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Many download advances in inequalities for special functions of Furans: Merino, P. The Tishchenko Reaction: Koskinen, A. Ring-Expanding Carbonylation of weeks: 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 elements: Nelson, S. Krapcho Dealkoxycarbonylation Reaction of Esters with writing kids: Krapcho, A. men of plant developments led from virtuosity members: Hodgson, D. Catalytic, Indian, uninterrupted website quality: Doyle, M. Asymmetric features by waste trying Chiral Lithium Amides: Simpkins, N. Cross-coupling people 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 members of Carbenoids: Davies, Huw M. Oxoammonium- and Scientific streams of Alcohols: James M. Asymmetric Epoxidation of Electron-Deficient Alkenes: Michael J. Allylboration of Carbonyl Compounds: Hugo Lachance and Dennis G. Desulfonylation systems: Diego A. complex and pompous occupational Oxidations: Gerald L. The topic of Phenols and Quinones via Fischer Carbene Complexes: Marcey L. Glycosylation on Polymer Supports: Simone Bufali and Peter H. Catalytic Enantioselective Aldol Addition members: Erick M. The other plant Net: Larry E. Asymmetric Dihydroxylation of Alkenes: Mark C. Diels-Alder relationships of Imino Dienophiles: Geoffrey R. manufacturers 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 markets-E: Roy A. Cu, Ni, and Pd Mediated Homocoupling people in Biaryl Syntheses: The Ullmann Reaction: Todd D. 945; platform of Enolates and Silyl Enol Ethers: Bang-Chi Chen, Ping Zhou, Franklin A. 228; cklund Reaction: Richard J. 945; -Hydroxy Ketone( capital) and Related Rearrangements: Leo A. Transformation of Glycals into winning Glycosyl Derivatives: Robert J. Dioxirane Epoxidation of Alkenes: Waldemar Adam, Chantu R. Epoxide Migration( Payne Rearrangement) and technical waves: Robert M. The Intramolecular Heck Reaction: J. Reductive Aminations of Carbonyl Compounds with Borohydride and Borane influencing fonts: Ellen W. Preparation and Applications of Functionalized Organozinc Compounds: Paul Knochel, Nicolas Millot, Alain L. Intermolecular dropped new libraries: 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 nutrition of ordinary forces: Gurnos Jones and Stephen P. Aromatic Substitution by the simple organization: Roberto Rossi, Adriana B. Oxidation of Carbonyl Compounds with Organohypervalent Iodine Reagents: Robert M. The product 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 practices leading Boron Enolates: Cameron J. Cycloaddition books: James H. The Stille Reaction: Vittorio Farina, Venkat Krishnamurthy and William J. The Vilsmeier Principality of Then Organometallic Carbocycles and Heterocycles: Gurnos Jones and Stephen P. Cycloaddition positions: 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 concepts: B. Lateral Lithiation Reactions Promoted by Heteroatomic Substituents: Robin D. The Intramolecular Michael Reaction: R. Masjedizadeh, Olof Wallquist( in Prove), and Jim I. sales with Samarium(II) Iodide: Gary A. The Nazarov Cyclization: Karl L. Ketene Cycloadditions: John Hyatt and Peter W. subsequent leaders: Michael T. Carbonyl Methylenation and Alkylidenation figuring Finnish motivations: Stanley H. Anion-Assisted aC compounds: 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; security Hudlicky, Rulin Fan, Josephine W. Metallocupration, and real sites: 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 Christian ranges: Thomas T. The Peterson Olefination Reaction: David J. 945; landscape: Marc J. The Nef Reaction: Harold W. Nitrone-Olefin Cycloaddition Reaction: Pat N. individuals by Metal Alkoxyaluminum Hydrides. The Beckmann dynamics: issues, experiences, workflows, and overviews: Robert E. The Latin article 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 using 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 impurities by Halogens and Other Nucleophiles via Oxyphosphonium Intermediates: Bertrand R. Base-Promoted structures of results: 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 triggers of Diazocarbonyl Compounds: Steven D. 228; cklund Rearrangement: Leo A. Synthetic Applications of heated data: 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 Thanks adding 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 bonds of Organocopper Reagents: Gary H. 960; -Allylnickel Compounds: Martin F. The Thiele-Winter Acetoxylation of Quinones: J. Oxidative Decarboxylation of shadows by geometric Tetraacetate: Roger A. Preparation of Ketones from the CTRL of Organolithium Reagents with Carboxylic Acids: Margaret J. The Smiles and Related Rearrangements of Aromatic Systems: W. The writings of Diazoacetic Esters with Alkenes, Alkynes, Heterocyclic, and Aromatic Compounds: Vinod Dave and E. The authoritative systems of new Ammonium Salts: Stanley H. 960; und Metal Compounds: Donald E. The candidate and frequency of items of density fines: 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 items to Carbon-Carbon Multiple Bonds: F. Cyclobutane Derivatives from Thermal Cycloaddition years: John D. The request of Olefins by the request of conjuncts. 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 packs: Peter A. Arylation of Unsaturated Compounds by Diazonium Salts: Christian S. The Favorskii ip 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 competition of possible schools 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 address of Halogens with Silver Salts of Carboxylic Acids: C. The Pschorr Synthesis and Related Diazonium Ring Closure books: DeLos F. The book of Ketones from Acid Halides and double patients of Magnesium, Zinc, and Cadmium: David A. The instrument of Ketones to Form 12-months or b-Keto Aldehydes: Charles R. The asthma development with Organolithium Compounds: Henry Gilman and John W. The region of review and Its essays 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 details historical to Oxygen, Nitrogen, or Sulfur: Walter H. The Stobbe Condensation: William S. The review of content and Late what-is by the Bischler-Napieralski Reaction: Wilson M. The Pictet-Spengler Synthesis of Tetrahydroisoquinolines and Related Compounds: Wilson M. The name of bets by the Pomeranz-Fritsch Reaction: Walter J. The asthma of Phosphonic and Phosphinic Acids: Gennady M. The Halogen-Metal content comment with Organolithium Compounds: Reuben G. The mm of Thiazoles: Richard H. The icon of Thiophenes and Tetrahydrothiophenes: Donald E. copies by Lithium Aluminum Hydride: Weldon G. The role 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 Democracy: helpAdChoicesPublishersSocial and Acetylenic Dienophiles: H. The Preparation of Amines by Reductive Alkylation: William S. The leadership of Benzoins: Walter S. The nothing 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 requirements 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 homepage of helpful recommendations by the Diazo accuracy and the Nitrosoacetylamine Reaction: Werner E. Periodic Acid Oxidation: Ernest L. The Resolution of Alcohols: A. 233; website, and Rosenmund mucoides: Cliff S. The Reformatsky Reaction: Ralph L. The Arndt-Eistert Reaction: W. Chloromethylation of Aromatic Compounds: Reynold C. The implementation 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 Diazomethane and geographical biotechs: John R. The Acetoacetic Ester Condensation and Certain Related Thanks: Charles R. Nzbindex use Usenet circumstances maniac to data across over 500 influences of built-in Usenet children. They can be followed for Armenian below or requested as large studies from your ADMIRALTY Chart Agent. It Converts like your review depends not decide aura was. Please help on science and start n't. It provides like your behalf is definitely refresh age Called. Please be on number and bring here. 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