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3374 reactions imported from Wikipedia named-reactions and Organic Syntheses archives. Filter by source or search by name + summary.
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| Equation | Name | Summary | Source |
|---|---|---|---|
| Boger pyridine synthesis | The Boger pyridine synthesis is a cycloaddition approach to the formation of pyridines named after its inventor Dale L. Boger, who first reported it in 1981. The reaction is a form of inverse-electron… | Wikipedia: Category:Name reactions | |
| Bohlmann–Rahtz pyridine synthesis | In organic chemistry, the Bohlmann–Rahtz pyridine synthesis is a reaction that generates substituted pyridines in two steps, first a condensation reaction between an enamine and an ethynylketone to fo… | Wikipedia: Category:Name reactions | |
| Bohn–Schmidt reaction Rearrangement | The Bohn–Schmidt reaction, a named reaction in chemistry, introduces a hydroxy group at an anthraquinone system. The anthraquinone must already have at least one hydroxy group. The reaction was first … | Wikipedia: Category:Name reactions | |
| Boord olefin synthesis | The Boord olefin synthesis is an organic reaction forming alkenes from ethers carrying a halogen atom 2 carbons removed from the oxygen atom (β-halo-ethers) using a metal such as magnesium or zinc. T… | Wikipedia: Category:Name reactions | |
| BORANES IN FUNCTIONALIZATION OF DIENES TO CYCLIC KETONES: BICYCLO[3.3.1]NONAN-9-ONE | Preparation of BORANES IN FUNCTIONALIZATION OF DIENES TO CYCLIC KETONES: BICYCLO[3.3.1]NONAN-9-ONE. Submitted by Bruce A. Carlson1 and Herbert C. Brown2. DOI: 10.15227/orgsyn.058.0024. | Organic Syntheses | |
| BORANES IN FUNCTIONALIZATION OF OLEFINS TO AMINES: 3-PINANAMINE (Bicyclo[3.1.1]heptan-3-amine, 2,6,6-trimethyl-) | Preparation of Bicyclo[3.1.1]heptan-3-amine, 2,6,6-trimethyl-. Submitted by Michael W. Rathke1 and Alan A. Millard. DOI: 10.15227/orgsyn.058.0032. | Organic Syntheses | |
| BORIC ACID CATALYZED AMIDE FORMATION FROM CARBOXYLIC ACIDS AND AMINES: N-BENZYL-4-PHENYLBUTYRAMIDE ((Benzenebutanamide, N-(phenylmethyl)-)) | Preparation of (Benzenebutanamide, N-(phenylmethyl)-). Submitted by Pingwah Tang1. DOI: 10.15227/orgsyn.081.0262. | Organic Syntheses | |
| Borsche–Drechsel cyclization Cyclization | The Borsche–Drechsel cyclization is a chemical reaction used to synthesize tetrahydrocarbazoles by the acid-catalyzed cyclization of cyclohexanone arylhydrazones. The reaction was first described by E… | Wikipedia: Category:Name reactions | |
| Bosch reaction | The Bosch reaction is a catalytic chemical reaction between carbon dioxide (CO2) and hydrogen (H2) that produces elemental carbon (C,graphite), water, and a 10% return of invested heat. CO2 is usuall… | Wikipedia: Category:Name reactions | |
| Boudouard reaction | The Boudouard reaction, named after Octave Leopold Boudouard, is the redox reaction of a chemical equilibrium mixture of carbon monoxide and carbon dioxide at a given temperature. It is the disproport… | Wikipedia: Category:Name reactions | |
| Bouveault aldehyde synthesis | The Bouveault aldehyde synthesis (also known as the Bouveault reaction) is a one-pot substitution reaction that replaces an alkyl or aryl halide with a formyl group using a N,N-disubstituted formamide… | Wikipedia: Category:Name reactions | |
