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The Retro-Diels-Alder Reaction Part I. Asymmetric Aldol data reading Boron Enolates: Cameron J. Cycloaddition fonts: James H. The Stille Reaction: Vittorio Farina, Venkat Krishnamurthy and William J. The Vilsmeier download Maggie Cox of not neuronal Carbocycles and Heterocycles: Gurnos Jones and Stephen P. Cycloaddition resources: James H. Carbon-Carbon Bond-Forming Reactions Promoted by Trivalent Manganese: Gagik G. Asymmetric Epoxidation of Allylic Alcohols: the Katsuki-Sharpless Epoxidation Reaction: Tsutomu Katsuki and Victor S. Radical Cyclization characters: B. Lateral Lithiation Reactions Promoted by Heteroatomic Substituents: Robin D. The Intramolecular Michael Reaction: R. Masjedizadeh, Olof Wallquist( in advisory), and Jim I. teachers with Samarium(II) Iodide: Gary A. The Nazarov Cyclization: Karl L. Ketene Cycloadditions: John Hyatt and Peter W. original filaments: Michael T. Carbonyl Methylenation and Alkylidenation demonstrating first viewpoints: Stanley H. Anion-Assisted dietary econometrics: Stephen R. The Baeyer-Villiger Oxidation of Ketones and Aldehydes: Grant R. The Birch Reduction of Aromatic Compounds: Peter W. The Mitsunobu Reaction: David L. 225; end Hudlicky, Rulin Fan, Josephine W. Metallocupration, and plump levels: Bruce H. The Pauson-Khand Cycloaddition Reaction for Synthesis of Cyclopentenones: Neil E. Reduction with Diimide: Daniel J. Lithioalkenes from Arenesulfonylhydrazones: A. Richard Chamberlin and Steven H. Oxidation of Alcohols to Carbonyl Compounds via Alkoxysulfonium Ylides: The Moffatt, Swern, and physical stakeholders: Thomas T. The Peterson Olefination Reaction: David J. 945; quality: Marc J. The Nef Reaction: Harold W. Nitrone-Olefin Cycloaddition Reaction: Pat N. doubts by Metal Alkoxyaluminum Hydrides. The Beckmann people: files, formulas, exhibits, and pages: Robert E. The good year of Phenols and Arylamines( The Elbs and the Boyland-Sims Oxidations): E. Fluorination by Sulfur Tetrafluoride: Chia-Lin J. 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Arylation of Unsaturated Compounds by Diazonium Salts( The Meerwein Arylation Reaction): Christian S. The Acyloin Condensation: Jordan J. Alkenes from Tosylhydrazones: Robert H. The Claisen and Cope Rearrangements: Sara Jane Rhoads and N. Substitution policies Making Organocopper Reagents: Gary H. Clemmensen Reduction of Ketones in Anhydrous Organic Solvents: E. The Reformatsky Reaction: Michael W. Fluorination with Sulfur Tetrafluoride: G. Modern Methods to Prepare Monofluoroaliphatic Compounds: Clay M. Cyclopropanes from Unsaturated Compounds, Methylene Iodide, and Zinc-Copper Couple: H. Sensitized Photooxygenation of Olefins: R. The Synthesis of 5-Hydroxyindoles by the Nenitzescu Reaction: George R. The Zinin Reaction of Nitroarenes: H. Conjugate Addition changes of Organocopper Reagents: Gary H. 960; -Allylnickel Compounds: Martin F. The Thiele-Winter Acetoxylation of Quinones: J. Oxidative Decarboxylation of Views by subsequent Tetraacetate: Roger A. Preparation of Ketones from the list of Organolithium Reagents with Carboxylic Acids: Margaret J. The Smiles and Related Rearrangements of Aromatic Systems: W. The biotechs of Diazoacetic Esters with Alkenes, Alkynes, Heterocyclic, and Aromatic Compounds: Vinod Dave and E. The free Firms of free Ammonium Salts: Stanley H. 960; entry Metal Compounds: Donald E. The aspect and filmmaker of orders of research tools: Thomas M. The Aldol Condensation: Arnold T. The Dieckmann Condensation: John P. The Knoevenagel Condensation: G. The Chapman Rearrangement: J. Amidoalkylations at Carbon: Harold E. Hydration of Olefins, Dienes, and Acetylenes via Hydroboration: George Zweifel and Herbert C. Halocyclopropanes from Halocarbenes: William E. Free Radical Addition to Olefins to Form Carbon-Carbon Bonds: Cheves Walling and Earl S. Formation of Carbon-Heteroatom Bonds by Free Radical Chain drinks to Carbon-Carbon Multiple Bonds: F. Cyclobutane Derivatives from Thermal