NEW FORMATION OF PYRROLIZINES BY INTRAMOLECULAR CYCLIZATION OF PHENACYL SUBSTITUTED TETRAHYDROPYRIDINES

Authors
CSUZDI E PALLAGI I JERKOVICH G SOLYOM S
Citation
E. Csuzdi et al., NEW FORMATION OF PYRROLIZINES BY INTRAMOLECULAR CYCLIZATION OF PHENACYL SUBSTITUTED TETRAHYDROPYRIDINES, Synlett, (6), 1994, pp. 429-430
Citations number
8
Categorie Soggetti
Chemistry Inorganic & Nuclear
Journal title
Synlett → ACNP
ISSN journal
09365214
Issue
6
Year of publication
1994
Pages
429 - 430
Database
ISI
SICI code
0936-5214(1994):6<429:NFOPBI>2.0.ZU;2-K
Abstract
Cyclization of 1 -phenacyl-4-phenyl- 1,2,5,6-tetrahydropyridines under acidic conditions resulted 1,7-bis-phenyl-5,7a-dihydro-3H-pyrrolizine s, and the originally expected 4,6-bis-phenyl-1-azabicyclo[3.2.1]octa- 3,6-diene system was produced as a minor product.