Burk et al., 1995 - Google Patents

Highly enantioselective hydrogenation of. beta.-keto esters under mild conditions

Burk et al., 1995

Document ID
7899505701236107804
Author
Burk M
Harper T
Kalberg C
Publication year
Publication venue
Journal of the American Chemical Society

External Links

Snippet

Reactions were carried outat 35 C with an initial H2 pressure of 60 psig and 0.25—0.10 M solutions of substrate in MeOH/H20 (9/1), using the catalyst precursor (R,/?)-/-Pr-BPE-RuBr2 (0.2 mol%), unless otherwise stated. Reactiontime allowed for complete (100%) conver-sion …
Continue reading at pubs.acs.org (other versions)

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/132Preparation 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
    • C07C29/136Preparation 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
    • C07C29/147Preparation 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 carboxylic acids or derivatives thereof
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/132Preparation 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
    • C07C29/136Preparation 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
    • C07C29/143Preparation 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 ketones
    • C07C29/145Preparation 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 ketones with hydrogen or hydrogen-containing gases
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/132Preparation 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
    • C07C29/136Preparation 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
    • C07C29/14Preparation 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
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C67/00Preparation of carboxylic acid esters
    • C07C67/30Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group
    • C07C67/333Preparation of carboxylic acid esters by modifying the acid moiety of the ester, such modification not being an introduction of an ester group by isomerisation; by change of size of the carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B53/00Asymmetric syntheses
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07BGENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
    • C07B2200/00Indexing scheme relating to specific properties of organic compounds
    • C07B2200/07Optical isomers
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C29/00Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring
    • C07C29/36Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by reactions with formation of hydroxy groups, which may occur via intermediates being derivatives of hydroxy, e.g. O-metal
    • C07C29/38Preparation of compounds having hydroxy or O-metal groups bound to a carbon atom not belonging to a six-membered aromatic ring increasing the number of carbon atoms by reactions with formation of hydroxy groups, which may occur via intermediates being derivatives of hydroxy, e.g. O-metal by reaction with aldehydes or ketones
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C45/00Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07CACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C227/00Preparation of compounds containing amino and carboxyl groups bound to the same carbon skeleton
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07FACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
    • C07F17/00Metallocenes
    • C07F17/02Metallocenes of metals of Groups 8, 9 or 10 of the Periodic System

Similar Documents

Publication Publication Date Title
Burk et al. Highly enantioselective hydrogenation of. beta.-keto esters under mild conditions
Ohkuma et al. Practical enantioselective hydrogenation of aromatic ketones
Burk et al. Asymmetric catalytic synthesis of. beta.-branched amino acids via highly enantioselective hydrogenation of. alpha.-enamides.
Ohta et al. Asymmetric hydrogenation of unsaturated carboxylic acids catalyzed by BINAP-ruthenium (II) complexes
Burk et al. Rh− DuPHOS-Catalyzed enantioselective hydrogenation of enol esters. Application to the synthesis of highly enantioenriched α-hydroxy esters and 1, 2-diols
Sawamura et al. Catalytic asymmetric synthesis by means of secondary interaction between chiral ligands and substrates
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.
Ohkuma et al. Preferential hydrogenation of aldehydes and ketones.
Li et al. Recent advances in developing new axially chiral phosphine ligands for asymmetric catalysis
Jiang et al. Highly enantioselective hydrogenation of cyclic enol acetates catalyzed by a Rh–PennPhos complex
Brunner Enantioselective synthesis with optically active transition-metal catalysts
Peach et al. Asymmetric transfer hydrogenation of α, β-unsaturated, α-tosyloxy and α-substituted ketones
Ratovelomanana-Vidal et al. Synthetic applications of the ruthenium-catalyzed hydrogenation via dynamic kinetic resolution
Marinetti et al. Chiral 1, 2‐Bis (phosphetano) benzenes: Preparation and Use in the Ru‐Catalyzed Hydrogenations of Carbonyl Derivatives
Elma et al. Screening of C2-symmetric chiral phosphinites as ligands for ruthenium (II)-catalyzed asymmetric transfer hydrogenation of prochiral aromatic ketones
Takaya et al. New chiral ruthenium complexes for asymmetric catalytic hydrogenations
Burk et al. Asymmetric intramolecular hydrosilylation of hydroxyketones
Kadyrov et al. Efficient enantioselective synthesis of optically active diols by asymmetric hydrogenation with modular chiral metal catalysts
Eshon et al. α-Tetrasubstituted aldehydes through electronic and strain-controlled branch-selective stereoselective hydroformylation
CA2353375C (en) Process for producing optically active alcohol
Hagemann et al. A General Method for the Enantioselective Hydrogenation of β‐Keto Esters using Monodentate Binaphthophosphepine Ligands
Ren et al. Ruthenium-Catalyzed Oxidation of Allyl Alcohols with Intermolecular Hydrogen Transfer: Synthesis of α, β-Unsaturated Carbonyl Compounds
Dubrovina et al. Economic preparation of 1, 3-diphenyl-1, 3-bis (diphenylphosphino) propane: a versatile chiral diphosphine ligand for enantioselective hydrogenations
Pautigny et al. Convenient general asymmetric synthesis of roche ester derivatives through catalytic asymmetric hydrogenation: steric and electronic effects of ligands
Bernard et al. Evidence for carbon-oxygen bond formation, aldehyde decarbonylation, and dimerization by reaction of formaldehyde and acetaldehyde with trans-ROIr (CO)(PPh3) 2