Regioselectivity and kinetics of hydride transfer in substituted 1-benzyl-3-quinolinecarboxamide redox reactions
- 1 October 1987
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 52 (20) , 4454-4459
- https://doi.org/10.1021/jo00229a005
Abstract
No abstract availableThis publication has 5 references indexed in Scilit:
- Efficient chirality transfer between a chiral 4-methyl-1,4-dihydropyridine and benzoylformic ester. An example of a pure intermolecular self-immolative processJournal of the American Chemical Society, 1986
- Kinetics of the reduction of C-9 substituted acridinium cations by 1,4-dihydronicotinamidesBioorganic Chemistry, 1984
- 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
- Regioselectivity of hydride transfer to and between NAD+ analogsThe Journal of Organic Chemistry, 1983
- Nicotinamide‐Dependent One‐Electron and Two‐Electron (Flavin) Oxidoreduction : Thermodynamics, Kinetics, and MechanismEuropean Journal of Biochemistry, 1976