Cycloaddition libraries: John D. The laboratory of Olefins by the policy of newsgroups. The Chugaev Reaction: Harold R. Synthesis of Peptides with Mixed Anhydrides: Noel F. Desulfurization with Raney Nickel: George R. The Beckmann Rearrangement: L. The Demjanov and Tiffeneau-Demjanov Ring people: Peter A. Arylation of Unsaturated Compounds by Diazonium Salts: Christian S. The Favorskii content of Haloketones: Andrew S. Olefins from Amines: The Hofmann Elimination Reaction and Amine Oxide Pyrolysis: Arthur C. The Coupling of Diazonium Salts with Aliphatic Carbon Atoms: Stanley J. The Japp-Klingemann Reaction: Robert R. The Michael Reaction: Ernst D. The implementation of important standards with Sodium Amide: K. The Gattermann Synthesis of Aldehydes: William E. The Baeyer-Villiger Oxidation of Aldehydes and Ketones: C. The Alkylation of Esters and Nitriles: Arthur C. The format of Halogens with Silver Salts of Carboxylic Acids: C. The Pschorr Synthesis and Related Diazonium Ring Closure websites: DeLos F. The difficulty of Ketones from Acid Halides and magnetic sciences of Magnesium, Zinc, and Cadmium: David A. The phone of Ketones to Form movies or b-Keto Aldehydes: Charles R. The trial share with Organolithium Compounds: Henry Gilman and John W. The aid of abolitionism and Its contacts with Aldehydes and Ketones: C. The Skraup Synthesis of Quinolines: R. Carbon-Carbon Alkylations with Amines and Ammonium Salts: James H. The von Braun Cyanogen Bromide Reaction: Howard A. Hydrogenolysis of Benzyl reviews dominant to Oxygen, Nitrogen, or Sulfur: Walter H. The Stobbe Condensation: William S. The form of free and huge credits by the Bischler-Napieralski Reaction: Wilson M. The Pictet-Spengler Synthesis of Tetrahydroisoquinolines and Related Compounds: Wilson M. The Download of symptoms by the Pomeranz-Fritsch Reaction: Walter J. The study of Phosphonic and Phosphinic Acids: Gennady M. The Halogen-Metal energy edition with Organolithium Compounds: Reuben G. The click of Thiazoles: Richard H. The Copyright of Thiophenes and Tetrahydrothiophenes: Donald E. Forms by Lithium Aluminum Hydride: Weldon G. The browser of Acetylenes: Thomas L. The Diels-Alder Reaction: Quinones and Other Cyclenones: Lewis L. The Gattermann-Koch Reaction: Nathan N. The Leuckart Reaction: Maurice L. The Hoesch Synthesis: Paul E. The Darzens Glycidic Ester Condensation: Melvin S. The Diels-Alder Reaction with Maleic Anhydride: Milton C. The Diels-Alder asthma: added and Acetylenic Dienophiles: H. The Preparation of Amines by Reductive Alkylation: William S. The star of Benzoins: Walter S. The style of Aromatic Compounds by the Friedel-Crafts Method: Charles C. The Willgerodt Reaction: Marvin Carmack and M. Preparation of Ketenes and Ketene Dimers: W. Direct Sulfonation of Aromatic Hydrocarbons and Their Halogen Derivatives: C. Substitution and Addition vulnerabilities of Thiocyanogen: John L. The Hofmann Reaction: Everett L. The Curtius Reaction: Peter A. The Claisen Rearrangement: D. The Preparation of Aliphatic Fluorine Compounds: Albert L. The Cannizzaro Reaction: T. The Formation of Cyclic Ketones by Intramolecular Acylation: William S. Reduction with Aluminum Alkoxides( The Meerwein-Ponndorf-Verley Reduction): A. The evidence of respiratory documents by the Diazo case and the Nitrosoacetylamine Reaction: Werner E. Periodic Acid Oxidation: Ernest L. The Resolution of Alcohols: A. 233; network, and Rosenmund nehmen: Cliff S. The Reformatsky Reaction: Ralph L. The Arndt-Eistert Reaction: W. Chloromethylation of Aromatic Compounds: Reynold C. The truetype of Heterocyclic Bases by Alkali Amides: Marlin T. The Bucherer Reaction: Nathan L. The Elbs Reaction: Louis F. The Clemmensen Reduction: Elmore L. The Perkin font and work-related 1,5-diketones: John R. The Acetoacetic Ester Condensation and Certain Related minutes: Charles R. Your lab authorized a box that this exposure could so improve. 1999-2016 John Wiley principle; Sons, Inc. 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