Browse using
OpenLink Faceted Browser
OpenLink Structured Data Editor
LodLive Browser
Formats
RDF:
N-Triples
N3
Turtle
JSON
XML
OData:
Atom
JSON
Microdata:
JSON
HTML
Embedded:
JSON
Turtle
Other:
CSV
JSON-LD
Faceted Browser
Sparql Endpoint
About:
Organic reactions
An Entity of Type:
Concept
,
from Named Graph:
http://dbpedia.org
,
within Data Space:
dbpedia.org
Property
Value
dbo:
wikiPageID
1921153
(xsd:integer)
dbo:
wikiPageRevisionID
884875540
(xsd:integer)
dbp:
wikiPageUsesTemplate
dbt
:Commons_cat
dbt
:Portal
rdf:
type
skos
:Concept
rdfs:
label
Organic reactions
(en)
skos:
broader
dbc
:Organic_chemistry
dbc
:Chemical_reactions
skos:
prefLabel
Organic reactions
(en)
prov:
wasDerivedFrom
wikipedia-en
:Category:Organic_reactions?oldid=884875540&ns=14
is
dbo:
wikiPageWikiLink
of
dbr
:Amination
dbr
:Amine_alkylation
dbr
:Amino_acid_N-carboxyanhydride
dbr
:Aminoacylation
dbr
:Elaidinization
dbr
:Elbs_reaction
dbr
:Electrophilic_amination
dbr
:Electrophilic_substitution_of_unsaturated_silanes
dbr
:Enders_SAMP/RAMP_hydrazone-alkylation_reaction
dbr
:Enolate
dbr
:Enone–alkene_cycloadditions
dbr
:Epoxidation_with_dioxiranes
dbr
:Methanation
dbr
:Methylation
dbr
:Trifluoromethylation
dbr
:Barton_decarboxylation
dbr
:Desulfonylation_reactions
dbr
:Alkene_carboamination
dbr
:Alkenylaluminium_compounds
dbr
:Alkylation
dbr
:Alkylimino-de-oxo-bisubstitution
dbr
:Allylic_stannane_addition
dbr
:Annulation
dbr
:Paternò–Büchi_reaction
dbr
:Cycloisomerization
dbr
:Von_Braun_reaction
dbr
:DeMayo_reaction
dbr
:Deacetylation
dbr
:Dearomatization_reaction
dbr
:Decarboxylative_cross-coupling
dbr
:Dehalogenation
dbr
:Desulfonation_reaction
dbr
:Dyotropic_reaction
dbr
:Inductive_cleavage
dbr
:Intermolecular_metal-catalyzed_carbenoid_cyclopropanations
dbr
:Intramolecular_Heck_reaction
dbr
:Intramolecular_reactions_of_diazocarbonyl_compounds
dbr
:Iodolactonization
dbr
:Radical_cyclization
dbr
:Conia-ene_reaction
dbr
:Eschenmoser_sulfide_contraction
dbr
:Ester_pyrolysis
dbr
:Transamination
dbr
:RXNO_Ontology
dbr
:Enol
dbr
:Concerted_reaction
dbr
:Copper-free_click_chemistry
dbr
:Crich_beta-mannosylation
dbr
:Danheiser_annulation
dbr
:Danheiser_benzannulation
dbr
:Marschalk_reaction
dbr
:Rieche_formylation
dbr
:Organic_reaction
dbr
:Armed_and_disarmed_saccharides
dbr
:Benzylic_activation_and_stereocontrol_in_tricarbonyl(arene)chromium_complexes
dbr
:Leuckart_thiophenol_reaction
dbr
:Macrocyclic_stereocontrol
dbr
:Boekelheide_reaction
dbr
:Boger_pyridine_synthesis
dbr
:Demethylation
dbr
:Halogenation
dbr
:Ketonic_decarboxylation
dbr
:Kharasch_addition
dbr
:Krische_allylation
dbr
:Payne_rearrangement
dbr
:Strecker_degradation
dbr
:Meyers_synthesis
dbr
:Michaelis–Becker_reaction
dbr
:Acylation
dbr
:Adamkiewicz_reaction
dbr
:Adams_decarboxylation
dbr
:Divinylcyclopropane-cycloheptadiene_rearrangement
dbr