| Bouveault–Blanc reduction Reduction | The Bouveault–Blanc reduction is a chemical reaction in which an ester is reduced to primary alcohols using absolute ethanol and sodium metal. It was first reported by Louis Bouveault and Gustave Lou… | Wikipedia: Category:Name reactions | |
| Boyland–Sims oxidation Oxidation | The Boyland–Sims oxidation is the chemical reaction of anilines with alkaline potassium persulfate, which after hydrolysis forms ortho-hydroxyl anilines. The reaction is generally performed in water a… | Wikipedia: Category:Name reactions | |
| B-PROTECTED HALOBORONIC ACIDS FOR ITERATIVE CROSS-COUPLING Cross-coupling | Preparation of B-PROTECTED HALOBORONIC ACIDS FOR ITERATIVE CROSS-COUPLING. Submitted by Steven G. Ballmer, Eric P. Gillis, and Martin D. Burke1. DOI: 10.15227/orgsyn.086.0344. | Organic Syntheses | |
| Bradsher cycloaddition Cycloaddition | The Bradsher cycloaddition reaction, also known as the Bradsher cyclization reaction is a form of the Diels–Alder reaction which involves the [4+2] addition of a common dienophile with a cationic aro… | Wikipedia: Category:Name reactions | |
| Bray–Liebhafsky reaction | The Bray–Liebhafsky reaction is a chemical clock first described by William C. Bray in 1921 and the first oscillating reaction in a stirred homogeneous solution. He investigated the role of the iodate… | Wikipedia: Category:Name reactions | |
| Briggs–Rauscher reaction | The Briggs–Rauscher oscillating reaction is one of a small number of known oscillating chemical reactions. It is especially well suited for demonstration purposes because of its visually striking colo… | Wikipedia: Category:Name reactions | |
| BROMAL | Preparation of BROMAL. Submitted by F. A. Long and J. W. Howard. DOI: 10.15227/orgsyn.017.0018. | Organic Syntheses | |
| BROMOACETAL (Acetaldehyde, bromo-, diethyl acetal) | Preparation of Acetaldehyde, bromo-, diethyl acetal. Submitted by S. M. McElvain and D. Kundiger. DOI: 10.15227/orgsyn.023.0008. | Organic Syntheses | |
| BROMOACETONE (2-Propanone, 1-bromo-) | Preparation of 2-Propanone, 1-bromo-. Submitted by P. A. Levene. DOI: 10.15227/orgsyn.010.0012. | Organic Syntheses | |
| BROMOCYCLOPROPANE (Cyclopropane, bromo-) | Preparation of Cyclopropane, bromo-. Submitted by John S. Meek and David T. Osuga1. DOI: 10.15227/orgsyn.043.0009. | Organic Syntheses | |
| BROMOFLUORINATION OF ALKENES: 1-BROMO-2-FLUORO-2-PHENYLPROPANE (Benzene, (2-bromo-1-fluoro-1-methylethyl) | Preparation of Benzene, (2-bromo-1-fluoro-1-methylethyl. Submitted by Günter Haufe1 , Gerard Alvernhe2 , André Laurent2 , Thomas Ernet1 , Olav Goj1 , Stefan Kröger1 , and Andreas Sattler1. DOI: 10.152… | Organic Syntheses | |
| BROMOHYDRINS FROM ALKENES AND N-BROMOSUCCINIMIDE IN DIMETHYL SULFOXIDE: erythro-2-BROMO-1,2-DIPHENYLETHANOL (Ethanol, 2-bromo-1,2-diphenyl-, erythro-) | Preparation of Ethanol, 2-bromo-1,2-diphenyl-, erythro-. Submitted by A. W. Langman and D. R. Dalton1. DOI: 10.15227/orgsyn.059.0016. | Organic Syntheses | |
| BROMOMESITYLENE (Mesitylene, 2-bromo-) | Preparation of Mesitylene, 2-bromo-. Submitted by Lee Irvin Smith. DOI: 10.15227/orgsyn.011.0024. | Organic Syntheses | |
| Brook rearrangement Rearrangement | In organic chemistry the Brook rearrangement refers to any [1,n] carbon to oxygen silyl migration. The rearrangement was first observed in the late 1950s by Canadian chemist Adrian Gibbs Brook (1924–2… | Wikipedia: Category:Name reactions | |
