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- Noyori_asymmetric_hydrogenation abstract "In chemistry, the Noyori asymmetric hydrogenation of ketones is a chemical reaction for the enantioselective hydrogenation of ketone, aldehydes, and imines. This reaction exploits using chiral ruthenium catalysts introduced by Ryoji Noyori. He shared half of the Nobel Prize in Chemistry in 2001 with William S. Knowles for the study of the asymmetric hydrogenation. BINAP-Ru catalyst is used for the asymmetric hydrogenation of functionalized ketones and BINAP/diamine-Ru catalyst is used for the asymmetric hydrogenation of simple ketones. These hydrogenations are used in the production of several drugs, such as the antibacterial levofloxin, the antibiotic carbapenem, and the antipsychotic agent BMS181100.".
- Noyori_asymmetric_hydrogenation thumbnail Noyoriintro.png?width=300.
- Noyori_asymmetric_hydrogenation wikiPageID "6845005".
- Noyori_asymmetric_hydrogenation wikiPageLength "12017".
- Noyori_asymmetric_hydrogenation wikiPageOutDegree "111".
- Noyori_asymmetric_hydrogenation wikiPageRevisionID "698478954".
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Aldehyde.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Alkene.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Alkoxide.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Aromaticity.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Asymmetric_hydrogenation.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Atom.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink BINAP.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Base_(chemistry).
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Carbapenem.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Catalysis.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Catalytic_cycle.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Category:Chemical_synthesis.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Category:Hydrogenation.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Category:Stereochemistry.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Chemistry.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Chemoselectivity.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Chirality.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Compressed_hydrogen.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Corey–Itsuno_reduction.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Dehydration.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Diamine.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Diastereomer.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Dicarboxylic_acid.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Diphosphane.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Dynamic_Kinetic_Resolution_In_Asymmetric_Synthesis.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Enantiomer.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Ester.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Flippin–Lodge_angle.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Halide.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Hydride.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Hydrogen.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Hydrogen_chloride.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Hydrogenation.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Imine.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Ketone.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Kinetic_resolution.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Levofloxacin.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Ligand.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Midland_Alpine_borane_reduction.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Nobel_Prize_in_Chemistry.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Olefinic.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Oxygen.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Phenyl_group.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Reaction_intermediate.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Ruthenium.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Ryōji_Noyori.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Stereoselectivity.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Steric_effects.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink Transition_state.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink William_Standish_Knowles.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink File:BINAPRupathway.png.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink File:BINAPdiamineRu_pathway.png.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink File:BINAPdiamineRuscope2.png.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink File:BMS181110.png.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink File:Carbapenems1.png.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink File:Chemoselectivity1.png.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink File:Diastereoselectivity1.png.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink File:Enantioselectivity1.png.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink File:Levofloxacin3.png.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink File:Noyoriintro.png.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink File:Rudihalide.png.
- Noyori_asymmetric_hydrogenation wikiPageWikiLink File:SbinapRudiamine.png.
- Noyori_asymmetric_hydrogenation wikiPageWikiLinkText "Noyori asymmetric hydrogenation".
- Noyori_asymmetric_hydrogenation wikiPageWikiLinkText "Noyori type reaction".
- Noyori_asymmetric_hydrogenation wikiPageWikiLinkText "Noyori’s asymmetric hydrogenation".
- Noyori_asymmetric_hydrogenation wikiPageWikiLinkText "asymmetric hydrogenation".
- Noyori_asymmetric_hydrogenation wikiPageUsesTemplate Template:Reflist.
- Noyori_asymmetric_hydrogenation subject Category:Chemical_synthesis.
- Noyori_asymmetric_hydrogenation subject Category:Hydrogenation.
- Noyori_asymmetric_hydrogenation subject Category:Stereochemistry.
- Noyori_asymmetric_hydrogenation hypernym Reaction.
- Noyori_asymmetric_hydrogenation type Disease.
- Noyori_asymmetric_hydrogenation type Process.
- Noyori_asymmetric_hydrogenation type Reaction.
- Noyori_asymmetric_hydrogenation comment "In chemistry, the Noyori asymmetric hydrogenation of ketones is a chemical reaction for the enantioselective hydrogenation of ketone, aldehydes, and imines. This reaction exploits using chiral ruthenium catalysts introduced by Ryoji Noyori. He shared half of the Nobel Prize in Chemistry in 2001 with William S. Knowles for the study of the asymmetric hydrogenation.".
- Noyori_asymmetric_hydrogenation label "Noyori asymmetric hydrogenation".
- Noyori_asymmetric_hydrogenation sameAs Q3119091.
- Noyori_asymmetric_hydrogenation sameAs هدرجة_نويوري_اللامتناظرة.
- Noyori_asymmetric_hydrogenation sameAs Hidrogenación_asimétrica_Noyori.
- Noyori_asymmetric_hydrogenation sameAs Hydrogénation_asymétrique_de_Noyori.
- Noyori_asymmetric_hydrogenation sameAs 野依不斉水素化反応.
- Noyori_asymmetric_hydrogenation sameAs m.0gs7qc.
- Noyori_asymmetric_hydrogenation sameAs Q3119091.
- Noyori_asymmetric_hydrogenation sameAs 野依不对称氢化反应.
- Noyori_asymmetric_hydrogenation wasDerivedFrom Noyori_asymmetric_hydrogenation?oldid=698478954.
- Noyori_asymmetric_hydrogenation depiction Noyoriintro.png.
- Noyori_asymmetric_hydrogenation isPrimaryTopicOf Noyori_asymmetric_hydrogenation.