Redox-photosensitized reactions. 13. Ru(bpy)32+-photosensitized reactions of an NADH model, 1-benzyl-1,4-dihydronicotinamide, with aromatic carbonyl compounds and comparison with thermal reactions
- 1 June 1987
- journal article
- research article
- Published by American Chemical Society (ACS) in The Journal of Organic Chemistry
- Vol. 52 (13) , 2790-2796
- https://doi.org/10.1021/jo00389a027
Abstract
No abstract availableThis publication has 4 references indexed in Scilit:
- Mechanism of the oxidation of NADH by quinones. Energetics of one-electron and hydride routesJournal of the American Chemical Society, 1985
- Redox-photosensitized reactions. 11. Ru(bpy)32+-photosensitized reactions of 1-benzyl-1,4-dihydronicotinamide with aryl-substituted enones, derivatives of methyl cinnamate, and substituted cinnamonitriles: electron-transfer mechanism and structure-reactivity relationshipsThe Journal of Organic Chemistry, 1984
- Hydride vs. electron transfer in the reduction of flavin and flavin radical by 1,4-dihydropyridinesJournal of the American Chemical Society, 1983
- 1-Benzyldihydronicotinamide—A Model for Reduced DPNJournal of the American Chemical Society, 1955