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About:
Name reactions
An Entity of Type:
Concept
,
from Named Graph:
http://dbpedia.org
,
within Data Space:
dbpedia.org
Property
Value
dbo:
wikiPageID
17870655
(xsd:integer)
dbo:
wikiPageRevisionID
971239196
(xsd:integer)
dbp:
wikiPageUsesTemplate
dbt
:Commons_cat
dbt
:CatAutoTOC
rdf:
type
skos
:Concept
rdfs:
label
Name reactions
(en)
skos:
broader
dbc
:Eponyms
dbc
:Inorganic_reactions
dbc
:Organic_reactions
skos:
prefLabel
Name reactions
(en)
prov:
wasDerivedFrom
wikipedia-en
:Category:Name_reactions?oldid=971239196&ns=14
is
dbo:
wikiPageWikiLink
of
dbr
:Cadiot–Chodkiewicz_coupling
dbr
:Cadogan–Sundberg_indole_synthesis
dbr
:Camps_quinoline_synthesis
dbr
:Cannizzaro_reaction
dbr
:Castro–Stephens_coupling
dbr
:Bechamp_reaction
dbr
:Bechamp_reduction
dbr
:Belousov–Zhabotinsky_reaction
dbr
:Benary_reaction
dbr
:Prilezhaev_reaction
dbr
:Prins_reaction
dbr
:Pschorr_cyclization
dbr
:Pummerer_rearrangement
dbr
:Robinson_annulation
dbr
:Rosenmund_reduction
dbr
:Rosenmund–von_Braun_reaction
dbr
:Roskamp_reaction
dbr
:Rubottom_oxidation
dbr
:Sandmeyer_reaction
dbr
:Sarett_oxidation
dbr
:Schmidt_reaction
dbr
:Scholl_reaction
dbr
:Schotten–Baumann_reaction
dbr
:Elbs_reaction
dbr
:Menke_nitration
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
:Blum–Ittah_aziridine_synthesis
dbr
:Bohlmann–Rahtz_pyridine_synthesis
dbr
:Borsche–Drechsel_cyclization
dbr
:Bouveault_aldehyde_synthesis
dbr
:Bouveault–Blanc_reduction
dbr
:Boyland–Sims_oxidation
dbr
:Davis_oxidation
dbr
:De_Kimpe_aziridine_synthesis
dbr
:Dess–Martin_oxidation
dbr
:Devarda's_alloy
dbr
:Algar–Flynn–Oyamada_reaction
dbr
:Allan–Robinson_reaction
dbr
:Allen–Millar–Trippett_rearrangement
dbr
:Andrussow_process
dbr
:Arens–van_Dorp_synthesis
dbr
:Hiyama_coupling
dbr
:Hofmann_elimination
dbr
:Hofmann_rearrangement
dbr
:Horner–Wadsworth–Emmons_reaction
dbr
:Hunsdiecker_reaction
dbr
:Hurd–Mori_1,2,3-thiadiazole_synthesis
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
:Riley_oxidation
dbr
:Ritter_reaction
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
:Davis–Beirut_reaction
dbr
:DeMayo_reaction
dbr
:Debus–Radziszewski_imidazole_synthesis
dbr
:Dowd–Beckwith_ring-expansion_reaction
dbr
:Duff_reaction
dbr
:Dötz_reaction
dbr
:Intramolecular_Diels–Alder_cycloaddition
dbr
:Inverse_electron-demand_Diels–Alder_reaction
dbr
:Ivanov_reaction
dbr
:Jacobsen_rearrangement
dbr
:Letts_nitrile_synthesis
dbr
:Ley_Oxidation
dbr
:Noyori_asymmetric_hydrogenation
dbr
:Prato_reaction
dbr
:Prévost_reaction
dbr
:Pudovik_reaction
dbr
:Zinin_reaction
dbr
:Widman–Stoermer_synthesis
dbr
:1,2-Wittig_rearrangement
dbr
:Collins_oxidation
dbr
:Cope_reaction
dbr
:Cope_rearrangement
dbr
:Corey–Fuchs_reaction
dbr
:Corey–Itsuno_reduction
dbr
:Corey–Kim_oxidation
dbr
:Corey–Seebach_reaction
dbr
:Criegee_oxidation
dbr
:McMurry_reaction
dbr
:Meerwein–Ponndorf–Verley_reduction
dbr
:Menshutkin_reaction
dbr
:Sakurai_reaction
dbr
:Eschenmoser_fragmentation
dbr
:Eschenmoser_sulfide_contraction
dbr
:Nef_isocyanide_reaction
dbr
:Norrish_reaction
dbr
:Midland_Alpine_borane_reduction
dbr
:Niementowski_quinazoline_synthesis
dbr
:Shi_epoxidation
dbr
:Pomeranz–Fritsch_reaction
dbr
:Robinson–Gabriel_synthesis
