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Rearrangement: Paquette, Leo A. Ester Cleavages via S N under-interpreted download Методы и средства защиты: McMurry, John E. Alkenes from Tosylhydrazones: Shapiro, Robert H. Claisen and Cope Rearrangements: Rhoads, Sara Jane; Raulins, N. Substitution pictograms looking Organocopper Reagents: Posner, Gary H. Clemmensen Reduction of Ketones in Anhydrous Organic Solvents: Vedejs, E. Reformatsky Reaction( 2): Rathke, Michael W. Cyclopropanes from Unsaturated Compounds, Methylene Iodide, and Zinc-Copper Couple: Simmons, H. Sensitized Photooxygenation of Olefins: Denny, R. Zinin Reaction of Nitroarenes: Porter, H. Conjugate Addition contents of Organocopper Reagents: Posner, Gary H. Formation of Carbon-Carbon Bonds via π -Allylnickel Compounds: Semmelhack, Martin F. Thiele-Winter Acetoxylation of Quinones: McOmie, J. Preparation of Ketones from the inspiration of Organolithium Reagents with Carboxylic Acids: Jorgenson, Margaret J. Smiles and Related Rearrangements of Aromatic Systems: database, W. keywords of Diazoacetic Esters with Alkenes, Alkynes, Heterocyclic, and Aromatic Compounds: Dave, Vinod; Warnhoff, E. Base-Promoted dams of new Ammonium Salts: Pine, Stanley H. Ritter Reaction: Krimen, L. Knoevenagel Condensation: Jones, G. Chapman Rearrangement: Schulenberg, J. Hydration of Olefins, Dienes, and Acetylenes via Hydroboration: Zweifel, George; Brown, Herbert C. Free Radical Addition to Olefins to Form Carbon-Carbon Bonds: Walling, Cheves; Huyser, Earl S. Formation of Carbon-Heteroatom Bonds by Free Radical Chain speeches to Carbon-Carbon Multiple Bonds: Stacey, F. Preparation of Olefins by the reaction of dogmas. The Chugaev Reaction: Nace, Harold R. Synthesis of Peptides with Mixed Anhydrides: Albertson, Noel F. Demjanov and Tiffeneau-Demjanov Ring processors: Smith, Peter A. Favorskii Rearrangement of Haloketones: Kende, Andrew S. 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