Statements (44)
| Predicate | Object |
|---|---|
| gptkbp:instanceOf |
chemical reaction
|
| gptkbp:appearsIn |
synthesis of amino acids
|
| gptkbp:contributedTo |
green chemistry
|
| gptkbp:developedBy |
1990s
|
| gptkbp:enhances |
reaction selectivity
|
| gptkbp:hasRelatedPatent |
material science
medicinal chemistry agricultural chemistry |
| https://www.w3.org/2000/01/rdf-schema#label |
Corey–Noyori reaction
|
| gptkbp:involves |
transition metal catalyst
iridium catalysts ruthenium catalysts |
| gptkbp:isCitedIn |
research papers
|
| gptkbp:isConsidered |
a breakthrough in chemistry
|
| gptkbp:isExploredIn |
academic research
|
| gptkbp:isInfluencedBy |
gptkb:Ryoji_Noyori
gptkb:Elias_J._Corey |
| gptkbp:isNotableFor |
broad substrate scope
mild reaction conditions high enantioselectivity |
| gptkbp:isPartOf |
asymmetric synthesis
modern organic synthesis techniques |
| gptkbp:isPublishedIn |
scientific journals
|
| gptkbp:isRecognizedBy |
gptkb:Nobel_Prize_in_Chemistry
|
| gptkbp:isRelatedTo |
gptkb:Noyori_asymmetric_hydrogenation
chiral auxiliary methods Corey–Bakshi–Shibata_reduction |
| gptkbp:isStudiedIn |
organic chemistry
catalysis research sustainable chemistry |
| gptkbp:isTaughtIn |
university courses
|
| gptkbp:isUsedFor |
alkene hydrogenation
ketone hydrogenation aldehyde_hydrogenation |
| gptkbp:isUsedIn |
industrial applications
|
| gptkbp:namedAfter |
gptkb:Ryoji_Noyori
gptkb:Elias_J._Corey |
| gptkbp:produces |
chiral compounds
|
| gptkbp:relatedTo |
chiral ligand chemistry
|
| gptkbp:requires |
specific reaction conditions
|
| gptkbp:significance |
important for pharmaceuticals
|
| gptkbp:type |
asymmetric hydrogenation
|
| gptkbp:usedIn |
organic synthesis
|
| gptkbp:utilizes |
hydrogen gas
|