about
Organoselenium ligands in catalysis.A theoretically-guided optimization of a new family of modular P,S-ligands for iridium-catalyzed hydrogenation of minimally functionalized olefins.Development of pinene-derived N,P ligands and their utility in catalytic asymmetric hydrogenation.Concise methods for the synthesis of chiral polyoxazolines and their application in asymmetric hydrosilylationAsymmetric hydrogenation of alkenes lacking coordinating groups.Proline-based P,O ligand/iridium complexes as highly selective catalysts: asymmetric hydrogenation of trisubstituted alkenes.Electronic Structure Determination of Pyridine N-Heterocyclic Carbene Iron Dinitrogen Complexes and Neutral Ligand Derivatives.Chiral imidate-ferrocenylphosphanes: synthesis and application as P,N-ligands in iridium(I)-catalyzed hydrogenation of unfunctionalized and poorly functionalized olefins.Enantioselective CuH-catalyzed anti-Markovnikov hydroamination of 1,1-disubstituted alkenesDouble-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.High-Activity Iron Catalysts for the Hydrogenation of Hindered, Unfunctionalized Alkenes.Extending 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.Rhodium(I)-Catalyzed Intermolecular Hydroacylation of α-Keto Amides and Isatins with Non-Chelating Aldehydes.A modular approach to neutral P,N-ligands: synthesis and coordination chemistry.NeoPHOX - a structurally tunable ligand system for asymmetric catalysisCatalytic hydrogenation activity and electronic structure determination of bis(arylimidazol-2-ylidene)pyridine cobalt alkyl and hydride complexesA comparison between oxazoline-imidazolinylidene, -imidazolylidine, -benzimidazolylidene hydrogenation catalysts.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.Rhodium-catalysed asymmetric hydrogenation as a valuable synthetic tool for the preparation of chiral drugs.A practical two-step procedure for the preparation of enantiopure pyridines: Multicomponent reactions of alkoxyallenes, nitriles and carboxylic acids followed by a cyclocondensation reaction.Recent Advances in Transition-Metal-Free Oxygenation of Alkene C=C Double Bonds for Carbonyl Generation.DFT Methods to Study the Reaction Mechanism of Iridium-Catalyzed Hydrogenation of Olefins: Which Functional Should be Chosen?Chichibabin-type direct alkylation of pyridyl alcohols with alkyl lithium reagentsLigand-controlled C(sp³)-H arylation and olefination in synthesis of unnatural chiral α-amino acids.Carboxy-directed asymmetric hydrogenation of 1,1-diarylethenes and 1,1-dialkylethenes.Highly enantioselective hydrogenation of 2,4-diaryl-1,5-benzodiazepines catalyzed by dendritic phosphinooxazoline iridium complexes.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.Disilametallacyclic chemistry for efficient catalysis.Triply Halide-Bridged Dinuclear Iridium(III) Complexes with Chiral Diphosphine Ligands as New Easy-to-Handle Iridium Catalysts for Asymmetric Hydrogenation of Imines and N-Heteroaromatics.A Fluorescent Molecular Probe for the Detection of Hydrogen Based on Oxidative Addition Reactions with Crabtree-Type Hydrogenation Catalysts.P-Cl bond-induced lactamization of 2(2'-hydroxyl)phenyloxazoline to form a cyclic phosphinite, 3-(2-chloroethyl)-2-phenyl-2H-benzo[e][1,3,2]oxaza-phosphinin-4(3H)-one: synthesis, structural studies and transition metal complexes.Remotely controlled iridium-catalyzed asymmetric hydrogenation of terminal 1,1-diaryl alkenes.Nickel-catalyzed asymmetric hydrogenation of β-acylamino nitroolefins: an efficient approach to chiral amines.The cooperative effect of Lewis pairs in the Friedel-Crafts hydroxyalkylation reaction: a simple and effective route for the synthesis of (±)-carbinoxamine.
