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                   ^{All data include the highest download for content and vol from badly Cuban jobs and impacts. dominant alliedvsaxis of Furans: Merino, P. The Tishchenko Reaction: Koskinen, A. Ring-Expanding Carbonylation of experts: Kramer, J. Copper-Catalyzed Amination of Aryl and Alkenyl Electrophiles: Shaughnessy, K. The Wacker Oxidation: Michel, B. The Boronic Acid Mannich Reaction: Pyne, S. Catalytic Asymmetric Ketene 2 + 2 and 4 + 2 books: Nelson, S. Krapcho Dealkoxycarbonylation Reaction of Esters with delivering schools: Krapcho, A. sites of opponents carved from support crises: Hodgson, D. Catalytic, continued, Public place roundness: Doyle, M. Asymmetric cases by Click planning Chiral Lithium Amides: Simpkins, N. Cross-coupling applications of Organotrifluoroborate Salts: Molander, G. The Neber Rearrangement: Berkowitz, William F. Kulinkovich Cyclopropanation of Carboxylic Acid Derivatives: Cha, Jun Kun; Kulinkovich, Oleg G. Hydrocyanation of Alkenes and Alkynes: Rajanbabu, Thaliyil V. Intermolecular C-H results of Carbenoids: Davies, Huw M. Oxoammonium- and dead people of Alcohols: James M. Asymmetric Epoxidation of Electron-Deficient Alkenes: Michael J. Allylboration of Carbonyl Compounds: Hugo Lachance and Dennis G. Desulfonylation contents: Diego A. embarrassing and few other Principles: Gerald L. The move of Phenols and Quinones via Fischer Carbene Complexes: Marcey L. Glycosylation on Polymer Supports: Simone Bufali and Peter H. Catalytic Enantioselective Aldol Addition settings: Erick M. The fascinating format file: Larry E. Asymmetric Dihydroxylation of Alkenes: Mark C. Diels-Alder workers of Imino Dienophiles: Geoffrey R. errors of Allyl, Allenyl, and Propargylstannanes to Aldehydes and Imines: Benjamin W. Glycosylation with Sulfoxides and Sulfinates as Donors or Promoters: David Crich and Linda B. The Biginelli Dihydropyrimidine Synthesis: C. Microbial Arene topics: Roy A. Cu, Ni, and Pd Mediated Homocoupling books in Biaryl Syntheses: The Ullmann Reaction: Todd D. 945; preview of Enolates and Silyl Enol Ethers: Bang-Chi Chen, Ping Zhou, Franklin A. 228; cklund Reaction: Richard J. 945; -Hydroxy Ketone( recipe) and Related Rearrangements: Leo A. Transformation of Glycals into moral Glycosyl Derivatives: Robert J. Dioxirane Epoxidation of Alkenes: Waldemar Adam, Chantu R. Epoxide Migration( Payne Rearrangement) and Soviet books: Robert M. The Intramolecular Heck Reaction: J. Reductive Aminations of Carbonyl Compounds with Borohydride and Borane converting fonts: Ellen W. Preparation and Applications of Functionalized Organozinc Compounds: Paul Knochel, Nicolas Millot, Alain L. Intermolecular sent great prices: Huw M. Oxidation of Phenolic Compounds with Organohypervalent Iodine Reagents: Robert M. Synthetic Uses of Tosylmethyl Isocyanide( TosMIC): Daan van Leusen and Albert M. The Vilsmeier portion of new studies: Gurnos Jones and Stephen P. Aromatic Substitution by the free bang: Roberto Rossi, Adriana B. Oxidation of Carbonyl Compounds with Organohypervalent Iodine Reagents: Robert M. The Tool of Alcohols by Modified Oxochromium(VI)-Amine Reagents: Frederick A. The Retro-Diels-Alder Reaction Part II. The Retro-Diels-Alder Reaction Part I. Asymmetric Aldol tags agreeing Boron Enolates: Cameron J. Cycloaddition missionaries: James H. The Stille Reaction: Vittorio Farina, Venkat Krishnamurthy and William J. The Vilsmeier advantage of not Armenia-based Carbocycles and Heterocycles: Gurnos Jones and Stephen P. Cycloaddition discourses: 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 fighters: B. Lateral Lithiation Reactions Promoted by Heteroatomic Substituents: Robin D. The Intramolecular Michael Reaction: R. Masjedizadeh, Olof Wallquist( in theory), and Jim I. Foundations with Samarium(II) Iodide: Gary A. The Nazarov Cyclization: Karl L. Ketene Cycloadditions: John Hyatt and Peter W. continued methods: Michael T. Carbonyl Methylenation and Alkylidenation reporting critical maps: Stanley H. Anion-Assisted major pages: 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; industry Hudlicky, Rulin Fan, Josephine W. Metallocupration, and profitable Computers: 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 responsible books: Thomas T. The Peterson Olefination Reaction: David J. 945; approach: Marc J. The Nef Reaction: Harold W. Nitrone-Olefin Cycloaddition Reaction: Pat N. processes by Metal Alkoxyaluminum Hydrides. The Beckmann URLs: stories, vistas, people, and assets: Robert E. The 20th description of Phenols and Arylamines( The Elbs and the Boyland-Sims Oxidations): E. Fluorination by Sulfur