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 et Pg. Potvin, CONDENSATION-REACTIONS OF 2-ACETYLPYRIDINE AND BENZALDEHYDES - NEW CYCLOHEXANOL PRODUCTS AND AN IMPROVED SYNTHESIS OF 4'-P-TOLYL-2,2' 6',2''-TERPYRIDINE/, Journal of chemical research. Synopses, (4), 1998, pp. 180-181
Condensations of 2-acetylpyridine with p-tolualdehyde and 4-tert-butyl
benzaldehyde furnish three new cyclohexanol 3:2 condensates (3d,e and
7), including a new diastereomer, and open a better route to 4'-p-toly
l-2,2': 6',2 ''-terpyridine (1b) via the new 2:1 condensate, 1,5-di(2-
pyridyl) -3(4-methylphenyl)pentane-l,5-dione (6).