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About:
http://dbpedia.org/class/yago/WikicatOrganicReactions
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Thing
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from Named Graph:
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rdfs:
subClassOf
yago
:ChemicalReaction113447361
owl:
equivalentClass
yago-res
:wikicat_Organic_reactions
is
rdf:
type
of
dbr
:Cadiot–Chodkiewicz_coupling
dbr
:Cannizzaro_reaction
dbr
:Castro–Stephens_coupling
dbr
:Amination
dbr
:Amine_alkylation
dbr
:Amino_sugar
dbr
:Aminoacylation
dbr
:Bechamp_reaction
dbr
:Benary_reaction
dbr
:Benedict's_reagent
dbr
:Robinson_annulation
dbr
:Schmidt_reaction
dbr
:Elaidinization
dbr
:Elbs_reaction
dbr
:Electrocyclic_reaction
dbr
:Electrophile
dbr
:Electrophilic_addition
dbr
:Electrophilic_amination
dbr
:Electrophilic_aromatic_substitution
dbr
:Electrophilic_halogenation
dbr
:Electrophilic_substitution_of_unsaturated_silanes
dbr
:Enantioselective_reduction_of_ketones
dbr
:Enders_SAMP/RAMP_hydrazone-alkylation_reaction
dbr
:Entner–Doudoroff_pathway
dbr
:Epoxidation_with_dioxiranes
dbr
:Nucleophilic_addition
dbr
:Salt_metathesis_reaction
dbr
:Methanation
dbr
:Methylation
dbr
:Zaitsev's_rule
dbr
:Takai_olefination
dbr
:Trifluoromethylation
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
:Betti_reaction
dbr
:Biginelli_reaction
dbr
:Bischler–Möhlau_indole_synthesis
dbr
:Blaise_reaction
dbr
:Blanc_chloromethylation
dbr
:Bouveault–Blanc_reduction
dbr
:Boyland–Sims_oxidation
dbr
:Desulfonylation_reactions
dbr
:Algar–Flynn–Oyamada_reaction
dbr
:Alkylation
dbr
:Alkylimino-de-oxo-bisubstitution
dbr
:Allan–Robinson_reaction
dbr
:Allylic_rearrangement
dbr
:Allylic_stannane_addition
dbr
:Andrussow_process
dbr
:Annulation
dbr
:Hofmann_elimination
dbr
:Hofmann_rearrangement
dbr
:Paternò–Büchi_reaction
dbr
:Perkow_reaction
dbr
:Petrenko-Kritschenko_piperidone_synthesis
dbr
:Pfitzinger_reaction
dbr
:Cumene_process
dbr
:Upjohn_dihydroxylation
dbr
:Von_Braun_reaction
dbr
:DeMayo_reaction
dbr
:Dehydration_reaction
dbr
:Duff_reaction
dbr
:Dyotropic_reaction
dbr
:Inductive_cleavage
dbr
:Initiation_(chemistry)
dbr
:Intermolecular_metal-catalyzed_carbenoid_cyclopropanations
dbr
:Intramolecular_Heck_reaction
dbr
:Intramolecular_reactions_of_diazocarbonyl_compounds
dbr
:Iodolactonization
dbr
:Ivanov_reaction
dbr
:Nucleophilic_conjugate_addition
dbr
:Radical_cyclization
dbr
:1,3-Dipolar_cycloaddition
dbr
:Corey–Itsuno_reduction
dbr
:Eschenmoser_fragmentation
dbr
:Eschenmoser_sulfide_contraction
dbr
:Ester_pyrolysis
dbr
:Gassman_indole_synthesis
dbr
:Nucleophilic_acyl_substitution
dbr
:Nucleophilic_aromatic_substitution
dbr
:Olah_reagent
dbr
:Keto–enol_tautomerism
dbr
:Chugaev_elimination
dbr
:Clemmensen_reduction
dbr
:Elbs_persulfate_oxidation
dbr
:Friedel–Crafts_reaction
dbr
:Fritsch–Buttenberg–Wiechell_rearrangement
dbr
:Fukuyama_reduction
dbr
