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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 |
|---|---|---|---|
| GLUTACONALDEHYDE SODIUM SALT FROM HYDROLYSIS OF PYRIDINIUM-1-SULFONATE (2-Pentenedial, ion (1−), sodium) Hydrolysis | Preparation of 2-Pentenedial, ion (1−), sodium. Submitted by Jan Becher1. DOI: 10.15227/orgsyn.059.0079. | Organic Syntheses | |
| GLUTARIC ACID ((A) (from Trimethylene Cyanide)) | Preparation of (A) (from Trimethylene Cyanide). Submitted by C. S. Marvel and W. F. Tuley. DOI: 10.15227/orgsyn.010.0058. | Organic Syntheses | |
| GLUTARIC ACID AND GLUTARIMIDE (1. FROM γ-BUTYROLACTONE) | Preparation of 1. FROM γ-BUTYROLACTONE. Submitted by G. Paris, L. Berlinguet, and R. Gaudry1. DOI: 10.15227/orgsyn.037.0047. | Organic Syntheses | |
| GLYCEROL α-MONOCHLOROHYDRIN (1,2-Propanediol, 3-chloro-) | Preparation of 1,2-Propanediol, 3-chloro-. Submitted by J. B. Conant and O. R. Quayle. DOI: 10.15227/orgsyn.002.0033. | Organic Syntheses | |
| GLYCEROL α,γ-DIBROMOHYDRIN (2-Propanol, 1,3-dibromo-) | Preparation of 2-Propanol, 1,3-dibromo-. Submitted by Géza Braun. DOI: 10.15227/orgsyn.014.0042. | Organic Syntheses | |
| GLYCEROL α,γ-DICHLOROHYDRIN (2-Propanol, 1,3-dichloro-) | Preparation of 2-Propanol, 1,3-dichloro-. Submitted by J. B. Conant and O. R. Quayle. DOI: 10.15227/orgsyn.002.0029. | Organic Syntheses | |
| GLYCINE ((A) (from Methyleneaminoacetonitrile)) | Preparation of (A) (from Methyleneaminoacetonitrile). Submitted by W. K. Anslow and Harold King. DOI: 10.15227/orgsyn.004.0031. | Organic Syntheses | |
| GLYCINE ETHYL ESTER HYDROCHLORIDE | Preparation of GLYCINE ETHYL ESTER HYDROCHLORIDE. Submitted by C. S. Marvel. DOI: 10.15227/orgsyn.014.0046. | Organic Syntheses | |
| GLYCINE t-BUTYL ESTER | Preparation of GLYCINE t-BUTYL ESTER. Submitted by A. T. Moore and H. N. Rydon1. DOI: 10.15227/orgsyn.045.0047. | Organic Syntheses | |
| Glycolonitrile | Preparation of Glycolonitrile. Submitted by Roger Gaudry. DOI: 10.15227/orgsyn.027.0041. | Organic Syntheses | |
| GLYOXAL BISULFITE | Preparation of GLYOXAL BISULFITE. Submitted by Anthony R. Ronzio and T. D. Waugh. DOI: 10.15227/orgsyn.024.0061. | Organic Syntheses | |
| Gold(I)-Catalyzed Decarboxylative Allylic Amination of Allylic N-Tosylcarbamates | Preparation of Gold(I)-Catalyzed Decarboxylative Allylic Amination of Allylic N-Tosylcarbamates. Submitted by Dong Xing and Dan Yang1. DOI: 10.15227/orgsyn.089.0450. | Organic Syntheses | |
| Gomberg–Bachmann reaction | The Gomberg–Bachmann reaction, named for the Russian-American chemist Moses Gomberg and the American chemist Werner Emmanuel Bachmann, is an aryl-aryl coupling reaction via a diazonium salt. | Wikipedia: Category:Name reactions | |
| Gould–Jacobs reaction | The Gould–Jacobs reaction is an organic synthesis for the preparation of quinolines and 4‐hydroxyquinoline derivatives. The Gould–Jacobs reaction is a series of reactions. The series of reactions begi… | Wikipedia: Category:Name reactions | |
| GRAM SCALE CATALYTIC ASYMMETRIC AZIRIDINATION: PREPARATION OF (2R,3R)-ETHYL 1-BENZHYDRYL-3-(4-BROMOPHENYL)AZIRIDINE 2-CARBOXYLATE | Preparation of GRAM SCALE CATALYTIC ASYMMETRIC AZIRIDINATION: PREPARATION OF (2R,3R)-ETHYL 1-BENZHYDRYL-3-(4-BROMOPHENYL)AZIRIDINE 2-CARBOXYLATE. Submitted by Aman A. Desai, Roberto Morán-Ramallal, an… | Organic Syntheses | |
| Grieco elimination Elimination | The Grieco elimination is an organic reaction describing the elimination reaction of an aliphatic primary alcohol through a selenide to a terminal alkene. It is named for Paul Grieco. | Wikipedia: Category:Name reactions | |
| Grieco three-component condensation Condensation | The Grieco three-component condensation is an organic chemistry reaction that produces nitrogen-containing six-member heterocycles via a multi-component reaction of an aldehyde, a nitrogen component, … | Wikipedia: Category:Name reactions | |
| Griesbaum coozonolysis Oxidation | The Griesbaum coozonolysis is a name reaction in organic chemistry that allows for the preparation of tetrasubstituted ozonides (1,2,4-trioxolanes) by the reaction of O-methyl oximes with a carbonyl c… | Wikipedia: Category:Name reactions | |
