Abstract <p>2-Styrylpyridinium salts containing adamantane or aromatic fragments were prepared via a substitution reaction. It was found that quaternized substituted 2-ethenylpyridines undergo intramolecular cyclization under the action of bases, leading to trisubstituted cyclopropanes, as well as mono-, di-, and trisubstituted indolizines. A plausible mechanism was proposed for the formation of pyridylcyclopropanes.</p>

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Synthesis of Pyridylcyclopropanes and Indolizines Based on Quaternized Substituted Styrilpyridines

  • Anastasiya N. Bogdanova,
  • Elizaveta A. Sokova,
  • Marat R. Baimuratov,
  • Ol’ga A. Lodochnikova,
  • Yuri N. Klimochkin

摘要

Abstract

2-Styrylpyridinium salts containing adamantane or aromatic fragments were prepared via a substitution reaction. It was found that quaternized substituted 2-ethenylpyridines undergo intramolecular cyclization under the action of bases, leading to trisubstituted cyclopropanes, as well as mono-, di-, and trisubstituted indolizines. A plausible mechanism was proposed for the formation of pyridylcyclopropanes.