Shvartsberg, I. L. Kotlyarevskii

Research output: Contribution to journalArticlepeer-review

5 Citations (Scopus)


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 languageEnglish
Pages (from-to)1346-1350
Number of pages5
JournalBulletin of the Academy of Sciences of the USSR Division of Chemical Science
Issue number8
Publication statusPublished - 1 Aug 1980
Externally publishedYes

ASJC Scopus subject areas

  • Chemistry(all)

Fingerprint Dive into the research topics of 'Synthesis of acetylenyl-N-methylpyrroles'. Together they form a unique fingerprint.

Cite this