Iridium Catalysts with Bicyclic Pyridine–Phosphinite Ligands: Asymmetric Hydrogenation of Olefins and Furan Derivatives
about
A theoretically-guided optimization of a new family of modular P,S-ligands for iridium-catalyzed hydrogenation of minimally functionalized olefins.Asymmetric hydrogenation of alkenes lacking coordinating groups.Proline-based P,O ligand/iridium complexes as highly selective catalysts: asymmetric hydrogenation of trisubstituted alkenes.Ruthenium NHC catalyzed highly asymmetric hydrogenation of benzofurans.Iridium-catalyzed asymmetric hydrogenation of pyridinium salts.Asymmetric hydrogenation of disubstituted furans.Double-asymmetric hydrogenation strategy for the reduction of 1,1-diaryl olefins applied to an improved synthesis of CuIPhEt, a C2-symmetric N-heterocyclic carbenoidComparison Of Asymmetric Hydrogenations Of Unsaturated- Carboxylic Acids And -Esters.Neutral iridium catalysts with chiral phosphine-carboxy ligands for asymmetric hydrogenation of unsaturated carboxylic acids.Asymmetric hydrogenation of minimally functionalised terminal olefins: an alternative sustainable and direct strategy for preparing enantioenriched hydrocarbons.Asymmetric homogeneous hydrogenations at scale.Developing ligands for palladium(II)-catalyzed C-H functionalization: intimate dialogue between ligand and substrate.P,N ligands in asymmetric catalysis.Palladacycle promoted base controlled regio- and enantioselective hydrophosphination of 2-pyridylacrylate/amide and the cytotoxicity of their gold complexes.Total synthesis of (+)-trans-trikentrin A.Ruthenium-NHC-catalyzed asymmetric hydrogenation of indolizines: access to indolizidine alkaloids.Chichibabin-type direct alkylation of pyridyl alcohols with alkyl lithium reagents5,6,7,8-Tetra-hydro-quinoline 1-oxide hemihydrate.A novel antifungal agent with broad spectrum: 1-(4-biphenylyl)-3-(1H-imidazol-1-yl)-1-propanone.Chiral N-heterocyclic carbene/pyridine ligands for the iridium-catalyzed asymmetric hydrogenation of olefins.Asymmetric ruthenium-catalyzed hydrogenation of 2- and 2,9-substituted 1,10-phenanthrolines.Asymmetric Hydrogenation of Isoxazolium Triflates with a Chiral Iridium Catalyst.The cooperative effect of Lewis pairs in the Friedel-Crafts hydroxyalkylation reaction: a simple and effective route for the synthesis of (±)-carbinoxamine.Asymmetric Hydrogenation of Azaindoles: Chemo- and Enantioselective Reduction of Fused Aromatic Ring Systems Consisting of Two Heteroarenes.Asymmetric Hydrogenation of In Situ Generated Isochromenylium Intermediates by Copper/Ruthenium Tandem Catalysis.Asymmetric ruthenium-catalyzed hydrogenation of 2,6-disubstituted 1,5-naphthyridines: access to chiral 1,5-diaza-cis-decalins.Iridium-catalyzed asymmetric hydrogenation of 3,3-disubstituted allylic alcohols in ethereal solvents.A highly stereoselective and flexible strategy for the convergent synthesis of long-chain polydeoxypropionates: application towards the synthesis of the glycolipid membrane components