SEARCH Articles Figures Tables 1- -ethanone one-electron reduction potential 1.2.4- Triazol-5-ones reduction 1.6.7.8- Tetrahydro-4//-pyrido pyrimidin-4-ones, reduction 2- Oxazolin-5-ones reduction 2- Pyrazolin-5-ones reduction 2-Amino-3-nitroso-4//-pyrido pyrimidin-4-ones, reduction 4- Nitropyrazol-3-ones, reduction 4//-Pyrido pyrimidin-4-ones reduction 9 perhydropyrido oxazin-1-ones, reduction And one-electron reduction potential C-Glycosyl compounds one-electron reduction Cholest-4-en-3-one reduction Cholest-4-en-3-one reductive elimination Concerted one-electron reductions Consecutive and Cascade One-Pot Reductions Imidazolidin-2-ones reduction One electron oxidation and reduction One-Electron Reduction and Oxidation in Nonaqueous Solvents One-Electron Reductions of Carbonyl Compounds and Esters Reductive Coupling One-electron enzymatic reduction One-electron oxidation/reduction One-electron reductants One-electron reduction One-electron reduction pathway One-electron reduction potential One-electron reduction process One-electron reduction product Oxadiazin-5-ones reduction Pyridazin-3-ones, reduction Pyrimidin-2 -ones reduction Reduction of Heterocycles Containing One Nitrogen Atom Reduction of a System on One Isolated Level Surface Reduction of azetidin-2-ones (3-lactams) Reduction of cholest-5-en-3-one Reduction to a One-Parameter Model Reductions of Other Heterocycles Containing One Nitrogen Atom Reversible one-electron reduction and Tetrahydro-1,3-oxazin-2-ones, reduction Triazine-3-ones, reduction Two- step one-electron reduction