Relative reactivities of heteroaromatic cations towards reduction by 1,4-dihydronicotinamides
- 1 January 1986
- journal article
- Published by Elsevier in Tetrahedron
- Vol. 42 (4) , 1007-1019
- https://doi.org/10.1016/s0040-4020(01)87506-2
Abstract
No abstract availableThis publication has 34 references indexed in Scilit:
- Effect of isotope scrambling and tunneling on the kinetic and product isotope effects for reduced nicotinamide adenine dinucleotide model hydride transfer reactionsJournal of the American Chemical Society, 1983
- Reinvestigation of NADH analog redox reactions in acetonitrile: consequences of isotope scrambling on kinetic and product isotope effectsJournal of the American Chemical Society, 1982
- Hydride transfer between NAD+ analoguesFaraday Discussions of the Chemical Society, 1982
- Reduction by a model of NAD(P)H. 30. Proof for the electron-proton-electron-transfer mechanismJournal of the American Chemical Society, 1981
- Coenzyme Models. XIII. Micellar Catalysis of 1,4-Dihydronicotinamide Reduction of Isoalloxazines and Acridinium IonBulletin of the Chemical Society of Japan, 1978
- Model dehydrogenase reactions. Catalysis of dihydronicotinamide reductions by noncovalent interactionsBiochemistry, 1977
- Influence of Mg2+ ion on the reduction of N-methylacridinium ion with 1,4-dihydronicotinamideJournal of the Chemical Society, Chemical Communications, 1977
- Model dehydrogenase reactions. Direct observation of a charge-transfer complex in a dihydronicotinamide reductionJournal of the American Chemical Society, 1976
- Model dehydrogenase reactions. Neighboring group effects in dihydronicotinamide reductionsJournal of the American Chemical Society, 1975
- Model dehydrogenase reactions. Reduction of N-methylacridinium by reduced nicotinamide adenine dinucleotide and its derivativesJournal of the American Chemical Society, 1973