List of organic reactions
From Wikipedia, the free encyclopedia
This page aims to list well-known chemical reactions, name reactions, name reagents, and name rules to stimulate the creation of Wikipedia articles.
This list is not necessarily complete or up to date – if you see an article that should be here but isn't (or one that shouldn't be here but is), please update the page accordingly.
The list has not yet been checked for entries or existing articles under a slightly different name (e.g. reaction instead of synthesis). I would suggest to give new articles a descriptive title if possible (e.g. Birch reduction instead of Birch reaction, Williamson ether synthesis instead of Williamson reaction).
Relevant links for chemical reactions are:
- http://www.organic-chemistry.org/namedreactions/
- http://www.stolaf.edu/depts/chemistry/courses/toolkits/247/practice/medialib/data/
- http://www.chem.wisc.edu/areas/reich/handouts/NameReagents/namedreag-cont.htm
[edit] See also
Wikimedia Commons has media related to:
- Chemical reaction
- List of organic compounds
- List of inorganic compounds
- List of biomolecules
- List of minerals
- Polyatomic ions
- Category:Organic reactions
- Category:Reaction images
- Organic reaction
[edit] Contents
| 1 A B C D E F G H I J K L M N O P Q R S T U V W X Y Z |
[edit] 1
(back up)
[edit] A
- Abramovitch-Shapiro tryptamine synthesis
- Acetoacetic ester condensation
- Acyloin condensation
- Adams catalyst
- Adkins catalyst
- Adkins-Peterson reaction
- Akabori amino acid reaction
- Alder ene reaction
- Alder-Rickert rule
- Alder-Stein rules
- Aldol addition
- Aldol condensation
- Algar-Flynn-Oyamada reaction
- Allan-Robinson reaction
- Allylic rearrangement
- Amadori rearrangement
- Andrussov oxidation
- Appel reaction
- Arbuzov reaction, Arbusow reaction
- Arens-van Dorp synthesis, Isler modification
- Arndt-Eistert synthesis
- Auwers synthesis
- Azo coupling
(back up)
[edit] B
- Baeyer-Drewson indigo synthesis
- Baeyer-Villiger oxidation
- Baeyer-Villiger rearrangement
- Bakeland process (Bakelite)
- Baker-Venkataraman rearrangement
- Baker-Venkataraman transformation
- Bally-Scholl synthesis
- Balz-Schiemann reaction
- Bamberger rearrangement
- Bamberger triazine synthesis
- Bamford-Stevens reaction
- Barbier-Wieland degradation
- Bardhan-Senguph phenanthrene synthesis
- Bartoli indole synthesis
- Bartoli reaction
- Barton reaction
- Barton-McCombie reaction, Barton deoxygenation
- Baudisch reaction
- Bayer test
- Baylis-Hilman reaction
- Bechamp reaction
- Beckmann rearrangement
- Bellus-Claisen rearrangement
- Belousov-Zhabotinsky reaction
- Benary reaction
- Benzidine rearrangement
- Benzilic acid rearrangement
- Benzoin condensation
- Bergman cyclization
- Bergmann azlactone peptide synthesis
- Bergmann degradation
- Bergmann-Zervas carbobenzoxy method
- Bernthsen acridine synthesis
- Bestmann's reagent
- Betti reaction
- Biginelli pyrimidine synthesis
- Biginelli reaction
- Birch reduction
- Bischler-Möhlau indole synthesis
- Bischler triazine synthesis
- Bischler-Napieralski reaction
- Blaise ketone synthesis
- Blaise reaction
- Blanc reaction
- Blanc chloromethylation
- Bodroux reaction
- Bodroux-Chichibabin aldehyde synthesis
- Bogert-Cook synthesis
- Bohn-Schmidt reaction
- Boord olefin synthesis
- Borodin reaction
- Borsche-Drechsel cyclization
- Bosch-Meiser urea process
- Bouveault aldehyde synthesis
- Bouveault-Blanc reduction
- Boyland-Sims oxidation
- Boyer Reaction
- Brown hydroboration
- Bucherer carbazole synthesis
- Bucherer reaction
- Bucherer-Bergs reaction
- Buchner ring enlargement
- Buchner-Curtius-Schlotterbeck reaction
- Buchwald-Hartwig amination
