About: http://dbpedia.org/class/yago/WikicatNameReactions

Property	Value
rdfs:subClassOf	yago:ChemicalReaction113447361
owl:equivalentClass	yago-res:wikicat_Name_reactions
is rdf:type of	dbr:Cadiot–Chodkiewicz_coupling dbr:Camps_quinoline_synthesis dbr:Cannizzaro_reaction dbr:Carbazole dbr:Castro–Stephens_coupling dbr:Bechamp_reaction dbr:Bechamp_reduction dbr:Benary_reaction dbr:Benedict's_reagent dbr:Prins_reaction dbr:Pummerer_rearrangement dbr:Robinson_annulation dbr:Rosenmund_reduction dbr:Rosenmund–von_Braun_reaction dbr:Rubottom_oxidation dbr:Sandmeyer_reaction dbr:Sarett_oxidation dbr:Schmidt_reaction dbr:Scholl_reaction dbr:Schotten–Baumann_reaction dbr:Elbs_reaction dbr:Ene_reaction dbr:Takai_olefination dbr:Bartoli_indole_synthesis dbr:Barton_decarboxylation dbr:Barton–Kellogg_reaction dbr:Barton–McCombie_deoxygenation dbr:Baudisch_reaction dbr:Baylis–Hillman_reaction dbr:Beckmann_rearrangement dbr:Bergman_cyclization dbr:Bergmann_azlactone_peptide_synthesis dbr:Betti_reaction dbr:Biginelli_reaction dbr:Birch_reduction dbr:Bischler–Möhlau_indole_synthesis dbr:Bischler–Napieralski_reaction dbr:Blaise_reaction dbr:Blanc_chloromethylation dbr:Bouveault_aldehyde_synthesis dbr:Bouveault–Blanc_reduction dbr:Boyland–Sims_oxidation dbr:Debus-Radziszewski_imidazole_synthesis dbr:Dess–Martin_periodinane dbr:Algar–Flynn–Oyamada_reaction dbr:Allan–Robinson_reaction dbr:Andrussow_process dbr:Hiyama_coupling dbr:Hofmann_elimination dbr:Hofmann_rearrangement dbr:Horner–Wadsworth–Emmons_reaction dbr:Hunsdiecker_reaction dbr:Johnson–Corey–Chaykovsky_reaction dbr:Jones_oxidation dbr:Julia_olefination dbr:Paternò–Büchi_reaction dbr:Pechmann_condensation dbr:Perkin_reaction dbr:Perkow_reaction dbr:Petasis_reaction dbr:Peterson_olefination dbr:Petrenko-Kritschenko_piperidone_synthesis dbr:Pfitzinger_reaction dbr:Reimer–Tiemann_reaction dbr:Ritter_reaction dbr:Cyclopropanation dbr:Dakin–West_reaction dbr:Ugi_reaction dbr:Ullmann_condensation dbr:Ullmann_reaction dbr:Upjohn_dihydroxylation dbr:Van_Leusen_reaction dbr:Vilsmeier–Haack_reaction dbr:Von_Braun_reaction dbr:Dowd–Beckwith_ring-expansion_reaction dbr:Duff_reaction dbr:Intramolecular_Diels–Alder_cycloaddition dbr:Iodine_clock_reaction dbr:Ivanov_reaction dbr:Jacobsen_rearrangement dbr:Letts_nitrile_synthesis dbr:Noyori_asymmetric_hydrogenation dbr:Prato_reaction dbr:Prévost_reaction dbr:Zinin_reaction dbr:1,2-Wittig_rearrangement dbr:Cope_reaction dbr:Cope_rearrangement dbr:Corey–Fuchs_reaction dbr:Corey–Itsuno_reduction dbr:Corey–Kim_oxidation dbr:McMurry_reaction dbr:Meerwein–Ponndorf–Verley_reduction dbr:Menshutkin_reaction dbr:Ruzicka_large-ring_synthesis dbr:Sakurai_reaction dbr:Eschenmoser_fragmentation