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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 |
|---|---|---|---|
| FLUORINATIONS WITH PYRIDINIUM POLYHYDROGEN FLUORIDE REAGENT: 1-FLUOROADAMANTANE (Tricyclo[3.3.1.13,7]decane, 1-fluoro-) | Preparation of Tricyclo[3.3.1.13,7]decane, 1-fluoro-. Submitted by George A. Olah1 and Michael Watkins. DOI: 10.15227/orgsyn.058.0075. | Organic Syntheses | |
| FLUOROBENZENE (Benzene, fluoro-) | Preparation of Benzene, fluoro-. Submitted by D. T. Flood. DOI: 10.15227/orgsyn.013.0046. | Organic Syntheses | |
| FORMAMIDINE ACETATE | Preparation of FORMAMIDINE ACETATE. Submitted by Edward C. Taylor, Wendell A. Ehrhart, and M. Kawanisi1. DOI: 10.15227/orgsyn.046.0039. | Organic Syntheses | |
| FORMATION AND PHOTOCHEMICAL WOLFF REARRANGEMENT OF CYCLIC α-DIAZO KETONES: D-NORANDROST-5-EN-3β-OL-16-CARBOXYLIC ACIDS (D-Norandrost-5-ene-16-carboxylic acids, 3β-hydroxy-, (3β,16α) and (3β,16β)-) Rearrangement | Preparation of D-Norandrost-5-ene-16-carboxylic acids, 3β-hydroxy-, (3β,16α) and (3β,16β)-. Submitted by Thomas N. Wheeler and J. Meinwald1. DOI: 10.15227/orgsyn.052.0053. | Organic Syntheses | |
| FORMATION OF γ-KETO ESTERS FROM β-KETO ESTERS: METHYL 5,5-DIMETHYL-4-OXOHEXANOATE (Hexanoic acid, 5,5-dimethyl-4-oxo-, methyl ester) | Preparation of Hexanoic acid, 5,5-dimethyl-4-oxo-, methyl ester. Submitted by Matthew D. Ronsheim, Ramona K. Hilgenkamp, and Charles K. Zercher1. DOI: 10.15227/orgsyn.079.0146. | Organic Syntheses | |
| Formose reaction | The formose reaction, discovered by Aleksandr Butlerov in 1861, and hence also known as the Butlerov reaction, involves the formation of sugars from formaldehyde. The term formose is a portmanteau of … | Wikipedia: Category:Name reactions | |
| FORMYL TRANSFER TO GRIGNARD REAGENTS WITH N-FORMYLPIPERIDINE: 3-PHENYLPROPIONALDEHYDE Organometallic addition | Preparation of FORMYL TRANSFER TO GRIGNARD REAGENTS WITH N-FORMYLPIPERIDINE: 3-PHENYLPROPIONALDEHYDE. Submitted by George A. Olah and Massoud Arvanaghi1. DOI: 10.15227/orgsyn.064.0114. | Organic Syntheses | |
| Forster–Decker method | The Forster–Decker method is a series of chemical reactions that have the effect of mono-alkylating a primary amine (1), forming a secondary amine (6). The process occurs by way of transient formation… | Wikipedia: Category:Name reactions | |
| FRAGMENTATION OF α,β-EPOXYKETONES TO ACETYLENIC ALDEHYDES AND KETONES: PREPARATION OF 2,3-EPOXYCYCLOHEXANONE AND ITS FRAGMENTATION TO 5-HEXYNAL (5-Hexynal) | Preparation of 5-Hexynal. Submitted by Dorothee Felix, Claude Wintner, and A. Eschenmoser1. DOI: 10.15227/orgsyn.055.0052. | Organic Syntheses | |
| FRAGMENTATION-RECOMBINATION NAZAROV CYCLIZATION: 3,4-DIMETHYLCYCLOPENT-2-EN-1-ONE Cyclization | Preparation of FRAGMENTATION-RECOMBINATION NAZAROV CYCLIZATION: 3,4-DIMETHYLCYCLOPENT-2-EN-1-ONE. Submitted by Keith D. Schwartz and James D. White1. DOI: 10.15227/orgsyn.083.0049. | Organic Syntheses | |
| Fráter–Seebach alkylation | In organic chemistry, the Fráter–Seebach alkylation (also known as Seebach–Fráter alkylation or Fráter–Seebach reaction) is a diastereoselective alkylation of chiral beta-hydroxy esters using strong b… | Wikipedia: Category:Name reactions | |
| FREE-RADICAL ALKYLATION OF QUINONES: 2-PHENOXYMETHYL-1,4-BENZOQUINONE (2,5-Cyclohexadiene-1,4-dione, 2-(phenoxymethyl)-) | Preparation of 2,5-Cyclohexadiene-1,4-dione, 2-(phenoxymethyl)-. Submitted by Niels Jacobsen1. DOI: 10.15227/orgsyn.056.0068. | Organic Syntheses | |