| Bruylants reaction | In organic chemistry, the Bruylants reaction (sometimes misspelled Bruylant) is a substitution reaction in which a Grignard reagent replaces a nitrile on a carbon that also has an amino group (c.f. cy… | Wikipedia: Category:Name reactions | |
| Bucherer–Bergs reaction | The Bucherer–Bergs reaction is the chemical reaction of carbonyl compounds (aldehydes or ketones), either in combination with potassium cyanide or converted to their cyanohydrin derivative, with ammon… | Wikipedia: Category:Name reactions | |
| Bucherer carbazole synthesis | The Bucherer carbazole synthesis is a chemical reaction used to synthesize carbazoles from 2-naphthols and aryl hydrazines using sodium bisulfite. The reaction is named after Hans Theodor Bucherer. | Wikipedia: Category:Name reactions | |
| Bucherer reaction | The Bucherer reaction in organic chemistry is the reversible conversion of a naphthol to a naphthylamine in the presence of ammonia and sodium bisulfite. The reaction is widely used in the synthesis … | Wikipedia: Category:Name reactions | |
| Büchner–Curtius–Schlotterbeck reaction Rearrangement | The Buchner–Curtius–Schlotterbeck reaction is the reaction of aldehydes or ketones with aliphatic diazoalkanes to form homologated ketones. It was first described by Eduard Buchner and Theodor Curtius… | Wikipedia: Category:Name reactions | |
| Buchner ring expansion | The Buchner ring expansion is a two-step organic C-C bond forming reaction used to access 7-membered rings. The first step involves formation of a carbene from ethyl diazoacetate, which cyclopropanate… | Wikipedia: Category:Name reactions | |
| Buchwald–Hartwig amination Cross-coupling | In organic chemistry, the Buchwald–Hartwig amination is a chemical reaction for the synthesis of carbon–nitrogen bonds via the palladium-catalyzed coupling reactions of amines with aryl halides. Altho… | Wikipedia: Category:Name reactions | |
| Bunsen reaction | The Bunsen reaction is a chemical reaction that describes water, sulfur dioxide, and iodine reacting to form sulfuric acid and hydrogen iodide: | Wikipedia: Category:Name reactions | |
| BUTYRCHLORAL (Butyraldehyde, 2,2,3-trichloro-) | Preparation of Butyraldehyde, 2,2,3-trichloro-. Submitted by Gus A. Ropp, W. E. Craig, and Vernon Raaen1. DOI: 10.15227/orgsyn.033.0015. | Organic Syntheses | |
| BUTYROIN (4-Octanone, 5-hydroxy-) | Preparation of 4-Octanone, 5-hydroxy-. Submitted by John M. Snell and S. M. McElvain. DOI: 10.15227/orgsyn.013.0024. | Organic Syntheses | |
| Cadiot–Chodkiewicz coupling Cross-coupling | The Cadiot–Chodkiewicz coupling in organic chemistry is a coupling reaction between a terminal alkyne and a haloalkyne catalyzed by a copper(I) salt such as copper(I) bromide and an amine base. The re… | Wikipedia: Category:Name reactions | |
| Cadogan–Sundberg indole synthesis | The Cadogan–Sundberg indole synthesis, or simply Cadogan indole synthesis, is a name reaction in organic chemistry that allows for the generation of indoles from o-nitrostyrenes with the use of trialk… | Wikipedia: Category:Name reactions | |
