Browse · Reactions
Reactions
3374 reactions imported from Wikipedia named-reactions and Organic Syntheses archives. Filter by source or search by name + summary.
Results
| Equation | Name | Summary | Source |
|---|---|---|---|
| ISONITROSOPROPIOPHENONE (1,2-Propanedione, 1-phenyl-, 2-oxime) | Preparation of 1,2-Propanedione, 1-phenyl-, 2-oxime. Submitted by Walter H. Hartung and Frank Crossley. DOI: 10.15227/orgsyn.016.0044. | Organic Syntheses | |
| ISOPHORONE OXIDE (Cyclohexanone, 2,3-epoxy-3,5,5-trimethyl-) | Preparation of Cyclohexanone, 2,3-epoxy-3,5,5-trimethyl-. Submitted by Richard L. Wasson and Herbert O. House1. DOI: 10.15227/orgsyn.037.0058. | Organic Syntheses | |
| ISOPHTHALALDEHYDE | Preparation of ISOPHTHALALDEHYDE. Submitted by J. H. Ackerman and A. R. Surrey1. DOI: 10.15227/orgsyn.047.0076. | Organic Syntheses | |
| (−)-ISOPINOCAMPHEOL (Bicyclo[3.1.1]heptan-3-ol, 2,6,6-trimethyl-, [1R-(1α,2β,3α,5α)]-) | Preparation of Bicyclo[3.1.1]heptan-3-ol, 2,6,6-trimethyl-, [1R-(1α,2β,3α,5α)]-. Submitted by C. F. Lane and J. J. Daniels1. DOI: 10.15227/orgsyn.052.0059. | Organic Syntheses | |
| ISOPRENE CYCLIC SULFONE (Thiophene, 2,5-dihydro-3-methyl-, 1-dioxide) | Preparation of Thiophene, 2,5-dihydro-3-methyl-, 1-dioxide. Submitted by Robert L. Frank and Raymond P. Seven1. DOI: 10.15227/orgsyn.029.0059. | Organic Syntheses | |
| ISOPROPYL LACTATE (Lactic acid, isopropyl ester) | Preparation of Lactic acid, isopropyl ester. Submitted by F. A. McDermott. DOI: 10.15227/orgsyn.010.0088. | Organic Syntheses | |
| ISOPROPYL THIOCYANATE (Thiocyanic acid, isopropyl ester) | Preparation of Thiocyanic acid, isopropyl ester. Submitted by R. L. Shriner. DOI: 10.15227/orgsyn.011.0092. | Organic Syntheses | |
| ISOXAZOLE ANNELATION REACTION: 1-METHYL-4,4a,5,6,7,8-HEXAHYDRONAPHTHALEN-2(3H)-ONE (2(3H)-Naphthalenone, 4,4a,5,6,7,8-hexahydro-1-methyl-) | Preparation of 2(3H)-Naphthalenone, 4,4a,5,6,7,8-hexahydro-1-methyl-. Submitted by John E. McMurry1. DOI: 10.15227/orgsyn.053.0070. | Organic Syntheses | |
| ITACONIC ANHYDRIDE AND ITACONIC ACID | Preparation of ITACONIC ANHYDRIDE AND ITACONIC ACID. Submitted by R. L. Shriner, S. G. Ford, and L. J. Roll. DOI: 10.15227/orgsyn.011.0070. | Organic Syntheses | |
| ITACONYL CHLORIDE | Preparation of ITACONYL CHLORIDE. Submitted by Henry Feuer and Stanley M. Pier1. DOI: 10.15227/orgsyn.033.0041. | Organic Syntheses | |
| Ivanov reaction | The Ivanov reaction is a carbon–carbon bond-forming chemical reaction involving the addition of dianions (endiolates) of aryl acetic acids (Ivanov reagents) with electrophilic substrates such as aldeh… | Wikipedia: Category:Name reactions | |
| Jacobsen epoxidation Oxidation | The Jacobsen epoxidation, sometimes also referred to as Jacobsen-Katsuki epoxidation is a chemical reaction which allows enantioselective epoxidation of unfunctionalized alkyl- and aryl- substituted a… | Wikipedia: Category:Name reactions | |
| Jacobsen rearrangement Rearrangement | The Jacobsen rearrangement is a chemical reaction, commonly described as the migration of an alkyl group in a sulfonic acid derived from a polyalkyl- or polyhalobenzene: | Wikipedia: Category:Name reactions | |
| Jaffe reaction | The Jaffe reaction is a colorimetric method used in clinical chemistry to determine creatinine levels in blood and urine. In 1886, Max Jaffe (1841–1911) wrote about its basic principles in the paper Ü… | Wikipedia: Category:Name reactions | |
| Japp–Klingemann reaction | The Japp–Klingemann reaction is a chemical reaction used to synthesize hydrazones from β-keto-acids (or β-keto-esters) and aryl diazonium salts. The reaction is named after the chemists Francis Robert… | Wikipedia: Category:Name reactions | |
| Japp–Maitland condensation Condensation | The Japp–Maitland condensation is an organic reaction and a type of Aldol reaction and a tandem reaction. In a reaction between the ketone 3-pentanone and the aldehyde benzaldehyde catalyzed by base t… | Wikipedia: Category:Name reactions | |
| Jocic reaction | In organic chemistry, the Jocic reaction, also called the Jocic–Reeve reaction (named after Zivojin Jocic and Wilkins Reeve) is a name reaction that generates α-substituted carboxylic acids from trich… | Wikipedia: Category:Name reactions | |
