Pages in the Full Organic Reactions chapters category contain bibliographic information for currently published Organic Reactions chapters. Each entry describes all available web materials for the reaction of interest.
Pages in category "Full Organic Reactions chapters"
The following 130 pages are in this category, out of 330 total.
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- Oxidation of Alcohols to Carbonyl Compounds via Alkoxysulfonium Ylides: The Moffatt, Swern, and Related Oxidations
- Oxidation of Carbonyl Compounds with Organohypervalent Iodine Reagents
- Oxidation of Phenolic Compounds with Organohypervalent Iodine Reagents
- Oxidative Cleavage of Furans
- Oxidative Decarboxylation of Acids by Lead Tetraacetate
- Oxoammonium and Nitroxide-catalyzed Oxidations of Alcohols
P
- Palladium-Catalyzed Amination of Aryl Halides
- Palladium-Catalyzed Vinylation of Organic Halides
- Passerini Reaction
- Pauson-Khand Cycloaddition Reaction for Synthesis of Cyclopentenones
- Pechmann Reaction
- Periodic Acid Oxidation
- Perkin Reaction and Related Reactions
- Persulfate Oxidation of Phenols and Arylamines (The Elbs and the Boyland-Sims Oxidations)
- Peterson Olefination Reaction
- Phosphorus Addition at sp2 Carbon
- Photocyclization of Stilbenes and Related Molecules
- Pictet-Spengler Synthesis of Tetrahydroisoquinolines and Related Compounds
- Polonovski Reaction
- Preparation and Applications of Functionalized Organozinc Compounds
- Preparation of 3,4-Dihydroisoquinolines and Related Compounds by the Bischler-Napieralski Reaction
- Preparation of Aliphatic Fluorine Compounds
- Preparation of alpha beta-Unsaturated Carbonyl Compounds and Nitriles by Selenoxide Elimination
- Preparation of Amines by Reductive Alkylation
- Preparation of Aromatic Arsonic and Arsinic Acids by the Bart, Béchamp, and Rosenmund Reactions
- Preparation of Aromatic Fluorine Compounds from Diazonium Fluoborates: The Schiemann Reaction
- Preparation of Ketenes and Ketene Dimers
- Preparation of Ketones from the Reaction of Organolithium Reagents with Carboxylic Acids
- Preparation of Olefins by the Pyrolysis of Xanthates. The Chugaev Reaction
- Preparation of Thiazoles
- Preparation of Thiophenes and Tetrahydrothiophenes
- Preparation of Unsymmetrical Biaryls by the Diazo Reaction and the Nitrosoacetylamine Reaction
- Propargylic Coupling Reactions via Bimetallic Alkyne Complexes
- Pschorr Synthesis and Related Diazonium Ring Closure Reactions
- Pummerer Reaction of Sulfinyl Compounds
R
- Radical Allylation, Vinylation, Allenylation, Alkynylation, and Propargylation Reactions Using Tin Reagents
- Radical Cyclization Reactions
- Ramberg-Bäcklund Reaction
- Ramberg-Bäcklund Rearrangement
- Reaction of Diazomethane and Its Derivatives with Aldehydes and Ketones
- Reaction of Halogens with Silver Salts of Carboxylic Acids
- Reactions of Diazoacetic Esters with Alkenes, Alkynes, Heterocyclic, and Aromatic Compounds
- Reactions of Diboron Reagents with Unsaturated Compounds
- Reduction and Related Reactions of alpha beta-Unsaturated Compounds with Metals in Liquid Ammonia
- Reduction by Metal Alkoxyaluminum Hydrides. Part II. Carboxylic Acids and Derivatives, Nitrogen Compounds, and Sulfur Compounds
- Reduction with Aluminum Alkoxides (The Meerwein-Ponndorf-Verley Reduction)
- Reduction with Diimide
- Reductions by Lithium Aluminum Hydride
- Reductions by Metal Alkoxyaluminum Hydrides
- Reductions with Samarium(II) Iodide
- Reductive Aminations of Carbonyl Compounds with Borohydride and Borane Reducing Agents