| FREE-RADICAL CYCLIZATION: ETHYL 1-CYANO-2-METHYLCYCLOHEXANECARBOXYLATE (Cyclohexanecarboxylic acid, 1-cyano-2-methyl-, ethyl ester) Cyclization | Preparation of Cyclohexanecarboxylic acid, 1-cyano-2-methyl-, ethyl ester. Submitted by Marc Julia and Michel Maumy1. DOI: 10.15227/orgsyn.055.0057. | Organic Syntheses | |
| Friedel-Crafts acylation: benzene + acetyl chloride → acetophenone Scale Electrophilic aromatic substitution | Textbook electrophilic aromatic substitution via the AlCl3-generated acylium ion. The product ketone (acetophenone) deactivates the ring toward further acylation, so unlike F-C alkylation, monoacylati… | Friedel-Crafts 1877 | |
| Friedel–Crafts reaction | The Friedel–Crafts reactions are a set of reactions developed by Charles Friedel and James Crafts in 1877 to attach substituents to an aromatic ring. Friedel–Crafts reactions are of two main types: al… | Wikipedia: Category:Name reactions | |
| Friedländer synthesis | The Friedländer synthesis is a chemical reaction of 2-aminobenzaldehydes with ketones to form quinoline derivatives. It is named after German chemist Paul Friedländer (1857–1923). | Wikipedia: Category:Name reactions | |
| Fries rearrangement Rearrangement | The Fries rearrangement, named for the German chemist Karl Theophil Fries, is a rearrangement reaction of a phenolic ester to a keto phenol. The reaction is induced by a Lewis acid. | Wikipedia: Category:Name reactions | |
| Fritsch–Buttenberg–Wiechell rearrangement Rearrangement | The Fritsch–Buttenberg–Wiechell rearrangement, named for Paul Ernst Moritz Fritsch (1859–1913), Wilhelm Paul Buttenberg, and Heinrich G. Wiechell, is a chemical reaction whereby a 1,1-diaryl-2-bromo-a… | Wikipedia: Category:Name reactions | |
| Fujimoto–Belleau reaction | The Fujimoto–Belleau reaction is a chemical reaction that forms cyclic α-substituted α,β-unsaturated ketones from enol lactones. The reaction was discovered in 1951 by George I. Fujimoto and Bernard B… | Wikipedia: Category:Name reactions | |
| Fujiwara–Moritani reaction | In organic chemistry, the Fujiwara–Moritani reaction is a type of cross coupling reaction where an aromatic C-H bond is directly coupled to an olefinic C-H bond, generating a new C-C bond. This reacti… | Wikipedia: Category:Name reactions | |
| Fukuyama coupling Cross-coupling | The Fukuyama coupling is a coupling reaction taking place between a thioester and an organozinc halide in the presence of a palladium catalyst. The reaction product is a ketone. This reaction was disc… | Wikipedia: Category:Name reactions | |
| Fukuyama indole synthesis | The Fukuyama indole synthesis is a versatile tin mediated chemical reaction that results in the formation of 2,3-disubstituted indoles. A practical one-pot reaction that can be useful for the creatio… | Wikipedia: Category:Name reactions | |
| Fukuyama reduction Reduction | The Fukuyama reduction is an organic reaction and an organic reduction in which a thioester is reduced to an aldehyde by a silyl hydride in presence of a catalytic amount of palladium. This reaction w… | Wikipedia: Category:Name reactions | |
| FUMARIC ACID | Preparation of FUMARIC ACID. Submitted by Nicholas A. Milas. DOI: 10.15227/orgsyn.011.0046. | Organic Syntheses | |
| FUMARONITRILE | Preparation of FUMARONITRILE. Submitted by David T. Mowry and John Mann Butler1. DOI: 10.15227/orgsyn.030.0046. | Organic Syntheses | |