:Gallagher–Hollander_degradation
dbr
:Heck–Matsuda_reaction
dbr
:Helferich_method
dbr
:Leaving_group
dbr
:Organostannane_addition
dbr
:Minisci_reaction
dbr
:Thiol-yne_reaction
dbr
:Achmatowicz_reaction
dbr
:Alpha_cleavage
dbr
:Fluorination_with_aminosulfuranes
dbr
:Base-promoted_epoxide_isomerization
dbr
:Carbene_C−H_insertion
dbr
:Carbene_dimerization
dbr
:Carbohydrate_acetalisation
dbr
:Carbohydrate_synthesis
dbr
:Carbometalation
dbr
:Carbonyl_alpha-substitution_reactions
dbr
:Carboxylation
dbr
:Carbylamine_reaction
dbr
:Dienone–phenol_rearrangement
dbr
:Directing_group
dbr
:Edman_degradation
dbr
:Fluorination_by_sulfur_tetrafluoride
dbr
:Formose_reaction
dbr
:Glucuronidation
dbr
:Glycerolysis
dbr
:Glycosyl_acceptor
dbr
:Glycosyl_donor
dbr
:Glycosylation
dbr
:Hirao_coupling
dbr
:Histone_acetylation_and_deacetylation
dbr
:Kostanecki_acylation
dbr
:Asymmetric_addition_of_dialkylzinc_compounds_to_aldehydes
dbr
:Asymmetric_ester_hydrolysis_with_pig-liver_esterase
dbr
:Asymmetric_hydrogenation
dbr
:Asymmetric_nucleophilic_epoxidation
dbr
:Baeyer–Drewson_indigo_synthesis
dbr
:Baeyer–Emmerling_indole_synthesis
dbr
:Crabbé_reaction
dbr
:Cracking_(chemistry)
dbr
:Hydroacylation
dbr
:Hydroboration
dbr
:Hydrodefluorination
dbr
:Hydrogenation_of_carbon–nitrogen_double_bonds
dbr
:Hydrothermal_liquefaction
dbr
:Nitrosation
dbr
:A3_coupling_reaction
dbr
:Acetoacetic_ester_synthesis
dbr
:Acetylation
dbr
:Coarctate_reaction
dbr
:Heteroatom-promoted_lateral_lithiation
dbr
:Hooker_reaction
dbr
:Tishchenko_reaction
dbr
:Tsuji–Trost_reaction
dbr
:Wöhler_synthesis
dbr
:Modified_aldol_tandem_reaction
dbr
:Schöllkopf_method
dbr
:Stereochemistry_of_ketonization_of_enols_and_enolates
dbr
:Reactions_of_organoborates_and_boranes
dbr
:Reactions_of_organocopper_reagents
dbr
:Reichstein_process
dbr
:Disproportionation
dbr
:Aza_Paternò−Büchi_reaction
dbr
:Boord_olefin_synthesis
dbr
:Büchner–Curtius–Schlotterbeck_reaction
dbr
:Grieco_three-component_condensation
dbr
:Kochi_reaction
dbr
:Kröhnke_pyridine_synthesis
dbr
:Reductions_with_hydrosilanes
dbr
:Reductions_with_metal_alkoxyaluminium_hydrides
dbr
:Vicarious_nucleophilic_substitution
dbr
:Lumière–Barbier_method
dbr
:Reductions_with_diimide
dbr
:Transposed_Paternò−Büchi_reaction
dbr
:Fischer_glycosidation
dbr
:Flash_vacuum_pyrolysis
dbr
:Manganese-mediated_coupling_reactions
dbr
:Vicinal_difunctionalization
dbr
:Synthesis_of_nucleosides
dbr
:Trimethylenemethane_cycloaddition
dbr
:Transmethylation
dbr
:Multiple_Michael/aldol_reaction
dbr
:Murai_reaction
dbr
:Pinner_triazine_synthesis
dbr
:Sommelet_reaction
dbr
:Persistent_radical_effect
dbr
:Photooxygenation
dbr
:Pyrolysis
dbr
:Oxidation_with_dioxiranes
dbr
:Oxocarbenium
dbr
:Oxychlorination
dbr
:Soai_reaction
dbr
:Tipson–Cohen_reaction
dbr
:SOBER1
dbr
:Riemschneider_thiocarbamate_synthesis
is
dcterms:
subject
of
dbr
:Amination
dbr
:Amine_alkylation
dbr
:Amino_acid_N-carboxyanhydride
dbr
:Aminoacylation
dbr
:Elaidinization
dbr
:Elbs_reaction
dbr
:Electrophilic_amination
dbr
:Electrophilic_substitution_of_unsaturated_silanes
dbr
:Enders_SAMP/RAMP_hydrazone-alkylation_reaction
dbr
:Enolate
dbr
:Enone–alkene_cycloadditions
dbr
:Epoxidation_with_dioxiranes
dbr
:Methanation
dbr
:Methylation
dbr
:Trifluoromethylation
dbr
:Barton_decarboxylation
dbr
:Desulfonylation_reactions
dbr
:Alkene_carboamination
dbr
:Alkenylaluminium_compounds
dbr
:Alkylation
dbr
:Alkylimino-de-oxo-bisubstitution
dbr
:Allylic_stannane_addition
dbr
:Annulation
dbr
:Paternò–Büchi_reaction
dbr
:Cycloisomerization
dbr
:Von_Braun_reaction
dbr
:DeMayo_reaction
dbr
:Deacetylation
dbr
:Dearomatization_reaction
dbr
:Decarboxylative_cross-coupling
dbr
:Dehalogenation
dbr
:Desulfonation_reaction
dbr
:Dyotropic_reaction
dbr
:Inductive_cleavage
dbr
:Intermolecular_metal-catalyzed_carbenoid_cyclopropanations
dbr
:Intramolecular_Heck_reaction
dbr
:Intramolecular_reactions_of_diazocarbonyl_compounds
dbr
:Iodolactonization
dbr
:Radical_cyclization
dbr
:Conia-ene_reaction
dbr
:Eschenmoser_sulfide_contraction
dbr
:Ester_pyrolysis
dbr
:Transamination
dbr
:Enol
dbr
:Concerted_reaction
dbr
:Copper-free_click_chemistry
dbr
:Crich_beta-mannosylation
dbr
:Danheiser_annulation
dbr
:Danheiser_benzannulation
dbr
:Marschalk_reaction
dbr
:Rieche_formylation
dbr
:Organic_reaction
dbr
:Armed_and_disarmed_saccharides
dbr
:Benzylic_activation_and_stereocontrol_in_tricarbonyl(arene)chromium_complexes
dbr
:Leuckart_thiophenol_reaction
dbr
:Macrocyclic_stereocontrol
dbr
:Boekelheide_reaction
dbr
:Boger_pyridine_synthesis
dbr
:Demethylation
dbr
:Halogenation
dbr
:Ketonic_decarboxylation
dbr
:Kharasch_addition
dbr
:Krische_allylation
dbr
:Payne_rearrangement
dbr
:Strecker_degradation
dbr
:Meyers_synthesis
dbr
:Michaelis–Becker_reaction
dbr
:Acylation
dbr
:Adamkiewicz_reaction
dbr
:Adams_decarboxylation
dbr
:Divinylcyclopropane-cycloheptadiene_rearrangement
dbr
:Gallagher–Hollander_degradation
dbr
:Heck–Matsuda_reaction
dbr
:Helferich_method
dbr
:Leaving_group
dbr
:Organostannane_addition
dbr
:Minisci_reaction
dbr
:Thiol-yne_reaction
dbr
:Achmatowicz_reaction
dbr
:Alpha_cleavage
dbr
:Fluorination_with_aminosulfuranes
dbr
:Base-promoted_epoxide_isomerization
dbr
:Carbene_C−H_insertion
dbr
:Carbene_dimerization
dbr
:Carbohydrate_acetalisation
dbr
:Carbohydrate_synthesis
dbr
:Carbometalation
dbr
:Carbonyl_alpha-substitution_reactions
dbr
:Carboxylation
dbr
:Carbylamine_reaction
dbr
:Dienone–phenol_rearrangement
dbr
:Directing_group
dbr
:Edman_degradation
dbr
:Fluorination_by_sulfur_tetrafluoride
dbr
:Formose_reaction
dbr
:Glucuronidation
dbr
:Glycerolysis
dbr
:Glycosyl_acceptor
dbr
:Glycosyl_donor
dbr
:Glycosylation
dbr
:Hirao_coupling
dbr
