http://dbpedia.org/ontology/abstract
|
The Danheiser benzannulation is a chemical reaction used in organic chemistry to generate highly substituted phenols in a single step. It is named after Rick L. Danheiser who developed the reaction.
|
http://dbpedia.org/ontology/thumbnail
|
http://commons.wikimedia.org/wiki/Special:FilePath/Scheme_1_Danheiser_Benzannulation.png?width=300 +
|
http://dbpedia.org/ontology/wikiPageID
|
44503117
|
http://dbpedia.org/ontology/wikiPageLength
|
18766
|
http://dbpedia.org/ontology/wikiPageRevisionID
|
1097200643
|
http://dbpedia.org/ontology/wikiPageWikiLink
|
http://dbpedia.org/resource/Indole +
, http://dbpedia.org/resource/Palladium +
, http://dbpedia.org/resource/Lithium +
, http://dbpedia.org/resource/Dehydrohalogenation +
, http://dbpedia.org/resource/Ether +
, http://dbpedia.org/resource/Dibenzylideneacetone +
, http://dbpedia.org/resource/Substitution_reaction +
, http://dbpedia.org/resource/Yield_%28chemistry%29 +
, http://dbpedia.org/resource/Wolff_rearrangement +
, http://dbpedia.org/resource/Wulff%E2%80%93D%C3%B6tz_reaction +
, http://dbpedia.org/resource/Metalation +
, http://dbpedia.org/resource/Regioselectivity +
, http://dbpedia.org/resource/Aniline +
, http://dbpedia.org/resource/Toluene +
, http://dbpedia.org/resource/Aromaticity +
, http://dbpedia.org/resource/Mercury-vapor_lamp +
, http://dbpedia.org/resource/Zinc +
, http://dbpedia.org/resource/Mycophenolic_acid +
, http://dbpedia.org/resource/Cobalt +
, http://dbpedia.org/resource/Thioethers +
, http://dbpedia.org/resource/Zinc_iodide +
, http://dbpedia.org/resource/Tetrahydrofuran +
, http://dbpedia.org/resource/Benzene +
, http://dbpedia.org/resource/Organic_chemistry +
, http://dbpedia.org/resource/Chemical_reaction +
, http://dbpedia.org/resource/Aldol +
, http://dbpedia.org/resource/Benzothiophene +
, http://dbpedia.org/resource/Benzofuran +
, http://dbpedia.org/resource/Carbazole +
, http://dbpedia.org/resource/Phenols +
, http://dbpedia.org/resource/Ketene +
, http://dbpedia.org/resource/Tetrahydrocannabinol +
, http://dbpedia.org/resource/Dichloroethane +
, http://dbpedia.org/resource/Olefin_metathesis +
, http://dbpedia.org/resource/Robinson_annulation +
, http://dbpedia.org/resource/Cycloaddition +
, http://dbpedia.org/resource/1%2C2-dichloroethane +
, http://dbpedia.org/resource/Category:Organic_reactions +
, http://dbpedia.org/resource/Enyne +
, http://dbpedia.org/resource/File:Scheme_8_Synthesis_of.png +
, http://dbpedia.org/resource/Arene_substitution_pattern +
, http://dbpedia.org/resource/File:Scheme_9_Formation_of.png +
, http://dbpedia.org/resource/File:Scheme_6_Formation_of.png +
, http://dbpedia.org/resource/File:Scheme_7_Synthesis_of.png +
, http://dbpedia.org/resource/File:Scheme10_Synthesis_of.png +
, http://dbpedia.org/resource/File:Scheme_11_Cobalt_catalyzed.png +
, http://dbpedia.org/resource/Carbene +
, http://dbpedia.org/resource/File:Shceme17.png +
, http://dbpedia.org/resource/Naphthalene +
, http://dbpedia.org/resource/The_Learning_Company +
, http://dbpedia.org/resource/Rick_Danheiser +
, http://dbpedia.org/resource/File:Scheme_15_Benzannulation_Towards.png +
, http://dbpedia.org/resource/File:Scheme_15_Benzannulation_Towards_b.png +
, http://dbpedia.org/resource/File:Scheme_13_Palladium_Catalyzed.png +
, http://dbpedia.org/resource/Phenol +
, http://dbpedia.org/resource/File:Scheme_14_Benzannulation_Toward.png +
, http://dbpedia.org/resource/1%2C3-bis%28diphenylphosphino%29propane +
, http://dbpedia.org/resource/File:Scheme_16_Benzannulation_Toward.png +
, http://dbpedia.org/resource/Ring-closing_metathesis +
, http://dbpedia.org/resource/Potassium_hydroxide +
, http://dbpedia.org/resource/Catalyst +
, http://dbpedia.org/resource/Electrocyclic +
, http://dbpedia.org/resource/In_situ +
, http://dbpedia.org/resource/Pericyclic_reaction +
, http://dbpedia.org/resource/Category:Name_reactions +
, http://dbpedia.org/resource/Dichloromethane +
