A name reaction is an chemical reaction named after its discoverer.
The naming is done for historical reasons, because of her probation in practice or because of the mnemonic benefits associated with the naming.
Knowledge of the individual names reactions are particularly useful for understanding of reaction mechanisms and for the planning of organic syntheses.
Below is a list of online available descriptions and mechanisms of the named chemical reactions.
Content, Topics
Details
Acetoacetic Ester Condensation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Acetoacetic Ester Synthesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Acid catalysed hydrolysis of esters . . .
Detail at the mechanism for the hydrolysis of esters in the presence of a dilute acid (such as hydrochloric acid or sulphuric acid) acting as the catalyst. Chemguide
Acyloin Condensation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Alder-Ene Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Aldol Addition
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Aldol Condensation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Appel Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Appel Reaction
... converts an alcohol to an alkyl halide
Arbuzov Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Arndt-Eistert Synthesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Azo Coupling
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Baddeley Reaction
Isomerization of 2,5-dialkylacetophenones in presence of aluminum chloride to 3,5- and 3,4-dialkylacetophenones
Baeyer-Villiger Oxidation
Baeyer-Villiger Rearrangement
Baeyer-Villiger Oxidation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Baker-Venkataraman Rearrangement
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Balz-Schiemann Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Bamford-Stevens Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Barton-McCombie Reaction (Barton Desoxigenation)
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Baylis-Hillman Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Beckmann Rearrangement
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Benzilic Acid Rearrangement
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Benzoin Condensation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Biginelli Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Birch Reduction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Bischler-Napieralski Reaction
Synthesis of 3,4-dihydroisoquinolines from the beta-ethylamides. Organic Chemistry Portal
Blaise Reaction
Synthesis of β-enamino esters or β-keto esters via the zinc-mediated reaction of nitriles with α-haloesters. Organic Chemistry Portal
Blanc Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Bouveault-Blanc Reduction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Brook Rearrangement
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Brown Hydroboration
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Bucherer-Bergs Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Buchwald-Hartwig Chemistry
Historical context; development of initial catalytic systems; mechanistic studies and rational design; reaction scope - Format: PDF
Buchwald-Hartwig Cross Coupling Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Cadiot-Chodkiewicz Coupling
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Cannizaro Oxidation Reduction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
CBS Reduction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Chan-Lam Coupling
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Claisen Condensation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Claisen Rearrangement
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Clemmensen Reduction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Conia-Ene Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Cope Elimination
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Cope Rearrangement
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Corey-Bakshi-Shibata Reduction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Corey-Fuchs Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Corey-Kim Oxidation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Corey-Winter Olefin Synthesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Coumarin Synthesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Cross Metathesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Curtius Rearrangement (Reaction)
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Dakin Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Dakin West Reaction
... converts an amino acid and an anhydride to an acylamino ketone
Dess-Martin Oxidation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Diazotation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Dieckmann Condensation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Diels-Alder Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Directed ortho Metalation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Doebner Modification
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Eglinton Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Ene Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Epoxidation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Eschweiler-Clarke Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Ester Pyrolysis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Esterification reaction
Detail at the mechanism for the formation of esters from carboxylic acids and alcohols in the presence of concentrated sulphuric acid acting as the catalyst. Chemguide
Favorskii Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Finkelstein Reaction
An alkyl halide is converted into another alkyl halide
Fischer Esterification
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Fischer Indole Synthesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Fischer Tropsch Reaction
The Molecular Basis of the Fischer Tropsch Reaction. Dissertation, 2002 - Format: PDF
Friedel-Crafts Acylation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Friedel-Crafts Alkylation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Friedlaender Synthesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Fries Rearrangement
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Fukuyama Coupling
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Gabriel Synthesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Gewald Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Glaser Coupling
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Grignard Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Grubbs Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Haloform Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Hantzsch Dihydropyridine Synthesis (Pyridine Synthesis)
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Hay Coupling
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Heck Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Hell-Volhard-Zelinsky Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Henry Reaktion
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Hofmann Elimination
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Hofmann Rearrangement
... converts a primary amide to a primary amine
Hofmann's Rule
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Horner-Wadsworth-Emmons Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Hosomi-Sakurai Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Hunsdiecker Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Hydration of ethene to make ethanol
The mechanism for the hydration of ethene to make ethanol using phosphoric(V) acid as the catalyst. Chemguide
Hydroboration
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Ireland-Claisen Rearrangement
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Iwanow Reaction (Reagent)
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Jones Oxidation
... oxidizes alcohols using chromic trioxide and acid in water
Julia Olefination
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Julia Olefination, modified
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Julia-Kocienski Olefination
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Julia-Lythgoe Olefination