| Grignard addition: phenylmagnesium bromide + benzaldehyde → diphenylmethanol Scale Organometallic addition | Textbook Grignard addition. Phenylmagnesium bromide (PhMgBr) attacks benzaldehyde's carbonyl carbon; aqueous acidic workup releases diphenylmethanol (benzhydrol). PhMgBr is bought as a 1 M or 3 M solu… | Grignard 1900 | |
| Grignard reaction Organometallic addition | The Grignard reaction (French: [ɡʁiɲaʁ]) is an organometallic chemical reaction in which, according to the classical definition, carbon alkyl, allyl, vinyl, or aryl magnesium halides (Grignard reagent… | Wikipedia: Category:Name reactions | |
| Grob fragmentation | A Grob fragmentation is an elimination reaction that breaks a neutral aliphatic chain into three fragments: a positive ion spanning atoms 1 and 2 (the "electrofuge"), an unsaturated neutral fragment s… | Wikipedia: Category:Name reactions | |
| Grundmann aldehyde synthesis | The Grundmann aldehyde synthesis is a chemical reaction that produces an aldehyde from an acyl halide. | Wikipedia: Category:Name reactions | |
| GUANIDINE NITRATE | Preparation of GUANIDINE NITRATE. Submitted by Tenney L. Davis. DOI: 10.15227/orgsyn.007.0046. | Organic Syntheses | |
| GUANIDOACETIC ACID (Glycocyamine) | Preparation of Glycocyamine. Submitted by E. Brand and F. C. Brand. DOI: 10.15227/orgsyn.022.0059. | Organic Syntheses | |
| GUANYLTHIOUREA (Urea, 1-amidino-2-thio-) | Preparation of Urea, 1-amidino-2-thio-. Submitted by Frederick Kurzer1. DOI: 10.15227/orgsyn.035.0069. | Organic Syntheses | |
| Guerbet reaction | The Guerbet reaction, named after Marcel Guerbet (1861–1938), is an organic reaction that converts a primary alcohol into its β-alkylated dimer alcohol with loss of one equivalent of water. The proces… | Wikipedia: Category:Name reactions | |
| Haber process | The Haber process, also called the Haber–Bosch process, is the main industrial procedure for the production of ammonia. It converts atmospheric nitrogen (N2) to ammonia (NH3) by a reaction with hydrog… | Wikipedia: Category:Name reactions | |
| Haber–Weiss reaction | The Haber–Weiss reaction generates •OH (hydroxyl radicals) from H2O2 (hydrogen peroxide) and superoxide (•O2−) catalyzed by iron ions. It was first proposed by Fritz Haber and his student Joseph Joshu… | Wikipedia: Category:Name reactions | |
| Hammick reaction | The Hammick reaction, named after Dalziel Hammick, is a chemical reaction in which the thermal decarboxylation of α-picolinic (or related) acids in the presence of carbonyl compounds forms 2-pyridyl-c… | Wikipedia: Category:Name reactions | |
| Hantzsch pyridine synthesis | The Hantzsch pyridine synthesis or Hantzsch dihydropyridine synthesis is a multi-component organic reaction between an aldehyde such as formaldehyde, 2 equivalents of a β-keto ester such as ethyl acet… | Wikipedia: Category:Name reactions | |
| Hantzsch pyrrole synthesis | The Hantzsch Pyrrole Synthesis, named for Arthur Rudolf Hantzsch, is the chemical reaction of β-ketoesters (1) with ammonia (or primary amines) and α-haloketones (2) to give substituted pyrroles (3). | Wikipedia: Category:Name reactions | |
| Hass–Bender oxidation Oxidation | In organic chemistry, the Hass–Bender oxidation (also called the Hass–Bender carbonyl synthesis) is an organic oxidation reaction that converts benzyl halides into benzaldehydes using the sodium salt … | Wikipedia: Category:Name reactions | |
| Hayashi rearrangement Rearrangement | The Hayashi rearrangement is the chemical reaction of ortho-benzoylbenzoic acids catalyzed by sulfuric acid or phosphorus pentoxide. | Wikipedia: Category:Name reactions | |
| Heck–Matsuda reaction Cross-coupling | The Heck–Matsuda (HM) reaction is an organic reaction and a type of palladium catalysed arylation of olefins that uses arenediazonium salts as an alternative to aryl halides and triflates. | Wikipedia: Category:Name reactions | |
