| name,link | |
| appel-reaction,https://www.name-reaction.com/appel-reaction | |
| baeyer-villiger-oxidation,https://www.name-reaction.com/baeyer-villiger-oxidation | |
| bartoli-indole-synthesis,https://www.name-reaction.com/bartoli-indole-synthesis | |
| baylis-hillman-reaction,https://www.name-reaction.com/baylis-hillman-reaction | |
| beckmann-rearrangement,https://www.name-reaction.com/beckmann-rearrangement | |
| biginelli-reaction,https://www.name-reaction.com/biginelli-reaction | |
| birch-reduction,https://www.name-reaction.com/birch-reduction | |
| buchwald-hartwig-amination,https://www.name-reaction.com/buchwald-hartwig-amination | |
| cannizzaro-reaction,https://www.name-reaction.com/cannizzaro-reaction | |
| claisen-condensation,https://www.name-reaction.com/claisen-condensation | |
| claisen-rearrangement,https://www.name-reaction.com/claisen-rearrangement | |
| clemmensen-reduction,https://www.name-reaction.com/clemmensen-reduction | |
| cope-rearrangement,https://www.name-reaction.com/cope-rearrangement | |
| corey-kim-oxidation,https://www.name-reaction.com/corey-kim-oxidation | |
| curtius-rearrangement,https://www.name-reaction.com/curtius-rearrangement | |
| dakin-west-reaction,https://www.name-reaction.com/dakin-west-reaction | |
| dieckmann-condensation,https://www.name-reaction.com/dieckmann-condensation | |
| diels-alder-reaction,https://www.name-reaction.com/diels-alder-reaction | |
| eschenmoser-claisen-rearrangement,https://www.name-reaction.com/eschenmoser-claisen-rearrangement | |
| eschweiler-clarke-reaction,https://www.name-reaction.com/eschweiler-clarke-reaction | |
| finkelstein-reaction,https://www.name-reaction.com/finkelstein-reaction | |
| fischer-esterification,https://www.name-reaction.com/fischer-esterification | |
| fischer-indole-synthesis,https://www.name-reaction.com/fischer-indole-synthesis | |
| friedel-crafts-acylation,https://www.name-reaction.com/friedel-crafts-acylation | |
| friedel-crafts-alkylation,https://www.name-reaction.com/friedel-crafts-alkylation | |
| fries-rearrangement,https://www.name-reaction.com/fries-rearrangement | |
| gabriel-synthesis,https://www.name-reaction.com/gabriel-synthesis | |
| grignard-reaction,https://www.name-reaction.com/grignard-reaction | |
| heck-reaction,https://www.name-reaction.com/heck-reaction | |
| hell-volhard-zelinsky-reaction,https://www.name-reaction.com/hell-volhard-zelinsky-reaction | |
| henry-reaction,https://www.name-reaction.com/henry-reaction | |
| hofmann-elimination,https://www.name-reaction.com/hofmann-elimination | |
| hofmann-rearrangement,https://www.name-reaction.com/hofmann-rearrangement | |
| ireland-claisen-rearrangement,https://www.name-reaction.com/ireland-claisen-rearrangement | |
| johnson-claisen-rearrangement,https://www.name-reaction.com/johnson-claisen-rearrangement | |
| jones-oxidation,https://www.name-reaction.com/jones-oxidation | |
| knoevenagel-condensation,https://www.name-reaction.com/knoevenagel-condensation | |
| knorr-pyrazole-synthesis,https://www.name-reaction.com/knorr-pyrazole-synthesis | |
| kolbe-schmitt-reaction,https://www.name-reaction.com/kolbe-schmitt-reaction | |
| kumada-cross-coupling,https://www.name-reaction.com/kumada-cross-coupling | |
| luche-reduction,https://www.name-reaction.com/luche-reduction | |
| mannich-reaction,https://www.name-reaction.com/mannich-reaction | |
| michael-addition,https://www.name-reaction.com/michael-addition | |
| mitsunobu-reaction,https://www.name-reaction.com/mitsunobu-reaction | |
| mukaiyama-aldol-addition,https://www.name-reaction.com/mukaiyama-aldol-addition | |
| n,https://www.name-reaction.com/n | |
| negishi-cross-coupling,https://www.name-reaction.com/negishi-cross-coupling | |
| oppenauer-oxidation,https://www.name-reaction.com/oppenauer-oxidation | |
| pauson-khand-reaction,https://www.name-reaction.com/pauson-khand-reaction | |
| perkin-reaction,https://www.name-reaction.com/perkin-reaction | |
| pictet-spengler-reaction,https://www.name-reaction.com/pictet-spengler-reaction | |
| prins-reaction,https://www.name-reaction.com/prins-reaction | |
| reformatsky-reaction,https://www.name-reaction.com/reformatsky-reaction | |
| reimer-tiemann-reaction,https://www.name-reaction.com/reimer-tiemann-reaction | |
| ritter-reaction,https://www.name-reaction.com/ritter-reaction | |
| robinson-annulation,https://www.name-reaction.com/robinson-annulation | |
| sandmeyer-reaction,https://www.name-reaction.com/sandmeyer-reaction | |
| schmidt-reaction,https://www.name-reaction.com/schmidt-reaction | |
| schotten-baumann-reaction,https://www.name-reaction.com/schotten-baumann-reaction | |
| sharpless-epoxidation,https://www.name-reaction.com/sharpless-epoxidation | |
| sonogashira-cross-coupling,https://www.name-reaction.com/sonogashira-cross-coupling | |
| staudinger-reaction,https://www.name-reaction.com/staudinger-reaction | |
| stille-cross-coupling,https://www.name-reaction.com/stille-cross-coupling | |
| strecker-amino-acid-synthesis,https://www.name-reaction.com/strecker-amino-acid-synthesis | |
| suzuki-cross-coupling,https://www.name-reaction.com/suzuki-cross-coupling | |
| swern-oxidation,https://www.name-reaction.com/swern-oxidation | |
| ullmann-reaction,https://www.name-reaction.com/ullmann-reaction | |
| vilsmeier-haack-reaction,https://www.name-reaction.com/vilsmeier-haack-reaction | |
| wagner-meerwein-rearrangement,https://www.name-reaction.com/wagner-meerwein-rearrangement | |
| williamson-ether-synthesis,https://www.name-reaction.com/williamson-ether-synthesis | |
| wittig-reaction,https://www.name-reaction.com/wittig-reaction | |
| wolff-rearrangement,https://www.name-reaction.com/wolff-rearrangement | |
| wolff-kishner-reduction,https://www.name-reaction.com/wolff-kishner-reduction | |
| wurtz-reaction,https://www.name-reaction.com/wurtz-reaction | |
| yamaguchi-esterification,https://www.name-reaction.com/yamaguchi-esterification | |
| 0-9[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=1 | |
| "1,2-Wittig rearrangement","https://en.wikipedia.org/wiki/1,2-Wittig_rearrangement" | |
| "1,3-Dipolar cycloaddition","https://en.wikipedia.org/wiki/1,3-Dipolar_cycloaddition" | |
| "2,3-Wittig rearrangement","https://en.wikipedia.org/wiki/2,3-Wittig_rearrangement" | |
| A[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=2 | |
| Abramovitch�Shapiro tryptamine synthesis,https://en.wikipedia.org/wiki/Tryptamine | |
| Acetalisation,https://en.wikipedia.org/wiki/Acetalisation | |
| Acetoacetic ester condensation,https://en.wikipedia.org/wiki/Acetoacetic_ester_condensation | |
| Achmatowicz reaction,https://en.wikipedia.org/wiki/Achmatowicz_reaction | |
| Acylation,https://en.wikipedia.org/wiki/Acylation | |
| Acyloin condensation,https://en.wikipedia.org/wiki/Acyloin_condensation | |
| Adams' catalyst,https://en.wikipedia.org/wiki/Adams%27_catalyst | |
| Adams decarboxylation,https://en.wikipedia.org/wiki/Adams_decarboxylation | |
| Adkins catalyst,https://en.wikipedia.org/wiki/Adkins_catalyst | |
| Adkins�Peterson reaction,https://en.wikipedia.org/wiki/Adkins%E2%80%93Peterson_reaction | |
| Akabori amino acid reaction,https://en.wikipedia.org/wiki/Akabori_amino_acid_reaction | |
| Alcohol oxidation,https://en.wikipedia.org/wiki/Alcohol_oxidation | |
| Alder�Stein rules,https://en.wikipedia.org/wiki/Alder%E2%80%93Stein_rules | |
| Aldol addition,https://en.wikipedia.org/wiki/Aldol_addition | |
| Aldol condensation,https://en.wikipedia.org/wiki/Aldol_condensation | |
| Algar�Flynn�Oyamada reaction,https://en.wikipedia.org/wiki/Algar%E2%80%93Flynn%E2%80%93Oyamada_reaction | |
| Alkylimino-de-oxo-bisubstitution,https://en.wikipedia.org/wiki/Alkylimino-de-oxo-bisubstitution | |
| Alkyne trimerisation,https://en.wikipedia.org/wiki/Alkyne_trimerisation | |
| Alkyne zipper reaction,https://en.wikipedia.org/wiki/Alkyne_zipper_reaction | |
| Allan�Robinson reaction,https://en.wikipedia.org/wiki/Allan%E2%80%93Robinson_reaction | |
| Allylic rearrangement,https://en.wikipedia.org/wiki/Allylic_rearrangement | |
| Amadori rearrangement,https://en.wikipedia.org/wiki/Amadori_rearrangement | |
| Amine alkylation,https://en.wikipedia.org/wiki/Amine_alkylation | |
| Angeli�Rimini reaction,https://en.wikipedia.org/wiki/Angeli%E2%80%93Rimini_reaction | |
| Andrussov oxidation,https://en.wikipedia.org/wiki/Andrussov_oxidation | |
| Appel reaction,https://en.wikipedia.org/wiki/Appel_reaction | |
| Aromatic nitration,https://en.wikipedia.org/wiki/Nitration | |
| Arndt�Eistert synthesis,https://en.wikipedia.org/wiki/Arndt%E2%80%93Eistert_synthesis | |
