Asymmetric catalysis: science and opportunities (Nobel lecture).
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Catalytic enantioselective synthesis of chiral organic compounds of ultra-high purity of >99% eeThe Structure of Glycerol Trinitrate Reductase NerA fromAgrobacterium radiobacterReveals the Molecular Reason for Nitro- and Ene-Reductase Activity in OYE HomologuesFrontiers, opportunities, and challenges in biochemical and chemical catalysis of CO2 fixationWeak coordination as a powerful means for developing broadly useful C-H functionalization reactions.Enantiomerically enriched, polycrystalline molecular sieves.Highly enantioselective synthesis of γ-, δ-, and ε-chiral 1-alkanols via Zr-catalyzed asymmetric carboalumination of alkenes (ZACA)-Cu- or Pd-catalyzed cross-coupling.A remarkably effective copper(II)-dipyridylphosphine catalyst system for the asymmetric hydrosilylation of ketones in air.Coordination chemistry of poly(thioether)borate ligands.An Overview of Stereoselective Synthesis of α-Aminophosphonic Acids and Derivatives(R)-1,1'-Binaphthalene-2,2'-diyl dicinnamate.Ruthenium-catalyzed C-C bond forming transfer hydrogenation: carbonyl allylation from the alcohol or aldehyde oxidation level employing acyclic 1,3-dienes as surrogates to preformed allyl metal reagents.Development of Chiral Bis-hydrazone Ligands for the Enantioselective Cross-Coupling Reactions of Aryldimethylsilanolates.Synthesis of chiral mono(N-heterocyclic carbene) palladium and gold complexes with a 1,1'-biphenyl scaffold and their applications in catalysis.Regioselective derivatizations of a tribrominated atropisomeric benzamide scaffold.Dihydrogen complexes as prototypes for the coordination chemistry of saturated moleculesHigh-Activity Iron Catalysts for the Hydrogenation of Hindered, Unfunctionalized Alkenes.Prediction of Stereochemistry using Q2MM.Pd and Mo Catalyzed Asymmetric Allylic Alkylation.A green chemistry approach to asymmetric catalysis: solvent-free and highly concentrated reactionsHighly efficient molybdenum-based catalysts for enantioselective alkene metathesisEnhanced hydrogenation activity and diastereomeric interactions of methyl pyruvate co-adsorbed with R-1-(1-naphthyl)ethylamine on Pd(111)Catalytic carbonyl addition through transfer hydrogenation: a departure from preformed organometallic reagents.Widely applicable synthesis of enantiomerically pure tertiary alkyl-containing 1-alkanols by zirconium-catalyzed asymmetric carboalumination of alkenes and palladium- or copper-catalyzed cross-coupling.Controlling the enantioselectivity of enzymes by directed evolution: practical and theoretical ramifications.Chiral biphenyl diphosphines for asymmetric catalysis: stereoelectronic design and industrial perspectives.Toward efficient asymmetric hydrogenation: architectural and functional engineering of chiral molecular catalystsStereoselectivity of supported alkene metathesis catalysts: a goal and a tool to characterize active sites.Asymmetric bioreduction of activated alkenes to industrially relevant optically active compounds.Developing ligands for palladium(II)-catalyzed C-H functionalization: intimate dialogue between ligand and substrate.Frustration across the periodic table: heterolytic cleavage of dihydrogen by metal complexes.On the concept of frustrated Lewis pairs.Cyclic C-amino phosphorus ylides as a source of bidentate heteroditopic ligands (phosphine/aminocarbene) for transition metalsCarbonyl propargylation from the alcohol or aldehyde oxidation level employing 1,3-enynes as surrogates to preformed allenylmetal reagents: a ruthenium-catalyzed C-C bond-forming transfer hydrogenation.Absolute structure determination of compounds with axial and planar chirality using the crystalline sponge method.Highly Efficient and Selective Hydrogenation of Aldehydes: A Well-Defined Fe(II) Catalyst Exhibits Noble-Metal Activity.Nitrile as Activating Group in the Asymmetric Bioreduction of β-Cyanoacrylic Acids Catalyzed by Ene-ReductasesDetermination of the absolute stereostructure of a cyclic azobenzene from the crystal structure of the precursor containing a heavy element.Syntheses, Characterization, Resolution, and Biological Studies of Coordination Compounds of Aspartic Acid and Glycine.Harnessing non-covalent interactions to exert control over regioselectivity and site-selectivity in catalytic reactions.Exploring the full catalytic cycle of rhodium(i)-BINAP-catalysed isomerisation of allylic amines: a graph theory approach for path optimisation.
P2860
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P2860
Asymmetric catalysis: science and opportunities (Nobel lecture).
description
2002 nî lūn-bûn
@nan
2002年の論文
@ja
2002年学术文章
@wuu
2002年学术文章
@zh
2002年学术文章
@zh-cn
2002年学术文章
@zh-hans
2002年学术文章
@zh-my
2002年学术文章
@zh-sg
2002年學術文章
@yue
2002年學術文章
@zh-hant
name
Asymmetric catalysis: science and opportunities (Nobel lecture).
@en
Asymmetric catalysis: science and opportunities
@nl
type
label
Asymmetric catalysis: science and opportunities (Nobel lecture).
@en
Asymmetric catalysis: science and opportunities
@nl
prefLabel
Asymmetric catalysis: science and opportunities (Nobel lecture).
@en
Asymmetric catalysis: science and opportunities
@nl
P1476
Asymmetric catalysis: science and opportunities (Nobel lecture)
@en
P2093
Ryoji Noyori
P304
P577
2002-06-01T00:00:00Z