Category:Name reactions
A name reaction is a chemical reaction named after its discoverers or developers.
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Pages in category "Name reactions"
The following 200 pages are in this category, out of approximately 534 total. This list may not reflect recent changes.
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- Abramov reaction
- Achmatowicz reaction
- Adams decarboxylation
- Adkins–Peterson reaction
- Akabori amino-acid reaction
- Albright–Goldman oxidation
- Alder ene reaction
- Aldol–Tishchenko reaction
- Algar–Flynn–Oyamada reaction
- Allan–Robinson reaction
- Allen–Millar–Trippett rearrangement
- Amadori rearrangement
- Andrussow process
- Angeli–Rimini reaction
- Appel reaction
- Arens–van Dorp synthesis
- Arndt–Eistert reaction
- Asinger reaction
- Aston–Greenburg rearrangement
- Atherton–Todd reaction
- Auwers synthesis
- Aza-Baylis–Hillman reaction
- Aza-Cope rearrangement
- Aza-Diels–Alder reaction
- Aza-Wittig reaction
- Azide-alkyne Huisgen cycloaddition
B
- Babler oxidation
- Baeyer–Drewsen indigo synthesis
- Baeyer–Emmerling indole synthesis
- Baeyer–Villiger oxidation
- Bailey peptide synthesis
- Baker–Venkataraman rearrangement
- Bamberger rearrangement
- Bamberger triazine synthesis
- Bamford–Stevens reaction
- Banert cascade
- Barbier reaction
- Barbier–Wieland degradation
- Bardhan–Sengupta phenanthrene synthesis
- Bargellini reaction
- Bartoli indole synthesis
- Barton decarboxylation
- Barton reaction
- Barton vinyl iodine procedure
- Barton–Kellogg reaction
- Barton–McCombie deoxygenation
- Barton–Zard reaction
- Baudisch reaction
- Baylis–Hillman reaction
- Bechamp reaction
- Béchamp reduction
- 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
- Birch reduction
- Birkeland–Eyde process
- Bischler–Möhlau indole synthesis
- Bischler–Napieralski reaction
- Blaise ketone synthesis
- Blaise reaction
- Blanc chloromethylation
- Blum–Ittah aziridine synthesis
- Bobbitt reaction
- Bodroux reaction
- Bodroux–Chichibabin aldehyde synthesis
- Boekelheide reaction
- Boger pyridine synthesis
- Bohlmann–Rahtz pyridine synthesis
- Bohn–Schmidt reaction
- Boord olefin synthesis
- Borodin reaction
- Borsche–Drechsel cyclization
- Bosch reaction
- Boudouard reaction
- Bouveault aldehyde synthesis
- Bouveault–Blanc reduction
- Boyland–Sims oxidation
- Bradsher cycloaddition
- Bray–Liebhafsky reaction
- Briggs–Rauscher reaction
- Brook rearrangement
- Bruylants reaction
- Bucherer carbazole synthesis
- Bucherer reaction
- Bucherer–Bergs reaction
- Buchner ring expansion
- Büchner–Curtius–Schlotterbeck reaction
- Buchwald–Hartwig amination
- Bunsen reaction
C
- Cadiot–Chodkiewicz coupling
- Cadogan–Sundberg indole synthesis
- Camps quinoline synthesis
- Cannizzaro reaction
- Carroll rearrangement
- Castro–Stephens coupling
- Chan rearrangement
- Chan–Lam coupling
- Chapman rearrangement
- Chichibabin pyridine synthesis
- Chugaev elimination
- Claisen condensation
- Claisen rearrangement
- Clemmensen reduction
- Collins oxidation
- 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–Link reaction
- Corey–Seebach reaction
- Corey–Winter olefin synthesis
- Corey–Nicolaou macrolactonization
- Cornforth rearrangement
- Crabbé reaction
- Creighton process
- Criegee oxidation
- Criegee rearrangement
- Curtius rearrangement
D
- Dakin oxidation
- Dakin–West reaction
- Danheiser annulation
- Danheiser benzannulation
- Darzens halogenation
- Darzens reaction
- Darzens tetralin synthesis
- Davis oxidation
- Davis–Beirut reaction
- De Kimpe aziridine 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
- Doering–LaFlamme allene synthesis
- Dötz reaction
- Wulff–Dötz reaction
- Dowd–Beckwith ring-expansion reaction
- Doyle–Kirmse reaction
- Duff reaction
E
- Edman degradation
- Einhorn–Brunner reaction
- Elbs persulfate oxidation
- Elbs reaction
- Emde degradation
- Enders SAMP/RAMP hydrazone-alkylation reaction
- Erlenmeyer–Plöchl azlactone and amino-acid synthesis
- Eschenmoser fragmentation
- Eschenmoser sulfide contraction
- Eschweiler–Clarke reaction
- Étard reaction
- Evans–Saksena reduction
- Evans–Tishchenko reaction
F
- Favorskii reaction
- Favorskii rearrangement
- Feist–Benary synthesis
- Fenton's reaction
- Fenton's reagent
- Ferrario–Ackermann reaction
- Ferrier carbocyclization
- Ferrier rearrangement
- Fétizon oxidation
- Fiesselmann thiophene synthesis
- 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
- Fráter–Seebach alkylation
- Freund reaction
- Friedel–Crafts reaction
- Friedländer synthesis