| FUMARYL CHLORIDE | Preparation of FUMARYL CHLORIDE. Submitted by L. P. Kyrides. DOI: 10.15227/orgsyn.020.0051. | Organic Syntheses | |
| FURAN | Preparation of FURAN. Submitted by W. C. Wilson. DOI: 10.15227/orgsyn.007.0040. | Organic Syntheses | |
| FURFURAL (2-Furaldehyde) | Preparation of 2-Furaldehyde. Submitted by Roger Adams and V. Voorhees. DOI: 10.15227/orgsyn.001.0049. | Organic Syntheses | |
| FURFURAL DIACETATE (2-Furanmethanediol, diacetate) | Preparation of 2-Furanmethanediol, diacetate. Submitted by R. T. Bertz1. DOI: 10.15227/orgsyn.033.0039. | Organic Syntheses | |
| FURYLACRYLIC ACID (2-Furanacrylic acid) | Preparation of 2-Furanacrylic acid. Submitted by S. Rajagopalan and P. V. A. Raman. DOI: 10.15227/orgsyn.025.0051. | Organic Syntheses | |
| Gabriel–Colman rearrangement Rearrangement | The Gabriel–Colman rearrangement is the chemical reaction of a saccharin or phthalimido ester with a strong base, such as an alkoxide, to form substituted isoquinolines. First described in 1900 by che… | Wikipedia: Category:Name reactions | |
| Gabriel synthesis | The Gabriel synthesis is a chemical reaction that transforms primary alkyl halides into primary amines. Traditionally, the reaction uses potassium phthalimide. The reaction is named after the German c… | Wikipedia: Category:Name reactions | |
| GALLACETOPHENONE | Preparation of GALLACETOPHENONE. Submitted by I. C. Badhwar and K. Venkataraman. DOI: 10.15227/orgsyn.014.0040. | Organic Syntheses | |
| Gallagher–Hollander degradation | In the Gallagher–Hollander degradation (1946) pyruvic acid is removed from a linear aliphatic carboxylic acid yielding a new acid with two carbon atoms fewer. The original publication concerns the con… | Wikipedia: Category:Name reactions | |
| Ganem oxidation Oxidation | In organic chemistry, the Ganem oxidation is a name reaction that allows for the preparation of carbonyls from primary or secondary alkyl halides with the use of trialkylamine N-oxides, such as N-meth… | Wikipedia: Category:Name reactions | |
| Gattermann reaction | The Gattermann reaction (also known as the Gattermann formylation and the Gattermann salicylaldehyde synthesis) is a chemical reaction in which aromatic compounds are formylated by a mixture of hydro… | Wikipedia: Category:Name reactions | |
| GEMINAL ACYLATION-ALKYLATION AT A CARBONYL CENTER USING DIETHYL N-BENZYLIDENEAMINOMETHYLPHOSPHONATE: 2-METHYL-2-PHENYL-4-PENTENAL (4-Pentenal, 2-methyl-2-phenyl-) | Preparation of 4-Pentenal, 2-methyl-2-phenyl-. Submitted by Steven K. Davidsen, Gerald W. Phllips, and Stephen F. Martin1. DOI: 10.15227/orgsyn.065.0119. | Organic Syntheses | |
| GENERATION AND [2+2] CYCLOADDITIONS OF THIO-SUBSTITUTED KETENES: trans-1-(4-METHOXYPHENYL)-4-PHENYL-3-(PHENYLTHIO)AZETIDIN-2-ONE ((2-Azetidinone, 1-(4-methoxyphenyl)-4-phenyl-3-(phenylthio)-, trans-)) Cycloaddition | Preparation of (2-Azetidinone, 1-(4-methoxyphenyl)-4-phenyl-3-(phenylthio)-, trans-). Submitted by Rick L. Danheiser, Iwao Okamoto, Michael D. Lawlor, and Thomas W. Lee.1. DOI: 10.15227/orgsyn.080.016… | Organic Syntheses | |
| GENERATION AND CYCLIZATION OF 5-HEXENYLLITHIUM: 2-CYCLOPENTYLACETOPHENONE (Ethanone, 2-cyclopentyl-1-phenyl-) Cyclization | Preparation of Ethanone, 2-cyclopentyl-1-phenyl-. Submitted by William F. Bailey, Matthew R. Luderer, Michael J. Mealy, and Eric R. Punzalan1. DOI: 10.15227/orgsyn.081.0121. | Organic Syntheses | |