| Johnson–Corey–Chaykovsky reaction | The Johnson–Corey–Chaykovsky reaction (sometimes referred to as the Corey–Chaykovsky reaction or CCR) is a chemical reaction used in organic chemistry for the synthesis of epoxides, aziridines, and cy… | Wikipedia: Category:Name reactions | |
| Jones oxidation Oxidation | The Jones oxidation is an organic reaction for the oxidation of primary and secondary alcohols to carboxylic acids and ketones, respectively. It is named after its discoverer, Sir Ewart Jones. The rea… | Wikipedia: Category:Name reactions | |
| Juliá–Colonna epoxidation Oxidation | The Juliá–Colonna epoxidation is an asymmetric poly-leucine catalyzed nucleophilic epoxidation of electron deficient olefins in a triphasic system. The reaction was reported by Sebastian Juliá at the … | Wikipedia: Category:Name reactions | |
| Julia olefination Olefination | The Julia olefination (also known as the Julia–Lythgoe olefination) is the chemical reaction used in organic chemistry of phenyl sulfones (1) with aldehydes (or ketones) to give alkenes (olefins)(3) a… | Wikipedia: Category:Name reactions | |
| JULOLIDINE (Benzo[ij]quinolizine, 1,2,3,5,6,7-hexahydro-) | Preparation of Benzo[ij]quinolizine, 1,2,3,5,6,7-hexahydro-. Submitted by D. B. Glass and A. Weissberger. DOI: 10.15227/orgsyn.026.0040. | Organic Syntheses | |
| Kabachnik–Fields reaction | In organophosphorus chemistry, the Kabachnik–Fields reaction is a three-component organic reaction forming α-aminomethylphosphonates from an amine, a carbonyl compound, and a dialkyl phosphonate, (RO)… | Wikipedia: Category:Name reactions | |
| Kauffmann olefination Olefination | The Kauffmann olefination is a chemical reaction to convert aldehydes and ketones to olefins with a terminal methylene group. This reaction was discovered by the German chemist Thomas Kauffmann and is… | Wikipedia: Category:Name reactions | |
| Keck asymmetric allylation | In organic chemistry, the Keck asymmetric allylation is a chemical reaction that involves the nucleophilic addition of an allyl group to an aldehyde. The catalyst is a chiral complex that contains tit… | Wikipedia: Category:Name reactions | |
| KETENE | Preparation of KETENE. Submitted by C. D. Hurd. DOI: 10.15227/orgsyn.004.0039. | Organic Syntheses | |
| KETENE | Preparation of KETENE. Submitted by S. Andreades and H. D. Carlson1. DOI: 10.15227/orgsyn.045.0050. | Organic Syntheses | |
| KETENE DI(2-METHOXYETHYL) ACETAL (Ketene bis(2-methoxyethyl) acetal) | Preparation of Ketene bis(2-methoxyethyl) acetal. Submitted by William C. Kuryla and John E. Hyre1. DOI: 10.15227/orgsyn.047.0078. | Organic Syntheses | |
| KETENE DIETHYLACETAL (Ketene, diethyl ketal) | Preparation of Ketene, diethyl ketal. Submitted by S. M. McElvain and D. Kundiger. DOI: 10.15227/orgsyn.023.0045. | Organic Syntheses | |
| KETENE DIMER (Acetylketene) | Preparation of Acetylketene. Submitted by Jonathan W. Williams and John A. Krynitsky. DOI: 10.15227/orgsyn.021.0064. | Organic Syntheses | |
| KETONES AND ALCOHOLS FROM ORGANOBORANES: PHENYL HEPTYL KETONE, 1-HEXANOL, AND 1-OCTANOL (1-Octanone, 1-phenyl-) | Preparation of 1-Octanone, 1-phenyl-. Submitted by Hiromichi Kono and John Hooz1. DOI: 10.15227/orgsyn.053.0077. | Organic Syntheses | |
| KETONES FROM CARBOXYLIC ACIDS AND GRIGNARD REAGENTS: METHYL 6-OXODECANOATE (Decanoic acid, 6-oxo-, methyl ester) Organometallic addition | Preparation of Decanoic acid, 6-oxo-, methyl ester. Submitted by Tamotsu Fujisawa and Toshio Sato1. DOI: 10.15227/orgsyn.066.0116. | Organic Syntheses | |
| Ketonic decarboxylation | Ketonic decarboxylation (also known as decarboxylative ketonization) is a type of organic reaction involving decarboxylation, converting two equivalents of a carboxylic acid (R−C(=O)OH) to a symmetric… | Wikipedia: Category:Name reactions | |
| Kharasch addition Addition | The Kharasch addition is an organic reaction and a metal-catalysed free radical addition of CXCl3 compounds (X = Cl, Br, H) to alkenes. The reaction is used to append trichloromethyl or dichloromethy… | Wikipedia: Category:Name reactions | |