| Heck reaction Cross-coupling | The Heck reaction (also called the Mizoroki–Heck reaction) is the chemical reaction of an unsaturated halide (or triflate) with an alkene in the presence of a base and a palladium catalyst to form a … | Wikipedia: Category:Name reactions | |
| HECK REACTIONS OF ARYL CHLORIDES CATALYZED BY PALLADIUM/TRI-tert-BUTYLPHOSPHINE: (E)-2-METHYL-3-PHENYLACRYLIC ACID BUTYL ESTER AND (E)-4-(2-PHENYLETHENYL)BENZONITRILE (2-Propenoic acid, 2-methyl-3-phenyl-, butyl ester and Benzonitrile, 4-[(1E)-2-phenylethenyl]) Cross-coupling | Preparation of 2-Propenoic acid, 2-methyl-3-phenyl-, butyl ester and Benzonitrile, 4-[(1E)-2-phenylethenyl]. Submitted by Adam F. Littke and Gregory C. Fu1. DOI: 10.15227/orgsyn.081.0063. | Organic Syntheses | |
| Hegedus indole synthesis | The Hegedus indole synthesis is a name reaction in organic chemistry that allows for the generation of indoles through palladium(II)-mediated oxidative cyclization of ortho-alkenyl anilines. The react… | Wikipedia: Category:Name reactions | |
| HELICENEBISQUINONES: SYNTHESIS OF A [7]HELICENEBISQUINONE ((Dinaphtho[2,1-c:1',2'-g]phenanthrene-1,4,15,18-tetrone, 9,10-dimethoxy-6,13-bis[[tris(1-methylethyl)silyl]oxy]-)) | Preparation of (Dinaphtho[2,1-c:1',2'-g]phenanthrene-1,4,15,18-tetrone, 9,10-dimethoxy-6,13-bis[[tris(1-methylethyl)silyl]oxy]-). Submitted by Kamil Paruch, Libor Vyklicky, and Thomas J. Katz1. DOI: 1… | Organic Syntheses | |
| Hell–Volhard–Zelinsky halogenation Halogenation | The Hell–Volhard–Zelinsky halogenation reaction is a chemical transformation that transforms an alkyl carboxylic acid to the α-bromo derivative. It is a specialized and rare kind of halogenation. | Wikipedia: Category:Name reactions | |
| Hemetsberger indole synthesis | The Hemetsberger indole synthesis (also called the Hemetsberger–Knittel synthesis) is a chemical reaction that thermally decomposes a 3-aryl-2-azido-propenoic ester into an indole-2-carboxylic ester. | Wikipedia: Category:Name reactions | |
| HEMIMELLITENE (Benzene, 1,2,3-trimethyl-) | Preparation of Benzene, 1,2,3-trimethyl-. Submitted by W. R. Brasen and C. R. Hauser1. DOI: 10.15227/orgsyn.034.0056. | Organic Syntheses | |
| HEMIN | Preparation of HEMIN. Submitted by Hans Fischer. DOI: 10.15227/orgsyn.021.0053. | Organic Syntheses | |
| HENDECANEDIOIC ACID (Undecanedioic acid) | Preparation of Undecanedioic acid. Submitted by Lois J. Durham, Donald J. McLeod, and James Cason1. DOI: 10.15227/orgsyn.038.0034. | Organic Syntheses | |
| Henry reaction | The Henry reaction is a classic carbon–carbon bond formation reaction in organic chemistry. Discovered in 1895 by the Belgian chemist Louis Henry (1834–1913), it is the combination of a nitroalkane an… | Wikipedia: Category:Name reactions | |
| Henry reaction (nitroaldol addition) Scale Addition | Base-catalysed addition of a nitroalkane to an aldehyde to give a β-nitro alcohol that dehydrates under Knoevenagel-Henry conditions to the conjugated nitroalkene. Default example here is the textbook… | Henry 1895 | |
| HEPTALDOXIME (Enanthaldehyde oxime) | Preparation of Enanthaldehyde oxime. Submitted by E. W. Bousquet. DOI: 10.15227/orgsyn.011.0054. | Organic Syntheses | |
| Herz reaction | The Herz reaction, named after the chemist Richard Herz, is the chemical conversion of an aniline to the benzodithiazolium salt by its reaction with disulfur dichloride. The salt is called a Herz sal… | Wikipedia: Category:Name reactions | |
| Hexadehydro Diels–Alder reaction | In organic chemistry, the hexadehydro-Diels–Alder (HDDA) reaction is an organic chemical reaction between a diyne (2 alkyne functional groups arranged in a conjugated system) and an alkyne to form a r… | Wikipedia: Category:Name reactions | |
| HEXAFLUOROACETONE (2-Propanone, 1,1,1,3,3,3-hexafluoro-) | Preparation of 2-Propanone, 1,1,1,3,3,3-hexafluoro-. Submitted by Michael Van Der Puy and Louis G. Anello1. DOI: 10.15227/orgsyn.063.0154. | Organic Syntheses | |
| HEXAFLUOROACETONE IMINE (2-Propanimine, 1,1,1,3,3,3-hexafluoro-) | Preparation of 2-Propanimine, 1,1,1,3,3,3-hexafluoro-. Submitted by W. J. Middleton1 and H. D. Carlson. DOI: 10.15227/orgsyn.050.0081. | Organic Syntheses |
