Catalytic homogeneous asymmetric hydrogenations of largely unfunctionalized alkenes.
about
A theoretically-guided optimization of a new family of modular P,S-ligands for iridium-catalyzed hydrogenation of minimally functionalized olefins.Highly modular P-OP ligands for asymmetric hydrogenation: synthesis, catalytic activity, and mechanism.Asymmetric hydrogenation of alkenes lacking coordinating groups.An additional coordination group leads to extremely efficient chiral iridium catalysts for asymmetric hydrogenation of ketones.Proline-based P,O ligand/iridium complexes as highly selective catalysts: asymmetric hydrogenation of trisubstituted alkenes.Chiral imidate-ferrocenylphosphanes: synthesis and application as P,N-ligands in iridium(I)-catalyzed hydrogenation of unfunctionalized and poorly functionalized olefins.Double-asymmetric hydrogenation strategy for the reduction of 1,1-diaryl olefins applied to an improved synthesis of CuIPhEt, a C2-symmetric N-heterocyclic carbenoidIridium catalysis: application of asymmetric reductive hydrogenation.Cobalt precursors for high-throughput discovery of base metal asymmetric alkene hydrogenation catalysts.Enantioselective small molecule synthesis by carbon dioxide fixation using a dual Brønsted acid/base organocatalyst.Asymmetric Synthesis of Deoxypropionate Derivatives via Catalytic Hydrogenolysis of Enantioenriched Z-Ketene HeterodimersExtending the Substrate Scope for the Asymmetric Iridium-Catalyzed Hydrogenation of Minimally Functionalized Olefins by Using Biaryl Phosphite-Based Modular Ligand Libraries.Adaptable P-X Biaryl Phosphite/Phosphoroamidite-Containing Ligands for Asymmetric Hydrogenation and C-X Bond-Forming Reactions: Ligand Libraries with Exceptionally Wide Substrate Scope.NeoPHOX - a structurally tunable ligand system for asymmetric catalysisA comparison between oxazoline-imidazolinylidene, -imidazolylidine, -benzimidazolylidene hydrogenation catalysts.Asymmetric hydrogenation of minimally functionalised terminal olefins: an alternative sustainable and direct strategy for preparing enantioenriched hydrocarbons.Transfer hydrogenation with Hantzsch esters and related organic hydride donors.Homogeneous palladium-catalyzed asymmetric hydrogenation.Polyaromatic N-heterocyclic carbene ligands and π-stacking. Catalytic consequences.DFT Methods to Study the Reaction Mechanism of Iridium-Catalyzed Hydrogenation of Olefins: Which Functional Should be Chosen?Asymmetric Synthesis of Dipropionate Derivatives through Catalytic Hydrogenation of Enantioenriched E-Ketene Heterodimers.General approach to the total synthesis of 9-methoxy-substituted indole alkaloids: synthesis of mitragynine, as well as 9-methoxygeissoschizol and 9-methoxy-N(b)-methylgeissoschizol.Hydrogenation of unactivated enamines to tertiary amines: rhodium complexes of fluorinated phosphines give marked improvements in catalytic activity.Carboxy-directed asymmetric hydrogenation of 1,1-diarylethenes and 1,1-dialkylethenes.Palladium-catalyzed asymmetric hydrogenation of α-acyloxy-1-arylethanones.A non-iterative, flexible, and highly stereoselective synthesis of polydeoxypropionates--synthesis of (+)-vittatalactone.Chiral N-heterocyclic carbene/pyridine ligands for the iridium-catalyzed asymmetric hydrogenation of olefins.A Fluorescent Molecular Probe for the Detection of Hydrogen Based on Oxidative Addition Reactions with Crabtree-Type Hydrogenation Catalysts.Development of new thiazole-based iridium catalysts and their applications in the asymmetric hydrogenation of trisubstituted olefins.Remotely controlled iridium-catalyzed asymmetric hydrogenation of terminal 1,1-diaryl alkenes.Evaluation of density functional methods on the geometric and energetic descriptions of species involved in Cu⁺-promoted catalysis.Effect of chelating ring size in catalytic ketone hydrogenation: facile synthesis of ruthenium(II) precatalysts containing an N-heterocyclic carbene with a primary amine donor for ketone hydrogenation and a DFT study of mechanisms.Regio- and Enantioselective Cobalt-Catalyzed Sequential Hydrosilylation/Hydrogenation of Terminal Alkynes.Asymmetric Hydrogenation of Vinylthioethers: Access to Optically Active 1,5-Benzothiazepine Derivatives.Pd Nanocubes@ZIF-8: Integration of Plasmon-Driven Photothermal Conversion with a Metal-Organic Framework for Efficient and Selective Catalysis.Phosphite-Thiother Ligands Derived from Carbohydrates allow the Enantioswitchable Hydrogenation of Cyclic β-Enamides by using either Rh or Ir Catalysts.Asymmetric synthesis of 4-aryl-1,2,5-thiadiazolidin-3-one 1,1-dioxides via Pd-catalyzed hydrogenation of cyclic ketimines.Iridium-catalyzed asymmetric hydrogenation of 3,3-disubstituted allylic alcohols in ethereal solvents.Nickel-catalyzed asymmetric transfer hydrogenation of conjugated olefins.Nickel-catalyzed asymmetric transfer hydrogenation of olefins for the synthesis of α- and β-amino acids.
