Asymmetric transfer hydrogenation: chiral ligands and applications.
about
Asymmetric transfer hydrogenation catalysed by hydrophobic dendritic DACH-rhodium complex in water.α-Amino-oximes based on optically pure limonene: a new ligands family for ruthenium-catalyzed asymmetric transfer hydrogenation.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.Ruthenium catalyzed C-C bond formation via transfer hydrogenation: branch-selective reductive coupling of allenes to paraformaldehyde and higher aldehydes.Transient Ru-methyl formate intermediates generated with bifunctional transfer hydrogenation catalysts.Selective Reduction of Halogenated Nitroarenes with Hydrazine Hydrate in the Presence of Pd/CBroader, greener, and more efficient: recent advances in asymmetric transfer hydrogenation.Catalytic carbonyl addition through transfer hydrogenation: a departure from preformed organometallic reagents.Studies on the Bisoxazoline and (-)-Sparteine Mediated Enantioselective Addition of Organolithium Reagents to Imines.Stable cyclic carbenes and related species beyond diaminocarbenes.Transfer hydrogenation with Hantzsch esters and related organic hydride donors.Asymmetric homogeneous hydrogenations at scale.Chiral ligands derived from monoterpenes: application in the synthesis of optically pure secondary alcohols via asymmetric catalysis.2-Azanorbornane--a versatile chiral aza-Diels-Alder cycloadduct: preparation, applications in stereoselective synthesis and biological activity.Heterogeneous and homogeneous catalysis for the hydrogenation of carboxylic acid derivatives: history, advances and future directions.Synthetic applications of hypophosphite derivatives in reduction.The contrasting catalytic efficiency and cancer cell antiproliferative activity of stereoselective organoruthenium transfer hydrogenation catalysts.N-Alkylation by Hydrogen Autotransfer Reactions.Metal-Catalysed Transfer Hydrogenation of Ketones.The Development of Phosphine-Free "Tethered" Ruthenium(II) Catalysts for the Asymmetric Reduction of Ketones and Imines.Imino Transfer Hydrogenation Reductions.Transition-Metal-Catalyzed Asymmetric Hydrogenation and Transfer Hydrogenation: Sustainable Chemistry to Access Bioactive Molecules.Easy To Synthesize, Robust Organo-osmium Asymmetric Transfer Hydrogenation Catalysts.Carbonyl 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.Synthesis and coordination chemistry of tri-substituted benzamidrazonesSynthesis of cruentaren AAnomalies in the asymmetric transfer hydrogenation of several polycyclic meso compounds.Selective cobalt nanoparticles for catalytic transfer hydrogenation of N-heteroarenes.Stereospecific cross-coupling of secondary organotrifluoroborates: potassium 1-(benzyloxy)alkyltrifluoroborates.Influence of Cofactor Regeneration Strategies on Preparative-Scale, Asymmetric Carbonyl Reductions by Engineered Escherichia coli.Chemoselective reduction of aldehydes by ruthenium trichloride and resin-bound formates.Large-scale ruthenium- and enzyme-catalyzed dynamic kinetic resolution of (rac)-1-phenylethanol.A practical access to highly enantiomerically pure flavanones by catalytic asymmetric transfer hydrogenation.Catalytic enantioselective amination of alcohols by the use of borrowing hydrogen methodology: cooperative catalysis by iridium and a chiral phosphoric acid.The mechanism for the hydrogenation of ketones catalyzed by Knölker's iron-catalyst.Iridium(I) N-heterocyclic carbene complexes of benzimidazol-2-ylidene: effect of electron donating groups on the catalytic transfer hydrogenation reaction.Ruthenium xantphos complexes in hydrogen transfer processes: reactivity and mechanistic studies.Dynamic kinetic resolution of beta-keto sulfones via asymmetric transfer hydrogenation.Asymmetric ruthenium-catalyzed hydrogenation of 2- and 2,9-substituted 1,10-phenanthrolines.Asymmetric reduction of ketones by biocatalysis using clementine mandarin (Citrus reticulata) fruit grown in Annaba or by ruthenium catalysis for access to both enantiomers.
P2860
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P2860
Asymmetric transfer hydrogenation: chiral ligands and applications.
description
2005 nî lūn-bûn
@nan
2005年の論文
@ja
2005年学术文章
@wuu
2005年学术文章
@zh-cn
2005年学术文章
@zh-hans
2005年学术文章
@zh-my
2005年学术文章
@zh-sg
2005年學術文章
@yue
2005年學術文章
@zh
2005年學術文章
@zh-hant
name
Asymmetric transfer hydrogenation: chiral ligands and applications.
@ast
Asymmetric transfer hydrogenation: chiral ligands and applications.
@en
type
label
Asymmetric transfer hydrogenation: chiral ligands and applications.
@ast
Asymmetric transfer hydrogenation: chiral ligands and applications.
@en
prefLabel
Asymmetric transfer hydrogenation: chiral ligands and applications.
@ast
Asymmetric transfer hydrogenation: chiral ligands and applications.
@en
P2860
P356
P1476
Asymmetric transfer hydrogenation: chiral ligands and applications.
@en
P2093
Elisabetta Alberico
Serafino Gladiali
P2860
P304
P356
10.1039/B513396C
P577
2005-12-19T00:00:00Z