dbr:Eschenmoser_sulfide_contraction dbr:Gassman_indole_synthesis dbr:Norrish_reaction dbr:Midland_Alpine_borane_reduction dbr:Niementowski_quinazoline_synthesis dbr:Shi_epoxidation dbr:Nitrophosphate_process dbr:Zeisel_determination dbr:Robinson–Gabriel_synthesis dbr:Chugaev_elimination dbr:Cinnoline dbr:Claisen_condensation dbr:Claisen_rearrangement dbr:Clemmensen_reduction dbr:Elbs_persulfate_oxidation dbr:Emde_degradation dbr:Friedel–Crafts_reaction dbr:Friedländer_synthesis dbr:Fries_rearrangement dbr:Fritsch–Buttenberg–Wiechell_rearrangement dbr:Fukuyama_coupling dbr:Fukuyama_reduction dbr:Gabriel_synthesis dbr:Gattermann_reaction dbr:Gewald_reaction dbr:Glaser_coupling dbr:Boudouard_reaction dbr:Bradsher_cycloaddition dbr:Mitsunobu_reaction dbr:Conrad–Limpach_synthesis dbr:Cook–Heilbron_thiazole_synthesis dbr:Corey–House_synthesis dbr:Corey–Winter_olefin_synthesis dbr:Creighton_process dbr:Criegee_rearrangement dbr:Danheiser_annulation dbr:Marschalk_reaction dbr:Martinet_dioxindole_synthesis dbr:Milas_hydroxylation dbr:Appel_reaction dbr:Benkeser_reaction dbr:Bergius_process dbr:Bergmann_degradation dbr:Bernthsen_acridine_synthesis dbr:Leuckart_reaction dbr:Liebeskind–Srogl_coupling dbr:Lindgren_oxidation dbr:Lobry_de_Bruyn–van_Ekenstein_transformation dbr:Lossen_rearrangement dbr:Luche_reduction dbr:Madelung_synthesis dbr:Bodroux–Chichibabin_aldehyde_synthesis dbr:Simmons–Smith_reaction dbr:Skraup_reaction dbr:Staudinger_reaction dbr:Steglich_esterification dbr:Stetter_reaction dbr:Stieglitz_rearrangement dbr:Stille_reaction dbr:Strecker_amino_acid_synthesis dbr:Combes_quinoline_synthesis dbr:Delépine_reaction dbr:Demjanov_rearrangement dbr:Zincke_nitration dbr:Favorskii_reaction dbr:Fráter–Seebach_alkylation dbr:Fujimoto–Belleau_reaction dbr:Fukuyama_indole_synthesis dbr:Hajos–Parrish–Eder–Sauer–Wiechert_reaction dbr:Hall–Héroult_process dbr:Hammick_reaction dbr:Hemetsberger_indole_synthesis dbr:Ketone dbr:Kharasch_addition dbr:Kowalski_ester_homologation dbr:Overman_rearrangement dbr:Payne_rearrangement dbr:Pellizzari_reaction dbr:Staudinger_synthesis dbr:Stickland_fermentation dbr:Strecker_degradation dbr:Marker_degradation dbr:Markó–Lam_deoxygenation dbr:McCormack_reaction dbr:McFadyen–Stevens_reaction dbr:McLafferty_rearrangement dbr:Meyers_synthesis dbr:Meyer–Schuster_rearrangement dbr:Michael_reaction dbr:Michaelis–Becker_reaction dbr:Auwers_synthesis dbr:Aza-Baylis–Hillman_reaction dbr:Aza-Diels–Alder_reaction dbr:Azide-alkyne_Huisgen_cycloaddition dbr:Baeyer–Villiger_oxidation dbr:Balz–Schiemann_reaction dbr:Barbier_reaction dbr:Bucherer–Bergs_reaction dbr:Buchwald–Hartwig_amination dbr:Adams_decarboxylation dbr:Adkins–Peterson_reaction