𝔖 Bobbio Scriptorium
✦   LIBER   ✦

The reactivity of 1,4-dihydronicotinamides towards reduction of 1,1′,1″-trifluoro-acetophenone : influence of methyl substitution on the pyridine ring.

✍ Scribed by Jan Bossaerts; Roger A. Dommisse; Frank C. Alderweireldt


Book ID
104232666
Publisher
Elsevier Science
Year
1984
Tongue
French
Weight
131 KB
Volume
25
Category
Article
ISSN
0040-4039

No coin nor oath required. For personal study only.


📜 SIMILAR VOLUMES


Reactivity of biologically important red
✍ Marcus E. Brewster; James J. kaminski; Zoltan Gabanyi; Klara Czako; Agnes Simay; 📂 Article 📅 1990 🏛 Elsevier Science 🌐 French ⚖ 436 KB

Bronsted-type analysis for the log of the reaction rates for fe~cyan~de-~diated oxidation for a series of l-(4-substituted phenyl)-1,4\_dihydronicotinamide and the pKa's for the corresponding component anilines produced a linear (rs0.993) relationship over the range of p-N(CH,), to p-CF,. This obser

Reactivity of biologically important red
✍ Marcus E. Brewster; Ming-Ju Huang; James J. Kaminski; Emil Pop; Nicholas Bodor 📂 Article 📅 1991 🏛 John Wiley and Sons 🌐 English ⚖ 438 KB

## Abstract Significant linear correlations were observed between AM1‐derived adiabatic, but not vertical, ionization potentials and the log of ferricyanide‐mediated oxidation of 3‐substituted‐1‐methyl‐1,4‐dihydropyridines. This result is consistent with a rate‐determining electron loss in the reac