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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. 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