Jendralla, 1994 - Google Patents
Asymmetric hydrogenation of 2-benzylidenesuccinic acid 4-[(4-BOC-amino)-1-piperidide] monoamide: key step in a process for large scale preparation of a renin …Jendralla, 1994
- Document ID
- 9441701717551836079
- Author
- Jendralla H
- Publication year
- Publication venue
- Synthesis
External Links
Snippet
The N-terminal component 4 of an orally active renin inhibitor is prepared on kg-scale by asymmetric hydrogenation of the title compound 3. Enantioselectivities of several homogeneous homochiral rhodium (I)-and ruthenium (lI)-diphosphine catalysts are …
- 238000009876 asymmetric hydrogenation reaction 0 title abstract description 13
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System compounds of the platinum group
- C07F15/0073—Rhodium compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C29/00—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
- C07C29/132—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group
- C07C29/136—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. -COOH
- C07C29/14—Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring by reduction of an oxygen containing functional group of >C=O containing groups, e.g. -COOH of a -CHO group
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B53/00—Asymmetric syntheses
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2531/00—Additional information regarding catalytic systems classified in B01J31/00
- B01J2531/80—Complexes comprising metals of Group VIII as the central metal
- B01J2531/82—Metals of the platinum group
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J2231/00—Catalytic reactions performed with catalysts classified in B01J31/00
- B01J2231/60—Reduction reactions, e.g. hydrogenation
- B01J2231/64—Reductions in general of organic substrates, e.g. hydride reductions or hydrogenations
- B01J2231/641—Hydrogenation of organic substrates, i.e. H2 or H-transfer hydrogenations, e.g. Fischer-Tropsch processes
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B2200/00—Indexing scheme relating to specific properties of organic compounds
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS, COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J31/00—Catalysts comprising hydrides, coordination complexes or organic compounds
- B01J31/16—Catalysts comprising hydrides, coordination complexes or organic compounds containing coordination complexes
- B01J31/22—Organic complexes
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| Burk et al. | Catalytic asymmetric reductive amination of ketones via highly enantioselective hydrogenation of the C N double bond | |
| Genet et al. | Enantioselective hydrogenation reactions with a full set of preformed and prepared in situ chiral diphosphine-ruthenium (II) catalysts. | |
| Genet et al. | Asymmetric synthesis. Practical production of D and L threonine. Dynamic kinetic resolution in rhodium and ruthenium catalyzed hydrogenation of 2-acylamino-3-oxobutyrates. | |
| Ojima et al. | Recent advances in catalytic asymmetric reactions promoted by transition metal complexes | |
| Zeiss | Enantioselective synthesis of both enantiomers of phosphinothricin via asymmetric hydrogenation of. alpha.-acylamido acrylates | |
| Madec et al. | Asymmetric hydrogenation reactions using a practical in situ generation of chiral ruthenium–diphosphine catalysts from anhydrous RuCl3 | |
| US6258979B1 (en) | Chiral ferrocene phosphines active in asymmetric catalysis | |
| EP0631571B1 (en) | Preparation of optically active hydrazines and amines | |
| CN101675020A (en) | Method for synthesizing optically active carbonyl compounds | |
| HK1000595B (en) | Preparation of optically active hydrazines and amines | |
| WO2001058588A1 (en) | Chiral ferrocene phosphines and their use in asymmetric catalytic reactions | |
| Chiba et al. | BICHEP Ru complexes, highly efficient catalysts for asymmetric hydrogenation of carbonyl compounds | |
| US6255493B1 (en) | Transition metal-catalyzed reactions based on chiral amine oxazolinyl ligands | |
| Gooßen et al. | A Practical and Effective Ruthenium Trichloride‐Based Protocol for the Regio‐and Stereoselective Catalytic Hydroamidation of Terminal Alkynes | |
| US4652657A (en) | Chiral rhodium-diphosphine complexes | |
| Dubrovina et al. | Economic preparation of 1, 3-diphenyl-1, 3-bis (diphenylphosphino) propane: a versatile chiral diphosphine ligand for enantioselective hydrogenations | |
| AU2007278274B2 (en) | Asymmetric hydrogenation of 1,1,1-trifluoroacetone | |
| Pàmies et al. | Phosphine–phosphite, a new class of auxiliaries in highly active and enantioselective hydrogenation | |
| DE602005003572T2 (en) | FERROCENYL LIGANDS FOR HOMOGENEOUS, ENANTIOSELECTIVE HYDROGENATION CATALYSTS | |
| WO1999059721A1 (en) | Catalytic asymmetric hydrogenation, hydroformylation, and hydrovinylation via transition metal catalysts with phosphines and phosphites | |
| KR20020009485A (en) | Process for producing optically active alcohol | |
| Jendralla | Asymmetric hydrogenation of 2-benzylidenesuccinic acid 4-[(4-BOC-amino)-1-piperidide] monoamide: key step in a process for large scale preparation of a renin inhibitor | |
| JP4427109B2 (en) | Phosphorane and diphosphorane, metal complexes thereof, use thereof and method of asymmetric hydrogenation | |
| Diéguez et al. | Chiral phosphite–phosphoroamidites: a new class of ligand for asymmetric catalytic hydrogenation | |
| EP1844061B1 (en) | Metallocene-based phosphorus chiral phosphines |