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- Q3119091 subject Q18698606.
- Q3119091 subject Q7565754.
- Q3119091 subject Q8692179.
- Q3119091 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.".
- Q3119091 thumbnail Noyoriintro.png?width=300.
- Q3119091 wikiPageWikiLink Q101487.
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- Q3119091 wikiPageWikiLink Q18698606.
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- Q3119091 wikiPageWikiLink Q7565754.
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- Q3119091 wikiPageWikiLink Q82264.
- Q3119091 wikiPageWikiLink Q8692179.
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- Q3119091 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.".
- Q3119091 label "Noyori asymmetric hydrogenation".
- Q3119091 depiction Noyoriintro.png.