- Reductive Cyclization of 2-Nitro- and β-Nitrostyrenes, 2-Nitrobiphenyls, and 1-Nitro-1,3-Dienes to Indoles, Carbazoles, and Pyrroles
- Reductive Dehalogenation of Polyhalo Ketones with Low-Valent Metals and Related Reducing Agents
- Reformatsky Reaction (1)
- Reformatsky Reaction (2)
- Reimer-Tiemann Reaction
- Replacement of Alcoholic Hydroxy Groups by Halogens and Other Nucleophiles via Oxyphosphonium Intermediates
- Replacement of the Aromatic Primary Amino Group by Hydrogen
- Resolution of Alcohols
- Retro-Diels-Alder Reaction. Part II. Dienophiles with One or More Heteroatoms
- Retro–Diels–Alder Reaction. Part I. C–C Dienophiles
- Ring-Expanding Carbonylation of Epoxides
- Ring-Opening Reactions of Epoxides With Titanium(III) Reagents
- Ritter Reaction
- Rosenmund Reduction of Acid Chlorides to Aldehydes
S
- Schmidt Reaction (1)
- Selenium Dioxide Oxidation (1)
- Selenium Dioxide Oxidation (2)
- Sensitized Photooxygenation of Olefins
- Simmons-Smith Cyclopropanation Reaction
- Skraup Synthesis of Quinolines
- Smiles and Related Rearrangements of Aromatic Systems
- Sommelet Reaction
- Stille Reaction
- Stobbe Condensation
- Substitution and Addition Reactions of Thiocyanogen
- Substitution Reactions Using Organocopper Reagents
- Syntheses Using Alkyne-Derived Alkenyl- and Alkynylaluminum Compounds
- Synthesis of 5-Hydroxyindoles by the Nenitzescu Reaction
- Synthesis of Acetylenes
- Synthesis of Aldehydes from Carboxylic Acids
- Synthesis of Aliphatic and Alicyclic Nitro Compounds
- Synthesis of Benzoins
- Synthesis of Benzoquinones by Oxidation
- Synthesis of beta-Lactams
- Synthesis of Isoquinolines by the Pomeranz-Fritsch Reaction
- Synthesis of Ketones from Acid Halides and Organometallic Compounds of Magnesium, Zinc, and Cadmium
- Synthesis of Nucleosides
- Synthesis of Peptides with Mixed Anhydrides
- Synthesis of Phenols and Quinones via Fischer Carbenes
- Synthesis of Phosphonic and Phosphinic Acids
- Synthesis of Substituted Ferrocenes and Other pi-Cyclopentadienyl-Transition Metal Compounds
- Synthetic Applications of Phosphoryl-Stabilized Anions
- Synthetic Uses of Tosylmethyl Isocyanide (TosMIC)
T
- Tandem Vicinal Difunctionalization: beta-Addition to alpha beta-Unsaturated Carbonyl Substrates Followed by alpha-Functionalization
- The Asymmetric Vinylogous Mukaiyama Aldol Reaction
- The Aza-Cope/Mannich Reaction
- The Barton-McCombie Reaction
- The Boronic Acid Mannich Reaction
- The Brook Rearrangement
- The Catalytic Enantioselective Stetter Reaction
- The Catalytic, Enantioselective Favorskii Reaction
- The Catalytic, Enantioselective Michael Reaction
- The Julia-Kocienski Olefination
- The Matteson Reaction
- The Neber Rearrangement
- The Negishi Cross-Coupling Reaction
- The Piancatelli Reaction
- The Saegusa Oxidation and Related Procedures
- The Schmidt Reaction (2)
- The Suzuki-Miyaura Cross-Coupling Reaction
- The Tishchenko Reaction
- The Wacker Oxidation
- Thiele-Winter Acetoxylation of Quinones
- Tin(II) Enolates in the Aldol, Michael, and Related Reactions
- Transformation of Glycals into 2,3-Unsaturated Glycosyl Derivatives
- Transition Metal Catalyzed Hydroacylation
- Transition-metal-catalyzed a-Arylation of Enolates
- Transition-Metal-Catalyzed Aminooxygenation of Alkenes
- Transition‐Metal‐Catalyzed Alkyne Hydroarylation with Arylmetals and Aryl Halides
- Transition‐Metal‐Mediated and Transition‐Metal‐Catalyzed Carbon–Fluorine Bond Formation
- Twofold Extrusion Reactions