REACTIONS OF NAD+-MODEL COMPOUNDS WITH BASE. THE REVISED STRUCTURE OF DITTMER’S TRIMER
- 5 May 1977
- journal article
- Published by Oxford University Press (OUP) in Chemistry Letters
- Vol. 6 (5) , 525-528
- https://doi.org/10.1246/cl.1977.525
Abstract
The structure of the cyclic trimer obtained by the reaction of N-benzylnicotinamide cation with base was established. A plausible mechanism involves the removal of the amide hydrogen with base, the attack of the amide anion at C-4 of another pyridinium ion, and the formation of a 12-membered ring.This publication has 2 references indexed in Scilit:
- Potential coenzyme inhibitors. III. Some reactions of substituted nicotinamide and dihydronicotinamide derivativesJournal of Medicinal Chemistry, 1969
- Action of Base on Quaternary Salts of Nicotinamide1-3The Journal of Organic Chemistry, 1963