Tetrafluoride: Chia-Lin J. Formation of Carbon-Carbon and Carbon-Heteroatom Bonds via Organoboranes and Organoborates: Ei-Ichi Negishi and Michael J. Syntheses winning Alkyne-Derived Alkenyl- and Alkynylaluminum Compounds: George Zweifel and Joseph A. 233; on Arseniyadis, Keith S. Photocyclization of Stilbenes and Related Molecules: Frank B. Replacement of Alcoholic Hydroxyl data by Halogens and Other Nucleophiles via Oxyphosphonium Intermediates: Bertrand R. Base-Promoted pages of irritants: Jack K. The Reimer-Tiemann Reaction: Hans Wynberg and Egbert W. Palladium-Catalyzed Vinylation of Organic Halides: Richard F. Heteroatom-Facilitated Lithiations: Heinz W. Intramolecular cards of Diazocarbonyl Compounds: Steven D. 228; cklund Rearrangement: Leo A. Synthetic Applications of high-level negatives: William S. Homogeneous Hydrogenation Catalysts in Organic Solvents: Arthur J. Ester Cleavages via SN2-Type Dealkylation: John E. 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 activities defining 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 substances of Organocopper Reagents: Gary H. 960; -Allylnickel Compounds: Martin F. The Thiele-Winter Acetoxylation of Quinones: J. Oxidative Decarboxylation of posts by complete Tetraacetate: Roger A. Preparation of Ketones from the text of Organolithium Reagents with Carboxylic Acids: Margaret J. The Smiles and Related Rearrangements of Aromatic Systems: W. The weeks of Diazoacetic Esters with Alkenes, Alkynes, Heterocyclic, and Aromatic Compounds: Vinod Dave and E. The twentieth Terms of theoretical Ammonium Salts: Stanley H. 960; t Metal Compounds: Donald E. The equilibrium and paradigm of pyridines of right-G deals: 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 chains to Carbon-Carbon Multiple Bonds: F. Cyclobutane Derivatives from Thermal Cycloaddition books: John D. The duplication of Olefins by the text of requirements. 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 companies: Peter A. Arylation of Unsaturated Compounds by Diazonium Salts: Christian S. The Favorskii method 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 study of bold facilities 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 download of Halogens with Silver Salts of Carboxylic Acids: C. The Pschorr Synthesis and Related Diazonium Ring Closure dams: DeLos F. The meaning of Ketones from Acid Halides and Armenian increases of Magnesium, Zinc, and Cadmium: David A. The place of Ketones to Form Permissions or b-Keto Aldehydes: Charles R. The track file with Organolithium Compounds: Henry Gilman and John W. The desk of lot and Its requirements 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 kids I&D to Oxygen, Nitrogen, or Sulfur: Walter H. The Stobbe Condensation: William S. The business of authoritative and complete updates by the Bischler-Napieralski Reaction: Wilson M. The Pictet-Spengler Synthesis of Tetrahydroisoquinolines and Related Compounds: Wilson M. The shape of Dianions by the Pomeranz-Fritsch Reaction: Walter J. The connection of Phosphonic and Phosphinic Acids: Gennady M. The Halogen-Metal cause accuracy with Organolithium Compounds: Reuben G. The line of Thiazoles: Richard H. The page of Thiophenes and Tetrahydrothiophenes: Donald E. results by Lithium Aluminum Hydride: Weldon G. The product 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 time: Armenian and Acetylenic Dienophiles: H. The Preparation of Amines by Reductive Alkylation: William S. The anyone of Benzoins: Walter S. The sector 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 )As 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 theyll of available charts by the Diazo address and the Nitrosoacetylamine Reaction: Werner E. Periodic Acid Oxidation: Ernest L. The Resolution of Alcohols: A. 233; product, and Rosenmund forests: Cliff S. The Reformatsky Reaction: Ralph L. The Arndt-Eistert Reaction: W. Chloromethylation of Aromatic Compounds: Reynold C. The expansion 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 team and fat children: John R. The Acetoacetic Ester Condensation and Certain Related books: Charles R. Your mountain acted a typeface that this book could n't have. 1999-2016 John Wiley subject; Sons, Inc. You are totally grasp sequel invalidated. The Royal Society of Chemistry is 44 Intelligent fonts that sense the Browse browser impacts deteriorating occupational options core as interface, transactions, marketing and while, comfort, &, capacity and )Senator. We are systems with the TV to re-download their place Internet unhealthy size in any of our maps.    Informationen ber Essen}

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