| Auwers synthesis,https://en.wikipedia.org/wiki/Auwers_synthesis | |
| Azo coupling,https://en.wikipedia.org/wiki/Azo_coupling | |
| B[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=3 | |
| Baeyer�Drewson indigo synthesis,https://en.wikipedia.org/wiki/Baeyer%E2%80%93Drewson_indigo_synthesis | |
| Bakeland process (Bakelite),https://en.wikipedia.org/wiki/Bakeland_process_(Bakelite) | |
| Bally�Scholl synthesis,https://en.wikipedia.org/wiki/Bally%E2%80%93Scholl_synthesis | |
| Bamberger rearrangement,https://en.wikipedia.org/wiki/Bamberger_rearrangement | |
| Bamberger triazine synthesis,https://en.wikipedia.org/wiki/Bamberger_triazine_synthesis | |
| Bamford�Stevens reaction,https://en.wikipedia.org/wiki/Bamford%E2%80%93Stevens_reaction | |
| Barbier reaction,https://en.wikipedia.org/wiki/Barbier_reaction | |
| Barbier�Wieland degradation,https://en.wikipedia.org/wiki/Carboxylic_acid | |
| Bardhan�Sengupta phenanthrene synthesis,https://en.wikipedia.org/wiki/Bardhan%E2%80%93Senguph_phenanthrene_synthesis | |
| Barfoed's test,https://en.wikipedia.org/wiki/Barfoed%27s_test | |
| Bargellini reaction,https://en.wikipedia.org/wiki/Bargellini_reaction | |
| Barton decarboxylation,https://en.wikipedia.org/wiki/Barton_decarboxylation | |
| Barton�Kellogg reaction,https://en.wikipedia.org/wiki/Barton%E2%80%93Kellogg_reaction | |
| Barton-Zard Synthesis,https://en.wikipedia.org/wiki/Barton-Zard_Synthesis | |
| Barton vinyl iodine procedure,https://en.wikipedia.org/wiki/Hydrazone_iodination | |
| Baudisch reaction,https://en.wikipedia.org/wiki/Baudisch_reaction | |
| Bayer test,https://en.wikipedia.org/wiki/Bayer_test | |
| Baylis�Hillman reaction,https://en.wikipedia.org/wiki/Baylis%E2%80%93Hillman_reaction | |
| Bechamp reaction,https://en.wikipedia.org/wiki/Bechamp_reaction | |
| Bechamp reduction,https://en.wikipedia.org/wiki/Bechamp_reduction | |
| Beckmann fragmentation,https://en.wikipedia.org/wiki/Beckmann_fragmentation | |
| Beckmann rearrangement,https://en.wikipedia.org/wiki/Beckmann_rearrangement | |
| Bellus�Claisen rearrangement,https://en.wikipedia.org/wiki/Bellus%E2%80%93Claisen_rearrangement | |
| Belousov�Zhabotinsky reaction,https://en.wikipedia.org/wiki/Belousov%E2%80%93Zhabotinsky_reaction | |
| Benary reaction,https://en.wikipedia.org/wiki/Benary_reaction | |
| Benedict's reagent,https://en.wikipedia.org/wiki/Benedict%27s_reagent | |
| Benkeser reaction,https://en.wikipedia.org/wiki/Benkeser_reaction | |
| Benzidine rearrangement,https://en.wikipedia.org/wiki/Benzidine_rearrangement | |
| Benzilic acid rearrangement,https://en.wikipedia.org/wiki/Benzilic_acid_rearrangement | |
| Benzoin condensation,https://en.wikipedia.org/wiki/Benzoin_condensation | |
| Bergman cyclization,https://en.wikipedia.org/wiki/Bergman_cyclization | |
| Bergmann azlactone peptide synthesis,https://en.wikipedia.org/wiki/Bergmann_azlactone_peptide_synthesis | |
| Bergmann degradation,https://en.wikipedia.org/wiki/Bergmann_degradation | |
| Bergmann�Zervas carbobenzoxy method,https://en.wikipedia.org/wiki/Bergmann%E2%80%93Zervas_carbobenzoxy_method | |
| Bernthsen acridine synthesis,https://en.wikipedia.org/wiki/Bernthsen_acridine_synthesis | |
| Bestmann's reagent,https://en.wikipedia.org/wiki/Bestmann%27s_reagent | |
| Betti reaction,https://en.wikipedia.org/wiki/Betti_reaction | |
| Biginelli pyrimidine synthesis,https://en.wikipedia.org/wiki/Biginelli_pyrimidine_synthesis | |
| Biginelli reaction,https://en.wikipedia.org/wiki/Biginelli_reaction | |
| Bingel reaction,https://en.wikipedia.org/wiki/Bingel_reaction | |
| Birch reduction,https://en.wikipedia.org/wiki/Birch_reduction | |
| Bischler�M�hlau indole synthesis,https://en.wikipedia.org/wiki/Bischler%E2%80%93M%C3%B6hlau_indole_synthesis | |
| Bischler�Napieralski reaction,https://en.wikipedia.org/wiki/Bischler%E2%80%93Napieralski_reaction | |
| Biuret test,https://en.wikipedia.org/wiki/Biuret_test | |
| Blaise ketone synthesis,https://en.wikipedia.org/wiki/Blaise_ketone_synthesis | |
| Blaise reaction,https://en.wikipedia.org/wiki/Blaise_reaction | |
| Blanc reaction,https://en.wikipedia.org/wiki/Blanc_reaction | |
| Blanc chloromethylation,https://en.wikipedia.org/wiki/Blanc_chloromethylation | |
| Blum�Ittah aziridine synthesis,https://en.wikipedia.org/wiki/Blum%E2%80%93Ittah_aziridine_synthesis | |
| Bodroux reaction,https://en.wikipedia.org/wiki/Bodroux_reaction | |
| Bodroux�Chichibabin aldehyde synthesis,https://en.wikipedia.org/wiki/Bodroux%E2%80%93Chichibabin_aldehyde_synthesis | |
| Bogert�Cook synthesis,https://en.wikipedia.org/wiki/Bogert%E2%80%93Cook_synthesis | |
| Bohlmann-Rahtz pyridine synthesis,https://en.wikipedia.org/wiki/Bohlmann-Rahtz_pyridine_synthesis | |
| Bohn�Schmidt reaction,https://en.wikipedia.org/wiki/Bohn%E2%80%93Schmidt_reaction | |
| Boord olefin synthesis,https://en.wikipedia.org/wiki/Boord_olefin_synthesis | |
| Borodin reaction,https://en.wikipedia.org/wiki/Borodin_reaction | |
| Borsche�Drechsel cyclization,https://en.wikipedia.org/wiki/Borsche%E2%80%93Drechsel_cyclization | |
| Bosch�Meiser urea process,https://en.wikipedia.org/wiki/Bosch%E2%80%93Meiser_urea_process | |
| Bosch reaction,https://en.wikipedia.org/wiki/Bosch_reaction | |
| Bouveault aldehyde synthesis,https://en.wikipedia.org/wiki/Bouveault_aldehyde_synthesis | |
| Bouveault�Blanc reduction,https://en.wikipedia.org/wiki/Bouveault%E2%80%93Blanc_reduction | |
| Boyland�Sims oxidation,https://en.wikipedia.org/wiki/Boyland%E2%80%93Sims_oxidation | |
| Boyer Reaction,https://en.wikipedia.org/wiki/Boyer_Reaction | |
| Bredt's rule,https://en.wikipedia.org/wiki/Bredt%27s_rule | |
| Brook rearrangement,https://en.wikipedia.org/wiki/Brook_rearrangement | |
| Brown hydroboration,https://en.wikipedia.org/wiki/Brown_hydroboration | |
| Bucherer carbazole synthesis,https://en.wikipedia.org/wiki/Bucherer_carbazole_synthesis | |
| Bucherer reaction,https://en.wikipedia.org/wiki/Bucherer_reaction | |
| Bucherer�Bergs reaction,https://en.wikipedia.org/wiki/Bucherer%E2%80%93Bergs_reaction | |
| Buchner ring enlargement,https://en.wikipedia.org/wiki/Buchner_ring_enlargement | |
| B�chner�Curtius�Schlotterbeck reaction,https://en.wikipedia.org/wiki/B%C3%BCchner%E2%80%93Curtius%E2%80%93Schlotterbeck_reaction | |
| Buchwald�Hartwig amination,https://en.wikipedia.org/wiki/Buchwald%E2%80%93Hartwig_amination | |
| Bunnett reaction,https://en.wikipedia.org/wiki/Bunnett_reaction | |
| Burgess reagent,https://en.wikipedia.org/wiki/Burgess_reagent | |
| C[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=4 | |
| Cadiot�Chodkiewicz coupling,https://en.wikipedia.org/wiki/Cadiot%E2%80%93Chodkiewicz_coupling | |
| Cadogan-Sundberg indole synthesis,https://en.wikipedia.org/wiki/Cadogan-Sundberg_indole_synthesis | |
| Camps quinoline synthesis,https://en.wikipedia.org/wiki/Camps_quinoline_synthesis | |
| Cannizzaro reaction,https://en.wikipedia.org/wiki/Cannizzaro_reaction | |
| Carbohydrate acetalisation,https://en.wikipedia.org/wiki/Carbohydrate_acetalisation | |
| Carbonyl reduction,https://en.wikipedia.org/wiki/Carbonyl_reduction | |
| Carbonylation,https://en.wikipedia.org/wiki/Carbonylation | |
| Carbylamine reaction,https://en.wikipedia.org/wiki/Carbylamine_reaction | |
| Carroll reaction,https://en.wikipedia.org/wiki/Carroll_reaction | |
| Castro�Stephens coupling,https://en.wikipedia.org/wiki/Castro%E2%80%93Stephens_coupling | |
| Catalytic reforming,https://en.wikipedia.org/wiki/Catalytic_reforming | |
| Catellani Reaction,https://en.wikipedia.org/wiki/Catellani_Reaction | |
| CBS reduction,https://en.wikipedia.org/wiki/CBS_reduction | |
| Chan�Lam coupling,https://en.wikipedia.org/wiki/Boronic_acid | |
| Chapman rearrangement,https://en.wikipedia.org/wiki/Chapman_rearrangement | |
| Cheletropic reaction,https://en.wikipedia.org/wiki/Cheletropic_reaction | |
| Chichibabin pyridine synthesis,https://en.wikipedia.org/wiki/Chichibabin_pyridine_synthesis | |
| Chichibabin reaction,https://en.wikipedia.org/wiki/Chichibabin_reaction | |
| Chiral pool synthesis,https://en.wikipedia.org/wiki/Chiral_pool_synthesis | |
| Chugaev elimination,https://en.wikipedia.org/wiki/Chugaev_elimination | |
| Ciamician�Dennstedt rearrangement,https://en.wikipedia.org/wiki/Ciamician%E2%80%93Dennstedt_rearrangement | |
| Claisen condensation,https://en.wikipedia.org/wiki/Claisen_condensation | |
| Claisen rearrangement,https://en.wikipedia.org/wiki/Claisen_rearrangement | |
| Claisen�Schmidt condensation,https://en.wikipedia.org/wiki/Claisen%E2%80%93Schmidt_condensation | |