hydroxyphthioceranic and phthioceranic acid.Iridium-Catalyzed Asymmetric Hydrogenation of Unfunctionalized Exocyclic C=C Bonds.Deuterium-Labeling Study of the Hydrogenation of 2-Methylfuran and 2,5-Dimethylfuran over Carbon-Supported Noble Metal Catalysts.Asymmetric transfer hydrogenation of 3-nitroquinolines: facile access to cyclic nitro compounds with two contiguous stereocenters.Pd-catalyzed asymmetric hydrogenation of fluorinated aromatic pyrazol-5-ols via capture of active tautomers.Dynamic kinetic resolution of 2,3-dihydrobenzo[b]furans: chemoenzymatic synthesis of analgesic agent BRL 37959
P2860
Q30840957-B8623E89-04BF-46E7-BD16-6E3EE04DD5A4Q34183895-662EBE7E-C4C4-48FA-A13E-37AA5E9802FBQ34212415-C1621EC1-BC06-43A6-99D0-4638171F5977Q34252605-FABADC42-8107-4376-BA82-56343E9F18E4Q34299154-2530D3DD-7719-4800-A835-29E73005D131Q34405561-702511FE-F587-43C6-8FEE-11BD6721CBCAQ34577374-D0D47360-5820-47E9-9125-6C930E14DE39Q37696509-0E12D7CA-C595-4B71-BF37-F8C8132BBBA1Q37741842-BB455079-BCBC-4E78-8D21-A9FA844C24B2Q37817868-C5BA5DB4-359D-4E05-8F57-97091BAD6CF2Q37982636-36D83A8A-DA57-4272-B836-4BB447A24410Q38097103-2F6543E8-9C7D-468F-881D-47D1B476E2ACQ38164480-705503F8-99EB-4E48-B97A-B4EE1F4D1F22Q38833790-E99F97B0-2900-49A8-81B5-99A4548B4DACQ39249722-3AD3E9CB-EDA5-4075-9E7C-280943F38B18Q40119605-4BD54D3D-D146-4980-BFC2-0FD1772EFFFAQ41678053-20BF2A67-FD25-49B7-ABB9-2416BE211FC5Q42131517-93BB1ADB-A3DD-4451-A75F-39040395F03DQ42713801-ACF1CB77-BD8D-4334-817D-7A3BE8B25A5CQ46158280-E67EED90-BCCD-4ED6-8B1F-B23944A69846Q46229905-34F22CC0-96CF-4AF8-9594-4F9BEB5BC335Q46559626-56688CDC-3E80-4918-A366-0CA93BA5B5B8Q47749655-F226A5DC-7FC7-48CA-A840-90E9427CECADQ48095133-B6880BF5-14F1-499B-979B-1EB581464DB1Q48123291-2BB5B8FE-A1CF-48F9-BBA9-5E2E8A423412Q50439233-3E1D066F-5B89-46DE-99AA-350999DF4255Q50462410-9ECB7DB4-79E9-4097-9AB7-C352867F9616Q51039397-9FB88A1B-42EE-4597-98D4-599B49776B13Q51129106-11CB128B-194B-4F50-B9D4-31975F4739F4Q51718921-2911BE2A-B34F-46FA-AF8C-11CC54AD2A35Q53748827-D760F85A-2F33-431A-9810-6242AAE98D2FQ54948512-E6D1F570-2241-4713-9349-63B6961B28DBQ56927629-529E7550-BF33-452C-BA0F-014A37707025
P2860
Iridium Catalysts with Bicyclic Pyridine–Phosphinite Ligands: Asymmetric Hydrogenation of Olefins and Furan Derivatives
description
wetenschappelijk artikel
@nl
наукова стаття, опублікована в серпні 2006
@uk
name
Iridium Catalysts with Bicycli ...... Olefins and Furan Derivatives
@en
Iridium Catalysts with Bicycli ...... Olefins and Furan Derivatives
@nl
type
label
Iridium Catalysts with Bicycli ...... Olefins and Furan Derivatives
@en
Iridium Catalysts with Bicycli ...... Olefins and Furan Derivatives
@nl
prefLabel
Iridium Catalysts with Bicycli ...... Olefins and Furan Derivatives
@en
Iridium Catalysts with Bicycli ...... Olefins and Furan Derivatives
@nl
P2093
P921
P356
P1476
Iridium Catalysts with Bicycli ...... Olefins and Furan Derivatives
@en
P2093
Andreas Pfaltz
Sebastian P. Smidt
Stefan Kaiser
P304
P356
10.1002/ANIE.200601529
P407
P577
2006-08-04T00:00:00Z