SEARCH Articles Figures Tables Alkenes in elimination reactions Alkoxide ions as bases in elimination Alkoxide ions substitution versus elimination in reactions with Anti Elimination in E2 Reactions Stereoelectronic Effects Anti conformation in elimination reactions Application in Heavy Metal Elimination from Crude Oil Application of Hofmann Elimination in Linker Design Assumptions in SO2 oxidation calculations elimination of this assumption Atomic Versus Molecular Elimination in Halogenated Hydrocarbons Bases in E2 elimination Bases in elimination reactions Bases used in elimination reactions Catalysis (cont in elimination reactions Catalysis in elimination reactions Conformation importance in elimination reaction Cyclohexyl systems elimination reactions in, stereochemistry E2 elimination in cyclic comps ElcB elimination in aldol dehydration ElcB elimination in benzyne formation Elcb Eliminations in protecting group chemistry Electrophile in elimination reactions Elimination Reactions in Pyrolysis Elimination in Furanuronate Derivatives Elimination in Plants, Animals, and Humans Elimination in Unsaturated, Hexopyranoid Systems Elimination in enamine formation Elimination in ester hydrolysis Elimination in synthesis Elimination in vicinal disubstituted substrates Elimination of diffusion contribution to the overpotential in chronoamperometry and chronopotentiometry Elimination of non-equilibrium effects in separate solutions Elimination reactions in preparation Elimination reactions in synthesis Elimination, and Halogenation Reactions in Polymers Eliminations and Rearrangements in Deamination of Open-Chain Amines Enolacetal-forming -Elimination in 6-Aldehyde Derivatives of Pyranosides Gauss Elimination in Formula Form Gauss Elimination in Matrix Form HOFMANN ELIMINATION, in alkenes HOFMANN ELIMINATION, in alkenes preparation In elimination reactions In situ elimination Intermediates in Elimination Reactions Isotope effects in elimination reactions Isotope effects in eliminations Leaving groups in elimination Leaving groups in elimination reactions Model Studies of Reductive Elimination in the Rh System Neutral Molecules Eliminated in the Mass Spectrometer Number of operations in the Gaussian elimination method Orientation Effects in Elimination Reactions Orientation in E2 elimination as a function of base strength Orientation in Pyrolytic Eliminations Ortho Elimination in the Fragmentation of Nitroarenes Oxidative Addition and Reductive Elimination in the Gilman Reaction Profiling of Drug Absorption, Distribution, Metabolism and Elimination in Man the hADME Study Pyrolytic eliminations in the gas phase Reactivity in the Addition-Elimination Route Silene-Type Species in Elimination-Addition Reactions Sodium alkoxides as bases in elimination reactions Sodium ethoxide in elimination reactions Stereochemistry at C-3 in nucleophilic 3-replacements and a,3-eliminations Stereoelectronic Effects in Elimination Reactions Steric effects in elimination Steric effects, in elimination reactions Steric hindrance in elimination reactions Substitution and Elimination Reactions in Synthesis The elimination of chlorines in catalyst Zinc-copper couple in reductive elimination