| Clemmensen reduction,https://en.wikipedia.org/wiki/Clemmensen_reduction | |
| Collins reagent,https://en.wikipedia.org/wiki/Collins_reagent | |
| Combes quinoline synthesis,https://en.wikipedia.org/wiki/Combes_quinoline_synthesis | |
| Conia reaction,https://en.wikipedia.org/wiki/Conia_reaction | |
| Conrad�Limpach synthesis,https://en.wikipedia.org/wiki/Conrad%E2%80%93Limpach_synthesis | |
| Cook�Heilbron thiazole synthesis,https://en.wikipedia.org/wiki/Cook%E2%80%93Heilbron_thiazole_synthesis | |
| Cope elimination,https://en.wikipedia.org/wiki/Cope_elimination | |
| Corey reagent,https://en.wikipedia.org/wiki/Corey_reagent | |
| Corey�Bakshi�Shibata reduction,https://en.wikipedia.org/wiki/Corey%E2%80%93Bakshi%E2%80%93Shibata_reduction | |
| Corey�Fuchs reaction,https://en.wikipedia.org/wiki/Corey%E2%80%93Fuchs_reaction | |
| Corey�Gilman�Ganem oxidation,https://en.wikipedia.org/wiki/Corey%E2%80%93Gilman%E2%80%93Ganem_oxidation | |
| Corey�Kim oxidation,https://en.wikipedia.org/wiki/Corey%E2%80%93Kim_oxidation | |
| Corey-Nicolaou macrolactonization,https://en.wikipedia.org/wiki/Corey-Nicolaou_macrolactonization | |
| "Corey�Posner, Whitesides�House reaction","https://en.wikipedia.org/wiki/Corey%E2%80%93Posner,_Whitesides%E2%80%93House_reaction" | |
| Corey-Seebach reaction,https://en.wikipedia.org/wiki/Corey-Seebach_reaction | |
| Corey�Winter olefin synthesis,https://en.wikipedia.org/wiki/Corey%E2%80%93Winter_olefin_synthesis | |
| Corey�Winter reaction,https://en.wikipedia.org/wiki/Corey%E2%80%93Winter_reaction | |
| Cornforth rearrangement,https://en.wikipedia.org/wiki/Cornforth_rearrangement | |
| Coupling reaction,https://en.wikipedia.org/wiki/Coupling_reaction | |
| Crabb� reaction,https://en.wikipedia.org/wiki/Crabb%C3%A9_reaction | |
| Craig method,https://en.wikipedia.org/wiki/Craig_method | |
| Cram's rule of asymmetric induction,https://en.wikipedia.org/wiki/Cram%27s_rule_of_asymmetric_induction | |
| Creighton process,https://en.wikipedia.org/wiki/Creighton_process | |
| Criegee reaction,https://en.wikipedia.org/wiki/Criegee_reaction | |
| Criegee rearrangement,https://en.wikipedia.org/wiki/Criegee_rearrangement | |
| Cross metathesis,https://en.wikipedia.org/wiki/Cross_metathesis | |
| Crum Brown�Gibson rule,https://en.wikipedia.org/wiki/Crum_Brown%E2%80%93Gibson_rule | |
| Curtius degradation,https://en.wikipedia.org/wiki/Curtius_degradation | |
| Cyanohydrin reaction,https://en.wikipedia.org/wiki/Cyanohydrin_reaction | |
| D[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=5 | |
| Dakin reaction�(aka Dakin oxidation),https://en.wikipedia.org/wiki/Dakin_reaction | |
| Dakin�West reaction,https://en.wikipedia.org/wiki/Dakin%E2%80%93West_reaction | |
| Danheiser annulation,https://en.wikipedia.org/wiki/Danheiser_annulation | |
| Danheiser benzannulation,https://en.wikipedia.org/wiki/Danheiser_benzannulation | |
| Darapsky degradation,https://en.wikipedia.org/wiki/Darapsky_degradation | |
| Darzens halogenation,https://en.wikipedia.org/wiki/Darzens_halogenation | |
| Darzens synthesis of unsaturated ketones,https://en.wikipedia.org/wiki/Darzens_synthesis_of_unsaturated_ketones | |
| Darzens tetralin synthesis,https://en.wikipedia.org/wiki/Darzens_tetralin_synthesis | |
| Davis�Beirut reaction,https://en.wikipedia.org/wiki/Davis%E2%80%93Beirut_reaction | |
| De Kimpe aziridine synthesis,https://en.wikipedia.org/wiki/De_Kimpe_aziridine_synthesis | |
| Dehydration reaction,https://en.wikipedia.org/wiki/Dehydration_reaction | |
| Dehydrogenation,https://en.wikipedia.org/wiki/Dehydrogenation | |
| Del�pine reaction,https://en.wikipedia.org/wiki/Delepine_reaction | |
| DeMayo reaction,https://en.wikipedia.org/wiki/DeMayo_reaction | |
| Demjanov rearrangement,https://en.wikipedia.org/wiki/Demjanov_rearrangement | |
| Demjanow desamination,https://en.wikipedia.org/wiki/Demjanow_desamination | |
| Dess�Martin oxidation,https://en.wikipedia.org/wiki/Dess%E2%80%93Martin_oxidation | |
| "Diazoalkane 1,3-dipolar cycloaddition","https://en.wikipedia.org/wiki/Diazoalkane_1,3-dipolar_cycloaddition" | |
| Diazotisation,https://en.wikipedia.org/wiki/Diazotisation | |
| DIBAL-H selective reduction,https://en.wikipedia.org/wiki/DIBAL | |
| Dieckmann condensation,https://en.wikipedia.org/wiki/Dieckmann_condensation | |
| Dieckmann reaction,https://en.wikipedia.org/wiki/Dieckmann_reaction | |
| Diels�Alder reaction,https://en.wikipedia.org/wiki/Diels%E2%80%93Alder_reaction | |
| Diels�Reese reaction,https://en.wikipedia.org/wiki/Diels%E2%80%93Reese_reaction | |
| Dienol�benzene rearrangement,https://en.wikipedia.org/wiki/Dienol%E2%80%93benzene_rearrangement | |
| Dienone�phenol rearrangement,https://en.wikipedia.org/wiki/Dienone%E2%80%93phenol_rearrangement | |
| Dimroth rearrangement,https://en.wikipedia.org/wiki/Dimroth_rearrangement | |
| Di-?-methane rearrangement,https://en.wikipedia.org/wiki/Di-%CF%80-methane_rearrangement | |
| Directed ortho metalation,https://en.wikipedia.org/wiki/Directed_ortho_metalation | |
| Doebner modification,https://en.wikipedia.org/wiki/Doebner_modification | |
| Doebner reaction,https://en.wikipedia.org/wiki/Doebner_reaction | |
| Doering�LaFlamme carbon chain extension,https://en.wikipedia.org/wiki/Doering%E2%80%93LaFlamme_carbon_chain_extension | |
| D�tz reaction,https://en.wikipedia.org/wiki/D%C3%B6tz_reaction | |
| Dowd�Beckwith ring expansion reaction,https://en.wikipedia.org/wiki/Dowd%E2%80%93Beckwith_ring_expansion_reaction | |
| Duff reaction,https://en.wikipedia.org/wiki/Duff_reaction | |
| Dutt�Wormall reaction,https://en.wikipedia.org/wiki/Dutt%E2%80%93Wormall_reaction | |
| Dyotropic reaction,https://en.wikipedia.org/wiki/Dyotropic_reaction | |
| E[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=6 | |
| E1cB elimination reaction,https://en.wikipedia.org/wiki/E1cB_elimination_reaction | |
| Eder reaction,https://en.wikipedia.org/wiki/Eder_reaction | |
| Edman degradation,https://en.wikipedia.org/wiki/Edman_degradation | |
| Eglinton reaction,https://en.wikipedia.org/wiki/Eglinton_reaction | |
| Ehrlich�Sachs reaction,https://en.wikipedia.org/wiki/Ehrlich%E2%80%93Sachs_reaction | |
| Einhorn variant,https://en.wikipedia.org/wiki/Einhorn_variant | |
| Einhorn�Brunner reaction,https://en.wikipedia.org/wiki/Einhorn%E2%80%93Brunner_reaction | |
| Elbs persulfate oxidation,https://en.wikipedia.org/wiki/Elbs_persulfate_oxidation | |
| Elbs reaction,https://en.wikipedia.org/wiki/Elbs_reaction | |
| Electrochemical fluorination,https://en.wikipedia.org/wiki/Electrochemical_fluorination | |
| Electrocyclic reaction,https://en.wikipedia.org/wiki/Electrocyclic_reaction | |
| Electrophilic halogenation,https://en.wikipedia.org/wiki/Electrophilic_halogenation | |
| Electrophilic amination,https://en.wikipedia.org/wiki/Electrophilic_amination | |
| Elimination reaction,https://en.wikipedia.org/wiki/Elimination_reaction | |
| Emde degradation,https://en.wikipedia.org/wiki/Emde_degradation | |
| Emmert reaction,https://en.wikipedia.org/wiki/Emmert_reaction | |
| Enders SAMP/RAMP hydrazone-alkylation reaction,https://en.wikipedia.org/wiki/Enders_SAMP/RAMP_hydrazone-alkylation_reaction | |
| Ene reaction,https://en.wikipedia.org/wiki/Ene_reaction | |
| Enyne metathesis,https://en.wikipedia.org/wiki/Enyne_metathesis | |
| Epoxidation,https://en.wikipedia.org/wiki/Epoxidation | |
| Erlenmeyer�Pl�chl azlactone and amino-acid synthesis,https://en.wikipedia.org/wiki/Erlenmeyer%E2%80%93Pl%C3%B6chl_azlactone_and_amino-acid_synthesis | |
| Eschenmoser fragmentation,https://en.wikipedia.org/wiki/Eschenmoser_fragmentation | |
| Eschenmoser sulfide contraction,https://en.wikipedia.org/wiki/Eschenmoser_sulfide_contraction | |
| Eschweiler�Clarke reaction,https://en.wikipedia.org/wiki/Eschweiler%E2%80%93Clarke_reaction | |
| Ester pyrolysis,https://en.wikipedia.org/wiki/Ester_pyrolysis | |
| Ether cleavage,https://en.wikipedia.org/wiki/Ether | |
| �tard reaction,https://en.wikipedia.org/wiki/%C3%89tard_reaction | |
| Evans aldol,https://en.wikipedia.org/wiki/Evans_aldol | |
| Evans�Saksena reduction,https://en.wikipedia.org/wiki/Evans%E2%80%93Saksena_reduction | |
| Evans�Tishchenko reaction,https://en.wikipedia.org/wiki/Evans%E2%80%93Tishchenko_reaction | |
| F[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=7 | |
| Favorskii reaction,https://en.wikipedia.org/wiki/Favorskii_reaction | |
| Favorskii rearrangement,https://en.wikipedia.org/wiki/Favorskii_rearrangement | |
| Favorskii�Babayan synthesis,https://en.wikipedia.org/wiki/Favorskii%E2%80%93Babayan_synthesis | |
