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 |
|---|---|---|---|
| ETHYL PYRUVATE (Pyruvic acid, ethyl ester) | Preparation of Pyruvic acid, ethyl ester. Submitted by J. W. Cornforth1. DOI: 10.15227/orgsyn.031.0059. | Organic Syntheses | |
| ETHYL (R)-2-AZIDOPROPIONATE (Propanoic acid, 2-azido-, ethyl ester, (R)-) | Preparation of Propanoic acid, 2-azido-, ethyl ester, (R)-. Submitted by Andrew S. Thompson, Frederick W. Hartner, Jr., and Edward J. J. Grabowski1. DOI: 10.15227/orgsyn.075.0031. | Organic Syntheses | |
| ETHYL tert-BUTYL MALONATE (Malonic acid, tert-butyl ethyl ester) | Preparation of Malonic acid, tert-butyl ethyl ester. Submitted by R. E. Strube1. DOI: 10.15227/orgsyn.037.0034. | Organic Syntheses | |
| ETHYL α-(1-PYRROLIDYL)PROPIONATE (1-Pyrrolidineacetic acid, α-methyl-, ethyl ester) | Preparation of 1-Pyrrolidineacetic acid, α-methyl-, ethyl ester. Submitted by Robert Bruce Moffett1. DOI: 10.15227/orgsyn.033.0035. | Organic Syntheses | |
| ETHYL α-ACETYL-β-(2,3-DIMETHOXYPHENYL)-PROPIONATE (Hydrocinnamic acid, α-acetyl-2,3-dimethoxy-, ethyl ester) | Preparation of Hydrocinnamic acid, α-acetyl-2,3-dimethoxy-, ethyl ester. Submitted by E. C. Horning, J. Koo, M. S. Fish, and G. N. Walker1. DOI: 10.15227/orgsyn.031.0056. | Organic Syntheses | |
| ETHYL α-(BROMOMETHYL)ACRYLATE (2-Propenoic acid, 2-(bromomethyl)-,ethyl ester) | Preparation of 2-Propenoic acid, 2-(bromomethyl)-,ethyl ester. Submitted by K. Ramarajan, K. Ramalingam, D. J. O'Donnell, and K. D. Berlin1. DOI: 10.15227/orgsyn.061.0056. | Organic Syntheses | |
| ETHYL α-(HEXAHYDROAZEPINYLIDENE-2)ACETATE FROM O-METHYLCAPROLACTIM AND MELDRUM'S ACID (Acetic acid, (hexahydro-2H-azepin-2-ylidene)-, ethyl ester, (Z)-) | Preparation of Acetic acid, (hexahydro-2H-azepin-2-ylidene)-, ethyl ester, (Z)-. Submitted by J. P. Celerier, E. Deloisy-Marchalant, G. Lhommet, and P. Maitte1. DOI: 10.15227/orgsyn.067.0170. | Organic Syntheses | |
| ETHYL α-(HYDROXYMETHYL)ACRYLATE (2-Propenoic acid, 2-(hydroxymethyl)-, ethyl ester) | Preparation of 2-Propenoic acid, 2-(hydroxymethyl)-, ethyl ester. Submitted by J. Villieras and M Rambaud1. DOI: 10.15227/orgsyn.066.0220. | Organic Syntheses | |
| ETHYL α-ISOPROPYLACETOACETATE (Isovaleric acid, α-acetyl, ethyl ester) | Preparation of Isovaleric acid, α-acetyl, ethyl ester. Submitted by Joe T. Adams, Robert Levine, and Charles R. Hauser. DOI: 10.15227/orgsyn.027.0035. | Organic Syntheses | |
| ETHYL α-NAPHTHOATE (1-Naphthoic acid, ethyl ester) | Preparation of 1-Naphthoic acid, ethyl ester. Submitted by Frank C. Whitmore and D. J. Loder. DOI: 10.15227/orgsyn.000.0003. | Organic Syntheses | |
| ETHYL α-NITROBUTYRATE (Butyric acid, 2-nitro-, ethyl ester) | Preparation of Butyric acid, 2-nitro-, ethyl ester. Submitted by Nathan Kornblum and Robert K. Blackwood1. DOI: 10.15227/orgsyn.037.0044. | Organic Syntheses | |
| ETHYL α-PHENYLACETOACETATE (α-Toluic acid, α-acetyl-, ethyl ester) | Preparation of α-Toluic acid, α-acetyl-, ethyl ester. Submitted by R. H. Kimball, George D. Jefferson, and Arthur B. Pike. DOI: 10.15227/orgsyn.018.0036. | Organic Syntheses | |
| ETHYL α,β-DIBROMO-β-PHENYLPROPIONATE (Hydrocinnamic acid, α,β-dibromo-, ethyl ester) | Preparation of Hydrocinnamic acid, α,β-dibromo-, ethyl ester. Submitted by T. W. Abbott and Darrell Althousen. DOI: 10.15227/orgsyn.012.0036. | Organic Syntheses | |