P2860
Q30840957-26698B26-8DC2-4053-9EBF-F1ADF2B91878Q33564648-C3488E8B-F4ED-4FD8-91E1-5F0129C904DBQ34183895-EC6F19DE-AC08-46A2-A7E8-7E57AEFB3083Q34200033-9A01981F-ECBE-4943-ABB3-0C9FD51FC83AQ34212415-015216D3-6A10-4FA5-ABAA-52ED4F299D98Q34421537-615B4D35-F760-4211-9008-01E1BB3A387FQ34577374-73F1DD96-00DE-4875-9B0D-3DBC6CE5FB11Q34940130-301FEF93-8FAE-4CB4-8342-6EF355DE2E62Q35056319-BD04552D-5926-48AF-9152-448A96185FF6Q35651649-A28EAC20-839B-4074-8667-2B6282443229Q35994711-9379ABAA-8233-4E9E-94A4-F9D2BADFC4CBQ36031815-145AB3B5-3893-4D96-A82E-D6A7B472F35CQ36057224-3CD21AE7-21C8-48C8-AEAC-C39DD1C96A7DQ37165363-102EBC57-6E0F-46B1-A57C-BFF31D7A7083Q37305566-4FCBF9BA-6C62-4234-8658-24E822B406AAQ37817868-E81B4244-C726-44B9-ABCB-F24BB05F0EB8Q37979197-4B60E501-BE35-4CCB-90E2-95BF56FFE632Q38058747-244258A9-1210-48DE-B76B-B498EBD49208Q38883312-50138DD3-D473-4643-BD02-ECD8EBB98B38Q38939712-D275CBBB-198A-4047-94B5-FDC6C6BFD18CQ41175352-53DA7790-1A8C-4EE4-B960-6E2DCDB8C2ABQ41866066-0EF027C5-9465-4B4E-9F87-DF7A0A325591Q42100750-D6420F85-CA8E-453D-B89C-F8A6A0EC723CQ44539934-AEEDB5BD-5214-4374-BD0C-359A965A0B90Q44754424-CD5F986B-100E-4DCE-B5AB-54D1A2C8D737Q46083028-29868E07-62DF-4A12-8BEA-9DDBB6D88849Q46158280-A75DEB73-DC93-417D-A150-37721D9D2F23Q46671375-199347BC-AFD0-46F2-812B-13748E6C6BD4Q46823433-FAACF36F-2B5A-4830-89A1-D9FE329E2718Q46966415-DFFA5285-86BC-4A33-A369-12830054D3C2Q46972528-57D06F9B-D0ED-410D-834B-8958F2E53787Q47302079-69DCD078-B18F-4241-8862-E01965CE58C2Q48188601-2F14F005-DD82-4978-B167-C7375DA26E2CQ48246490-517AF6AD-CC5A-48FD-AA9F-BC1BFEF368F3Q48255957-A0463082-7C90-4F97-B549-92CAFA0A49E7Q48304499-4A2315AE-DDFC-4E07-8D4E-CE11972ED94AQ48335898-060223CB-0193-4913-ADE7-AF0987213501Q50462410-9F46A724-1868-47DC-AA61-BF13428C08C3Q50890662-F82DA24D-08C1-4D38-BCF9-EB20A1C20A35Q51037539-F11C8E84-1230-4539-9E20-2D4E15BA7983
P2860
Catalytic homogeneous asymmetric hydrogenations of largely unfunctionalized alkenes.
description
2005 nî lūn-bûn
@nan
2005 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2005 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2005年の論文
@ja
2005年論文
@yue
2005年論文
@zh-hant
2005年論文
@zh-hk
2005年論文
@zh-mo
2005年論文
@zh-tw
2005年论文
@wuu
name
Catalytic homogeneous asymmetric hydrogenations of largely unfunctionalized alkenes.
@ast
Catalytic homogeneous asymmetric hydrogenations of largely unfunctionalized alkenes.
@en
Catalytic homogeneous asymmetric hydrogenations of largely unfunctionalized alkenes.
@nl
type
label
Catalytic homogeneous asymmetric hydrogenations of largely unfunctionalized alkenes.
@ast
Catalytic homogeneous asymmetric hydrogenations of largely unfunctionalized alkenes.
@en
Catalytic homogeneous asymmetric hydrogenations of largely unfunctionalized alkenes.
@nl
prefLabel
Catalytic homogeneous asymmetric hydrogenations of largely unfunctionalized alkenes.
@ast
Catalytic homogeneous asymmetric hydrogenations of largely unfunctionalized alkenes.
@en
Catalytic homogeneous asymmetric hydrogenations of largely unfunctionalized alkenes.
@nl
P356
P1433
P1476
Catalytic homogeneous asymmetric hydrogenations of largely unfunctionalized alkenes
@en
P2093
Xiuhua Cui
P304
P356
10.1021/CR0500131
P50
P577
2005-09-01T00:00:00Z