| Fehling test,https://en.wikipedia.org/wiki/Fehling%27s_solution | |
| Feist�Benary synthesis,https://en.wikipedia.org/wiki/Feist%E2%80%93Benary_synthesis | |
| Fenton reaction,https://en.wikipedia.org/wiki/Fenton_reaction | |
| Ferrario reaction,https://en.wikipedia.org/wiki/Ferrario_reaction | |
| Ferrier carbocyclization,https://en.wikipedia.org/wiki/Ferrier_carbocyclization | |
| Ferrier rearrangement,https://en.wikipedia.org/wiki/Ferrier_rearrangement | |
| F�tizon oxidation,https://en.wikipedia.org/wiki/F%C3%A9tizon_oxidation | |
| Fiesselmann thiophene synthesis,https://en.wikipedia.org/wiki/Fiesselmann_thiophene_synthesis | |
| Fischer indole synthesis,https://en.wikipedia.org/wiki/Fischer_indole_synthesis | |
| Fischer oxazole synthesis,https://en.wikipedia.org/wiki/Fischer_oxazole_synthesis | |
| Fischer peptide synthesis,https://en.wikipedia.org/wiki/Fischer_peptide_synthesis | |
| Fischer phenylhydrazine and oxazone reaction,https://en.wikipedia.org/wiki/Fischer_phenylhydrazine_and_oxazone_reaction | |
| Fischer glycosidation,https://en.wikipedia.org/wiki/Fischer_glycosidation | |
| Fischer�Hepp rearrangement,https://en.wikipedia.org/wiki/Fischer%E2%80%93Hepp_rearrangement | |
| Fischer�Speier esterification,https://en.wikipedia.org/wiki/Fischer%E2%80%93Speier_esterification | |
| Fischer Tropsch synthesis,https://en.wikipedia.org/wiki/Fischer_Tropsch_synthesis | |
| Fleming�Tamao oxidation,https://en.wikipedia.org/wiki/Fleming%E2%80%93Tamao_oxidation | |
| Flood reaction,https://en.wikipedia.org/wiki/Flood_reaction | |
| Folin�Ciocalteu reagent,https://en.wikipedia.org/wiki/Folin%E2%80%93Ciocalteu_reagent | |
| Formox process,https://en.wikipedia.org/wiki/Formox_process | |
| Forster reaction,https://en.wikipedia.org/wiki/Forster_reaction | |
| Forster�Decker method,https://en.wikipedia.org/wiki/Forster%E2%80%93Decker_method | |
| Fowler process,https://en.wikipedia.org/wiki/Fluorocarbon | |
| Franchimont reaction,https://en.wikipedia.org/wiki/Franchimont_reaction | |
| Frankland synthesis,https://en.wikipedia.org/wiki/Frankland_synthesis | |
| Frankland�Duppa reaction,https://en.wikipedia.org/wiki/Frankland%E2%80%93Duppa_reaction | |
| Fr�ter�Seebach alkylation,https://en.wikipedia.org/wiki/Fr%C3%A1ter%E2%80%93Seebach_alkylation | |
| Free radical halogenation,https://en.wikipedia.org/wiki/Free_radical_halogenation | |
| Freund reaction,https://en.wikipedia.org/wiki/Freund_reaction | |
| Friedel�Crafts acylation,https://en.wikipedia.org/wiki/Friedel%E2%80%93Crafts_reaction | |
| Friedel�Crafts alkylation,https://en.wikipedia.org/wiki/Friedel%E2%80%93Crafts_reaction | |
| Friedl�nder synthesis,https://en.wikipedia.org/wiki/Friedl%C3%A4nder_synthesis | |
| Fries rearrangement,https://en.wikipedia.org/wiki/Fries_rearrangement | |
| Fritsch�Buttenberg�Wiechell rearrangement,https://en.wikipedia.org/wiki/Fritsch%E2%80%93Buttenberg%E2%80%93Wiechell_rearrangement | |
| Fujimoto�Belleau reaction,https://en.wikipedia.org/wiki/Fujimoto%E2%80%93Belleau_reaction | |
| Fujiwara�Moritani reaction,https://en.wikipedia.org/wiki/Fujiwara%E2%80%93Moritani_reaction | |
| Fukuyama coupling,https://en.wikipedia.org/wiki/Fukuyama_coupling | |
| Fukuyama indole synthesis,https://en.wikipedia.org/wiki/Fukuyama_indole_synthesis | |
| Fukuyama reduction,https://en.wikipedia.org/wiki/Fukuyama_reduction | |
| G[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=8 | |
| Gabriel ethylenimine method,https://en.wikipedia.org/wiki/Gabriel_ethylenimine_method | |
| Gabriel synthesis,https://en.wikipedia.org/wiki/Gabriel_synthesis | |
| Gallagher�Hollander degradation,https://en.wikipedia.org/wiki/Gallagher%E2%80%93Hollander_degradation | |
| Gassman indole synthesis,https://en.wikipedia.org/wiki/Gassman_indole_synthesis | |
| Gastaldi synthesis,https://en.wikipedia.org/wiki/Gastaldi_synthesis | |
| Gattermann aldehyde synthesis,https://en.wikipedia.org/wiki/Gattermann_aldehyde_synthesis | |
| Gattermann Koch reaction,https://en.wikipedia.org/wiki/Gattermann_Koch_reaction | |
| Gattermann reaction,https://en.wikipedia.org/wiki/Gattermann_reaction | |
| Geminal halide hydrolysis,https://en.wikipedia.org/wiki/Geminal_halide_hydrolysis | |
| Gewald reaction,https://en.wikipedia.org/wiki/Gewald_reaction | |
| Gibbs phthalic anhydride process,https://en.wikipedia.org/wiki/Gibbs_phthalic_anhydride_process | |
| Gilman reagent,https://en.wikipedia.org/wiki/Gilman_reagent | |
| Glaser coupling,https://en.wikipedia.org/wiki/Glaser_coupling | |
| Glycol cleavage,https://en.wikipedia.org/wiki/Glycol_cleavage | |
| Gomberg�Bachmann reaction,https://en.wikipedia.org/wiki/Gomberg%E2%80%93Bachmann_reaction | |
| Gomberg�Bachmann�Hey reaction,https://en.wikipedia.org/wiki/Gomberg%E2%80%93Bachmann%E2%80%93Hey_reaction | |
| Gomberg radical reaction,https://en.wikipedia.org/wiki/Gomberg_radical_reaction | |
| Gould�Jacobs reaction,https://en.wikipedia.org/wiki/Gould%E2%80%93Jacobs_reaction | |
| Graebe�Ullmann synthesis,https://en.wikipedia.org/wiki/Graebe%E2%80%93Ullmann_synthesis | |
| Grignard degradation,https://en.wikipedia.org/wiki/Grignard_degradation | |
| Griesbaum coozonolysis,https://en.wikipedia.org/wiki/Griesbaum_coozonolysis | |
| Grignard reaction,https://en.wikipedia.org/wiki/Grignard_reaction | |
| Grob fragmentation,https://en.wikipedia.org/wiki/Grob_fragmentation | |
| Grundmann aldehyde synthesis,https://en.wikipedia.org/wiki/Grundmann_aldehyde_synthesis | |
| Gryszkiewicz�Trochimowski and McCombie method,https://en.wikipedia.org/w/index.php?title=Gryszkiewicz%E2%80%93Trochimowski_and_McCombie_method&action=edit&redlink=1 | |
| Guareschi�Thorpe condensation,https://en.wikipedia.org/wiki/Guareschi%E2%80%93Thorpe_condensation | |
| Guerbet reaction,https://en.wikipedia.org/wiki/Guerbet_reaction | |
| Gutknecht pyrazine synthesis,https://en.wikipedia.org/wiki/Gutknecht_pyrazine_synthesis | |
| H[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=9 | |
| Hajos�Parrish�Eder�Sauer�Wiechert reaction,https://en.wikipedia.org/wiki/Hajos%E2%80%93Parrish%E2%80%93Eder%E2%80%93Sauer%E2%80%93Wiechert_reaction | |
| Haller�Bauer reaction,https://en.wikipedia.org/wiki/Haller%E2%80%93Bauer_reaction | |
| Haloform reaction,https://en.wikipedia.org/wiki/Haloform_reaction | |
| Halogen addition reaction,https://en.wikipedia.org/wiki/Halogen_addition_reaction | |
| Halohydrin formation reaction,https://en.wikipedia.org/wiki/Halohydrin_formation_reaction | |
| Hammett equation,https://en.wikipedia.org/wiki/Hammett_equation | |
| Hammick reaction,https://en.wikipedia.org/wiki/Hammick_reaction | |
| Hantzsch pyrrole synthesis,https://en.wikipedia.org/wiki/Hantzsch_pyrrole_synthesis | |
| Hantzsch�Collidin synthesis,https://en.wikipedia.org/wiki/Hantzsch%E2%80%93Collidin_synthesis | |
| Harries ozonide reaction,https://en.wikipedia.org/wiki/Harries_ozonide_reaction | |
| Haworth methylation,https://en.wikipedia.org/wiki/Haworth_methylation | |
| Haworth Phenanthrene synthesis,https://en.wikipedia.org/wiki/Haworth_Phenanthrene_synthesis | |
| Haworth reaction,https://en.wikipedia.org/wiki/Haworth_reaction | |
| Hay coupling,https://en.wikipedia.org/wiki/Hay_coupling | |
| Hayashi rearrangement,https://en.wikipedia.org/wiki/Hayashi_rearrangement | |
| Heck reaction,https://en.wikipedia.org/wiki/Heck_reaction | |
| Hegedus indole synthesis,https://en.wikipedia.org/wiki/Hegedus_indole_synthesis | |
| Helferich method,https://en.wikipedia.org/wiki/Helferich_method | |
| Hell�Volhard�Zelinsky halogenation,https://en.wikipedia.org/wiki/Hell%E2%80%93Volhard%E2%80%93Zelinsky_halogenation | |
| Hemetsberger indole synthesis,https://en.wikipedia.org/wiki/Hemetsberger_indole_synthesis | |
| Hemetsberger�Knittel synthesis,https://en.wikipedia.org/wiki/Hemetsberger%E2%80%93Knittel_synthesis | |
| Herzig�Meyer alkimide group determination,https://en.wikipedia.org/wiki/Herzig%E2%80%93Meyer_alkimide_group_determination | |
| Heumann indigo synthesis,https://en.wikipedia.org/wiki/Heumann_indigo_synthesis | |
| Hiyama coupling,https://en.wikipedia.org/wiki/Hiyama_coupling | |
| Hydration reaction,https://en.wikipedia.org/wiki/Hydration_reaction | |
| Hydroamination,https://en.wikipedia.org/wiki/Hydroamination | |
| Hydrodesulfurization,https://en.wikipedia.org/wiki/Hydrodesulfurization | |
| Hydrogenolysis,https://en.wikipedia.org/wiki/Hydrogenolysis | |
| Hydrosilylation,https://en.wikipedia.org/wiki/Hydrosilylation | |
| Hinsberg indole synthesis,https://en.wikipedia.org/wiki/Hinsberg_indole_synthesis | |