- Bunnett reaction
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[edit] C
- Cadiot-Chodkiewicz coupling
- Camps quinoline synthesis
- Cannizzaro reaction
- Carroll reaction
- Catalytic reforming
- CBS reduction
- Chan-Lam coupling
- Chapman rearrangement
- Chichibabin pyridine synthesis
- Chichibabin reaction
- Chugaev elimination
- Ciamician-Dennstedt rearrangement
- Claisen condensation
- Claisen rearrangement
- Claisen-Schmidt condensation
- Clemmensen reduction
- Collins-Reagent
- Combes quinoline synthesis
- Conia reaction
- Conrad-Limpach synthesis
- Cope elimination
- Cope rearrangement
- Corey reagent
- Corey-Bakshi-Shibata reduction
- Corey-Fuchs reaction
- Corey-Kim oxidation
- Corey-Posner, Whitesides-House reaction
- Corey-Winter olefin synthesis
- Corey-Winter reaction
- Coupling reaction
- Craig method
- Cram's rule of asymmetric induction
- Creighton process
- Criegee reaction
- Criegee rearrangement
- Cross metathesis
- Crum Brown-Gibson rule
- Curtius degradation
- Curtius rearrangement, Curtius reaction
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[edit] D
- Dakin reaction
- Dakin-West reaction
- Danheiser Benzannulation reaction
- Danheiser Cyclopentene annulation reaction
- Darapsky degradation
- Darzens condensation, Darzens-Claisen reaction, Glycidic ester condensation
- Darzens synthesis of unsaturated ketones
- Darzens tetralin synthesis
- Delepine reaction
- Demjanov rearrangement
- Demjanow desamination
- Dess-Martin oxidation
- Dewer-Evans-Zimmermann reaction
- Diazotisation
- Dieckmann condensation
- Dieckmann reaction
- Diels-Alder reaction
- Diels Reese reaction
- Dienol benzene rearrangement
- Dienone phenol rearrangement
- Dimroth rearrangement
- Di-pi-methane rearrangement
- Directed ortho metalation
- Doebner modification
- Doebner-Miller reaction, Beyer method for quinolines
- Doering-LaFlamme carbon chain extension
- Dötz reaction
- Dowd-Beckwith ring expansion reaction
- Duff reaction
- Dutt-Wormall reaction
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[edit] E
- E1 is an Elimination reaction mechanism
- E1cb
- E2 is an Elimination reaction mechanism
- Eder reaction
- Edman degradation
- Egling coupling
- Eglinton reaction
- Ehrlich-Sachs reaction
- Einhorn variant
- Einhorn-Brunner reaction
- Elbs persulfate oxidation
- Elbs reaction
- Elimination reaction
- Eltekoff reaction
- Emde degradation
- Emmert reaction
- Ene reaction
- Epoxidation
- Erlenmeyer synthesis, Azlactone synthesis
- Erlenmeyer-Plochl azlactone and amino acid synthesis
- Eschenmoser fragmentation
- Eschweiler-Clarke reaction
- Ester pyrolysis
- Étard reaction
- Evans aldol
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[edit] F
- Favorskii reaction
- Favorskii rearrangement
- Favorskii-Babayan synthesis
- Feist-Benary synthesis
- Fenton reaction
- Ferrario reaction
- Ferrier rearrangement
- Finkelstein reaction
- Fischer indole synthesis
- Fischer oxazole synthesis
- Fischer peptide synthesis
- Fischer phenylhydrazine and oxazone reaction
- Fischer reduction
- Fischer glycosidation
- Fischer-Hepp rearrangement
- Fischer-Speier esterification
- Fischer Tropsch synthesis
- Flood reaction
- Forster reaction
- Forster-Decker method
- Franchimont reaction
- Frankland synthesis
- Frankland-Duppa reaction
- Freund reaction
- Friedel-Crafts Acylation
- Friedel-Crafts Alkylation
- Friedländer synthesis
- Fries rearrangement
- Fritsch-Buttenberg-Wiechell rearrangement
- Fujimoto-Belleau reaction
- Fukuyama coupling
(back up)
[edit] G
- Gabriel ethylenimine method
- Gabriel synthesis
- Gabriel-Colman rearrangement, Gabriel isoquinoline synthesis
