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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 |
|---|---|---|---|
| MACROLIDES FROM CYCLIZATION OF ω-BROMOCARBOXYLIC ACIDS: 11-HYDROXYUNDECANOIC LACTONE (Oxacyclododecan-2-one) Cyclization | Preparation of Oxacyclododecan-2-one. Submitted by C. Galli and L. Mandolini1. DOI: 10.15227/orgsyn.058.0098. | Organic Syntheses | |
| Madelung synthesis | In organic chemistry, Madelung synthesis is a chemical reaction that produces (substituted or unsubstituted) indoles by the intramolecular cyclization of N-phenylamides using strong base at high tempe… | Wikipedia: Category:Name reactions | |
| MAGNESIATION OF WEAKLY ACTIVATED ARENES USING tmp2Mg·2LiCl: SYNTHESIS OF TERT-BUTYL ETHYL PHTHALATE | Preparation of MAGNESIATION OF WEAKLY ACTIVATED ARENES USING tmp2Mg·2LiCl: SYNTHESIS OF TERT-BUTYL ETHYL PHTHALATE. Submitted by Christoph J. Rohbogner1, Andreas J. Wagner1, Giuliano C. Clososki2, and… | Organic Syntheses | |
| Maillard reaction | The Maillard reaction ( MY-ar; French: [majaʁ]) is a chemical reaction between amino acids and reducing sugars to create melanoidins, the compounds that give browned food its distinctive flavor. Seare… | Wikipedia: Category:Name reactions | |
| Malaprade reaction | In organic chemistry, the Malaprade reaction or Malaprade oxidation is a reaction that converts vicinal diols by periodic acid or a periodate salt to give a pair of carbonyl derivatives. The reaction … | Wikipedia: Category:Name reactions | |
| Mallory reaction | In organic chemistry, the Mallory reaction is a photochemical-cyclization–elimination reaction of diaryl-ethylene structures to form phenanthrenes and other polycyclic form polycyclic aromatic hydroca… | Wikipedia: Category:Name reactions | |
| MALONIC ACID | Preparation of MALONIC ACID. Submitted by Nathan Weiner. DOI: 10.15227/orgsyn.018.0050. | Organic Syntheses | |
| MALONONITRILE | Preparation of MALONONITRILE. Submitted by Alexander R. Surrey. DOI: 10.15227/orgsyn.025.0063. | Organic Syntheses | |
| MALONONITRILE | Preparation of MALONONITRILE. Submitted by B. B. Corson, R. W. Scott, and C. E. Vose. DOI: 10.15227/orgsyn.010.0066. | Organic Syntheses | |
| m-AMINOBENZALDEHYDE DIMETHYLACETAL (Benzaldehyde, m-amino-, dimethylacetal) | Preparation of Benzaldehyde, m-amino-, dimethylacetal. Submitted by Roland N. Icke, C. Ernst Redemann, Burnett B. Wisegarver, and Gordon A. Alles. DOI: 10.15227/orgsyn.029.0006. | Organic Syntheses | |
| MANDELAMIDE | Preparation of MANDELAMIDE. Submitted by L. F. Audrieth and M. Sveda. DOI: 10.15227/orgsyn.020.0062. | Organic Syntheses | |
| MANDELIC ACID | Preparation of MANDELIC ACID. Submitted by J. G. Aston, J. D. Newkirk, D. M. Jenkins, and Julian Dorsky. DOI: 10.15227/orgsyn.023.0048. | Organic Syntheses | |
| MANDELIC ACID | Preparation of MANDELIC ACID. Submitted by B. B. Corson, Ruth A. Dodge, S. A. Harris, and J. S. Yeaw. DOI: 10.15227/orgsyn.006.0058. | Organic Syntheses | |
| MANGANESE-COPPER-CATALYZED CONJUGATE ADDITION OF ORGANOMAGNESIUM REAGENTS TO α,β-ETHYLENIC KETONES: 2-(1,1-DIMETHYLPENTYL)-5-METHYL-CYCLOHEXANONE FROM PULEGONE (Cyclohexanone, 2-(1,1-dimethylpentyl)-5-methyl-) Addition | Preparation of Cyclohexanone, 2-(1,1-dimethylpentyl)-5-methyl-. Submitted by S. Marquais, M. Alami, and G. Cahiez1. DOI: 10.15227/orgsyn.072.0135. | Organic Syntheses | |
| Mannich reaction Addition | In organic chemistry, the Mannich reaction is a three-component organic reaction that involves the amino alkylation of the α-position of a ketone or aldehyde with an aldehyde and a nullary, primary, o… | Wikipedia: Category:Name reactions | |
| Marker degradation | The Marker degradation is a three-step synthetic route in steroid chemistry developed by American chemist Russell Earl Marker in 1938–1940. It is used for the production of cortisone and mammalian sex… | Wikipedia: Category:Name reactions | |