, http://dbpedia.org/resource/Resorcinol +
, http://dbpedia.org/resource/File:4-octyne_reaction.png +
, http://dbpedia.org/resource/Triphenylphosphine +
, http://dbpedia.org/resource/File:Scheme_18_Benzannulation_towards.png +
, http://dbpedia.org/resource/File:Scheme_1_Danheiser_Benzannulation.png +
, http://dbpedia.org/resource/File:Dictyodendrin_synthesis.tif +
, http://dbpedia.org/resource/File:Mechanism_of_the_Reaction.png +
, http://dbpedia.org/resource/Cylindrocyclophanes +
, http://dbpedia.org/resource/File:Scheme_5_Mechanism_for.png +
, http://dbpedia.org/resource/Annulation +
, http://dbpedia.org/resource/File:Scheme_5_Mechanism_for_b.png +
, http://dbpedia.org/resource/Chloroform +
, http://dbpedia.org/resource/File:Scheme_2_Danheiser_Benzannulation.png +
, http://dbpedia.org/resource/Allene +
, http://dbpedia.org/resource/File:Scheme_3_Reaction_Mechanism.png +
, http://dbpedia.org/resource/Saponify +
, http://dbpedia.org/resource/Octyne +
, http://dbpedia.org/resource/Penicillium +
, http://dbpedia.org/resource/Michael_Addition +
, http://dbpedia.org/resource/Open-chain_compound +
|
http://dbpedia.org/property/wikiPageUsesTemplate
|
http://dbpedia.org/resource/Template:Reflist +
, http://dbpedia.org/resource/Template:Organic_reactions +
|
http://purl.org/dc/terms/subject
|
http://dbpedia.org/resource/Category:Organic_reactions +
, http://dbpedia.org/resource/Category:Name_reactions +
|
http://purl.org/linguistics/gold/hypernym
|
http://dbpedia.org/resource/Reaction +
|
http://www.w3.org/ns/prov#wasDerivedFrom
|
http://en.wikipedia.org/wiki/Danheiser_benzannulation?oldid=1097200643&ns=0 +
|
http://xmlns.com/foaf/0.1/depiction
|
http://commons.wikimedia.org/wiki/Special:FilePath/Scheme_16_Benzannulation_Toward.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/Scheme_18_Benzannulation_towards.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/Scheme_5_Mechanism_for_b.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/Scheme_6_Formation_of.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/Scheme_3_Reaction_Mechanism.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/Scheme_5_Mechanism_for.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/Scheme_11_Cobalt_catalyzed.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/Shceme17.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/Scheme10_Synthesis_of.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/Scheme_15_Benzannulation_Towards.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/Scheme_15_Benzannulation_Towards_b.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/Scheme_13_Palladium_Catalyzed.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/Scheme_14_Benzannulation_Toward.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/Scheme_9_Formation_of.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/Scheme_7_Synthesis_of.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/Scheme_8_Synthesis_of.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/4-octyne_reaction.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/Mechanism_of_the_Reaction.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/Scheme_1_Danheiser_Benzannulation.png +
, http://commons.wikimedia.org/wiki/Special:FilePath/Scheme_2_Danheiser_Benzannulation.png +
|
http://xmlns.com/foaf/0.1/isPrimaryTopicOf
|
http://en.wikipedia.org/wiki/Danheiser_benzannulation +
|
owl:sameAs |
http://dbpedia.org/resource/Danheiser_benzannulation +
, https://global.dbpedia.org/id/2MaWj +
, http://www.wikidata.org/entity/Q24963007 +
, http://yago-knowledge.org/resource/Danheiser_benzannulation +
, http://rdf.freebase.com/ns/m.012c5w_g +
|
rdf:type |
http://dbpedia.org/ontology/Disease +
|
rdfs:comment |
The Danheiser benzannulation is a chemical reaction used in organic chemistry to generate highly substituted phenols in a single step. It is named after Rick L. Danheiser who developed the reaction.
|
rdfs:label |
Danheiser benzannulation
|