- Gallagher-Hollander degradation
- Gassman indole synthesis
- Gastaldi synthesis
- Gattermann aldehyde synthesis
- Gattermann Koch reaction
- Gattermann reaction
- Gewald reaction
- Gibbs phthalic anhydride process
- Gilman reagent
- Glaser coupling
- Glycol cleavage
- Gogte synthesis
- Gomberg-Bachmann reaction
- Gomberg-Bachmann-Hey reaction
- Gomberg-Free radical reaction
- Gould-Jacobs reaction
- Graebe-Ullmann synthesis
- Grignard degradation
- Grignard reaction
- Grob fragmentation
- Grubbs' catalyst in Olefin metathesis
- Grundmann aldehyde synthesis
- Gryszkiewicz-Trochimowski and McCombie method
- Guareschi-Thorpe condensation
- Guerbet reaction
- Gutknecht pyrazine synthesis
(back up)
[edit] H
- Haller-Bauer reaction
- Haloform reaction
- Hammett equation
- Hammick reaction
- Hammond-Principle or Hammond postulate
- Hantzch pyrrole synthesis
- Hantzsch dihydropyridine synthesis, Hantzsch pyridine synthesis
- Hantzsch Pyridine synthesis, Gattermann-Skita synthesis, Guareschi-Thorpe condensation, Knoevenagel-Fries modification
- Hantzsch-Collidin-synthesis
- Harber-Weiss reaction
- Harries Ozonide reaction
- Haworth Methylation
- Haworth Phenanthrene synthesis
- Haworth-reaction
- Hay coupling
- Hayashi rearrangement
- Heck reaction
- Helferich method
- Hell-Volhard-Zelinsky halogenation
- Hemetsberger indole synthesis
- Henkel reaction, Raecke process, Henkel process
- Henry reaction, Kamlet reaction
- Herz reaction, Herz compounds
- Herzig-Meyer alkimide group determination
- Heumann indigo synthesis
- Hinsberg indole synthesis
- Hinsberg reaction
- Hinsberg separation
- Hinsberg sulfone synthesis
- Hoch-Campbell ethylenimine synthesis
- Hofmann degradation, Exhaustive methylation
- Hofmann Elimination
- Hofmann Isonitrile synthesis, Carbylamine reaction
- Hofmann produkt
- Hofmann rearrangement
- Hofmann-Löffler reaction, Löffler-Freytag reaction, Hofmann-Löffler-Freytag reaction
- Hofmann-Martius rearrangement
- Hofmann's Rule
- Hofmann-Sand reaction
- Homo rearrangement of steroids
- Hooker reaction
- Horner-Wadsworth-Emmons reaction
- Hösch reaction
- Hosomi-Sakurai reaction
- Houben-Fischer synthesis
- Hunsdiecker reaction
- Hydroboration
(back up)
[edit] I
- Ing-Manske procedure
- Ipatieff reaction
- Ipso substitution
- Ivanov reagent, Ivanov reaction
(back up)
[edit] J
- Jacobsen rearrangement
- Janovsky reaction
- Japp-Klingemann reaction
- Japp-Maitland condensation
- Jones oxidation
- Jordan-Ullmann-Goldberg synthesis
- Julia olefination
- Julia-Lythgoe olefination
(back up)
[edit] K
- Kabachnik-Fields reaction
- Kendall-Mattox reaction
- Kiliani-Fischer synthesis
- Kindler reaction
- Kishner cyclopropane synthesis
- Knoevenagel condensation
- Knoop-Oesterlin amino acid synthesis
- Knorr pyrazole synthesis
- Knorr pyrrole synthesis
- Knorr quinoline synthesis
- Koch-Haaf reaction
- Kochi reaction
- Koenigs-Knorr reaction
- Kolbe electrolysis
- Kolbe-Schmitt reaction
- Kondakov rule
- Kontanecki acylation
- Kornblum oxidation
- Krafft degradation
- Kröhnke aldehyde synthesis
- Kröhnke oxidation
- Kröhnke pyridine synthesis
- Kucherov reaction
- Kuhn-Winterstein reaction
- Kulinkovich reaction
- Kumada coupling
(back up)
[edit] L
- Larock indole synthesis
- Lebedev process
- Lehmstedt-Tanasescu reaction
- Leimgruber-Batcho indole synthesis
- Letts nitrile synthesis
- Leuckart reaction
- Leuckart thiophenol reaction
- Leuckart-Wallach reaction
- Leuckert amide synthesis
- Levinstein process
- Lieben iodoform reaction, Haloform reaction
- Lindlar catalyst
- Lobry-de Bruyn-van Ekenstein transformation
- Lossen rearrangement
- Luche reduction
(back up)
[edit] M
- Madelung synthesis