| Markó–Lam deoxygenation | The Markó–Lam deoxygenation is an organic chemistry reaction where the hydroxy functional group in an organic compound is replaced by a hydrogen atom to give an alkyl group. The Markó-Lam reaction is … | Wikipedia: Category:Name reactions | |
| Marschalk reaction | The Marschalk reaction in chemistry is the sodium dithionite promoted reaction of a phenolic anthraquinone with an aldehyde to yield a substituted phenolic anthraquinone after the addition of acid. | Wikipedia: Category:Name reactions | |
| Marsh test | The Marsh test is a highly sensitive method in the detection of arsenic, especially useful in the field of forensic toxicology when arsenic was used as a poison. It was developed by the chemist James … | Wikipedia: Category:Name reactions | |
| Martinet dioxindole synthesis | The Martinet dioxindole synthesis was first reported in 1913 by J. Martinet. It is a chemical reaction in which a primary or secondary aniline or substituted aromatic amine is condensed with ethyl or … | Wikipedia: Category:Name reactions | |
| m-BROMONITROBENZENE (Benzene, 1-bromo-3-nitro-) | Preparation of Benzene, 1-bromo-3-nitro-. Submitted by John R. Johnson and C. G. Gauerke. DOI: 10.15227/orgsyn.008.0046. | Organic Syntheses | |
| m-BROMOTOLUENE (Toluene, m-bromo-) | Preparation of Toluene, m-bromo-. Submitted by L. A. Bigelow, J. R. Johnson, and L. T. Sandborn. DOI: 10.15227/orgsyn.006.0016. | Organic Syntheses | |
| McCormack reaction | The McCormack reaction is a method for the synthesis of organophosphorus compounds. In this reaction, a 1,3-diene and a source of R2P+ are combined to give phospholenium cation. The reaction is named … | Wikipedia: Category:Name reactions | |
| McFadyen–Stevens reaction | The McFadyen–Stevens reaction is a chemical reaction best described as a base-catalyzed thermal decomposition of acylsulfonylhydrazides to aldehydes.[1][2] | Wikipedia: Category:Name reactions | |
| m-CHLOROBENZALDEHYDE (Benzaldehyde, m-chloro-) | Preparation of Benzaldehyde, m-chloro-. Submitted by Johannes S. Buck and Walter S. Ide. DOI: 10.15227/orgsyn.013.0028. | Organic Syntheses | |
| m-CHLORONITROBENZENE (Benzene, 1-chloro-3-nitro-) | Preparation of Benzene, 1-chloro-3-nitro-. Submitted by W. W. Hartman and M. R. Brethen. DOI: 10.15227/orgsyn.003.0079. | Organic Syntheses | |
| m-CHLOROPERBENZOIC ACID (Benzenecarboperoxoic acid, 3-chloro-) | Preparation of Benzenecarboperoxoic acid, 3-chloro-. Submitted by Richard N. McDonald1, Richard N. Steppel, and James E. Dorsey. DOI: 10.15227/orgsyn.050.0015. | Organic Syntheses | |
| m-CHLOROPHENYLMETHYLCARBINOL (Benzyl alcohol, m-chloro-α-methyl-) | Preparation of Benzyl alcohol, m-chloro-α-methyl-. Submitted by C. G. Overberger, J. H. Saunders, R. E. Allen, and Robert Gander. DOI: 10.15227/orgsyn.028.0028. | Organic Syntheses | |
| m-CHLOROSTYRENE (Styrene, m-chloro-) | Preparation of Styrene, m-chloro-. Submitted by C. G. Overberger and J. H. Saunders. DOI: 10.15227/orgsyn.028.0031. | Organic Syntheses | |
| McLafferty rearrangement Rearrangement | The McLafferty rearrangement is a fragmentation reaction observed in mass spectrometry of organic molecules in which the parent radical cation splits into daughter radical cation and neutral spin-pair… | Wikipedia: Category:Name reactions | |
| McMurry reaction | The McMurry reaction is an organic reaction in which two ketone or aldehyde groups are coupled to form an alkene using a titanium chloride compound such as titanium(III) chloride and a reducing agent.… | Wikipedia: Category:Name reactions | |
| m-CYMENE (m-Isopropyltoluene) | Preparation of m-Isopropyltoluene. Submitted by D. E. Pearson, Robert D. Wysong, and J. M. Finkel1. DOI: 10.15227/orgsyn.047.0040. | Organic Syntheses | |
| Meerwein arylation | The Meerwein arylation is an organic reaction involving the addition of an aryl diazonium salt (ArN2X) to an electron-poor alkene usually supported by a metal salt. The reaction product is an alkylate… | Wikipedia: Category:Name reactions | |