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Kabachnik-Fields Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Kindler Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Knoevenagel Condensation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Kochi Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Kolbe Electrolysis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Kolbe-Schmitt Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Kumada Coupling
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Lawesson’s Reagent
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Leuckart Thiophenol Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Luche Reduction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Malonic Ester Synthesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Mannich Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Markovnikov's Rule
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Markovnikov's Rule
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
McMurry Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Meerwein-Ponndorf-Verley Reduction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Michael Addition
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Michaelis-Arbuzov Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Mitsunobu Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Modified Julia Olefination
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Mukaiyama Aldol Addition
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Multicomponent Reactions
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Nef Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Nef Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Negishi Coupling
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Newman-Kwart Rearrangement
In the NKR a intramolecular aryl migration of O-thiocarbamates at high temperatures leads to S-thiocarbamates. Organic Chemistry Portal
Nitroaldol Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Nozaki-Hiyama Coupling
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Olefin Metathesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Olefin Metathesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Oppenauer Oxidation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Organosilicon Reactions
Named Organosilicon Reactions - Format: PDF
Overman Rearrangement
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Oxy-Cope Rearrangement
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Paal-Knorr Furan Synthesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Paal-Knorr Pyrrole Synthesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Paal-Knorr Thiophene Synthesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Passerini Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Paterno-Büchi Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Pauson-Khand Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Pechmann Condensation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Perkin Reaction
Perkin Condensation
Peterson Olefination
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Pictet-Spengler Reaction
Pictet-Spengler tetrahydroisoquinoline synthesis
Pinacol Coupling Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Pinacol Rearrangement
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Pinner Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Prilezhaev Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Prins Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Pschorr Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Reformatsky Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Reimer-Tiemann Reaction
... converts a phenol to an o-hydroxy benzaldehyde
Ring Opening Metathesis (Polymerization)
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Ritter Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Robinson Anellation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Rosenmund Reduction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Rubottom Oxidation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Sakurai Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Sandmeyer Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Saytzeff's Rule
Description and mechanism. Organic Chemistry Portal
Schiemann Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Schlosser Modification
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Schmidt Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Schotten-Baumann Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Shapiro Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Sharpless Epoxidation
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Simmons-Smith Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Sonogashira Coupling
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Staudinger Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Steglich Esterification
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Stetter Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Stille Coupling
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Strecker Synthesis
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Suzuki Coupling
The palladium-catalysed cross coupling between organoboronic acid and halides. Organic Chemistry Portal
Swern Oxidation
Synthesis of aldehydes and ketones from primary or secondary alcohols. Organic Chemistry Portal
Tebbe Olefination
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Tishhenko Reaction
Synthesis of esters from two equivalents of an aldehyde. Organic Chemistry Portal
Tusji-Trost Allylation
The palladium-catalyzed allylation of nucleophiles. Organic Chemistry Portal
Ugi Reaction
Rapid preparation of α-aminoacyl amide derivatives. Organic Chemistry Portal
Ullmann Reaction
Description of the reaction and detail at the mechanism. Organic Chemistry Portal
Upjohn Dihydroxylation
Syn-selective preparation of 1,2-diols from alkenes. Organic Chemistry Portal
Vilsmeier Reaction
Formylation of electron-rich arenes. Organic Chemistry Portal
Wacker-Tsuji Oxidation
Synthesis of ethanal from ethene by palladium-catalyzed oxidation with oxygen. Organic Chemistry Portal
Wagner-Meerwein Rearrangement
... converts an alcohol to an olefin
Weinreb Ketone Synthesis
Conversion of carboxylic acids to ketones or aldehydes. Organic Chemistry Portal
Wenker Synthesis
The synthesis of aziridines from 1,2-amino alcohols. Organic Chemistry Portal
Willgerodt-Kindler Reaction
The synthesis of amides from aryl ketones. Organic Chemistry Portal
Williamson Synthesis
The preparation of a wide variety of unsymmetric ethers. Organic Chemistry Portal
Wittig Reaction
The preparation of an alkene by the reaction of an aldehyde or ketone. Organic Chemistry Portal
Wittig: [1,2]-Wittig Rearrangement
A base-promoted reaction of ethers to yield secondary or tertiary alcohols. Organic Chemistry Portal
Wittig: [2,3]-Wittig Rearrangement
Synthesis of homoallylic alcohols. Organic Chemistry Portal
Wittig-Horner Reaction
The reaction of aldehydes or ketones leads to olefins with excellent E-selectivity. Organic Chemistry Portal
Wohl-Ziegler Reaction
The bromination of allylic positions with N-bromosuccinimide. Organic Chemistry Portal
Wolff Rearrangement
The generation of ketenes from α-diazoketones. Organic Chemistry Portal
Wolff-Kishner Reduction
The reduction of aldehydes and ketones to alkanes. Organic Chemistry Portal
Wurtz Reaction
The Wurtz Coupling produces the simple dimer derived from two equivalents of alkyl halide. Organic Chemistry Portal
Wurtz-Fittig Reaction
Alkylation of aryl halides. Organic Chemistry Portal
Yamaguchi Esterification
... converts a carboxylic acid and an alcohol to an ester
Other Directories
Illustrated Glossary of Organic Chemistry
Named reactions
Named Reactions
Named Reactions without mechanisms
Named Reactions
Named Reactions in Organic Chemistry
Name-Reaction.com
Comprehensive and visually dynamic, Name-Reaction.com is a tool to quickly and easily learn organic reactions. Name-Reaction.com provides clear and concise reaction schematics and mechanisms that students can easily understand.
Name-Reaction.com is aimed at educating chemists on organic reactions in an interactive, dynamic and easy to understand format in order to better visualize the abstract world of chemistry and facilitate learning.
Last update: 15.02.2020.
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