:Gabriel_synthesis
dbr
:Gattermann_reaction
dbr
:Gewald_reaction
dbr
:Glaser_coupling
dbr
:Boudouard_reaction
dbr
:Concerted_reaction
dbr
:Condensation_reaction
dbr
:Copper-free_click_chemistry
dbr
:Corey–House_synthesis
dbr
:Creighton_process
dbr
:Crich_beta-mannosylation
dbr
:Danheiser_annulation
dbr
:Marschalk_reaction
dbr
:Rieche_formylation
dbr
:Milas_hydroxylation
dbr
:Organic_reaction
dbr
:Organic_redox_reaction
dbr
:Appel_reaction
dbr
:Benzilic_acid_rearrangement
dbr
:Bergmann_degradation
dbr
:Bernthsen_acridine_synthesis
dbr
:Leuckart_thiophenol_reaction
dbr
:Luche_reduction
dbr
:Bodroux–Chichibabin_aldehyde_synthesis
dbr
:Staudinger_reaction
dbr
:Strecker_amino_acid_synthesis
dbr
:Demethylation
dbr
:Deoxygenation
dbr
:Zincke_nitration
dbr
:Fujimoto–Belleau_reaction
dbr
:Fukuyama_indole_synthesis
dbr
:Halogen_addition_reaction
dbr
:Halogenation
dbr
:Hammick_reaction
dbr
:Hemetsberger_indole_synthesis
dbr
:Ketone_halogenation
dbr
:Ketonic_decarboxylation
dbr
:Kharasch_addition
dbr
:Payne_rearrangement
dbr
:Pellizzari_reaction
dbr
:Organic_synthesis
dbr
:Strecker_degradation
dbr
:McFadyen–Stevens_reaction
dbr
:Meyers_synthesis
dbr
:Michaelis–Becker_reaction
dbr
:Oligonucleotide_synthesis
dbr
:Auwers_synthesis
dbr
:Azide-alkyne_Huisgen_cycloaddition
dbr
:Baeyer–Villiger_oxidation
dbr
:Balz–Schiemann_reaction
dbr
:Barbier_reaction
dbr
:Buchwald–Hartwig_amination
dbr
:Adamkiewicz_reaction
dbr
:Adams_decarboxylation
dbr
:Adkins–Peterson_reaction
dbr
:Transesterification
dbr
:Weinreb_ketone_synthesis
dbr
:Wenker_synthesis
dbr
:Willgerodt_rearrangement
dbr
:Williamson_ether_synthesis
dbr
:Divinylcyclopropane-cycloheptadiene_rearrangement
dbr
:Gabriel–Colman_rearrangement
dbr
:Gallagher–Hollander_degradation
dbr
:Hayashi_rearrangement
dbr
:Heck–Matsuda_reaction
dbr
:Helferich_method
dbr
:Leaving_group
dbr
:Nitrosylation
dbr
:Organostannane_addition
dbr
:Minisci_reaction
dbr
:Thiol-yne_reaction
dbr
:Nitration
dbr
:Achmatowicz_reaction
dbr
:Acyloin_condensation
dbr
:2+2_photocycloaddition
dbr
:Curtius_rearrangement
dbr
:Darzens_reaction
dbr
:Alpha_cleavage
dbr
:Favorskii_rearrangement
dbr
:Fischer–Hepp_rearrangement
dbr
:Fischer–Speier_esterification
dbr
:Fleming–Tamao_oxidation
dbr
:Fluorination_with_aminosulfuranes
dbr
:Bamberger_rearrangement
dbr
:Bamberger_triazine_synthesis
dbr
:Barton–Zard_reaction
dbr
:Base-promoted_epoxide_isomerization
dbr
:Oxidation_with_chromium(VI)-amine_complexes
dbr
:Ozonolysis
dbr
:Carbene_C−H_insertion
dbr
:Carbene_dimerization
dbr
:Carbohydrate_acetalisation
dbr
:Carbometalation
dbr
:Carbonyl_alpha-substitution_reactions
dbr
:Carbonylation
dbr
:Carbon–hydrogen_bond_activation
dbr
:Carboxylation
dbr
:Diazoalkane_1,3-dipolar_cycloaddition
dbr
:Dimroth_rearrangement
dbr
:Edman_degradation
dbr
:Fluid_catalytic_cracking
dbr
:Fluorination_by_sulfur_tetrafluoride
dbr
:Formylation_reaction
dbr
:Forster–Decker_method
dbr
:Fowler_process
dbr