| GENERATION AND REACTIONS OF ALKENYLLITHIUM REAGENTS: 2-BUTYLBORNENE | Preparation of GENERATION AND REACTIONS OF ALKENYLLITHIUM REAGENTS: 2-BUTYLBORNENE. Submitted by A. Richard Chamberlin, Ellen L. Liotta, and F. Thomas Bond1. DOI: 10.15227/orgsyn.061.0141. | Organic Syntheses | |
| GENERATION AND USE OF LITHIUM PENTAFLUOROPROPEN-2-OLATE: 4-HYDROXY-1,1,1,3,3-PENTAFLUORO-2-HEXANONE HYDRATE (2,2,4-Hexanetriol, 1,1,1,3,3-pentafluoro- from 1-Propen-2-ol, 1,1,3,3,3-pentafluoro-, lithium salt) | Preparation of 2,2,4-Hexanetriol, 1,1,1,3,3-pentafluoro- from 1-Propen-2-ol, 1,1,3,3,3-pentafluoro-, lithium salt. Submitted by Cheng-Ping Qian, Yu-Zhong Liu, Katsuhiko Tomooka, and Takeshi Nakai1. DO… | Organic Syntheses | |
| GENERATION OF 1-PROPYNYLLITHIUM FROM (Z/E)-1-BROMO-1-PROPENE: 6-PHENYLHEX-2-YN-5-EN-4-OL (1-Hexen-4-yn-3-ol, 1-phenyl-, (E)-) | Preparation of 1-Hexen-4-yn-3-ol, 1-phenyl-, (E)-. Submitted by Dominique Toussaint and Jean Suffert1. DOI: 10.15227/orgsyn.076.0214. | Organic Syntheses | |
| GENERATION OF AN ACETYLENE-TITANIUM ALKOXIDE COMPLEX: PREPARATION OF (Z)-1,2-DIDEUTERIO-1-(TRIMETHYLSILYL)-1-HEXENE ((Silane, (1,2-dideuterio-1-hexenyl)trimethyl-, (Z)-)) | Preparation of (Silane, (1,2-dideuterio-1-hexenyl)trimethyl-, (Z)-). Submitted by Hirokazu Urabe, Daisuke Suzuki, and Fumie Sato1. DOI: 10.15227/orgsyn.080.0120. | Organic Syntheses | |
| GENERATION OF N,N-DIETHYLCARBAMOYLLITHIUM VIA LITHIUM-TELLURIUM EXCHANGE AND ITS REACTION WITH 3-PHENYLPROPANAL: N,N-DIETHYL-2-HYDROXY-4-PHENYLBUTANAMIDE (Benzenebutanamide, N,N-diethyl-α-hydroxy-) | Preparation of Benzenebutanamide, N,N-diethyl-α-hydroxy-. Submitted by Nobuaki Kambe, Toru Inoue, and Noboru Sonoda1. DOI: 10.15227/orgsyn.072.0154. | Organic Syntheses | |
| GENERATION OF NONRACEMIC 2-(t-BUTYLDIMETHYLSILYLOXY)-3-BUTYNYLLITHIUM FROM (S)-ETHYL LACTATE: ((S)-4-(t-BUTYLDIMETHYLSILYLOXY)-2-PENTYN-1-OL) | Preparation of (S)-4-(t-BUTYLDIMETHYLSILYLOXY)-2-PENTYN-1-OL. Submitted by James A. Marshall, Mathew M. Yanik, Nicholas D. Adams, Keith C. Ellis, and Harry R. Chobanian1. DOI: 10.15227/orgsyn.081.0157… | Organic Syntheses | |
| GENERATION OF YNOLATE AND Z-SELECTIVE OLEFINATION OF ACYLSILANES: (Z)-2-METHYL-3-TRIMETHYLSILYL-2-BUTENOIC ACID ((Z)-2-Butenoic acid, 2-methyl-3-trimethylsilyl-) Olefination | Preparation of (Z)-2-Butenoic acid, 2-methyl-3-trimethylsilyl-. Submitted by Mitsuru Shindo1, Kenji Matsumoto2, and Kozo Shishido2. DOI: 10.15227/orgsyn.084.0011. | Organic Syntheses | |
| GERANYL CHLORIDE (2,6-Octadiene, 1-chloro-3,7-dimethyl-, (E)-) | Preparation of 2,6-Octadiene, 1-chloro-3,7-dimethyl-, (E)-. Submitted by Jose G. Calzada and John Hooz1. DOI: 10.15227/orgsyn.054.0063. | Organic Syntheses | |
| Gewald reaction | The Gewald reaction (or the Gewald aminothiophene synthesis) is an organic reaction involving the condensation of a ketone (or aldehyde when R2 = H) with a α-cyanoester in the presence of elemental su… | Wikipedia: Category:Name reactions | |
| Girdler sulfide process | The Girdler sulfide (GS) process, also known as the Geib–Spevack (GS) process, is an industrial production method for extracting heavy water (deuterium oxide, D2O) from natural water. Heavy water is … | Wikipedia: Category:Name reactions | |
| Glaser coupling Cross-coupling | The Glaser coupling is a type of coupling reaction. It is by far one of the oldest coupling reactions and is based on copper compounds like copper(I) chloride or copper(I) bromide and an additional ox… | Wikipedia: Category:Name reactions |