- Malaprade reaction, Periodic acid oxidation
- Malonic ester synthesis
- Mannich reaction
- Markovnikov's rule, Markownikoff rule, Markownikow rule
- Martinet dioxindole synthesis
- McFadyen-Stevens reaction
- McLafferty rearrangement
- McMurry reaction
- Meerwein arylation
- Meerwein-Ponndorf-Verley reduction
- Meisenheimer rearrangement
- Meissenheimer complex
- Menshutkin reaction
- Mentzer pyrone synthesis
- Merckwald asymmetric synthesis
- Meyer and Hartmann reaction
- Meyer reaction
- Meyer synthesis
- Meyer-Schuster rearrangement
- Michael addition
- Michael addition, Michael system
- Michael condensation
- Michaelis-Arbuzov reaction
- Miescher degradation
- Mignonac reaction
- Milas hydroxylation of olefins
- Mitsunobu reaction
- Mukaiyama aldol addition
- Mukaiyama reaction
(back up)
[edit] N
- Nametkin rearrangement
- Nazarov cyclization reaction
- Neber rearrangement
- Nef reaction
- Negishi coupling
- Negishi-Zipper reaction
- Nenitzescu indole synthesis
- Nenitzescu reductive acylation
- Niementowski quinazoline synthesis
- Niementowski quinoline synthesis
- Nierenstein reaction
- Nitroaldol reaction
- Normant reagents
- Noyori asymmetric hydrogenation
- Nozaki-Hiyama-Kishi Nickel/Chromium Coupling reaction
- Nucleophilic acyl substitution
(back up)
[edit] O
- Olefin metathesis
- Oppenauer oxidation
- Ostromyslenskii reaction, Ostromisslenskii reaction
- Oxidative decarboxylation
- Oxo synthesis
- Oxy-Cope rearrangement
- Oxymercuration
- Ozonolysis
(back up)
[edit] P
- Paal-Knorr pyrrole synthesis
- Paal-Knorr synthesis
- Paneth technique
- Paolini reaction
- Passerini reaction
- Paterno-Büchi reaction
- Pauson-Khand reaction
- Pechmann condensation
- Pechmann pyrazole synthesis
- Pellizzari reaction
- Pelouze synthesis
- Perkin alicyclic synthesis
- Perkin reaction
- Perkin rearrangement
- Perkow reaction
- Petasis reaction
- Petasis reagent
- Peterson olefination
- Peterson reaction
- Petrenko-Kritschenko piperidone synthesis
- Pfan-Plattner azulene synthesis
- Pfitzinger reaction
- Pfitzner-Moffatt oxidation
- Pictet-Gams isoquinoline synthesis
- Pictet-Hubert reaction
- Pictet-Spengler isoquinoline synthesis
- Pictet-Spengler reaction
- Piloty alloxazine synthesis
- Piloty-Robinson pyrrole synthesis
- Pinacol coupling reaction
- Pinacol rearrangement
- Pinner amidine synthesis
- Pinner method for ortho esters
- Pinner reaction
- Pinner triazine synthesis
- Piria reaction
- Pitzer strain
- Polonovski reaction
- Pomeranz-Fritsch reaction
- Ponzio reaction
- Prelog strain
- Prevost reaction
- Prileschajew reaction
- Prilezhaev reaction
- Prins reaction
- Prinzbach synthesis
- Pschorr reaction
- Pummerer rearrangement
- Purdie methylation, Irvine-Purdie methylation
(back up)
[edit] Q
- Quelet reaction
(back up)
[edit] R
- Ramberg-Backlund reaction
- Raney-Nickel
- Rap-Stoermer condensation
- Raschig phenol process
- Reed reaction
- Reformatskii reaction
- Reilly-Hickinbottom rearrangement
- Reimer-Tiemann reaction
- Reissert indole synthesis
- Reissert reaction, Reissert compound
- Reppe synthesis
- Retropinacol rearrangement
- Reverdin reaction
- Riehm quinoline synthesis
- Riemschneider thiocarbamate synthesis
- Riley oxidations
- Ring closing metathesis
- Ring opening metathesis
- Ritter reaction
- Robinson annulation
- Robinson-Gabriel synthesis
- Robinson Schopf reaction
- Rosenmund reaction
- Rosenmund reduction
- Rosenmund-von Braun synthesis
- Rothemund reaction
- Rowe rearrangement
- Rupe reaction
- Rubottom oxidation
- Ruff-Fenton degradation
- Ruzicka large ring synthesis
(back up)
[edit] S
- Sakurai reaction
- Salol reaction
- Sandheimer
- Sandmeyer diphenylurea isatin synthesis