:Glycosyl_acceptor
dbr
:Glycosyl_donor
dbr
:Gomberg–Bachmann_reaction
dbr
:Hantzsch_pyrrole_synthesis
dbr
:Hinsberg_oxindole_synthesis
dbr
:Ishikawa_reagent
dbr
:Kabachnik–Fields_reaction
dbr
:Kiliani–Fischer_synthesis
dbr
:Kornblum_oxidation
dbr
:Kostanecki_acylation
dbr
:Lehmstedt–Tanasescu_reaction
dbr
:Rearrangement_reaction
dbr
:Steam_reforming
dbr
:Haloform_reaction
dbr
:Hantzsch_pyridine_synthesis
dbr
:Heck_reaction
dbr
:Asymmetric_ester_hydrolysis_with_pig-liver_esterase
dbr
:Asymmetric_nucleophilic_epoxidation
dbr
:Baeyer–Drewson_indigo_synthesis
dbr
:Baeyer–Emmerling_indole_synthesis
dbr
:Baker–Venkataraman_rearrangement
dbr
:Cracking_(chemistry)
dbr
:Hydration_reaction
dbr
:Hydroacylation
dbr
:Hydroboration
dbr
:Hydrodefluorination
dbr
:Hydrogenation_of_carbon–nitrogen_double_bonds
dbr
:Hydrohalogenation
dbr
:Hydrothermal_liquefaction
dbr
:Hydroxylation
dbr
:Nitrosation
dbr
:Westphalen–Lettré_rearrangement
dbr
:Zincke_reaction
dbr
:Arndt–Eistert_reaction
dbr
:Acetoacetic_ester_synthesis
dbr
:Alcohol_oxidation
dbr
:Aldol–Tishchenko_reaction
dbr
:Bingel_reaction
dbr
:Blaise_ketone_synthesis
dbr
:Swern_oxidation
dbr
:Einhorn–Brunner_reaction
dbr
:Herz_reaction
dbr
:Heteroatom-promoted_lateral_lithiation
dbr
:Hoesch_reaction
dbr
:Hooker_reaction
dbr
:Tishchenko_reaction
dbr
:Tsuji–Trost_reaction
dbr
:Whiting_reaction
dbr
:Wohl_degradation
dbr
:Wohl–Aue_reaction
dbr
:Wöhler_synthesis
dbr
:Schöllkopf_method
dbr
:Reactions_of_organocopper_reagents
dbr
:Reichstein_process
dbr
:Disproportionation
dbr
:Azo_coupling
dbr
:Mannich_reaction
dbr
:Boord_olefin_synthesis
dbr
:Büchner–Curtius–Schlotterbeck_reaction
dbr
:Sonogashira_coupling
dbr
:Grundmann_aldehyde_synthesis
dbr
:Guerbet_reaction
dbr
:Kochi_reaction
dbr
:Krapcho_decarboxylation
dbr
:Bucherer_carbazole_synthesis
dbr
:Bucherer_reaction
dbr
:Nef_reaction
dbr
:Oppenauer_oxidation
dbr
:Carroll_rearrangement
dbr
:Reductions_with_hydrosilanes
dbr
:Reductions_with_metal_alkoxyaluminium_hydrides
dbr
:Reductions_with_samarium(II)_iodide
dbr
:Reductive_amination
dbr
:Chain_propagation
dbr
:Chain_termination
dbr
:Sharpless_asymmetric_dihydroxylation
dbr
:Wittig_reaction
dbr
:Wolff_rearrangement
dbr
:Wolff–Kishner_reduction
dbr
:Wurtz_reaction
dbr
:Mineral_hydration
dbr
:Maillard_reaction
dbr
:Markovnikov's_rule
dbr
:Wagner–Meerwein_rearrangement
dbr
:Schlenk_equilibrium
dbr
:Sharpless_oxyamination
dbr
:Vicarious_nucleophilic_substitution
dbr
:Wallach_rearrangement
dbr
:Neber_rearrangement
dbr
:Nitroaldol_reaction
dbr
:Stephen_aldehyde_synthesis
dbr
:Varrentrapp_reaction
dbr
:Lumière–Barbier_method
dbr
:PEGylation
dbr
:Reductions_with_diimide
dbr
:Fischer_glycosidation
dbr
:Fischer_oxazole_synthesis
dbr
:Manganese-mediated_coupling_reactions
dbr
:Vicinal_difunctionalization
dbr
:Walden_inversion
dbr
:Synthesis_of_nucleosides
dbr
:Trimethylenemethane_cycloaddition
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