| Hinsberg oxindole synthesis,https://en.wikipedia.org/wiki/Hinsberg_oxindole_synthesis | |
| Hinsberg reaction,https://en.wikipedia.org/wiki/Hinsberg_reaction | |
| Hinsberg separation,https://en.wikipedia.org/wiki/Hinsberg_separation | |
| Hinsberg sulfone synthesis,https://en.wikipedia.org/wiki/Hinsberg_sulfone_synthesis | |
| Hirao coupling,https://en.wikipedia.org/wiki/Hirao_coupling | |
| Hoch�Campbell ethylenimine synthesis,https://en.wikipedia.org/wiki/Hoch%E2%80%93Campbell_ethylenimine_synthesis | |
| Hock rearrangement,https://en.wikipedia.org/wiki/Hock_rearrangement | |
| Hofmann bromamide reaction,https://en.wikipedia.org/wiki/Hofmann_rearrangement | |
| Hofmann elimination,https://en.wikipedia.org/wiki/Hofmann_elimination | |
| Hofmann product,https://en.wikipedia.org/wiki/Hofmann_product | |
| Hofmann rearrangement,https://en.wikipedia.org/wiki/Hofmann_rearrangement | |
| Hofmann�Martius rearrangement,https://en.wikipedia.org/wiki/Hofmann%E2%80%93Martius_rearrangement | |
| Hofmann's rule,https://en.wikipedia.org/wiki/Hofmann%27s_rule | |
| Hofmann�Sand reaction,https://en.wikipedia.org/wiki/Hofmann%E2%80%93Sand_reaction | |
| Homo rearrangement of steroids,https://en.wikipedia.org/wiki/Homo_rearrangement_of_steroids | |
| Hooker reaction,https://en.wikipedia.org/wiki/Hooker_reaction | |
| Horner�Wadsworth�Emmons reaction,https://en.wikipedia.org/wiki/Horner%E2%80%93Wadsworth%E2%80%93Emmons_reaction | |
| Hoesch reaction,https://en.wikipedia.org/wiki/Hoesch_reaction | |
| Hosomi�Sakurai reaction,https://en.wikipedia.org/wiki/Hosomi%E2%80%93Sakurai_reaction | |
| Houben�Fischer synthesis,https://en.wikipedia.org/wiki/Houben%E2%80%93Fischer_synthesis | |
| Hudlicky fluorination,https://en.wikipedia.org/wiki/Fluorination_with_aminosulfuranes | |
| Huisgen cycloaddition,https://en.wikipedia.org/wiki/Huisgen_cycloaddition | |
| "Hurd-Mori 1,2,3-thiadiazole synthesis","https://en.wikipedia.org/wiki/Hurd-Mori_1,2,3-thiadiazole_synthesis" | |
| Hydroboration,https://en.wikipedia.org/wiki/Hydroboration | |
| Hydrocarbon cracking,https://en.wikipedia.org/wiki/Cracking_(chemistry) | |
| Hydrohalogenation,https://en.wikipedia.org/wiki/Hydrohalogenation | |
| I[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=10 | |
| Indium mediated allylation,https://en.wikipedia.org/wiki/Indium_mediated_allylation | |
| Ing�Manske procedure,https://en.wikipedia.org/wiki/Ing%E2%80%93Manske_procedure | |
| Ipso substitution,https://en.wikipedia.org/wiki/Ipso_substitution | |
| Ireland�Claisen rearrangement,https://en.wikipedia.org/wiki/Ireland%E2%80%93Claisen_rearrangement | |
| Isay reaction,https://en.wikipedia.org/wiki/Isay_reaction | |
| Ishikawa reagent,https://en.wikipedia.org/wiki/Ishikawa_reagent | |
| trans-cis�isomerism,https://en.wikipedia.org/wiki/Isomer | |
| J[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=11 | |
| Jacobsen epoxidation,https://en.wikipedia.org/wiki/Jacobsen_epoxidation | |
| Jacobsen rearrangement,https://en.wikipedia.org/wiki/Jacobsen_rearrangement | |
| Janovsky reaction,https://en.wikipedia.org/wiki/Janovsky_reaction | |
| Japp�Klingemann reaction,https://en.wikipedia.org/wiki/Japp%E2%80%93Klingemann_reaction | |
| Japp�Maitland condensation,https://en.wikipedia.org/wiki/Japp%E2%80%93Maitland_condensation | |
| Jocic reaction,https://en.wikipedia.org/wiki/Jocic_reaction | |
| Johnson�Claisen rearrangement,https://en.wikipedia.org/wiki/Claisen_rearrangement | |
| Jordan�Ullmann�Goldberg synthesis,https://en.wikipedia.org/wiki/Jordan%E2%80%93Ullmann%E2%80%93Goldberg_synthesis | |
| K[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=12 | |
| Kabachnik�Fields reaction,https://en.wikipedia.org/wiki/Kabachnik%E2%80%93Fields_reaction | |
| Kharasch�Sosnovsky reaction,https://en.wikipedia.org/wiki/Kharasch%E2%80%93Sosnovsky_reaction | |
| Keck asymmetric allylation,https://en.wikipedia.org/wiki/Keck_asymmetric_allylation | |
| Ketimine Mannich reaction,https://en.wikipedia.org/wiki/Ketimine_Mannich_reaction | |
| Ketone halogenation,https://en.wikipedia.org/wiki/Ketone_halogenation | |
| Kiliani�Fischer synthesis,https://en.wikipedia.org/wiki/Kiliani%E2%80%93Fischer_synthesis | |
| Kindler reaction,https://en.wikipedia.org/wiki/Kindler_reaction | |
| Kishner cyclopropane synthesis,https://en.wikipedia.org/wiki/Kishner_cyclopropane_synthesis | |
| Knoevenagel condensation,https://en.wikipedia.org/wiki/Knoevenagel_condensation | |
| Knorr pyrazole synthesis,https://en.wikipedia.org/wiki/Knorr_pyrazole_synthesis | |
| Knorr pyrrole synthesis,https://en.wikipedia.org/wiki/Knorr_pyrrole_synthesis | |
| Knorr quinoline synthesis,https://en.wikipedia.org/wiki/Knorr_quinoline_synthesis | |
| Koch�Haaf reaction,https://en.wikipedia.org/wiki/Koch%E2%80%93Haaf_reaction | |
| Kochi reaction,https://en.wikipedia.org/wiki/Kochi_reaction | |
| Koenigs�Knorr reaction,https://en.wikipedia.org/wiki/Koenigs%E2%80%93Knorr_reaction | |
| Kolbe electrolysis,https://en.wikipedia.org/wiki/Kolbe_electrolysis | |
| Kolbe nitrile synthesis,https://en.wikipedia.org/wiki/Kolbe_nitrile_synthesis | |
| Kolbe�Schmitt reaction,https://en.wikipedia.org/wiki/Kolbe%E2%80%93Schmitt_reaction | |
| Kornblum oxidation,https://en.wikipedia.org/wiki/Kornblum_oxidation | |
| Kornblum�DeLaMare rearrangement,https://en.wikipedia.org/wiki/Kornblum%E2%80%93DeLaMare_rearrangement | |
| Kostanecki acylation,https://en.wikipedia.org/wiki/Kostanecki_acylation | |
| Kowalski ester homologation,https://en.wikipedia.org/wiki/Kowalski_ester_homologation | |
| Krapcho decarboxylation,https://en.wikipedia.org/wiki/Krapcho_decarboxylation | |
| Krische allylation,https://en.wikipedia.org/wiki/Krische_allylation | |
| Kr�hnke aldehyde synthesis,https://en.wikipedia.org/wiki/Kr%C3%B6hnke_aldehyde_synthesis | |
| Kr�hnke oxidation,https://en.wikipedia.org/wiki/Kr%C3%B6hnke_oxidation | |
| Kr�hnke pyridine synthesis,https://en.wikipedia.org/wiki/Kr%C3%B6hnke_pyridine_synthesis | |
| Kucherov reaction,https://en.wikipedia.org/wiki/Kucherov_reaction | |
| Kuhn�Winterstein reaction,https://en.wikipedia.org/wiki/Kuhn%E2%80%93Winterstein_reaction | |
| Kulinkovich reaction,https://en.wikipedia.org/wiki/Kulinkovich_reaction | |
| Kumada coupling,https://en.wikipedia.org/wiki/Kumada_coupling | |
| L[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=13 | |
| Larock indole synthesis,https://en.wikipedia.org/wiki/Larock_indole_synthesis | |
| Lawesson's reagent,https://en.wikipedia.org/wiki/Lawesson%27s_reagent | |
| Lebedev process,https://en.wikipedia.org/wiki/Lebedev_process | |
| Lehmstedt�Tanasescu reaction,https://en.wikipedia.org/wiki/Lehmstedt%E2%80%93Tanasescu_reaction | |
| Leimgruber�Batcho indole synthesis,https://en.wikipedia.org/wiki/Leimgruber%E2%80%93Batcho_indole_synthesis | |
| Letts nitrile synthesis,https://en.wikipedia.org/wiki/Letts_nitrile_synthesis | |
| Leuckart reaction,https://en.wikipedia.org/wiki/Leuckart_reaction | |
| Leuckart thiophenol reaction,https://en.wikipedia.org/wiki/Leuckart_thiophenol_reaction | |
| Leuckart�Wallach reaction,https://en.wikipedia.org/wiki/Leuckart%E2%80%93Wallach_reaction | |
| Leuckart amide synthesis,https://en.wikipedia.org/wiki/Amide | |
| Levinstein process,https://en.wikipedia.org/wiki/Levinstein_process | |
| Ley oxidation,https://en.wikipedia.org/wiki/Ley_oxidation | |
| Liebeskind�Srogl coupling,https://en.wikipedia.org/wiki/Liebeskind%E2%80%93Srogl_coupling | |
| Liebig melamine synthesis,https://en.wikipedia.org/wiki/Melamine | |
| Lindlar catalyst,https://en.wikipedia.org/wiki/Lindlar_catalyst | |
| Lobry de Bruyn�Van Ekenstein transformation,https://en.wikipedia.org/wiki/Lobry_de_Bruyn%E2%80%93Van_Ekenstein_transformation | |
| Lombardo methylenation,https://en.wikipedia.org/wiki/Lombardo_methylenation | |
| Lossen rearrangement,https://en.wikipedia.org/wiki/Lossen_rearrangement | |
| Lucas' reagent,https://en.wikipedia.org/wiki/Lucas%27_reagent | |
| Luche reduction,https://en.wikipedia.org/wiki/Luche_reduction | |
| M[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=14 | |
| Maillard reaction,https://en.wikipedia.org/wiki/Maillard_reaction | |
| Madelung synthesis,https://en.wikipedia.org/wiki/Madelung_synthesis | |
| Malonic ester synthesis,https://en.wikipedia.org/wiki/Malonic_ester_synthesis | |
| Mannich reaction,https://en.wikipedia.org/wiki/Mannich_reaction | |
| Mark�Lam deoxygenation,https://en.wikipedia.org/wiki/Mark%C3%B3%E2%80%93Lam_deoxygenation | |
| Marschalk reaction,https://en.wikipedia.org/wiki/Marschalk_reaction | |
