JPS5639097A - Optically active n-carbamoylpyrrolidinodiphosphine ligand and its preparation - Google Patents
Optically active n-carbamoylpyrrolidinodiphosphine ligand and its preparationInfo
- Publication number
- JPS5639097A JPS5639097A JP11413979A JP11413979A JPS5639097A JP S5639097 A JPS5639097 A JP S5639097A JP 11413979 A JP11413979 A JP 11413979A JP 11413979 A JP11413979 A JP 11413979A JP S5639097 A JPS5639097 A JP S5639097A
- Authority
- JP
- Japan
- Prior art keywords
- optically active
- formula
- ligand
- expressed
- carbamoylpyrrolidinodiphosphine
- 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.)
- Granted
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
- Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
- Low-Molecular Organic Synthesis Reactions Using Catalysts (AREA)
Abstract
NEW MATERIAL:The titled ligand expressed by formula I (R is aliphatic, aromatic or organic sulfonyl group;* is optically active site).
EXAMPLE: (2S, 4S)-(N-Phenylcarbamoyl)-4-diphenylphosphinomethulpyrrolidine.
USE: An asymmetric catalyst for preparing optically active α-amino acids having a high crystallinity, good handleability and a very high optical yield.
PROCESS: An optically active pyrrolidinodiphosphine expressed by formula II is reacted with an isocyanate expressed by the formula R-N=C=O to give the compound of formula I.
COPYRIGHT: (C)1981,JPO&Japio
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11413979A JPS5639097A (en) | 1979-09-07 | 1979-09-07 | Optically active n-carbamoylpyrrolidinodiphosphine ligand and its preparation |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP11413979A JPS5639097A (en) | 1979-09-07 | 1979-09-07 | Optically active n-carbamoylpyrrolidinodiphosphine ligand and its preparation |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS5639097A true JPS5639097A (en) | 1981-04-14 |
JPS6210516B2 JPS6210516B2 (en) | 1987-03-06 |
Family
ID=14630107
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP11413979A Granted JPS5639097A (en) | 1979-09-07 | 1979-09-07 | Optically active n-carbamoylpyrrolidinodiphosphine ligand and its preparation |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPS5639097A (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2521145A1 (en) * | 1982-02-05 | 1983-08-12 | Hoffmann La Roche | CHIRAL PHOSPHINS, PROCESSES FOR THEIR PREPARATION, INTERMEDIATE PRODUCTS OF THEIR PREPARATION, RHODIUM COMPLEXES OF THESE PHOSPHINS AND USE THEREOF IN ASYMMETRIC HYDROGENATIONS |
-
1979
- 1979-09-07 JP JP11413979A patent/JPS5639097A/en active Granted
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2521145A1 (en) * | 1982-02-05 | 1983-08-12 | Hoffmann La Roche | CHIRAL PHOSPHINS, PROCESSES FOR THEIR PREPARATION, INTERMEDIATE PRODUCTS OF THEIR PREPARATION, RHODIUM COMPLEXES OF THESE PHOSPHINS AND USE THEREOF IN ASYMMETRIC HYDROGENATIONS |
Also Published As
Publication number | Publication date |
---|---|
JPS6210516B2 (en) | 1987-03-06 |
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