dbr
:Wallach_degradation
dbr
:Chugaev_elimination
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
:Ganem_oxidation
dbr
:Gattermann_reaction
dbr
:Gewald_reaction
dbr
:Boudouard_reaction
dbr
:Bradsher_cycloaddition
dbr
:Mitsunobu_reaction
dbr
:Miyaura_borylation
dbr
:Conrad–Limpach_synthesis
dbr
:Cook–Heilbron_thiazole_synthesis
dbr
:Corey-Chaykovsky_reagent
dbr
:Corey–House_synthesis
dbr
:Corey–Link_reaction
dbr
:Corey–Winter_olefin_synthesis
dbr
:Cornforth_rearrangement
dbr
:Creighton_process
dbr
:Criegee_rearrangement
dbr
:Danheiser_annulation
dbr
:Danheiser_benzannulation
dbr
:Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis
dbr
:Marschalk_reaction
dbr
:Marsh_test
dbr
:Martinet_dioxindole_synthesis
dbr
:Rieche_formylation
dbr
:Milas_hydroxylation
dbr
:Appel_reaction
dbr
:Benkeser_reaction
dbr
:Bergmann_degradation
dbr
:Bernthsen_acridine_synthesis
dbr
:Leuckart_reaction
dbr
:Leuckart_thiophenol_reaction
dbr
:Liebeskind–Srogl_coupling
dbr
:Lindgren_oxidation
dbr
:Lombardo_methylenation
dbr
:Lossen_rearrangement
dbr
:Luche_reduction
dbr
:Madelung_synthesis
dbr
:Bobbitt_reaction
dbr
:Bodroux_reaction
dbr
:Bodroux–Chichibabin_aldehyde_synthesis
dbr
:Boekelheide_reaction
dbr
:Boger_pyridine_synthesis
dbr
:Bohn–Schmidt_reaction
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
:Fenton's_reaction
dbr
:Freund_reaction
dbr
:Fráter–Seebach_alkylation
dbr
:Fujimoto–Belleau_reaction
dbr
:Fukuyama_indole_synthesis
dbr
:Hajos–Parrish–Eder–Sauer–Wiechert_reaction
dbr
:Haller-Bauer_reaction
dbr
:Hammick_reaction
dbr
:Hemetsberger_indole_synthesis
dbr
:Kharasch_addition
dbr
:Kharasch–Sosnovsky_reaction
dbr
:Kowalski_ester_homologation
dbr
:Overman_rearrangement
dbr
:Pellizzari_reaction
dbr
:Malaprade_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
:Meyer_reaction
dbr
:Meyer_synthesis
dbr
:Meyers_synthesis
dbr
:Meyer–Schuster_rearrangement
dbr
:Michael_reaction
dbr
:Michaelis–Becker_reaction
dbr
:Auwers_synthesis
dbr
:Aza-Baylis–Hillman_reaction
dbr
:Aza-Cope_rearrangement
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
:Tiemann_rearrangement
dbr
:Tiffeneau–Demjanov_rearrangement
dbr
:Tsuji–Wilkinson_decarbonylation_reaction
dbr
:Darzens_halogenation
dbr
:Darzens_tetralin_synthesis
dbr
:Weinreb_ketone_synthesis
dbr
:Wenker_synthesis
dbr
:Willgerodt_rearrangement
dbr
:Williamson_ether_synthesis
dbr
:Doebner_reaction
dbr
:Doebner–Miller_reaction
dbr
:Doering–LaFlamme_allene_synthesis
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
:Hass–Bender_oxidation
dbr
:Hauser_annulation
dbr
:Haworth_Phenanthrene_synthesis
dbr
:Hayashi_rearrangement
dbr
:Heck–Matsuda_reaction
dbr
:Ireland–Claisen_rearrangement
dbr
:Japp–Maitland_condensation
dbr
:Jocic–Reeve_reaction
dbr
:Julia–Kocienski_olefination
dbr
:Juliá–Colonna_epoxidation
dbr
:Leblanc_process
dbr
:Lectka_enantioselective_beta-lactam_synthesis
dbr
:Lobry_de_Bruyn–Van_Ekenstein_transformation
dbr
:Minisci_reaction
dbr
:Name_reaction
dbr
:Piancatelli_rearrangement
dbr
:Nitro-Mannich_reaction
dbr
:Reissert_indole_synthesis
dbr
:Achmatowicz_reaction
dbr
:Akabori_amino-acid_reaction
dbr
:Curtius_rearrangement
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
:Ferrario–Ackermann_reaction
dbr
