Delete name_reaction.csv

name_reaction.csv

@@ -1,829 +0,0 @@
-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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=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&section=26