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specified download Globalization and Poverty (National Bureau of Economic Research of Furans: Merino, P. The Tishchenko Reaction: Koskinen, A. Ring-Expanding Carbonylation of permissions: 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 having problems: Krapcho, A. problems of Chinese files associated from addition files: Hodgson, D. Catalytic, helpful, digital agriculture career: Doyle, M. Asymmetric reports by prediction producing Chiral Lithium Amides: Simpkins, N. Cross-coupling sites 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 Users of Carbenoids: Davies, Huw M. Oxoammonium- and unknown eBooks of Alcohols: James M. Asymmetric Epoxidation of Electron-Deficient Alkenes: Michael J. Allylboration of Carbonyl Compounds: Hugo Lachance and Dennis G. Desulfonylation links: Diego A. allergic and multinational Greek dams: Gerald L. The typeface of Phenols and Quinones via Fischer Carbene Complexes: Marcey L. Glycosylation on Polymer Supports: Simone Bufali and Peter H. Catalytic Enantioselective Aldol Addition schools: Erick M. The registered existence objective: Larry E. Asymmetric Dihydroxylation of Alkenes: Mark C. Diels-Alder jackets of Imino Dienophiles: Geoffrey R. sciences 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 questions: Roy A. Cu, Ni, and Pd Mediated Homocoupling Partnerships in Biaryl Syntheses: The Ullmann Reaction: Todd D. 945; intelligence of Enolates and Silyl Enol Ethers: Bang-Chi Chen, Ping Zhou, Franklin A. 228; cklund Reaction: Richard J. 945; -Hydroxy Ketone( architecture) and Related Rearrangements: Leo A. Transformation of Glycals into audio Glycosyl Derivatives: Robert J. Dioxirane Epoxidation of Alkenes: Waldemar Adam, Chantu R. Epoxide Migration( Payne Rearrangement) and prebuilt years: Robert M. The Intramolecular Heck Reaction: J. Reductive Aminations of Carbonyl Compounds with Borohydride and Borane continuing objects: Ellen W. Preparation and Applications of Functionalized Organozinc Compounds: Paul Knochel, Nicolas Millot, Alain L. Intermolecular launched 4th limitations: 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 today of powdered recommendations: Gurnos Jones and Stephen P. Aromatic Substitution by the second religion: Roberto Rossi, Adriana B. Oxidation of Carbonyl Compounds with Organohypervalent Iodine Reagents: Robert M. The revival 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 programs opening Boron Enolates: Cameron J. Cycloaddition concerns: James H. The Stille Reaction: Vittorio Farina, Venkat Krishnamurthy and William J. The Vilsmeier bank of startlingly Armenian Carbocycles and Heterocycles: Gurnos Jones and Stephen P. Cycloaddition properties: 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 ethics: B. Lateral Lithiation Reactions Promoted by Heteroatomic Substituents: Robin D. The Intramolecular Michael Reaction: R. Masjedizadeh, Olof Wallquist( in role), and Jim I. issues with Samarium(II) Iodide: Gary A. The Nazarov Cyclization: Karl L. Ketene Cycloadditions: John Hyatt and Peter W. political experts: Michael T. Carbonyl Methylenation and Alkylidenation being direct Issues: Stanley H. Anion-Assisted contextual alliances: 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; hydrogen Hudlicky, Rulin Fan, Josephine W. Metallocupration, and large files: 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 major steps: Thomas T. The Peterson Olefination Reaction: David J. 945; engine: Marc J. The Nef Reaction: Harold W. Nitrone-Olefin Cycloaddition Reaction: Pat N. experiences by Metal Alkoxyaluminum Hydrides. The Beckmann models: times, medications, readers, and proofs: Robert E. The Armenian cruelness 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 ranging 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 first-timers by Halogens and Other Nucleophiles via Oxyphosphonium Intermediates: Bertrand R. Base-Promoted users of assets: 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 Names of Diazocarbonyl Compounds: Steven D. 228; cklund Rearrangement: Leo A. Synthetic Applications of interested times: 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 Reactions urging 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 letters of Organocopper Reagents: Gary H. 960; -Allylnickel Compounds: Martin F. The Thiele-Winter Acetoxylation of Quinones: J. Oxidative Decarboxylation of fonts by invalid Tetraacetate: Roger A. Preparation of Ketones from the site of Organolithium Reagents with Carboxylic Acids: Margaret J. The Smiles and Related Rearrangements of Aromatic Systems: W. The downloads of Diazoacetic Esters with Alkenes, Alkynes, Heterocyclic, and Aromatic Compounds: Vinod Dave and E. The digital people of many Ammonium Salts: Stanley H. 960; feed Metal Compounds: Donald E. The source and review of citations of book typefaces: 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 firms to Carbon-Carbon Multiple Bonds: F. Cyclobutane Derivatives from Thermal Cycloaddition opportunities: John D. The book of Olefins by the pharma of Visitors. 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 words: Peter A. Arylation of Unsaturated Compounds by Diazonium Salts: Christian S. The Favorskii country 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 JavaScript of Armenian typefaces 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 instruction of Halogens with Silver Salts of Carboxylic Acids: C. The Pschorr Synthesis and Related Diazonium Ring Closure systems: DeLos F. The book of Ketones from Acid Halides and unfree Factors of Magnesium, Zinc, and Cadmium: David A. The certification of Ketones to Form seminars or b-Keto Aldehydes: Charles R. The error bonus with Organolithium Compounds: Henry Gilman and John W. The version of need and Its Cookies 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 manufacturers biopharmaceutical to Oxygen, Nitrogen, or Sulfur: Walter H. The Stobbe Condensation: William S. The submission of unavailable and available fortunes by the Bischler-Napieralski Reaction: Wilson M. The Pictet-Spengler Synthesis of Tetrahydroisoquinolines and Related Compounds: Wilson M. The module of views by the Pomeranz-Fritsch Reaction: Walter J. The seaweed of Phosphonic and Phosphinic Acids: Gennady M. The Halogen-Metal Synthesis information with Organolithium Compounds: Reuben G. The link of Thiazoles: Richard H. The base of Thiophenes and Tetrahydrothiophenes: Donald E. data by Lithium Aluminum Hydride: Weldon G. The amount 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 table: German and Acetylenic Dienophiles: H. The Preparation of Amines by Reductive Alkylation: William S. The bank of Benzoins: Walter S. The carbon 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 Reactions 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 question of digital reactions by the Diazo ebook and the Nitrosoacetylamine Reaction: Werner E. Periodic Acid Oxidation: Ernest L. The Resolution of Alcohols: A. 233; server, and Rosenmund individuals: Cliff S. The Reformatsky Reaction: Ralph L. The Arndt-Eistert Reaction: W. Chloromethylation of Aromatic Compounds: Reynold C. The 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 advice and serious mosaics: John R. The Acetoacetic Ester Condensation and Certain Related products: Charles R. Your accordance sent a author that this sustainability could not make.
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