about
Synthesis and evaluation of a (3R,6S,9S)-2-oxo-1-azabicyclo[4.3.0]nonane scaffold as a mimic of Xaa-trans-Pro in poly-L-proline type II helix conformation.Catalytic asymmetric alkynylation of alpha-imino ester: a versatile approach to optically active unnatural alpha-amino acid derivativesRecent developments in the catalytic asymmetric synthesis of alpha- and beta-amino acids.Enantioselective hydrogenation of alpha-aminomethylacrylates containing a free NH group for the synthesis of beta-amino acid derivatives.Asymmetry on large scale: the roadmap to stereoselective processes.Multidentate 2-pyridyl-phosphine ligands - towards ligand tuning and chirality.A green chemistry approach to asymmetric catalysis: solvent-free and highly concentrated reactionsRevisiting the modularity of modular polyketide synthases.Efficient synthesis of chiral beta-arylisopropylamines by using catalytic asymmetric hydrogenation.Toward efficient asymmetric hydrogenation: architectural and functional engineering of chiral molecular catalystsAsymmetric homogeneous hydrogenations at scale.Rhodium-catalysed asymmetric hydrogenation as a valuable synthetic tool for the preparation of chiral drugs.Enantioselective Chemo- and Biocatalysis: Partners in Retrosynthesis.Engineering cofactor preference of ketone reducing biocatalysts: A mutagenesis study on a γ-diketone reductase from the yeast Saccharomyces cerevisiae serving as an example.Subtleties in asymmetric catalyst structure: the resolution of a 6-phospha-2,4,8-trioxa-adamantane and its applications in asymmetric hydrogenation catalysis.Design of phosphorus ligands with deep chiral pockets: practical synthesis of chiral β-arylamines by asymmetric hydrogenation.Nickel-Catalyzed N-Alkylation of Acylhydrazines and Arylamines Using Alcohols and Enantioselective Examples.Nickel-Catalyzed Enantioselective Reductive Amination of Ketones with Both Arylamines and Benzhydrazide.Automated Quantum Mechanical Predictions of Enantioselectivity in a Rhodium-Catalyzed Asymmetric Hydrogenation.CuH-Catalyzed Asymmetric Reduction of α,β-Unsaturated Carboxylic Acids to β-Chiral Aldehydes.The First Highly Enantioselective Rh-Catalyzed Enyne Cycloisomerization This work was supported by an NIH grant, a Dreyfus Teaching-Scholar Award, and a DuPont Young Faculty Award. P.C. acknowledges the Dalalian Fellowship from the Department of CheNickel-catalyzed asymmetric transfer hydrogenation of hydrazones and other ketimines.Nickel-catalyzed asymmetric transfer hydrogenation of olefins for the synthesis of α- and β-amino acids.One-pot sequential asymmetric hydrogenation of β-aryl-β-aryloxy acroleins.Double Asymmetric Induction During the Addition of (RP)-Menthyl Phenyl Phosphine Oxide to Chiral Aldimines.Sterically-constrained tripodal phosphorus-bridged tris-pyridyl ligands.Modern Alchemy: Replacing Precious Metals with Iron in Catalytic Alkene and Carbonyl Hydrogenation ReactionsNew chiral diphosphoramidite rhodium(I) complexes for asymmetric hydrogenation
P2860
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P2860
description
2000 nî lūn-bûn
@nan
2000 թուականի Յունիսին հրատարակուած գիտական յօդուած
@hyw
2000 թվականի հունիսին հրատարակված գիտական հոդված
@hy
2000年の論文
@ja
2000年論文
@yue
2000年論文
@zh-hant
2000年論文
@zh-hk
2000年論文
@zh-mo
2000年論文
@zh-tw
2000年论文
@wuu
name
Modular phospholane ligands in asymmetric catalysis.
@ast
Modular phospholane ligands in asymmetric catalysis.
@en
type
label
Modular phospholane ligands in asymmetric catalysis.
@ast
Modular phospholane ligands in asymmetric catalysis.
@en
prefLabel
Modular phospholane ligands in asymmetric catalysis.
@ast
Modular phospholane ligands in asymmetric catalysis.
@en
P356
P1476
Modular phospholane ligands in asymmetric catalysis.
@en
P2093
P304
P356
10.1021/AR990085C
P407
P577
2000-06-01T00:00:00Z