Category:Name reactions
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A name reaction is a chemical reaction named after its discoverers or developers. Script error: No such module "Side box". Template:CatAutoTOC
Script error: No such module "anchor".Pages in category "Name reactions"
The following 200 pages are in this category, out of approximately 403 total. This list may not reflect recent changes.
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- Achmatowicz reaction
- Adkins–Peterson reaction
- Akabori amino-acid reaction
- Alder ene reaction
- Aldol–Tishchenko reaction
- Algar–Flynn–Oyamada reaction
- Allan–Robinson reaction
- Amadori rearrangement
- Andrussow process
- Angeli–Rimini reaction
- Appel reaction
- Arndt–Eistert reaction
- Asinger reaction
- Auwers synthesis
- Aza-Baylis–Hillman reaction
- Aza-Diels–Alder reaction
- Azide-alkyne Huisgen cycloaddition
B
- Baeyer–Drewsen indigo synthesis
- Baeyer–Emmerling indole synthesis
- Baeyer–Villiger oxidation
- Baker–Venkataraman rearrangement
- Bamberger rearrangement
- Bamberger triazine synthesis
- Bamford–Stevens reaction
- Banert cascade
- Barbier reaction
- Bardhan–Sengupta phenanthrene synthesis
- Bartoli indole synthesis
- Barton reaction
- Barton–Kellogg reaction
- Barton–McCombie deoxygenation
- Barton–Zard reaction
- Baudisch reaction
- Bechamp reaction
- Beckmann rearrangement
- Belousov–Zhabotinsky reaction
- Benary reaction
- Benkeser reaction
- Bergman cyclization
- Bergmann azlactone peptide synthesis
- Bergmann degradation
- Bernthsen acridine synthesis
- Betti reaction
- Biginelli reaction
- Bingel reaction
- Birkeland–Eyde process
- Bischler–Möhlau indole synthesis
- Bischler–Napieralski reaction
- Blaise ketone synthesis
- Blaise reaction
- Blanc chloromethylation
- Bodroux reaction
- Bodroux–Chichibabin aldehyde synthesis
- Boord olefin synthesis
- Borodin reaction
- Bosch reaction
- Boudouard reaction
- Bouveault aldehyde synthesis
- Bouveault–Blanc reduction
- Boyland–Sims oxidation
- Bray–Liebhafsky reaction
- Briggs–Rauscher reaction
- Brook rearrangement
- Bucherer carbazole synthesis
- Bucherer reaction
- Bucherer–Bergs reaction
- Buchwald–Hartwig amination
- Bunsen reaction
- Béchamp reduction
C
- Cadiot–Chodkiewicz coupling
- Camps quinoline synthesis
- Cannizzaro reaction
- Carroll rearrangement
- Castro–Stephens coupling
- Chan rearrangement
- Chapman rearrangement
- Chichibabin pyridine synthesis
- Chugaev elimination
- Claisen condensation
- Claisen rearrangement
- Clemmensen reduction
- Combes quinoline synthesis
- Conrad–Limpach synthesis
- Cook–Heilbron thiazole synthesis
- Cope reaction
- Cope rearrangement
- Corey–Fuchs reaction
- Corey–House synthesis
- Corey–Itsuno reduction
- Corey–Kim oxidation
- Corey–Winter olefin synthesis
- Creighton process
- Criegee rearrangement
- Curtius rearrangement
D
- Dakin oxidation
- Dakin–West reaction
- Danheiser annulation
- Darzens reaction
- Darzens tetralin synthesis
- Debus–Radziszewski imidazole synthesis
- Delépine reaction
- DeMayo reaction
- Demjanov rearrangement
- Dess–Martin oxidation
- Devarda's alloy
- Dieckmann condensation
- Diels–Alder reaction
- Diels–Reese reaction
- Dimroth rearrangement
- Doebner reaction
- Doebner–Miller reaction
- Dötz reaction
- Wulff–Dötz reaction
- Dowd–Beckwith ring-expansion reaction
- Duff reaction
E
F
- Favorskii reaction
- Favorskii rearrangement
- Feist–Benary synthesis
- Fenton's reagent
- Ferrier carbocyclization
- Ferrier rearrangement
- Finkelstein reaction
- Fischer assay
- Fischer–Speier esterification
- Fischer glycosidation
- Fischer indole synthesis
- Fischer oxazole synthesis
- Fischer–Hepp rearrangement
- Fischer–Tropsch process
- Fleming–Tamao oxidation
- Formose reaction
- Forster–Decker method
- Freund reaction
- Friedel–Crafts reaction
- Friedländer synthesis
- Fries rearrangement
- Fritsch–Buttenberg–Wiechell rearrangement
- Fujimoto–Belleau reaction
- Fukuyama coupling
- Fukuyama indole synthesis
- Fukuyama reduction
G
- Gabriel synthesis
- Gabriel–Colman rearrangement
- Gallagher–Hollander degradation
- Gattermann reaction
- Gewald reaction
- Girdler sulfide process
- Glaser coupling
- Goldberg reaction
- Gomberg–Bachmann reaction
- Gould–Jacobs reaction
- Grieco elimination
- Grignard reaction
- Grob fragmentation
- Grundmann aldehyde synthesis
- Guerbet reaction
H
- Haber process
- Haber–Weiss reaction
- Haller-Bauer reaction
- Hammick reaction
- Hantzsch pyrrole synthesis
- Haworth Phenanthrene synthesis
- Hayashi rearrangement
- Heck reaction
- Hell–Volhard–Zelinsky halogenation
- Hemetsberger indole synthesis
- Henry reaction
- Herz reaction
- Hinsberg oxindole synthesis
- Hiyama coupling
- Hoesch reaction
- Hofmann elimination
- Hofmann rearrangement
- Hofmann–Löffler reaction
- Hooker reaction
- Horner–Wadsworth–Emmons reaction
- Hunsdiecker reaction