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