| ETHYL β-ANILINOCROTONATE (Crotonic acid, β-anilino-, ethyl ester) | Preparation of Crotonic acid, β-anilino-, ethyl ester. Submitted by George A. Reynolds and Charles R. Hauser. DOI: 10.15227/orgsyn.029.0042. | Organic Syntheses | |
| ETHYL β-BROMOPROPIONATE (Propionic acid, β-bromo-, ethyl ester) | Preparation of Propionic acid, β-bromo-, ethyl ester. Submitted by E. C. Kendall and B. McKenzie. DOI: 10.15227/orgsyn.003.0051. | Organic Syntheses | |
| ETHYL β-HYDROXY-β,β-DIPHENYLPROPIONATE (Hydracrylic acid, 3,3-diphenyl, ethyl ester) | Preparation of Hydracrylic acid, 3,3-diphenyl, ethyl ester. Submitted by W. R. Dunnavant and Charles R. Hauser1. DOI: 10.15227/orgsyn.044.0056. | Organic Syntheses | |
| ETHYL β-PHENYL-β-HYDROXYPROPIONATE (Hydracrylic acid, β-phenyl-, ethyl ester) | Preparation of Hydracrylic acid, β-phenyl-, ethyl ester. Submitted by Charles R. Hauser and David S. Breslow. DOI: 10.15227/orgsyn.021.0051. | Organic Syntheses | |
| ETHYL β,β-PENTAMETHYLENEGLYCIDATE (1-Oxaspiro[2.5]octane-2-carboxylic acid, ethyl ester) | Preparation of 1-Oxaspiro[2.5]octane-2-carboxylic acid, ethyl ester. Submitted by Richard H. Hunt, Leland J. Chinn, and William S. Johnson1. DOI: 10.15227/orgsyn.034.0054. | Organic Syntheses | |
| ETHYL γ-BROMOBUTYRATE (Butyric acid, γ-bromo-, ethyl ester) | Preparation of Butyric acid, γ-bromo-, ethyl ester. Submitted by J. Lavety and G. R. Proctor1. DOI: 10.15227/orgsyn.045.0042. | Organic Syntheses | |
| ETHYNYL p-TOLYL SULFONE (Benzene, 1-(ethynylsulfonyl)-4-methyl-) | Preparation of Benzene, 1-(ethynylsulfonyl)-4-methyl-. Submitted by Liladhar Waykole and Leo A. Paquette1. DOI: 10.15227/orgsyn.067.0149. | Organic Syntheses | |
| Evans–Saksena reduction Reduction | The Saksena–Evans reduction is a diastereoselective reduction of β-hydroxy ketones to the corresponding anti-dialcohols, employing the reagent tetramethylammonium triacetoxyborohydride (Me4NHB(OAc)3).… | Wikipedia: Category:Name reactions | |
| Evans–Tishchenko reaction Disproportionation | The Evans–Tishchenko reaction is the diastereoselective reduction of β-hydroxy ketones to the corresponding 1,3-anti diol monoesters. The reaction employs a Lewis acid, often samarium iodide, and an a… | Wikipedia: Category:Name reactions | |
| exo-cis-BICYCLO[3.3.0]OCTANE-2-CARBOXYLIC ACID (1-Pentalenecarboxylic acid, octahydro-) | Preparation of 1-Pentalenecarboxylic acid, octahydro-. Submitted by R. Dowbenko1. DOI: 10.15227/orgsyn.047.0010. | Organic Syntheses | |
| exo/endo-7-NORCARANOL | Preparation of exo/endo-7-NORCARANOL. Submitted by U. Schöllkopf, J. Paust, and M. R. Patsch1. DOI: 10.15227/orgsyn.049.0086. | Organic Syntheses | |
| (E,Z)-1-METHOXY-2-METHYL-3-(TRIMETHYLSILOXY)-1,3-PENTADIENE (Silane, [[1-(2-methoxy-1-methylethenyl)-1-propenyl]oxy]trimethyl-, (Z,E)-) | Preparation of Silane, [[1-(2-methoxy-1-methylethenyl)-1-propenyl]oxy]trimethyl-, (Z,E)-. Submitted by David C. Myles and Mathew H. Bigham1,2. DOI: 10.15227/orgsyn.070.0231. | Organic Syntheses | |
