JPS55121837A - Asymmetric hydrogenation catalyst - Google Patents
Asymmetric hydrogenation catalystInfo
- Publication number
- JPS55121837A JPS55121837A JP2849279A JP2849279A JPS55121837A JP S55121837 A JPS55121837 A JP S55121837A JP 2849279 A JP2849279 A JP 2849279A JP 2849279 A JP2849279 A JP 2849279A JP S55121837 A JPS55121837 A JP S55121837A
- Authority
- JP
- Japan
- Prior art keywords
- hydrogeneation
- optically active
- catalyst
- asymmetric
- ligand
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Classifications
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P20/00—Technologies relating to chemical industry
- Y02P20/50—Improvements relating to the production of bulk chemicals
- Y02P20/52—Improvements relating to the production of bulk chemicals using catalysts, e.g. selective catalysts
Landscapes
- Catalysts (AREA)
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
PURPOSE: To obtain chiral compounds in good yield by using a rhorium complex having the optically active substance of a specific phosphine derivative as a ligand as a catalyst for the hydrogeneation reaction of prochiral carbon double bonds.
CONSTITUTION: In the hydrogeneation reaction of an organic compound having prochiral C-C double bonds, an asymmetric hydrogeneation catalyst consisting of a rhodium complex having as a ligand a chiral phosphine, e.g., the optically active substance of phosphine derivative of the formula, (R is an alkyl, aryl or aralkyl group). Thus, chiral compounds can be obtained in good yield and also the asymmetric hydrogeneation catalyst is excellently applicable to the synthesis of optically active amino acids.
COPYRIGHT: (C)1980,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2849279A JPS55121837A (en) | 1979-03-12 | 1979-03-12 | Asymmetric hydrogenation catalyst |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP2849279A JPS55121837A (en) | 1979-03-12 | 1979-03-12 | Asymmetric hydrogenation catalyst |
Publications (1)
Publication Number | Publication Date |
---|---|
JPS55121837A true JPS55121837A (en) | 1980-09-19 |
Family
ID=12250157
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP2849279A Pending JPS55121837A (en) | 1979-03-12 | 1979-03-12 | Asymmetric hydrogenation catalyst |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS55121837A (en) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0083332A2 (en) * | 1981-12-28 | 1983-07-06 | Monsanto Company | Asymmetric reduction of nitro-containing prochiral compounds |
CN1047597C (en) * | 1997-06-02 | 1999-12-22 | 厦门大学 | Chiral phosphine aminate-metal coordinate compound, the prepn. method thereof and the application in the asymmetrically catalytic hydrogenation |
-
1979
- 1979-03-12 JP JP2849279A patent/JPS55121837A/en active Pending
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0083332A2 (en) * | 1981-12-28 | 1983-07-06 | Monsanto Company | Asymmetric reduction of nitro-containing prochiral compounds |
EP0083332A3 (en) * | 1981-12-28 | 1985-03-27 | Monsanto Company | Asymmetric reduction of nitro-containing prochiral compounds |
CN1047597C (en) * | 1997-06-02 | 1999-12-22 | 厦门大学 | Chiral phosphine aminate-metal coordinate compound, the prepn. method thereof and the application in the asymmetrically catalytic hydrogenation |
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