dbr:Tiffeneau–Demjanov_rearrangement dbr:Weinreb_ketone_synthesis dbr:Wenker_synthesis dbr:Willgerodt_rearrangement dbr:Williamson_ether_synthesis dbr:Doebner_reaction dbr:Doebner–Miller_reaction dbr:Doyle–Kirmse_reaction dbr:Fétizon_oxidation dbr:Gabriel–Colman_rearrangement dbr:Gallagher–Hollander_degradation dbr:Girdler_sulfide_process dbr:Haber_process dbr:Haber–Weiss_reaction dbr:Hayashi_rearrangement dbr:Heck–Matsuda_reaction dbr:Ireland–Claisen_rearrangement dbr:Japp–Maitland_condensation dbr:Juliá–Colonna_epoxidation dbr:Leblanc_process dbr:Lectka_enantioselective_beta-lactam_synthesis dbr:Minisci_reaction dbr:Ostwald_process dbr:Name_reaction dbr:Piancatelli_rearrangement dbr:Pinacol_coupling_reaction dbr:Reissert_indole_synthesis dbr:Achmatowicz_reaction dbr:Amide dbr:Akabori_amino-acid_reaction dbr:Curtius_rearrangement dbr:Cyclopropane dbr:Dakin_oxidation dbr:Darzens_reaction dbr:Amadori_rearrangement dbr:Eschweiler–Clarke_reaction dbr:Favorskii_rearrangement dbr:Feist–Benary_synthesis dbr:Fenton's_reagent dbr:Finkelstein_reaction dbr:Fischer_indole_synthesis dbr:Fischer–Hepp_rearrangement dbr:Fischer–Speier_esterification dbr:Fleming–Tamao_oxidation dbr:Angeli–Rimini_reaction dbr:Bamberger_rearrangement dbr:Bamberger_triazine_synthesis dbr:Bamford–Stevens_reaction dbr:Banert_cascade dbr:Barton_reaction dbr:Barton–Zard_reaction dbr:Bray–Liebhafsky_reaction dbr:Briggs–Rauscher_reaction dbr:Brook_rearrangement dbr:Nitrite dbr:Nitro_compound dbr:Nozaki–Hiyama–Kishi_reaction dbr:Oxo-Diels–Alder_reaction dbr:Passerini_reaction dbr:Carbonylation dbr:Diels–Alder_reaction dbr:Diels–Reese_reaction dbr:Dimroth_rearrangement dbr:Direct_process dbr:Edman_degradation dbr:Forster–Decker_method dbr:Gomberg–Bachmann_reaction dbr:Gould–Jacobs_reaction dbr:Hantzsch_pyrrole_synthesis dbr:Hinsberg_oxindole_synthesis dbr:Isay_reaction dbr:Kabachnik–Fields_reaction dbr:Kauffmann_olefination dbr:Kiliani–Fischer_synthesis dbr:Koch_reaction dbr:Koenigs–Knorr_reaction dbr:Kolbe_electrolysis dbr:Kornblum_oxidation dbr:Kornblum–DeLaMare_rearrangement dbr:Kostanecki_acylation dbr:Lehmstedt–Tanasescu_reaction dbr:Leimgruber–Batcho_indole_synthesis dbr:Lemieux–Johnson_oxidation dbr:Rauhut–Currier_reaction dbr:Povarov_reaction dbr:Reed_reaction dbr:2,3-Wittig_rearrangement dbr:Hantzsch_pyridine_synthesis dbr:Heck_reaction dbr:Hell–Volhard–Zelinsky_halogenation dbr:Jacobsen_epoxidation dbr:Japp–Klingemann_reaction dbr:Baeyer–Drewson_indigo_synthesis dbr:Baeyer–Emmerling_indole_synthesis dbr:Baker–Venkataraman_rearrangement dbr:Tetralin dbr:Tetrapropylammonium_perruthenate dbr:Hydrazone_iodination dbr:Hydroboration dbr:Narasaka–Prasad_reduction dbr:Westphalen–Lettré_rearrangement dbr:Zincke_reaction