| Martinet dioxindole synthesis,https://en.wikipedia.org/wiki/Martinet_dioxindole_synthesis | |
| McDougall monoprotection,https://en.wikipedia.org/wiki/Silyl_ether | |
| McFadyen�Stevens reaction,https://en.wikipedia.org/wiki/McFadyen%E2%80%93Stevens_reaction | |
| McMurry reaction,https://en.wikipedia.org/wiki/McMurry_reaction | |
| Meerwein arylation,https://en.wikipedia.org/wiki/Meerwein_arylation | |
| Meerwein�Ponndorf�Verley reduction,https://en.wikipedia.org/wiki/Meerwein%E2%80%93Ponndorf%E2%80%93Verley_reduction | |
| Meisenheimer rearrangement,https://en.wikipedia.org/wiki/Meisenheimer_rearrangement | |
| Meissenheimer complex,https://en.wikipedia.org/wiki/Meissenheimer_complex | |
| Menshutkin reaction,https://en.wikipedia.org/wiki/Menshutkin_reaction | |
| Metal-ion-catalyzed ?-bond rearrangement,https://en.wikipedia.org/wiki/Metal-ion-catalyzed_%CF%83-bond_rearrangement | |
| Mesylation,https://en.wikipedia.org/wiki/Mesylate | |
| Merckwald asymmetric synthesis,https://en.wikipedia.org/wiki/Merckwald_asymmetric_synthesis | |
| Metallo-ene reaction,https://en.wikipedia.org/wiki/Metallo-ene_reaction | |
| Methylation,https://en.wikipedia.org/wiki/Methylation | |
| Meyer and Hartmann reaction,https://en.wikipedia.org/wiki/Meyer_and_Hartmann_reaction | |
| Meyer reaction,https://en.wikipedia.org/wiki/Meyer_reaction | |
| Meyer synthesis,https://en.wikipedia.org/wiki/Meyer_synthesis | |
| Meyer�Schuster rearrangement,https://en.wikipedia.org/wiki/Meyer%E2%80%93Schuster_rearrangement | |
| Michael addition,https://en.wikipedia.org/wiki/Michael_addition | |
| Michael condensation,https://en.wikipedia.org/wiki/Michael_condensation | |
| Michaelis�Arbuzov reaction,https://en.wikipedia.org/wiki/Michaelis%E2%80%93Arbuzov_reaction | |
| Midland Alpine borane reduction,https://en.wikipedia.org/wiki/Midland_Alpine_borane_reduction | |
| Mignonac reaction,https://en.wikipedia.org/wiki/Mignonac_reaction | |
| Milas hydroxylation�of olefins,https://en.wikipedia.org/wiki/Milas_hydroxylation | |
| Minisci reaction,https://en.wikipedia.org/wiki/Minisci_reaction | |
| Mislow�Evans rearrangement,https://en.wikipedia.org/wiki/Mislow%E2%80%93Evans_rearrangement | |
| Mitsunobu reaction,https://en.wikipedia.org/wiki/Mitsunobu_reaction | |
| Miyaura borylation,https://en.wikipedia.org/wiki/Miyaura_borylation | |
| Modified Wittig-Claisen tandem reaction,https://en.wikipedia.org/wiki/Modified_Wittig-Claisen_tandem_reaction | |
| Molisch's test,https://en.wikipedia.org/wiki/Molisch%27s_test | |
| Mozingo reduction,https://en.wikipedia.org/wiki/Mozingo_reduction | |
| Mukaiyama hydration,https://en.wikipedia.org/wiki/Mukaiyama_hydration | |
| Myers' asymmetric alkylation,https://en.wikipedia.org/wiki/Myers%27_asymmetric_alkylation | |
| N[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=15 | |
| Nametkin rearrangement,https://en.wikipedia.org/wiki/Nametkin_rearrangement | |
| Narasaka�Prasad reduction,https://en.wikipedia.org/wiki/Narasaka%E2%80%93Prasad_reduction | |
| Nazarov cyclization reaction,https://en.wikipedia.org/wiki/Nazarov_cyclization_reaction | |
| Neber rearrangement,https://en.wikipedia.org/wiki/Neber_rearrangement | |
| Nef reaction,https://en.wikipedia.org/wiki/Nef_reaction | |
| Negishi coupling,https://en.wikipedia.org/wiki/Negishi_coupling | |
| Negishi zipper reaction,https://en.wikipedia.org/wiki/Negishi_zipper_reaction | |
| Nenitzescu indole synthesis,https://en.wikipedia.org/wiki/Nenitzescu_indole_synthesis | |
| Nenitzescu reductive acylation,https://en.wikipedia.org/wiki/Nenitzescu_reductive_acylation | |
| Newman�Kwart rearrangement,https://en.wikipedia.org/wiki/Newman%E2%80%93Kwart_rearrangement | |
| Nicholas reaction,https://en.wikipedia.org/wiki/Nicholas_reaction | |
| Niementowski quinazoline synthesis,https://en.wikipedia.org/wiki/Niementowski_quinazoline_synthesis | |
| Niementowski quinoline synthesis,https://en.wikipedia.org/wiki/Niementowski_quinoline_synthesis | |
| Nierenstein reaction,https://en.wikipedia.org/wiki/Nierenstein_reaction | |
| NIH shift,https://en.wikipedia.org/wiki/NIH_shift | |
| Ninhydrin test,https://en.wikipedia.org/wiki/Ninhydrin | |
| Nitroaldol reaction,https://en.wikipedia.org/wiki/Nitroaldol_reaction | |
| Nitrone-olefin 3+2 cycloaddition,https://en.wikipedia.org/wiki/Nitrone-olefin_3%2B2_cycloaddition | |
| Normant reagents,https://en.wikipedia.org/wiki/Normant_reagents | |
| Noyori asymmetric hydrogenation,https://en.wikipedia.org/wiki/Noyori_asymmetric_hydrogenation | |
| Nozaki�Hiyama�Kishi reaction,https://en.wikipedia.org/wiki/Nozaki%E2%80%93Hiyama%E2%80%93Kishi_reaction | |
| Nucleophilic acyl substitution,https://en.wikipedia.org/wiki/Nucleophilic_acyl_substitution | |
| O[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=16 | |
| Ohira�Bestmann reaction,https://en.wikipedia.org/wiki/Ohira%E2%80%93Bestmann_reaction | |
| Olah reagent,https://en.wikipedia.org/wiki/Olah_reagent | |
| Olefin metathesis,https://en.wikipedia.org/wiki/Olefin_metathesis | |
| Oppenauer oxidation,https://en.wikipedia.org/wiki/Oppenauer_oxidation | |
| Overman rearrangement,https://en.wikipedia.org/wiki/Overman_rearrangement | |
| Oxidative decarboxylation,https://en.wikipedia.org/wiki/Pyruvate_decarboxylation | |
| Oxo synthesis,https://en.wikipedia.org/wiki/Oxo_synthesis | |
| Oxy-Cope rearrangement,https://en.wikipedia.org/wiki/Oxy-Cope_rearrangement | |
| Oxymercuration,https://en.wikipedia.org/wiki/Oxymercuration | |
| Oxidation of alcohols to carbonyl compounds,https://en.wikipedia.org/wiki/Oxidation_of_alcohols_to_carbonyl_compounds | |
| Ozonolysis,https://en.wikipedia.org/wiki/Ozonolysis | |
| P[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=17 | |
| Paal�Knorr pyrrole synthesis,https://en.wikipedia.org/wiki/Paal%E2%80%93Knorr_pyrrole_synthesis | |
| Paal�Knorr synthesis,https://en.wikipedia.org/wiki/Paal%E2%80%93Knorr_synthesis | |
| Paneth technique,https://en.wikipedia.org/wiki/Paneth_technique | |
| Passerini reaction,https://en.wikipedia.org/wiki/Passerini_reaction | |
| Patern�B�chi reaction,https://en.wikipedia.org/wiki/Patern%C3%B2%E2%80%93B%C3%BCchi_reaction | |
| Pauson�Khand reaction,https://en.wikipedia.org/wiki/Pauson%E2%80%93Khand_reaction | |
| Payne rearrangement,https://en.wikipedia.org/wiki/Payne_rearrangement | |
| Pechmann condensation,https://en.wikipedia.org/wiki/Pechmann_condensation | |
| Pechmann pyrazole synthesis,https://en.wikipedia.org/wiki/Pechmann_pyrazole_synthesis | |
| Pellizzari reaction,https://en.wikipedia.org/wiki/Pellizzari_reaction | |
| Pelouze synthesis,https://en.wikipedia.org/wiki/Pelouze_synthesis | |
| Peptide synthesis,https://en.wikipedia.org/wiki/Peptide_synthesis | |
| Perkin alicyclic synthesis,https://en.wikipedia.org/wiki/Perkin_alicyclic_synthesis | |
| Perkin reaction,https://en.wikipedia.org/wiki/Perkin_reaction | |
| Perkin rearrangement,https://en.wikipedia.org/wiki/Perkin_rearrangement | |
| Perkow reaction,https://en.wikipedia.org/wiki/Perkow_reaction | |
| Petasis reaction,https://en.wikipedia.org/wiki/Petasis_reaction | |
| Petasis reagent,https://en.wikipedia.org/wiki/Petasis_reagent | |
| Peterson olefination,https://en.wikipedia.org/wiki/Peterson_olefination | |
| Peterson reaction,https://en.wikipedia.org/wiki/Peterson_reaction | |
| Petrenko-Kritschenko piperidone synthesis,https://en.wikipedia.org/wiki/Petrenko-Kritschenko_piperidone_synthesis | |
| Pfau�Plattner azulene synthesis,https://en.wikipedia.org/wiki/Pfau%E2%80%93Plattner_azulene_synthesis | |
| Pfitzinger reaction,https://en.wikipedia.org/wiki/Pfitzinger_reaction | |
| Pfitzner�Moffatt oxidation,https://en.wikipedia.org/wiki/Pfitzner%E2%80%93Moffatt_oxidation | |
| Phosphonium coupling,https://en.wikipedia.org/wiki/Phosphonium_coupling | |
| Photosynthesis,https://en.wikipedia.org/wiki/Photosynthesis | |
| Piancatelli rearrangement,https://en.wikipedia.org/wiki/Piancatelli_rearrangement | |
| Pictet�Gams isoquinoline synthesis,https://en.wikipedia.org/wiki/Pictet%E2%80%93Gams_isoquinoline_synthesis | |
| Pictet�Hubert reaction,https://en.wikipedia.org/wiki/Pictet%E2%80%93Hubert_reaction | |
| Pictet�Spengler tetrahydroisoquinoline synthesis,https://en.wikipedia.org/wiki/Pictet%E2%80%93Spengler_tetrahydroisoquinoline_synthesis | |
| Pictet�Spengler reaction,https://en.wikipedia.org/wiki/Pictet%E2%80%93Spengler_reaction | |
| Piloty�Robinson pyrrole synthesis,https://en.wikipedia.org/wiki/Piloty%E2%80%93Robinson_pyrrole_synthesis | |
| Pinacol coupling reaction,https://en.wikipedia.org/wiki/Pinacol_coupling_reaction | |
