name_reaction.csv

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