| Kharasch–Sosnovsky reaction | The Kharasch–Sosnovsky reaction is a method that involves using a copper or cobalt salt as a catalyst to oxidize olefins at the allylic position, subsequently condensing a peroxy ester (e.g. tert-Buty… | Wikipedia: Category:Name reactions | |
| Kiliani–Fischer synthesis | The Kiliani–Fischer synthesis, named for German chemists Heinrich Kiliani and Emil Fischer, is a method for synthesizing monosaccharides. It proceeds via synthesis and hydrolysis of a cyanohydrin, fo… | Wikipedia: Category:Name reactions | |
| Kinnear–Perren reaction | In organophosphorus chemistry, the Kinnear–Perren reaction (sometimes the Clay-Kinnear-Perren reaction) is used to prepare alkylphosphonyl dichlorides (RP(O)Cl2) and alkylphosphonate esters (RP(O)(OR'… | Wikipedia: Category:Name reactions | |
| Kirsanov reaction | The Kirsanov reaction is a method for the synthesis of certain organophosphorus compounds. In this reaction a tertiary phosphine is combined with a halogen and then an amine to give the iminophosphin… | Wikipedia: Category:Name reactions | |
| Knoevenagel condensation Condensation | In organic chemistry, the Knoevenagel condensation (pronounced [ˈknøːvənaːɡl̩]) reaction is a type of chemical reaction named after German chemist Emil Knoevenagel. It is a modification of the aldol c… | Wikipedia: Category:Name reactions | |
| Knorr pyrrole synthesis | The Knorr pyrrole synthesis is a widely used chemical reaction that synthesizes substituted pyrroles (3). The method involves the reaction of an α-amino-ketone (1) and a compound containing an electro… | Wikipedia: Category:Name reactions | |
| Knorr quinoline synthesis | The Knorr quinoline synthesis is an intramolecular organic reaction converting a β-ketoanilide to a 2-hydroxyquinoline using sulfuric acid. This reaction was first described by Ludwig Knorr (1859–1921… | Wikipedia: Category:Name reactions | |
| Kochi reaction | The Kochi reaction is an organic reaction for the decarboxylation of carboxylic acids to alkyl halides with lead(IV) acetate and a lithium halide. | Wikipedia: Category:Name reactions | |
| Koch reaction | The Koch reaction is an organic reaction for the synthesis of tertiary carboxylic acids from alcohols or alkenes and carbon monoxide. Some commonly industrially produced Koch acids include pivalic aci… | Wikipedia: Category:Name reactions | |
| Koenigs–Knorr reaction | The Koenigs–Knorr reaction is the substitution reaction of a glycosyl halide with an alcohol to give a glycoside. It is one of the oldest glycosylation reactions. It is named after Wilhelm Koenigs (18… | Wikipedia: Category:Name reactions | |
| Kolbe electrolysis | The Kolbe electrolysis or Kolbe reaction is an organic reaction named after Hermann Kolbe. The Kolbe reaction is formally a decarboxylative dimerisation of two carboxylic acids (or carboxylate ions). … | Wikipedia: Category:Name reactions | |
| Kolbe nitrile synthesis | The Kolbe nitrile synthesis, named for Hermann Kolbe, is a method for the preparation of alkyl nitriles by reaction of the corresponding alkyl halide with a metal cyanide. A side product for this reac… | Wikipedia: Category:Name reactions | |
| Kolbe–Schmitt reaction | The Kolbe–Schmitt reaction or Kolbe process (named after Hermann Kolbe and Rudolf Schmitt) is a carboxylation chemical reaction that proceeds by treating phenol with sodium hydroxide to form sodium ph… | Wikipedia: Category:Name reactions | |
| Kornblum–DeLaMare rearrangement Rearrangement | The Kornblum–DeLaMare rearrangement is a rearrangement reaction in organic chemistry in which a primary or secondary organic peroxide is converted to the corresponding ketone and alcohol under acid or… | Wikipedia: Category:Name reactions | |
| Kornblum oxidation Oxidation | The Kornblum oxidation, named after Nathan Kornblum, is an organic oxidation reaction that converts alkyl halides and tosylates into carbonyl compounds. | Wikipedia: Category:Name reactions | |
| Kostanecki acylation | The Kostanecki acylation is a method used in organic synthesis to form chromones or coumarins by acylation of O-hydroxyaryl ketones with aliphatic acid anhydrides, followed by cyclization. If benzoic … | Wikipedia: Category:Name reactions |