:Fiesselmann_thiophene_synthesis
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
:Barbier–Wieland_degradation
dbr
:Bardhan–Sengupta_phenanthrene_synthesis
dbr
:Bargellini_reaction
dbr
:Barton_reaction
dbr
:Barton_vinyl_iodine_procedure
dbr
:Barton–Zard_reaction
is
dcterms:
subject
of
dbr
:Cadiot–Chodkiewicz_coupling
dbr
:Cadogan–Sundberg_indole_synthesis
dbr
:Camps_quinoline_synthesis
dbr
:Cannizzaro_reaction
dbr
:Castro–Stephens_coupling
dbr
:Bechamp_reaction
dbr
:Bechamp_reduction
dbr
:Belousov–Zhabotinsky_reaction
dbr
:Benary_reaction
dbr
:Prilezhaev_reaction
dbr
:Prins_reaction
dbr
:Pschorr_cyclization
dbr
:Pummerer_rearrangement
dbr
:Robinson_annulation
dbr
:Rosenmund_reduction
dbr
:Rosenmund–von_Braun_reaction
dbr
:Roskamp_reaction
dbr
:Rubottom_oxidation
dbr
:Sandmeyer_reaction
dbr
:Sarett_oxidation
dbr
:Schmidt_reaction
dbr
:Scholl_reaction
dbr
:Schotten–Baumann_reaction
dbr
:Elbs_reaction
dbr
:Menke_nitration
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
:Blum–Ittah_aziridine_synthesis
dbr
:Bohlmann–Rahtz_pyridine_synthesis
dbr
:Borsche–Drechsel_cyclization
dbr
:Bouveault_aldehyde_synthesis
dbr
:Bouveault–Blanc_reduction
dbr
:Boyland–Sims_oxidation
dbr
:Davis_oxidation
dbr
:De_Kimpe_aziridine_synthesis
dbr
:Dess–Martin_oxidation
dbr
:Devarda's_alloy
dbr
:Algar–Flynn–Oyamada_reaction
dbr
:Allan–Robinson_reaction
dbr
:Allen–Millar–Trippett_rearrangement
dbr
:Andrussow_process
dbr
:Arens–van_Dorp_synthesis
dbr
:Hiyama_coupling
dbr
:Hofmann_elimination
dbr
:Hofmann_rearrangement
dbr
:Horner–Wadsworth–Emmons_reaction
dbr
:Hunsdiecker_reaction
dbr
:Hurd–Mori_1,2,3-thiadiazole_synthesis
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
:Riley_oxidation
dbr
:Ritter_reaction
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
:Davis–Beirut_reaction
dbr
:DeMayo_reaction
dbr
:Debus–Radziszewski_imidazole_synthesis
dbr
:Dowd–Beckwith_ring-expansion_reaction
dbr
:Duff_reaction
dbr
:Dötz_reaction
dbr
:Intramolecular_Diels–Alder_cycloaddition
dbr
:Inverse_electron-demand_Diels–Alder_reaction
dbr
:Ivanov_reaction
dbr
:Jacobsen_rearrangement
dbr
:Letts_nitrile_synthesis
dbr
:Ley_Oxidation
dbr
:Noyori_asymmetric_hydrogenation
dbr
:Prato_reaction
dbr
:Prévost_reaction
dbr
:Pudovik_reaction
dbr
:Zinin_reaction
dbr
:Widman–Stoermer_synthesis
dbr
:1,2-Wittig_rearrangement
dbr
:Collins_oxidation
dbr
:Cope_reaction
dbr
:Cope_rearrangement
dbr
:Corey–Fuchs_reaction
dbr
:Corey–Itsuno_reduction
dbr
:Corey–Kim_oxidation
dbr
:Corey–Seebach_reaction
dbr
:Criegee_oxidation
dbr
:McMurry_reaction
dbr
:Meerwein–Ponndorf–Verley_reduction
dbr
:Menshutkin_reaction
dbr
:Sakurai_reaction
dbr
:Eschenmoser_fragmentation
dbr
:Eschenmoser_sulfide_contraction
dbr
:Nef_isocyanide_reaction
dbr
:Norrish_reaction
dbr
:Midland_Alpine_borane_reduction
dbr
:Niementowski_quinazoline_synthesis
dbr
:Shi_epoxidation
dbr
:Pomeranz–Fritsch_reaction
dbr
:Robinson–Gabriel_synthesis
dbr
:Wallach_degradation
dbr
:Chugaev_elimination
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
:Ganem_oxidation
dbr
:Gattermann_reaction
dbr
:Gewald_reaction
dbr
:Boudouard_reaction
dbr
:Bradsher_cycloaddition
dbr
:Mitsunobu_reaction
dbr
:Miyaura_borylation
dbr
:Conrad–Limpach_synthesis
dbr
