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Synlett 1994; 1994(6): 429-430
DOI: 10.1055/s-1994-22876
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New Formation of Pyrrolizines by Intramolecular Cyclization of Phenacyl Substituted Tetrahydropyridines

Emese Csuzdi* , István Pallagi, Gyula Jerkovich, Sándor Sólyom
  • *Institute for Drug Research Ltd, H-1045 Budapest, Berlini u. 47-49, Hungary
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Publication History

Publication Date:
18 September 2002 (online)

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Cyclization of 1-phenacyl-4-phenyl-1,2,5,6-tetrahydropyridines under acidic conditions resulted 1,7-bis-phenyl-5,7a-dihydro-3H-pyrrolizines, and the originally expected 4,6-bis-phenyl-1-azabicyclo[3.2.1]octa-3,6-diene system was produced as a minor product.

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