- Sandmeyer isonitrosoacetanilide isatin synthesis
- Sandmeyer reaction
- Sanger reagent
- Sarett oxidation
- Saytzeff rule, Saytzeff's Rule
- Schiemann reaction
- Schlenk equilibrium
- Schlosser modification
- Schlosser variant
- Schlosser-Lochmann reaction
- Schmidlin ketene synthesis
- Schmidt degradation
- Schmidt reaction
- Scholl reaction
- Schorigin Shorygin reaction, Shorygin reaction, Wanklyn reaction
- Schotten-Baumann reaction
- Screttas-Yus reaction
- Semidine rearrangement
- Semmler-Wolff reaction
- Serini reaction
- Seyferth-Gilbert homologation
- Shapiro reaction
- Sharpless asymmetric dihydroxylation
- Sharpless epoxidation
- Sharpless oxyamination or aminohydroxylation
- Simmons-Smith reaction
- Simonini reaction
- Simonis chromone cyclization
- Skraup chinolin synthesis
- Skraup reaction
- Smiles rearrangement
- SNAr nucleophilic aromatic substitution
- SN1
- SN2
- SNi
- Sommelet reaction
- Sonn-Müller method
- Sonogashira coupling
- Sørensen formol titration
- Staedel-Rugheimer pyrazine synthesis
- Staudinger reaction
- Stephen aldehyde synthesis
- Stetter reaction
- Stevens rearrangement
- Stieglitz rearrangement
- Stille coupling
- Stobbe condensation
- Stollé synthesis
- Stork acylation
- Stork enamine alkylation
- Strecker amino acid synthesis
- Strecker degradation
- Strecker sulfite alkylation
- Strecker synthesis
- Stuffer disulfone hydrolysis rule
- Süs reaction
- Suzuki coupling
- Swain equation
- Swarts reaction
- Swern oxidation
(back up)
[edit] T
- Tafel rearrangement
- Takai olefination
- Tebbe olefination
- ter Meer reaction
- Thermite reactions
- Thiele reaction
- Thorpe reaction
- Tiemann rearrangement
- Tiffeneau ring enlargement reaction
- Tiffeneau-Demjanow rearrangement
- Tischtschenko reaction
- Tishchenko reaction, Tischischenko-Claisen reaction
- Tollens reagent
- Trapp mixture
- Traube purine synthesis
- Truce-Smiles rearrangement
- Tscherniac-Einhorn reaction
- Tschitschibabin reaction
- Tschugajeff reaction
- Twitchell process
- Tyrer sulfonation process
(back up)
[edit] U
- Ugi reaction
- Ullmann reaction
- Upjohn dihydroxylation
- Urech cyanohydrin method
- Urech Hydantoin synthesis
(back up)
[edit] V
- Van Slyke determination
- Varrentrapp reaction
- Vilsmeier reaction
- Vilsmeier-Haack reaction
- Voight amination
- Volhard-Erdmann cyclization
- von Braun amide degradation
- von Braun reaction
- von Meyer reduction
- von Richter cinnoline synthesis
- von Richter reaction
(back up)
[edit] W
- Wacker-Tsuji oxidation
- Wagner-Jauregg reaction
- Wagner-Meerwein rearrangement
- Walden inversion
- Wallach rearrangement
- Weerman degradation
- Weinreb ketone synthesis
- Wenker ring closure
- Wenker synthesis
- Wessely-Moser rearrangement
- Westphalen-Lettré rearrangement
- Wharton reaction
- Whiting reaction
- Wichterle reaction
- Widman-Stoermer synthesis
- Wilkinson catalyst
- Willgerodt rearrangement
- Willgerodt-Kindler reaction
- Williamson ether synthesis
- Winstein reaction
- Wittig reaction
- Wittig rearrangement
- Wittig-Horner reaction
- Wohl degradation
- Wohl-Aue reaction
- Wohler synthesis
- Wohl-Ziegler reaction
- Wolfenstein-Boters reaction
- Wolff rearrangement
- Wolff-Kishner reduction
- Woodward cis-hydroxylation
- Woodward-Hoffmann rule
- Wurtz coupling, Wurtz reaction
- Wurtz-Fittig reaction
(back up)
[edit] X
(back up)
[edit] Y
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[edit] Z
- Zeisel determination
- Zerevitinov determination, Zerewitinoff determination
- Ziegler condensation
- Ziegler method
- Zimmermann reaction
- Zincke disulfide cleavage
- Zinke nitration
- Zincke reaction
- Zincke-Suhl reaction
(back up)