:Cook–Heilbron_thiazole_synthesis
dbr
:Corey-Chaykovsky_reagent
dbr
:Corey–House_synthesis
dbr
:Corey–Link_reaction
dbr
:Corey–Winter_olefin_synthesis
dbr
:Cornforth_rearrangement
dbr
:Creighton_process
dbr
:Criegee_rearrangement
dbr
:Danheiser_annulation
dbr
:Danheiser_benzannulation
dbr
:Erlenmeyer–Plöchl_azlactone_and_amino-acid_synthesis
dbr
:Marschalk_reaction
dbr
:Marsh_test
dbr
:Martinet_dioxindole_synthesis
dbr
:Rieche_formylation
dbr
:Milas_hydroxylation
dbr
:Appel_reaction
dbr
:Benkeser_reaction
dbr
:Bergmann_degradation
dbr
:Bernthsen_acridine_synthesis
dbr
:Leuckart_reaction
dbr
:Leuckart_thiophenol_reaction
dbr
:Liebeskind–Srogl_coupling
dbr
:Lindgren_oxidation
dbr
:Lombardo_methylenation
dbr
:Lossen_rearrangement
dbr
:Luche_reduction
dbr
:Madelung_synthesis
dbr
:Bobbitt_reaction
dbr
:Bodroux_reaction
dbr
:Bodroux–Chichibabin_aldehyde_synthesis
dbr
:Boekelheide_reaction
dbr
:Boger_pyridine_synthesis
dbr
:Bohn–Schmidt_reaction
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
:Fenton's_reaction
dbr
:Freund_reaction
dbr
:Fráter–Seebach_alkylation
dbr
:Fujimoto–Belleau_reaction
dbr
:Fukuyama_indole_synthesis
dbr
:Hajos–Parrish–Eder–Sauer–Wiechert_reaction
dbr
:Haller-Bauer_reaction
dbr
:Hammick_reaction
dbr
:Hemetsberger_indole_synthesis
dbr
:Kharasch_addition
dbr
:Kharasch–Sosnovsky_reaction
dbr
:Kowalski_ester_homologation
dbr
:Overman_rearrangement
dbr
:Pellizzari_reaction
dbr
:Malaprade_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
:Meyer_reaction
dbr
:Meyer_synthesis
dbr
:Meyers_synthesis
dbr
:Meyer–Schuster_rearrangement
dbr
:Michael_reaction
dbr
:Michaelis–Becker_reaction
dbr
:Auwers_synthesis
dbr
:Aza-Baylis–Hillman_reaction
dbr
:Aza-Cope_rearrangement
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
:Tiemann_rearrangement
dbr
:Tiffeneau–Demjanov_rearrangement
dbr
:Tsuji–Wilkinson_decarbonylation_reaction
dbr
:Darzens_halogenation
dbr
:Darzens_tetralin_synthesis
dbr
:Weinreb_ketone_synthesis
dbr
:Wenker_synthesis
dbr
:Willgerodt_rearrangement
dbr
:Williamson_ether_synthesis
dbr
:Doebner_reaction
dbr
:Doebner–Miller_reaction
dbr
:Doering–LaFlamme_allene_synthesis
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
:Hass–Bender_oxidation
dbr
:Hauser_annulation
dbr
:Haworth_Phenanthrene_synthesis
dbr
:Hayashi_rearrangement
dbr
:Heck–Matsuda_reaction
dbr
:Ireland–Claisen_rearrangement
dbr
:Japp–Maitland_condensation
dbr
:Jocic–Reeve_reaction
dbr
:Julia–Kocienski_olefination
dbr
:Juliá–Colonna_epoxidation
dbr
:Leblanc_process
dbr
:Lectka_enantioselective_beta-lactam_synthesis
dbr
:Lobry_de_Bruyn–Van_Ekenstein_transformation
dbr
:Minisci_reaction
dbr
:Name_reaction
dbr
:Piancatelli_rearrangement
dbr
:Nitro-Mannich_reaction
dbr
:Reissert_indole_synthesis
dbr
:Achmatowicz_reaction
dbr
:Akabori_amino-acid_reaction
dbr
:Curtius_rearrangement
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
:Ferrario–Ackermann_reaction
dbr
:Fiesselmann_thiophene_synthesis
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
:Barbier–Wieland_degradation
dbr
:Bardhan–Sengupta_phenanthrene_synthesis
dbr
:Bargellini_reaction
dbr
:Barton_reaction
dbr
:Barton_vinyl_iodine_procedure
dbr
:Barton–Zard_reaction
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