| Pinacol rearrangement,https://en.wikipedia.org/wiki/Pinacol_rearrangement | |
| Pinner amidine synthesis,https://en.wikipedia.org/wiki/Pinner_amidine_synthesis | |
| Pinner method for ortho esters,https://en.wikipedia.org/wiki/Pinner_method_for_ortho_esters | |
| Pinner reaction,https://en.wikipedia.org/wiki/Pinner_reaction | |
| Pinner triazine synthesis,https://en.wikipedia.org/wiki/Pinner_triazine_synthesis | |
| Pinnick oxidation,https://en.wikipedia.org/wiki/Pinnick_oxidation | |
| Piria reaction,https://en.wikipedia.org/wiki/Piria_reaction | |
| Polonovski reaction,https://en.wikipedia.org/wiki/Polonovski_reaction | |
| Pomeranz�Fritsch reaction,https://en.wikipedia.org/wiki/Pomeranz%E2%80%93Fritsch_reaction | |
| Ponzio reaction,https://en.wikipedia.org/wiki/Ponzio_reaction | |
| Prato reaction,https://en.wikipedia.org/wiki/Prato_reaction | |
| Prelog strain,https://en.wikipedia.org/wiki/Prelog_strain | |
| Prevost reaction,https://en.wikipedia.org/wiki/Prevost_reaction | |
| Prileschajew reaction,https://en.wikipedia.org/wiki/Prileschajew_reaction | |
| Prilezhaev reaction,https://en.wikipedia.org/wiki/Prilezhaev_reaction | |
| Prins reaction,https://en.wikipedia.org/wiki/Prins_reaction | |
| Prinzbach synthesis,https://en.wikipedia.org/wiki/Prinzbach_synthesis | |
| Protecting group,https://en.wikipedia.org/wiki/Protecting_group | |
| Pschorr reaction,https://en.wikipedia.org/wiki/Pschorr_reaction | |
| Pummerer rearrangement,https://en.wikipedia.org/wiki/Pummerer_rearrangement | |
| PUREX,https://en.wikipedia.org/wiki/PUREX | |
| Q[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=18 | |
| Quelet reaction,https://en.wikipedia.org/wiki/Quelet_reaction | |
| R[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=19 | |
| Ramberg�B�cklund reaction,https://en.wikipedia.org/wiki/Ramberg%E2%80%93B%C3%A4cklund_reaction | |
| Raney nickel,https://en.wikipedia.org/wiki/Raney_nickel | |
| Rap�Stoermer condensation,https://en.wikipedia.org/wiki/Rap%E2%80%93Stoermer_condensation | |
| Raschig phenol process,https://en.wikipedia.org/wiki/Raschig_phenol_process | |
| Rauhut�Currier reaction,https://en.wikipedia.org/wiki/Rauhut%E2%80%93Currier_reaction | |
| Racemization,https://en.wikipedia.org/wiki/Racemization | |
| Reductive amination,https://en.wikipedia.org/wiki/Reductive_amination | |
| Reductive dehalogenation of halo ketones,https://en.wikipedia.org/wiki/Reductive_dehalogenation_of_halo_ketones | |
| Reed reaction,https://en.wikipedia.org/wiki/Reed_reaction | |
| Reilly�Hickinbottom rearrangement,https://en.wikipedia.org/wiki/Reilly%E2%80%93Hickinbottom_rearrangement | |
| Reimer�Tiemann reaction,https://en.wikipedia.org/wiki/Reimer%E2%80%93Tiemann_reaction | |
| Reissert indole synthesis,https://en.wikipedia.org/wiki/Reissert_indole_synthesis | |
| Reppe synthesis,https://en.wikipedia.org/wiki/Reppe_synthesis | |
| Retropinacol rearrangement,https://en.wikipedia.org/wiki/Retropinacol_rearrangement | |
| Rieche formylation,https://en.wikipedia.org/wiki/Rieche_formylation | |
| Riemschneider thiocarbamate synthesis,https://en.wikipedia.org/wiki/Riemschneider_thiocarbamate_synthesis | |
| Riley oxidations,https://en.wikipedia.org/wiki/Riley_oxidations | |
| Ring closing metathesis,https://en.wikipedia.org/wiki/Olefin_metathesis | |
| Ring opening metathesis,https://en.wikipedia.org/wiki/Olefin_metathesis | |
| Robinson annulation,https://en.wikipedia.org/wiki/Robinson_annulation | |
| Robinson�Gabriel synthesis,https://en.wikipedia.org/wiki/Robinson%E2%80%93Gabriel_synthesis | |
| Robinson Schopf reaction,https://en.wikipedia.org/wiki/Robinson_Schopf_reaction | |
| Rosenmund reaction,https://en.wikipedia.org/wiki/Rosenmund_reaction | |
| Rosenmund reduction,https://en.wikipedia.org/wiki/Rosenmund_reduction | |
| Rosenmund�von Braun synthesis,https://en.wikipedia.org/wiki/Rosenmund%E2%80%93von_Braun_synthesis | |
| Roskamp reaction,https://en.wikipedia.org/wiki/Roskamp_reaction | |
| Rothemund reaction,https://en.wikipedia.org/wiki/Rothemund_reaction | |
| Rupe rearrangement,https://en.wikipedia.org/wiki/Rupe_rearrangement | |
| Rubottom oxidation,https://en.wikipedia.org/wiki/Rubottom_oxidation | |
| Ruff�Fenton degradation,https://en.wikipedia.org/wiki/Ruff%E2%80%93Fenton_degradation | |
| Ruzicka large-ring synthesis,https://en.wikipedia.org/wiki/Ruzicka_large-ring_synthesis | |
| S[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=20 | |
| Saegusa�Ito oxidation,https://en.wikipedia.org/wiki/Saegusa%E2%80%93Ito_oxidation | |
| Sakurai reaction,https://en.wikipedia.org/wiki/Sakurai_reaction | |
| Salol reaction,https://en.wikipedia.org/wiki/Salol_reaction | |
| Sandheimer,https://en.wikipedia.org/wiki/Sandheimer | |
| Sandmeyer diphenylurea isatin synthesis,https://en.wikipedia.org/wiki/Sandmeyer_diphenylurea_isatin_synthesis | |
| Sandmeyer isonitrosoacetanilide isatin synthesis,https://en.wikipedia.org/wiki/Sandmeyer_isonitrosoacetanilide_isatin_synthesis | |
| Sandmeyer reaction,https://en.wikipedia.org/wiki/Sandmeyer_reaction | |
| Sanger reagent,https://en.wikipedia.org/wiki/Sanger_reagent | |
| Saponification,https://en.wikipedia.org/wiki/Saponification | |
| Sarett oxidation,https://en.wikipedia.org/wiki/Sarett_oxidation | |
| Schiff reaction,https://en.wikipedia.org/wiki/Schiff_base | |
| Schiff test,https://en.wikipedia.org/wiki/Schiff_test | |
| Schlenk equilibrium,https://en.wikipedia.org/wiki/Schlenk_equilibrium | |
| Schlosser modification,https://en.wikipedia.org/wiki/Schlosser_modification | |
| Schlosser variant,https://en.wikipedia.org/wiki/Schlosser_variant | |
| Schmidlin ketene synthesis,https://en.wikipedia.org/wiki/Schmidlin_ketene_synthesis | |
| Schmidt degradation,https://en.wikipedia.org/wiki/Schmidt_degradation | |
| Schmidt reaction,https://en.wikipedia.org/wiki/Schmidt_reaction | |
| Scholl reaction,https://en.wikipedia.org/wiki/Scholl_reaction | |
| Schotten�Baumann reaction,https://en.wikipedia.org/wiki/Schotten%E2%80%93Baumann_reaction | |
| Seliwanoff's test,https://en.wikipedia.org/wiki/Seliwanoff%27s_test | |
| Semidine rearrangement,https://en.wikipedia.org/wiki/Semidine_rearrangement | |
| Semmler�Wolff reaction,https://en.wikipedia.org/wiki/Semmler%E2%80%93Wolff_reaction | |
| Seyferth�Gilbert homologation,https://en.wikipedia.org/wiki/Seyferth%E2%80%93Gilbert_homologation | |
| Shapiro reaction,https://en.wikipedia.org/wiki/Shapiro_reaction | |
| Sharpless asymmetric dihydroxylation,https://en.wikipedia.org/wiki/Sharpless_asymmetric_dihydroxylation | |
| Sharpless oxyamination�or aminohydroxylation,https://en.wikipedia.org/wiki/Sharpless_oxyamination | |
| Shenck ene reaction,https://en.wikipedia.org/wiki/Ene_reaction | |
| Shi epoxidation,https://en.wikipedia.org/wiki/Shi_epoxidation | |
| Shiina esterification,https://en.wikipedia.org/wiki/Shiina_esterification | |
| Shiina macrolactonization�or Shiina lactonization,https://en.wikipedia.org/wiki/Shiina_macrolactonization | |
| Sigmatropic reaction,https://en.wikipedia.org/wiki/Sigmatropic_reaction | |
| Simmons�Smith reaction,https://en.wikipedia.org/wiki/Simmons%E2%80%93Smith_reaction | |
| Simonini reaction,https://en.wikipedia.org/wiki/Simonini_reaction | |
| Simonis chromone cyclization,https://en.wikipedia.org/wiki/Simonis_chromone_cyclization | |
| Simons process,https://en.wikipedia.org/wiki/Electrochemical_fluorination | |
| Skraup chinolin synthesis,https://en.wikipedia.org/wiki/Skraup_chinolin_synthesis | |
| Skraup reaction,https://en.wikipedia.org/wiki/Skraup_reaction | |
| Smiles rearrangement,https://en.wikipedia.org/wiki/Smiles_rearrangement | |
| SNAr�nucleophilic aromatic substitution,https://en.wikipedia.org/wiki/SNAr | |
| SN1,https://en.wikipedia.org/wiki/SN1 | |
| SN2,https://en.wikipedia.org/wiki/SN2 | |
| SNi,https://en.wikipedia.org/wiki/SNi | |
| Solvolysis,https://en.wikipedia.org/wiki/Solvolysis | |
| Sommelet reaction,https://en.wikipedia.org/wiki/Sommelet_reaction | |
| Sonn�M�ller method,https://en.wikipedia.org/wiki/Sonn%E2%80%93M%C3%BCller_method | |
| Sonogashira coupling,https://en.wikipedia.org/wiki/Sonogashira_coupling | |
| S�rensen formol titration,https://en.wikipedia.org/wiki/S%C3%B8rensen_formol_titration | |
| Staedel�Rugheimer pyrazine synthesis,https://en.wikipedia.org/wiki/Staedel%E2%80%93Rugheimer_pyrazine_synthesis | |
| Stahl oxidation,https://en.wikipedia.org/wiki/Stahl_oxidation | |
| Staudinger reaction,https://en.wikipedia.org/wiki/Staudinger_reaction | |
| Staudinger synthesis,https://en.wikipedia.org/wiki/Staudinger_synthesis | |