:Histone_acetylation_and_deacetylation
dbr
:Kostanecki_acylation
dbr
:Asymmetric_addition_of_dialkylzinc_compounds_to_aldehydes
dbr
:Asymmetric_ester_hydrolysis_with_pig-liver_esterase
dbr
:Asymmetric_hydrogenation
dbr
:Asymmetric_nucleophilic_epoxidation
dbr
:Baeyer–Drewson_indigo_synthesis
dbr
:Baeyer–Emmerling_indole_synthesis
dbr
:Crabbé_reaction
dbr
:Cracking_(chemistry)
dbr
:Hydroacylation
dbr
:Hydroboration
dbr
:Hydrodefluorination
dbr
:Hydrogenation_of_carbon–nitrogen_double_bonds
dbr
:Hydrothermal_liquefaction
dbr
:Nitrosation
dbr
:A3_coupling_reaction
dbr
:Acetoacetic_ester_synthesis
dbr
:Acetylation
dbr
:Coarctate_reaction
dbr
:Heteroatom-promoted_lateral_lithiation
dbr
:Hooker_reaction
dbr
:Tishchenko_reaction
dbr
:Tsuji–Trost_reaction
dbr
:Wöhler_synthesis
dbr
:Modified_aldol_tandem_reaction
dbr
:Schöllkopf_method
dbr
:Stereochemistry_of_ketonization_of_enols_and_enolates
dbr
:Reactions_of_organoborates_and_boranes
dbr
:Reactions_of_organocopper_reagents
dbr
:Reichstein_process
dbr
:Disproportionation
dbr
:Aza_Paternò−Büchi_reaction
dbr
:Boord_olefin_synthesis
dbr
:Büchner–Curtius–Schlotterbeck_reaction
dbr
:Grieco_three-component_condensation
dbr
:Kochi_reaction
dbr
:Kröhnke_pyridine_synthesis
dbr
:Reductions_with_hydrosilanes
dbr
:Reductions_with_metal_alkoxyaluminium_hydrides
dbr
:Vicarious_nucleophilic_substitution
dbr
:Lumière–Barbier_method
dbr
:Reductions_with_diimide
dbr
:Transposed_Paternò−Büchi_reaction
dbr
:Fischer_glycosidation
dbr
:Flash_vacuum_pyrolysis
dbr
:Manganese-mediated_coupling_reactions
dbr
:Vicinal_difunctionalization
dbr
:Synthesis_of_nucleosides
dbr
:Trimethylenemethane_cycloaddition
dbr
:Transmethylation
dbr
:Multiple_Michael/aldol_reaction
dbr
:Murai_reaction
dbr
:Pinner_triazine_synthesis
dbr
:Sommelet_reaction
dbr
:Persistent_radical_effect
dbr
:Photooxygenation
dbr
:Pyrolysis
dbr
:Oxidation_with_dioxiranes
dbr
:Oxocarbenium
dbr
:Oxychlorination
dbr
:Soai_reaction
dbr
:Tipson–Cohen_reaction
dbr
:SOBER1
dbr
:Riemschneider_thiocarbamate_synthesis
is
skos:
broader
of
dbc
:Amide_synthesis_reactions
dbc
:Joining_reactions
dbc
:Heterocycle_forming_reactions
dbc
:Ring_forming_reactions
dbc
:Chemical_reactions_of_ethers
dbc
:Name_reactions
dbc
:Rearrangement_reactions
dbc
:Functional_modification_reactions
dbc
:Ring_contraction_reactions
dbc
:Condensation_reactions
dbc
:Organic_redox_reactions
dbc
:Olefination_reactions
dbc
:Degradation_reactions
dbc
:Free_radical_reactions
dbc
:Pericyclic_reactions
dbc
:Esterification_reactions
dbc
:Organic_oxidation_reactions
dbc
:Coupling_reactions
dbc
:Carbon-carbon_bond_forming_reactions
dbc
:Pyrolysis
dbc
:Ring_expansion_reactions
dbc
:Carbon-heteroatom_bond_forming_reactions
This content was extracted from
Wikipedia
and is licensed under the
Creative Commons Attribution-ShareAlike 3.0 Unported License