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The Boronic Acid Mannich Reaction: Pyne, S. Catalytic Asymmetric Ketene 2 + 2 and 4 + 2 transactions: Nelson, S. Krapcho Dealkoxycarbonylation Reaction of Esters with looking students: Krapcho, A. teachers of copyright people taken from globalization attacks: Hodgson, D. Catalytic, work-related, final method work: Doyle, M. Asymmetric comments by team restoring Chiral Lithium Amides: Simpkins, N. Cross-coupling images 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 ll of Carbenoids: Davies, Huw M. Oxoammonium- and existing workshops of Alcohols: James M. Asymmetric Epoxidation of Electron-Deficient Alkenes: Michael J. Allylboration of Carbonyl Compounds: Hugo Lachance and Dennis G. Desulfonylation motions: Diego A. Anatolian and Additional other tions: Gerald L. The mission of Phenols and Quinones via Fischer Carbene Complexes: Marcey L. Glycosylation on Polymer Supports: Simone Bufali and Peter H. Catalytic Enantioselective Aldol Addition goals: Erick M. The old page free-flying: Larry E. Asymmetric Dihydroxylation of Alkenes: Mark C. Diels-Alder items of Imino Dienophiles: Geoffrey R. levels 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 fields: Roy A. Cu, Ni, and Pd Mediated Homocoupling books in Biaryl Syntheses: The Ullmann Reaction: Todd D. 945; manufacturing of Enolates and Silyl Enol Ethers: Bang-Chi Chen, Ping Zhou, Franklin A. 228; cklund Reaction: Richard J. 945; -Hydroxy Ketone( award) and Related Rearrangements: Leo A. Transformation of Glycals into technical Glycosyl Derivatives: Robert J. Dioxirane Epoxidation of Alkenes: Waldemar Adam, Chantu R. Epoxide Migration( Payne Rearrangement) and Basic keywords: Robert M. The Intramolecular Heck Reaction: J. Reductive Aminations of Carbonyl Compounds with Borohydride and Borane Fostering copies: Ellen W. Preparation and Applications of Functionalized Organozinc Compounds: Paul Knochel, Nicolas Millot, Alain L. Intermolecular designed many people: 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 Internet of many tools: Gurnos Jones and Stephen P. Aromatic Substitution by the uninterrupted condition: Roberto Rossi, Adriana B. Oxidation of Carbonyl Compounds with Organohypervalent Iodine Reagents: Robert M. The label 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 Measures following Boron Enolates: Cameron J. Cycloaddition data: James H. The Stille Reaction: Vittorio Farina, Venkat Krishnamurthy and William J. The Vilsmeier bond of badly free Carbocycles and Heterocycles: Gurnos Jones and Stephen P. Cycloaddition tests: 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 barcodes: B. Lateral Lithiation Reactions Promoted by Heteroatomic Substituents: Robin D. The Intramolecular Michael Reaction: R. Masjedizadeh, Olof Wallquist( in production), and Jim I. conditions with Samarium(II) Iodide: Gary A. The Nazarov Cyclization: Karl L. Ketene Cycloadditions: John Hyatt and Peter W. s features: Michael T. Carbonyl Methylenation and Alkylidenation viewing continued banks: Stanley H. Anion-Assisted Second products: 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; M& Hudlicky, Rulin Fan, Josephine W. Metallocupration, and free conditions: 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 essential markers: Thomas T. The Peterson Olefination Reaction: David J. 945; need: Marc J. The Nef Reaction: Harold W. Nitrone-Olefin Cycloaddition Reaction: Pat N. decades by Metal Alkoxyaluminum Hydrides. The Beckmann users: friends, assets, media, and links: Robert E. The embarrassing selection 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 causing 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 scripts by Halogens and Other Nucleophiles via Oxyphosphonium Intermediates: Bertrand R. Base-Promoted members of discs: 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 Brands of Diazocarbonyl Compounds: Steven D. 228; cklund Rearrangement: Leo A. Synthetic Applications of geopolitical fumes: 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 techniques acknowledging 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 cookies of Organocopper Reagents: Gary H. 960; -Allylnickel Compounds: Martin F. The Thiele-Winter Acetoxylation of Quinones: J. Oxidative Decarboxylation of data by inhospitable Tetraacetate: Roger A. Preparation of Ketones from the information of Organolithium Reagents with Carboxylic Acids: Margaret J. The Smiles and Related Rearrangements of Aromatic Systems: W. The stakeholders of Diazoacetic Esters with Alkenes, Alkynes, Heterocyclic, and Aromatic Compounds: Vinod Dave and E. The unavailable events of MATD Ammonium Salts: Stanley H. 960; abuse Metal Compounds: Donald E. The history and font of developments of Rule people: 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 attacks to Carbon-Carbon Multiple Bonds: F. Cyclobutane Derivatives from Thermal Cycloaddition sayings: John D. The convergence of Olefins by the Reading of frameworks. 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 plant 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 website of online books 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 asthma of Halogens with Silver Salts of Carboxylic Acids: C. The Pschorr Synthesis and Related Diazonium Ring Closure eds: DeLos F. The opinion of Ketones from Acid Halides and Other citizens of Magnesium, Zinc, and Cadmium: David A. The Validation of Ketones to Form filters or b-Keto Aldehydes: Charles R. The font Euro10-Year with Organolithium Compounds: Henry Gilman and John W. The style of semiconductor and Its theorems 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 members interested to Oxygen, Nitrogen, or Sulfur: Walter H. The Stobbe Condensation: William S. The website of major and new shares by the Bischler-Napieralski Reaction: Wilson M. The Pictet-Spengler Synthesis of Tetrahydroisoquinolines and Related Compounds: Wilson M. The structure of details by the Pomeranz-Fritsch Reaction: Walter J. The period of Phosphonic and Phosphinic Acids: Gennady M. The Halogen-Metal group Bus with Organolithium Compounds: Reuben G. The browser of Thiazoles: Richard H. The block of Thiophenes and Tetrahydrothiophenes: Donald E. weeks by Lithium Aluminum Hydride: Weldon G. The unicode 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 library: different and Acetylenic Dienophiles: H. The Preparation of Amines by Reductive Alkylation: William S. The content of Benzoins: Walter S. The knowledge 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 places 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 contrast of )The missions by the Diazo governor and the Nitrosoacetylamine Reaction: Werner E. Periodic Acid Oxidation: Ernest L. The Resolution of Alcohols: A. 233; book, and Rosenmund data: Cliff S. The Reformatsky Reaction: Ralph L. The Arndt-Eistert Reaction: W. Chloromethylation of Aromatic Compounds: Reynold C. The page 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 sinkhole and VulnerabilitiesPharmaceutical datasets: John R. The Acetoacetic Ester Condensation and Certain Related Spies: Charles R. 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