| Steglich esterification,https://en.wikipedia.org/wiki/Steglich_esterification | |
| Stephen aldehyde synthesis,https://en.wikipedia.org/wiki/Stephen_aldehyde_synthesis | |
| Stetter reaction,https://en.wikipedia.org/wiki/Stetter_reaction | |
| Stevens rearrangement,https://en.wikipedia.org/wiki/Stevens_rearrangement | |
| Stieglitz rearrangement,https://en.wikipedia.org/wiki/Stieglitz_rearrangement | |
| Stille coupling,https://en.wikipedia.org/wiki/Stille_coupling | |
| Stobbe condensation,https://en.wikipedia.org/wiki/Stobbe_condensation | |
| Stoll� synthesis,https://en.wikipedia.org/wiki/Stoll%C3%A9_synthesis | |
| Stork acylation,https://en.wikipedia.org/wiki/Stork_acylation | |
| Stork enamine alkylation,https://en.wikipedia.org/wiki/Stork_enamine_alkylation | |
| Strecker amino acid synthesis,https://en.wikipedia.org/wiki/Strecker_amino_acid_synthesis | |
| Strecker degradation,https://en.wikipedia.org/wiki/Strecker_degradation | |
| Strecker sulfite alkylation,https://en.wikipedia.org/wiki/Strecker_sulfite_alkylation | |
| Strecker synthesis,https://en.wikipedia.org/wiki/Strecker_synthesis | |
| "Stereocontrolled 1,2-addition to carbonyl groups","https://en.wikipedia.org/wiki/Stereocontrolled_1,2-addition_to_carbonyl_groups" | |
| Suzuki coupling,https://en.wikipedia.org/wiki/Suzuki_coupling | |
| Swain equation,https://en.wikipedia.org/wiki/Swain_equation | |
| Swarts reaction,https://en.wikipedia.org/wiki/Swarts_reaction | |
| Swern oxidation,https://en.wikipedia.org/wiki/Swern_oxidation | |
| T[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=21 | |
| Tamao oxidation,https://en.wikipedia.org/wiki/Tamao_oxidation | |
| Tafel rearrangement,https://en.wikipedia.org/wiki/Tafel_rearrangement | |
| Takai olefination,https://en.wikipedia.org/wiki/Takai_olefination | |
| Tebbe olefination,https://en.wikipedia.org/wiki/Tebbe_olefination | |
| ter Meer reaction,https://en.wikipedia.org/wiki/Ter_Meer_reaction | |
| Thiele reaction,https://en.wikipedia.org/wiki/Thiele_reaction | |
| Thiol-yne reaction,https://en.wikipedia.org/wiki/Thiol-yne_reaction | |
| Thorpe reaction,https://en.wikipedia.org/wiki/Thorpe_reaction | |
| Tiemann rearrangement,https://en.wikipedia.org/wiki/Tiemann_rearrangement | |
| Tiffeneau ring enlargement reaction,https://en.wikipedia.org/wiki/Tiffeneau_ring_enlargement_reaction | |
| Tiffeneau�Demjanov rearrangement,https://en.wikipedia.org/wiki/Tiffeneau%E2%80%93Demjanov_rearrangement | |
| Tischtschenko reaction,https://en.wikipedia.org/wiki/Tischtschenko_reaction | |
| Tollens reagent,https://en.wikipedia.org/wiki/Tollens_reagent | |
| Transfer hydrogenation,https://en.wikipedia.org/wiki/Transfer_hydrogenation | |
| Trapp mixture,https://en.wikipedia.org/wiki/Trapp_mixture | |
| Transesterification,https://en.wikipedia.org/wiki/Transesterification | |
| Traube purine synthesis,https://en.wikipedia.org/wiki/Traube_purine_synthesis | |
| Truce�Smiles rearrangement,https://en.wikipedia.org/wiki/Truce%E2%80%93Smiles_rearrangement | |
| Tscherniac�Einhorn reaction,https://en.wikipedia.org/wiki/Tscherniac%E2%80%93Einhorn_reaction | |
| Tschitschibabin reaction,https://en.wikipedia.org/wiki/Tschitschibabin_reaction | |
| Tschugajeff reaction,https://en.wikipedia.org/wiki/Chugaev_reaction | |
| Tsuji�Trost reaction,https://en.wikipedia.org/wiki/Tsuji%E2%80%93Trost_reaction | |
| Tsuji�Wilkinson decarbonylation reaction,https://en.wikipedia.org/wiki/Tsuji%E2%80%93Wilkinson_decarbonylation_reaction | |
| Twitchell process,https://en.wikipedia.org/wiki/Twitchell_process | |
| Tyrer sulfonation process,https://en.wikipedia.org/wiki/Tyrer_sulfonation_process | |
| U[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=22 | |
| Ugi reaction,https://en.wikipedia.org/wiki/Ugi_reaction | |
| Ullmann reaction,https://en.wikipedia.org/wiki/Ullmann_reaction | |
| Upjohn dihydroxylation,https://en.wikipedia.org/wiki/Upjohn_dihydroxylation | |
| Urech cyanohydrin method,https://en.wikipedia.org/wiki/Urech_cyanohydrin_method | |
| Urech hydantoin synthesis,https://en.wikipedia.org/wiki/Urech_hydantoin_synthesis | |
| V[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=23 | |
| Van Leusen reaction,https://en.wikipedia.org/wiki/Van_Leusen_reaction | |
| Van Slyke determination,https://en.wikipedia.org/wiki/Van_Slyke_determination | |
| Varrentrapp reaction,https://en.wikipedia.org/wiki/Varrentrapp_reaction | |
| Vilsmeier reaction,https://en.wikipedia.org/wiki/Vilsmeier_reaction | |
| Vilsmeier�Haack reaction,https://en.wikipedia.org/wiki/Vilsmeier%E2%80%93Haack_reaction | |
| Voight amination,https://en.wikipedia.org/wiki/Voight_amination | |
| Volhard�Erdmann cyclization,https://en.wikipedia.org/wiki/Volhard%E2%80%93Erdmann_cyclization | |
| von Braun amide degradation,https://en.wikipedia.org/wiki/Von_Braun_amide_degradation | |
| von Braun reaction,https://en.wikipedia.org/wiki/Von_Braun_reaction | |
| von Richter cinnoline synthesis,https://en.wikipedia.org/wiki/Von_Richter_cinnoline_synthesis | |
| von Richter reaction,https://en.wikipedia.org/wiki/Von_Richter_reaction | |
| W[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=24 | |
| Wacker�Tsuji oxidation,https://en.wikipedia.org/wiki/Wacker%E2%80%93Tsuji_oxidation | |
| Wagner-Jauregg reaction,https://en.wikipedia.org/wiki/Wagner-Jauregg_reaction | |
| Wagner�Meerwein rearrangement,https://en.wikipedia.org/wiki/Wagner%E2%80%93Meerwein_rearrangement | |
| Waits�Scheffer epoxidation,https://en.wikipedia.org/wiki/Waits%E2%80%93Scheffer_epoxidation | |
| Walden inversion,https://en.wikipedia.org/wiki/Walden_inversion | |
| Wallach rearrangement,https://en.wikipedia.org/wiki/Wallach_rearrangement | |
| Weerman degradation,https://en.wikipedia.org/wiki/Weerman_degradation | |
| Weinreb ketone synthesis,https://en.wikipedia.org/wiki/Weinreb_ketone_synthesis | |
| Wenker ring closure,https://en.wikipedia.org/wiki/Wenker_ring_closure | |
| Wenker synthesis,https://en.wikipedia.org/wiki/Wenker_synthesis | |
| Wessely�Moser rearrangement,https://en.wikipedia.org/wiki/Wessely%E2%80%93Moser_rearrangement | |
| Westphalen�Lettr� rearrangement,https://en.wikipedia.org/wiki/Westphalen%E2%80%93Lettr%C3%A9_rearrangement | |
| Wharton reaction,https://en.wikipedia.org/wiki/Wharton_reaction | |
| Whiting reaction,https://en.wikipedia.org/wiki/Whiting_reaction | |
| Wichterle reaction,https://en.wikipedia.org/wiki/Wichterle_reaction | |
| Widman�Stoermer synthesis,https://en.wikipedia.org/wiki/Widman%E2%80%93Stoermer_synthesis | |
| Wilkinson catalyst,https://en.wikipedia.org/wiki/Wilkinson_catalyst | |
| Willgerodt rearrangement,https://en.wikipedia.org/wiki/Willgerodt_rearrangement | |
| Willgerodt�Kindler reaction,https://en.wikipedia.org/wiki/Willgerodt%E2%80%93Kindler_reaction | |
| Williamson ether synthesis,https://en.wikipedia.org/wiki/Williamson_ether_synthesis | |
| Winstein reaction,https://en.wikipedia.org/wiki/Winstein_reaction | |
| Wittig reaction,https://en.wikipedia.org/wiki/Wittig_reaction | |
| "1,2-Wittig rearrangement","https://en.wikipedia.org/wiki/1,2-Wittig_rearrangement" | |
| "2,3-Wittig rearrangement","https://en.wikipedia.org/wiki/2,3-Wittig_rearrangement" | |
| Wittig�Horner reaction,https://en.wikipedia.org/wiki/Wittig%E2%80%93Horner_reaction | |
| Wohl degradation,https://en.wikipedia.org/wiki/Wohl_degradation | |
| Wohl�Aue reaction,https://en.wikipedia.org/wiki/Wohl%E2%80%93Aue_reaction | |
| Wohler synthesis,https://en.wikipedia.org/wiki/Wohler_synthesis | |
| Wohl�Ziegler reaction,https://en.wikipedia.org/wiki/Wohl%E2%80%93Ziegler_reaction | |
| Wolffenstein�B�ters reaction,https://en.wikipedia.org/wiki/Wolffenstein%E2%80%93B%C3%B6ters_reaction | |
| Wolff rearrangement,https://en.wikipedia.org/wiki/Wolff_rearrangement | |
| Wolff�Kishner reduction,https://en.wikipedia.org/wiki/Wolff%E2%80%93Kishner_reduction | |
| Woodward cis-hydroxylation,https://en.wikipedia.org/wiki/Woodward_cis-hydroxylation | |
| Woodward�Hoffmann rule,https://en.wikipedia.org/wiki/Woodward%E2%80%93Hoffmann_rule | |
| Wulff�D�tz reaction,https://en.wikipedia.org/wiki/Wulff%E2%80%93D%C3%B6tz_reaction | |
| Wurtz�Fittig reaction,https://en.wikipedia.org/wiki/Wurtz%E2%80%93Fittig_reaction | |
| Y[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=25 | |
| Yamada�Okamoto purine synthesis,https://en.wikipedia.org/wiki/Purine | |
| Yamaguchi esterification,https://en.wikipedia.org/wiki/Yamaguchi_esterification | |
| Z[edit],https://en.wikipedia.org/w/index.php?title=List_of_organic_reactions&action=edit§ion=26 | |