| Meerwein–Ponndorf–Verley reduction Reduction | The Meerwein–Ponndorf–Verley (MPV) reduction in organic chemistry is the reduction of ketones and aldehydes to their corresponding alcohols utilizing aluminium alkoxide catalysis in the presence of a … | Wikipedia: Category:Name reactions | |
| Meisenheimer rearrangement Rearrangement | In organic chemistry, the Meisenheimer rearrangement is the conversion of a tertiary amine oxide to a alkoxylamine. The reaction is most common for benzylic or allylic amine oxides. The reaction is … | Wikipedia: Category:Name reactions | |
| Menke nitration | The Menke nitration is the nitration of electron rich aromatic compounds with cupric nitrate and acetic anhydride. The reaction introduces the nitro group predominantly in the ortho position to the a… | Wikipedia: Category:Name reactions | |
| Menshutkin reaction | In organic chemistry, the Menshutkin reaction converts a tertiary amine into a quaternary ammonium salt by reaction with an alkyl halide. Similar reactions occur when tertiary phosphines are treated … | Wikipedia: Category:Name reactions | |
| MERCAPTANS FROM THIOKETALS: CYCLODODECYL MERCAPTAN | Preparation of MERCAPTANS FROM THIOKETALS: CYCLODODECYL MERCAPTAN. Submitted by S. R. Wilson1 and G. M. Georgiadis. DOI: 10.15227/orgsyn.061.0074. | Organic Syntheses | |
| MERCURY DI-β-NAPHTHYL (Mercury, di-2-naphthyl-) | Preparation of Mercury, di-2-naphthyl-. Submitted by A. N. Nesmajanow and E. D. Kohn. DOI: 10.15227/orgsyn.012.0046. | Organic Syntheses | |
| MERCURY(II) OXIDE-MODIFIED HUNSDIECKER REACTION: 1-BROMO-3-CHLOROCYCLOBUTANE | Preparation of MERCURY(II) OXIDE-MODIFIED HUNSDIECKER REACTION: 1-BROMO-3-CHLOROCYCLOBUTANE. Submitted by Gary M. Lampman and James C. Aumiller1. DOI: 10.15227/orgsyn.051.0106. | Organic Syntheses | |
| MESACONIC ACID | Preparation of MESACONIC ACID. Submitted by R. L. Shriner, S. G. Ford, and L. J. Roll. DOI: 10.15227/orgsyn.011.0074. | Organic Syntheses | |
| MESITALDEHYDE (Benzaldehyde, 2,4,6-trimethyl-) | Preparation of Benzaldehyde, 2,4,6-trimethyl-. Submitted by R. C. Fuson, E. C. Horning, S. P. Rowland, and M. L. Ward. DOI: 10.15227/orgsyn.023.0057. | Organic Syntheses | |
| MESITOIC ACID (Benzoic acid, 2,4,6-trimethyl-) | Preparation of Benzoic acid, 2,4,6-trimethyl-. Submitted by Phillip E. Sokol1. DOI: 10.15227/orgsyn.044.0069. | Organic Syntheses | |
| MESITOIC ACID (β-Isodurylic acid) | Preparation of β-Isodurylic acid. Submitted by Douglas M. Bowen. DOI: 10.15227/orgsyn.021.0077. | Organic Syntheses | |
| MESITYLACETIC ACID (Acetic acid, mesityl-) | Preparation of Acetic acid, mesityl-. Submitted by Reynold C. Fuson and Norman Rabjohn. DOI: 10.15227/orgsyn.025.0065. | Organic Syntheses | |
| MESITYLENE | Preparation of MESITYLENE. Submitted by Roger Adams and R. W. Hufferd. DOI: 10.15227/orgsyn.002.0041. | Organic Syntheses | |
| MESITYLENESULFONYLHYDRAZINE, AND (1α,2α,6β)-2,6-DIMETHYLCYCLOHEXANECARBONITRILE AND (1α,2β,6α)-2,6-DIMETHYLCYCLOHEXANECARBONITRILE AS A RACEMIC MIXTURE (Benzenesulfonic acid, 2,4,6-trimethyl-, hydrazide) | Preparation of Benzenesulfonic acid, 2,4,6-trimethyl-, hydrazide. Submitted by Jack R. Reid, Richard F. Dufresne, and John J. Chapman1. DOI: 10.15227/orgsyn.074.0217. | Organic Syntheses | |
| MESITYL OXIDE | Preparation of MESITYL OXIDE. Submitted by J. B. Conant and Neal Tuttle. DOI: 10.15227/orgsyn.001.0053. | Organic Syntheses | |
| METALATION OF 2-METHYLPYRIDINE DERIVATIVES: ETHYL 6-METHYLPYRIDINE-2-ACETATE (Pyridineacetic acid, 6-methyl-, ethyl ester) | Preparation of Pyridineacetic acid, 6-methyl-, ethyl ester. Submitted by William G. Kofron1 and Leona M. Baclawski. DOI: 10.15227/orgsyn.052.0075. | Organic Syntheses | |
| METAL-FREE ONE-POT OXIDATIVE AMINATION OF AROMATIC ALDEHYDES: CONVERSION OF BENZALDEHYDE TO N-BENZOYL PYRROLIDINE | Preparation of METAL-FREE ONE-POT OXIDATIVE AMINATION OF AROMATIC ALDEHYDES: CONVERSION OF BENZALDEHYDE TO N-BENZOYL PYRROLIDINE. Submitted by Kekeli Ekoue-Kovi and Christian Wolf1. DOI: 10.15227/orgs… | Organic Syntheses |
