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INTRODUCTION
BIOGRAPHICAL
OF
RYOJI NOYORI
•Born : on September 3, 1938
•in a suburb of Kobe (now Ashiya), Japan
•the first son of Kaneki and Suzuko Noyori
RYOJI NOY...
RESEARCH
• Noyori believes strongly in the power of catalysis and of green chemistry
• Noyori is most famous for asymmetri...
NOYORI CATALYSTS
MECHANISM
EXAMPLE:
NOYORI ASYMMETRIC HYDROGENATION
ASSYMETRICHYDROGENATION
chemical reaction that adds two atoms
of hydrogen to a target (sub...
NOYORI CATALYSTS
MECHANISM
Noyori asymmetric hydrogenation.
• Chemical reaction for the enantioselective
hydrogenation of ketones, aldehydes and imin...
Industrial application
• An antibacterial levofloxacin is synthesized
using (R)-1,2-propandiol, which is synthesized
from ...
• An antibiotic carbapenem is also prepared
using Noyori asymmetric hydrogenation via
(2S,3R)-methyl 2-(benzamidomethyl)-3...
• An antipsychotic agent BMS 181100 is
synthesized using BINAP/diamine-Ru catalyst.
REFERENCES
• http://www.chem.harvard.edu/groups/myers/
handouts/22_Noyori_Asymmetric_Hydrog.pdf
• http://www.synarchive.co...
Noyori asymmetric hydrogenation
Noyori asymmetric hydrogenation
Noyori asymmetric hydrogenation
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Noyori asymmetric hydrogenation

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Noyori asymmetric hydrogenation

  1. 1. INTRODUCTION BIOGRAPHICAL OF RYOJI NOYORI
  2. 2. •Born : on September 3, 1938 •in a suburb of Kobe (now Ashiya), Japan •the first son of Kaneki and Suzuko Noyori RYOJI NOYORI •won the Nobel Prize in Chemistry in 2001 •He shared the prize of study of chirally catalyzed hydrogenations WITH William S. Knowles ; the 2nd half went to K. Barry Sharpless for his study in chirally catalyzed oxidation reactions •Prize motivation: "for their work on chirally catalysed hydrogenation reactions“. •Field: Organic chemistry, industrial chemistry ACHIEVEMENT
  3. 3. RESEARCH • Noyori believes strongly in the power of catalysis and of green chemistry • Noyori is most famous for asymmetric hydrogenation using as catalysts complexes of rhodium and ruthenium, particularly those based on the BINAP ligand. • Asymmetric hydrogenation of an alkene in the presence of ((S)- BINAP)Ru(OAc)2 is used for the commercial production of enantiomerically pure (97% ee) naproxen, used as an anti-inflammatory drug. • The antibacterial agent levofloxacin is manufactured by asymmetric hydrogenation of ketones in the presence of a Ru(II) BINAP halide complex. • He has also worked on other asymmetric processes. Each year 3000 tones (after new expansion) of menthol are produced (in 94% ) by Takasago International Co., using Noyori's method for isomerization of allylic amines
  4. 4. NOYORI CATALYSTS
  5. 5. MECHANISM
  6. 6. EXAMPLE:
  7. 7. NOYORI ASYMMETRIC HYDROGENATION ASSYMETRICHYDROGENATION chemical reaction that adds two atoms of hydrogen to a target (substrate) molecule with three dimensional spatial selectivity. characterized by asymmetry in the spatial arrangement or placement of parts or components. THEREFORE NOYORIASSYMETRICHYDROGENATION ASYMMETRICAL ? chemical reaction for the enantioselective hydrogenation of ketone, aldehydes, and imines.
  8. 8. NOYORI CATALYSTS
  9. 9. MECHANISM
  10. 10. Noyori asymmetric hydrogenation. • Chemical reaction for the enantioselective hydrogenation of ketones, aldehydes and imines. • BINAP-Ru catalyst – functionalized ketones. • BINAP/diamine-Ru catalyst – simple ketones. • Used in production of several drugs, such as the antibacterial levofloxin, the antibiotic carbapenem and the antipsychotic agent BMS181100. APPLICATION
  11. 11. Industrial application • An antibacterial levofloxacin is synthesized using (R)-1,2-propandiol, which is synthesized from hydroxyacteone using Noyori asymmetric hydrogenation(Takasago Co./Daiichi Pharmaceutical Co.).
  12. 12. • An antibiotic carbapenem is also prepared using Noyori asymmetric hydrogenation via (2S,3R)-methyl 2-(benzamidomethyl)-3- hydroxybutanoate, which is synthesized from racemic methyl 2-(benzamidomethyl)-3- oxobutanoate by dynamic kinetic resolution.
  13. 13. • An antipsychotic agent BMS 181100 is synthesized using BINAP/diamine-Ru catalyst.
  14. 14. REFERENCES • http://www.chem.harvard.edu/groups/myers/ handouts/22_Noyori_Asymmetric_Hydrog.pdf • http://www.synarchive.com/named- reactions/Noyori_Asymmetric_Hydrogenation

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