Condensation of Ketones with Acylpyridinium Salts1

WE Doering, WE McEwen

Index: Doering; McEwen Journal of the American Chemical Society, 1951 , vol. 73, p. 2104,2108

Full Text: HTML

Citation Number: 44

Abstract

Claisen's product, C20HllN02, of the reaction of pyridine, benzoyl chloride and acetophenone has been shown to be 1-benzoyl-4-phenacyl-1, 4-dihydropyridine. The product from pyridine, acetic anhydride and acenaphthenone does not have the structure assigned to it by E. Ghigi but rather is 1-acetoxy-2-(l'-acetyl-l', 4'-dihydro-4'-pyridyl)- acenaphthylene. These interesting reactions of acylpyridinium salts at the-pposition of ...

Related Articles:

Synthesis of Benzo-fused Heterocycles by Intramolecular α-Arylation of Ketone Enolate Anions

[Lee, Cheuk Man; Sammes, Michael P.; Katritzky, Alan R. Journal of the Chemical Society, Perkin Transactions 1: Organic and Bio-Organic Chemistry (1972-1999), 1980 , p. 2458 - 2462]

More Articles...