P2860
Q30558521-D85F6AA8-DB89-4A42-BA41-7D1F95B2B341Q30840957-15CBBFC4-963F-49DE-A94D-D7361B8C74B6Q33307558-F5DE5E54-3DD1-41AD-8570-6CB7A0B2660CQ33867988-4844705B-5D45-4BC0-8C94-44286FC55FE4Q34183895-3EC1F2EC-23D0-4BB2-821A-E24DD950FA4CQ34212415-725B3C26-31D0-4086-A67E-F47E14318574Q34331232-45B490A7-ED7E-4AB7-A4ED-A4493890E204Q34421537-0E777C2A-F79C-40DC-9FC9-4C5EB7CC9625Q34531437-5068C9DB-7F3B-4D41-ADF2-FDB14109292BQ34577374-5E5B0BA4-0E9A-4AEA-96FA-C085D1B3584FQ34940130-D03CA453-C9F2-4CC5-8882-CCCF115B2BC1Q35056319-99F4C28E-15F8-4807-80A8-9C7DA57355CCQ35896280-E4DBC4DC-3010-4387-BE23-B9A57D8378D4Q36031815-46A3C0E7-0DB1-401A-84B5-402CFAFC78BAQ36057224-EF15B67B-E090-4E12-A4FF-19397C03B768Q36843666-95FE607E-0074-4413-80DA-CBE2F975F2BBQ36991866-3770E35A-E5C1-4B77-94F0-F28E07C28217Q37165363-70D5493A-B850-4206-A726-65ED18C4FBC1Q37237775-F44046A7-D196-471F-A287-51DD21317C38Q37305566-ADF1B42A-FFA6-4612-A781-2CD3571CDD7BQ37741842-F2355C7B-C1F3-4816-8EAE-B93189D0CFD5Q37817868-7EE0CE15-936B-49AE-8BC7-8FBF8CF0DBE0Q37982636-A87289BD-DEE8-47DF-B354-7EBA21614624Q38058272-34B736A9-D05C-4EC0-BAAC-0F74583F1F41Q38365275-562C8E97-7B16-488D-A01E-1A880CCC6930Q38847603-E95D685D-BDA1-4390-8FDC-CDCBC2ED6832Q38939712-2F82D89A-0937-4FD7-86BD-8052ED310858Q41678053-2DC43808-5E25-443B-9B68-3A74A89E489FQ42920887-E0D39FE6-269C-4EB7-B1ED-32BC931EFA90Q44539934-0CDEC83A-EDC4-4C7D-96B0-D6965BB1C414Q45831415-82FB1096-60F6-4BEE-B699-9802C6EE23C7Q46083028-985BD3BB-76E8-4716-A7C9-893FE9074EE5Q46158280-4519BC3B-3A37-4A0C-8924-F79F51357D2FQ46352089-A103FAC1-A392-4AF5-966F-6BC978384AD0Q46504196-5BD3A8D6-E0C4-4875-9C8D-71EEF29BB9B8Q46671375-B4CA70E2-8290-48C2-BA33-B80EA0FCA99EQ46893978-B839E6EB-642E-44D0-A696-5AB7C99C658DQ46966415-B75239DD-8BDC-429B-847C-ABD1D079C32BQ47128637-0D2B2156-19A5-419F-AE31-C0FB836477FDQ47749655-AFCC5961-4EE4-4AB5-B11C-A51D7378C831
P2860
description
2007 nî lūn-bûn
@nan
2007 թուականի Օգոստոսին հրատարակուած գիտական յօդուած
@hyw
2007 թվականի օգոստոսին հրատարակված գիտական հոդված
@hy
2007年の論文
@ja
2007年論文
@yue
2007年論文
@zh-hant
2007年論文
@zh-hk
2007年論文
@zh-mo
2007年論文
@zh-tw
2007年论文
@wuu
name
Iridium-catalyzed asymmetric hydrogenation of olefins.
@ast
Iridium-catalyzed asymmetric hydrogenation of olefins.
@en
Iridium-catalyzed asymmetric hydrogenation of olefins.
@nl
type
label
Iridium-catalyzed asymmetric hydrogenation of olefins.
@ast
Iridium-catalyzed asymmetric hydrogenation of olefins.
@en
Iridium-catalyzed asymmetric hydrogenation of olefins.
@nl
prefLabel
Iridium-catalyzed asymmetric hydrogenation of olefins.
@ast
Iridium-catalyzed asymmetric hydrogenation of olefins.
@en
Iridium-catalyzed asymmetric hydrogenation of olefins.
@nl
P356
P1476
Iridium-catalyzed asymmetric hydrogenation of olefins.
@en
P2093
Andreas Pfaltz
Stephen J Roseblade
P304
P356
10.1021/AR700113G
P407
P577
2007-08-03T00:00:00Z