Phanephos (original) (raw)

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dbo:abstract Phanephos is an organophosphorus compound with the chemical formula (C2H4)2(C6H3PPh2)2 (Ph = C6H5). It is a white solid that is soluble in organic solvents. It is an example of a chiral C2-symmetric diphosphine ligand used in asymmetric hydrogenation. Many substituents have been introduced in place of the phenyl groups, e.g., i-Pr, C6H11, etc and a variety of chiral diphosphine ligands have been reported in asymmetric catalysis since the 1960s. (en)
dbo:alternativeName (S)-Phanephos; (R)-Phanephos (en)
dbo:iupacName (S)-(+)-4,12-Bis(diphenylphosphino)-[2.2]-paracyclophane; (R)-(−)-4,12-Bis(diphenylphosphino)-[2.2]-paracyclophane (en)
dbo:thumbnail wiki-commons:Special:FilePath/Diphosphino_phanephos.png?width=300
dbo:wikiPageID 40708524 (xsd:integer)
dbo:wikiPageLength 3280 (xsd:nonNegativeInteger)
dbo:wikiPageRevisionID 1118577879 (xsd:integer)
dbo:wikiPageWikiLink dbr:Rhodium dbr:Ruthenium dbc:Chelating_agents dbc:Diphosphines dbc:Phenyl_compounds dbr:N-Butyllithium dbc:Cyclophanes dbr:Atropisomer dbr:Hydrogenation dbr:Chlorodiphenylphosphine dbr:C2-Symmetric_ligands dbr:Organophosphorus_compound dbr:Paracyclophane dbr:Phenyl dbr:Diphosphine dbr:File:Phanphos_preparation.png
dbp:imagefile Diphosphino phanephos.png (en)
dbp:imagesize 150 (xsd:integer)
dbp:iupacname --4,12-Bis-[2.2]-paracyclophane; --4,12-Bis-[2.2]-paracyclophane (en)
dbp:othernames -Phanephos; -Phanephos (en)
dbp:wikiPageUsesTemplate dbt:Chembox dbt:Chembox_Hazards dbt:Chembox_Identifiers dbt:Chembox_Properties dbt:Clear-left dbt:Cascite
dct:subject dbc:Chelating_agents dbc:Diphosphines dbc:Phenyl_compounds dbc:Cyclophanes
gold:hypernym dbr:Compound
rdf:type owl:Thing dul:ChemicalObject dbo:ChemicalSubstance wikidata:Q11173 yago:WikicatChelatingAgents yago:Agent109190918 yago:CausalAgent100007347 yago:PhysicalEntity100001930 dbo:ChemicalCompound
rdfs:comment Phanephos is an organophosphorus compound with the chemical formula (C2H4)2(C6H3PPh2)2 (Ph = C6H5). It is a white solid that is soluble in organic solvents. It is an example of a chiral C2-symmetric diphosphine ligand used in asymmetric hydrogenation. Many substituents have been introduced in place of the phenyl groups, e.g., i-Pr, C6H11, etc and a variety of chiral diphosphine ligands have been reported in asymmetric catalysis since the 1960s. (en)
rdfs:label Phanephos (en)
owl:sameAs freebase:Phanephos yago-res:Phanephos wikidata:Phanephos https://global.dbpedia.org/id/ZFLs
prov:wasDerivedFrom wikipedia-en:Phanephos?oldid=1118577879&ns=0
foaf:depiction wiki-commons:Special:FilePath/Diphosphino_phanephos.png wiki-commons:Special:FilePath/Phanphos_preparation.png
foaf:isPrimaryTopicOf wikipedia-en:Phanephos
is foaf:primaryTopic of wikipedia-en:Phanephos