Issue 4, 1998

Condensation Reactions of 2-Acetylpyridine and Benzaldehydes: New Cyclohexanol Products and an Improved Synthesis of 4′-p-Tolyl-2,2′:6′,2″-terpyridine

Abstract

Condensations of 2-acetylpyridine with p-tolualdehyde and 4-tert-butylbenzaldehyde furnish three new cyclohexanol 3:2 condensates (3d,e and 7), including a new diastereomer, and open a better route to 4′-p-tolyl-2,2′:6′,2″-terpyridine (1b) via the new 2:1 condensate, 1,5-di(2-pyridyl)-3(4-methylphenyl)pentane-1,5-dione (6).

Article information

Article type
Paper

J. Chem. Res. (S), 1998, 180-181

Condensation Reactions of 2-Acetylpyridine and Benzaldehydes: New Cyclohexanol Products and an Improved Synthesis of 4′-p-Tolyl-2,2′:6′,2″-terpyridine

C. Chamchoumis and P. G. Potvin, J. Chem. Res. (S), 1998, 180 DOI: 10.1039/A708518D

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