| FACILE SYNTHESES OF AMINOCYCLOPROPANES: N,N-DIBENZYL-N-(2-ETHENYLCYCLOPROPYL)AMINE ((Benzenemethanamine, N-(2-ethenylcyclopropyl)-N-(phenylmethyl)-) | Preparation of (Benzenemethanamine, N-(2-ethenylcyclopropyl)-N-(phenylmethyl)-. Submitted by Armin de Meijere, Harald Winsel, and Björn Stecker1. DOI: 10.15227/orgsyn.081.0014. | Organic Syntheses | |
| FACILE SYNTHESIS OF 2-ETHYL-3-QUINOLINECARBOXYLIC ACID HYDROCHLORIDE | Preparation of FACILE SYNTHESIS OF 2-ETHYL-3-QUINOLINECARBOXYLIC ACID HYDROCHLORIDE. Submitted by Brian R. McNaughton and Benjamin L. Miller1. DOI: 10.15227/orgsyn.085.0027. | Organic Syntheses | |
| Favorskii reaction | The Favorskii reaction is an organic chemistry reaction between an alkyne and a carbonyl group, under basic conditions. The reaction was discovered in the early 1900s by the Russian chemist Alexei Yev… | Wikipedia: Category:Name reactions | |
| Favorskii rearrangement Rearrangement | In organic chemistry, the Favorskii rearrangement is a reaction of α-halo ketones with a nucleophilic base to acyl derivatives. In the rearrangement, the substrate extrudes the carbonyl carbon to a p… | Wikipedia: Category:Name reactions | |
| Feist–Benary synthesis | The Feist–Benary synthesis is an organic reaction between α-halo ketones and β-dicarbonyl compounds to produce substituted furan compounds. This condensation reaction is catalyzed by amines such as am… | Wikipedia: Category:Name reactions | |
| Fenton's reagent | Fenton's reagent is a solution of hydrogen peroxide (H2O2) and an iron catalyst (typically iron(II) sulfate, FeSO4). It is used to oxidize contaminants or waste water as part of an advanced oxidation … | Wikipedia: Category:Name reactions | |
| Ferrario–Ackermann reaction | In organic chemistry, the Ferrario–Ackermann reaction or simply the Ferrario reaction is a name reaction that allow for the generation of phenoxathiin from diphenyl ether and sulfur in the presence of… | Wikipedia: Category:Name reactions | |
| Ferrier carbocyclization Cyclization | The Ferrier carbocyclization (or Ferrier II reaction) is an organic reaction that was first reported by the carbohydrate chemist Robert J. Ferrier in 1979. It is a metal-mediated rearrangement of eno… | Wikipedia: Category:Name reactions | |
| Ferrier rearrangement Rearrangement | The Ferrier rearrangement is an organic reaction that involves a nucleophilic substitution reaction combined with an allylic shift in a glycal (a 2,3-unsaturated glycoside). It was discovered by the c… | Wikipedia: Category:Name reactions | |
| FERROCENE (Iron, dicyclopentadienyl-) | Preparation of Iron, dicyclopentadienyl-. Submitted by G. Wilkinson1. DOI: 10.15227/orgsyn.036.0031. | Organic Syntheses | |
| FERROCENYLACETONITRILE (Iron, [(cyanomethyl)cyclopentadienyl]cyclopentadienyl) | Preparation of Iron, [(cyanomethyl)cyclopentadienyl]cyclopentadienyl. Submitted by Daniel Lednicer and Charles R. Hauser1. DOI: 10.15227/orgsyn.040.0045. | Organic Syntheses | |
| Fétizon oxidation Oxidation | Fétizon oxidation is the oxidation of primary and secondary alcohols utilizing the compound silver(I) carbonate absorbed onto the surface of celite also known as Fétizon's reagent first employed by Ma… | Wikipedia: Category:Name reactions | |
| Fiesselmann thiophene synthesis | The Fiesselmann thiophene synthesis is a name reaction in organic chemistry that allows for the generation of 3-hydroxy-2-thiophenecarboxylic acid derivatives from α,β-acetylenic esters with thioglyco… | Wikipedia: Category:Name reactions | |