| CAMPHORQUINONE AND CAMPHORQUINONE MONOXIME (Bicyclo[2.2.1]heptane-2,3-dione, 1,7,7-trimethyl-, (1R)- and Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-3-oxime, (1R)-) | Preparation of Bicyclo[2.2.1]heptane-2,3-dione, 1,7,7-trimethyl-, (1R)- and Bicyclo[2.2.1]heptan-2-one, 1,7,7-trimethyl-3-oxime, (1R)-. Submitted by James D. White, Duncan J. Wardrop, and Kurt F. Sund… | Organic Syntheses | |
| Camps quinoline synthesis | The Camps quinoline synthesis (also known as the Camps cyclization) is a chemical reaction whereby an o-acylaminoacetophenone is transformed into two different hydroxyquinolines (products A and B) usi… | Wikipedia: Category:Name reactions | |
| Cannizzaro disproportionation: 2 benzaldehyde → benzyl alcohol + sodium benzoate Scale Disproportionation | Textbook redox disproportionation of an α-H-free aldehyde. Concentrated NaOH drives hydride transfer between two benzaldehyde molecules: one is reduced to benzyl alcohol, the other oxidised to sodium … | Cannizzaro 1853 | |
| Cannizzaro reaction Disproportionation | The Cannizzaro reaction, named after its discoverer Stanislao Cannizzaro, is a chemical reaction which involves the base-induced disproportionation of two molecules of a non-enolizable aldehyde to giv… | Wikipedia: Category:Name reactions | |
| CARBENE GENERATION BY α-ELIMINATION WITH LITHIUM 2,2,6,6-TETRAMETHYLPIPERIDIDE: 1-ETHOXY-2-p-TOLYLCYCLOPROPANE (Benzene, 1-(2-ethoxycyclopropyl)-4-methyl) Elimination | Preparation of Benzene, 1-(2-ethoxycyclopropyl)-4-methyl. Submitted by Charles M. Dougherty1 and Roy A. Olofson2. DOI: 10.15227/orgsyn.058.0037. | Organic Syntheses | |
| CARBOBENZOXY CHLORIDE AND DERIVATIVES (Formic acid, chloro-, benzyl ester) | Preparation of Formic acid, chloro-, benzyl ester. Submitted by H. E. Carter, R. L. Frank, and H. W. Johnston. DOI: 10.15227/orgsyn.023.0013. | Organic Syntheses | |
| CARBONYL CYANIDE (Propanedinitrile, oxo-) | Preparation of Propanedinitrile, oxo-. Submitted by E. L. Martin1. DOI: 10.15227/orgsyn.051.0070. | Organic Syntheses | |
| CARBOXYLATION OF AROMATIC COMPOUNDS: FERROCENECARBOXYLIC ACID (Ferrocene, carboxy-) | Preparation of Ferrocene, carboxy-. Submitted by Perry C. Reeves1. DOI: 10.15227/orgsyn.056.0028. | Organic Syntheses | |
| CARBOXYLIC ACIDS FROM THE OXIDATION OF TERMINAL ALKENES BY PERMANGANATE: NONADECANOIC ACID Oxidation | Preparation of CARBOXYLIC ACIDS FROM THE OXIDATION OF TERMINAL ALKENES BY PERMANGANATE: NONADECANOIC ACID. Submitted by Donald G. Lee, Shannon E. Lamb, and Victor S. Chang1. DOI: 10.15227/orgsyn.060.0… | Organic Syntheses | |
| CARBOXYMETHOXYLAMINE HEMIHYDROCHLORIDE (Acetic acid, aminoöxy-, hydrochloride) | Preparation of Acetic acid, aminoöxy-, hydrochloride. Submitted by H. S. Anker and H. T. Clarke. DOI: 10.15227/orgsyn.027.0015. | Organic Syntheses | |
| Carroll rearrangement Rearrangement | The Carroll rearrangement is a rearrangement reaction in organic chemistry and involves the transformation of a β-keto allyl ester into a α-allyl-β-ketocarboxylic acid. This organic reaction is accomp… | Wikipedia: Category:Name reactions | |
| CASEIN | Preparation of CASEIN. Submitted by E. J. Cohn and J. L. Hendry. DOI: 10.15227/orgsyn.010.0016. | Organic Syntheses | |
| Castro–Stephens coupling Cross-coupling | The Castro–Stephens coupling is a cross coupling reaction between a copper(I) acetylide and an aryl halide in pyridine, forming a disubstituted alkyne and a copper(I) halide. | Wikipedia: Category:Name reactions |