| Finkelstein reaction Substitution | The Finkelstein reaction, named after the German chemist Hans Finkelstein, is a type of SN2 reaction (substitution nucleophilic bimolecular reaction) that involves the exchange of one halogen atom for… | Wikipedia: Category:Name reactions | |
| Fischer assay | The Fischer assay is a standardized laboratory test for determining the oil yield from oil shale to be expected from a conventional shale oil extraction. A 100 gram oil shale sample crushed to <2.38 … | Wikipedia: Category:Name reactions | |
| Fischer glycosidation | Fischer glycosidation (or Fischer glycosylation) refers to the formation of a glycoside by the reaction of an aldose or ketose with an alcohol in the presence of an acid catalyst. The reaction is name… | Wikipedia: Category:Name reactions | |
| Fischer–Hepp rearrangement Rearrangement | In organic chemistry, the Fischer–Hepp rearrangement is a rearrangement reaction in which an aromatic N-nitroso (−N=O) or secondary nitrosamine (>N−N=O) converts to a carbon nitroso compound: | Wikipedia: Category:Name reactions | |
| Fischer indole synthesis | The Fischer indole synthesis is a chemical reaction that produces the aromatic heterocycle indole from a (substituted) phenylhydrazine and an aldehyde or ketone under acidic conditions. The reaction w… | Wikipedia: Category:Name reactions | |
| Fischer oxazole synthesis | The Fischer oxazole synthesis is a chemical synthesis of an oxazole from a cyanohydrin and an aldehyde in the presence of anhydrous hydrochloric acid. This method was discovered by Emil Fischer in 189… | Wikipedia: Category:Name reactions | |
| Fischer–Speier esterification | Fischer esterification or Fischer–Speier esterification is a special type of esterification by refluxing a carboxylic acid and an alcohol in the presence of an acid catalyst. The reaction was first de… | Wikipedia: Category:Name reactions | |
| Fischer–Tropsch process | The Fischer–Tropsch process (FT) is a collection of chemical reactions that converts a mixture of carbon monoxide and hydrogen, known as syngas, into liquid hydrocarbons. These reactions occur in the … | Wikipedia: Category:Name reactions | |
| FLAVONE (Method 1) | Preparation of Method 1. Submitted by T. S. Wheeler1. DOI: 10.15227/orgsyn.032.0072. | Organic Syntheses | |
| Fleming–Tamao oxidation Oxidation | The Fleming–Tamao oxidation, or Tamao–Kumada–Fleming oxidation, converts a carbon–silicon bond to a carbon–oxygen bond with a peroxy acid or hydrogen peroxide. Fleming–Tamao oxidation refers to two sl… | Wikipedia: Category:Name reactions | |
| FLUORENONE-2-CARBOXYLIC ACID (2-Fluorenecarboxylic acid, 9-oxo-) | Preparation of 2-Fluorenecarboxylic acid, 9-oxo-. Submitted by George Rieveschl, Jr. and F. E. Ray. DOI: 10.15227/orgsyn.028.0063. | Organic Syntheses | |
| Fluoride Ring-Opening Kinetic Resolution of Terminal Epoxides: Preparation of (S)-2-Fluoro-1-Phenylethanol | Preparation of Fluoride Ring-Opening Kinetic Resolution of Terminal Epoxides: Preparation of (S)-2-Fluoro-1-Phenylethanol. Submitted by Travis W.Shaw, Julia A.Kalow, and Abigail G.Doyle1. DOI: 10.1522… | Organic Syntheses |
