Catalytic Asymmetric Hydrogenation of Heteroaromatic Compounds, Indoles
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Enantioselective hydrogenations of arylalkenes mediated by [Ir(cod) (JM-Phos) ]+ complexes.Ligand-controlled highly regioselective and asymmetric hydrogenation of quinoxalines catalyzed by ruthenium N-heterocyclic carbene complexes.Direct asymmetric hydrosilylation of indoles: combined Lewis base and Brønsted acid activation.Ruthenium NHC catalyzed highly asymmetric hydrogenation of benzofurans.Brønsted acid activation strategy in transition-metal catalyzed asymmetric hydrogenation of N-unprotected imines, enamines, and N-heteroaromatic compounds.Iridium-catalyzed asymmetric hydrogenation of pyridinium salts.Asymmetric homogeneous hydrogenations at scale.Ruthenium-NHC-catalyzed asymmetric hydrogenation of indolizines: access to indolizidine alkaloids.(+)-trans-Chlorido-{2-[(Rp)-2-(methyl-sulfan-yl)ferro-cen-yl]-2,5,6,7-tetra-hydro-pyrrolo-[1,2-c]imidazol-3-yl-idene}bis(tri-phenyl-phosphane-κP)palladium(II) hexa-fluorido-phosphate di-chloro-form disolvateRh-catalyzed highly enantioselective hydrogenation of nitroalkenes under basic conditions.Asymmetric ruthenium-catalyzed hydrogenation of 2- and 2,9-substituted 1,10-phenanthrolines.Asymmetric Hydrogenation of Isoxazolium Triflates with a Chiral Iridium Catalyst.Enantioselective Borylative Dearomatization of Indoles through Copper(I) Catalysis.Enhancing effects of salt formation on catalytic activity and enantioselectivity for asymmetric hydrogenation of isoquinolinium salts by dinuclear halide-bridged iridium complexes bearing chiral diphosphine ligands.Selective reduction of condensed N-heterocycles using water as a solvent and a hydrogen source.Asymmetric Hydrogenation of Azaindoles: Chemo- and Enantioselective Reduction of Fused Aromatic Ring Systems Consisting of Two Heteroarenes.Asymmetric Hydrogenation of In Situ Generated Isochromenylium Intermediates by Copper/Ruthenium Tandem Catalysis.Asymmetric ruthenium-catalyzed hydrogenation of 2,6-disubstituted 1,5-naphthyridines: access to chiral 1,5-diaza-cis-decalins.Chiral Phosphoric Acid Catalyzed Kinetic Resolution of Indolines Based on a Self-Redox Reaction.Highly Enantioselective Synthesis of Indolines: Asymmetric Hydrogenation at Ambient Temperature and Pressure with Cationic Ruthenium Diamine Catalysts.Highly Enantioselective Direct Synthesis of Endocyclic Vicinal Diamines through Chiral Ru(diamine)-Catalyzed Hydrogenation of 2,2'-Bisquinoline Derivatives.Asymmetric hydrogenation of quinazolinium salts catalysed by halide-bridged dinuclear iridium complexes bearing chiral diphosphine ligands.Asymmetric Synthesis of Optically Active Spirocyclic Indoline Scaffolds through an Enantioselective Reduction of Indoles.Asymmetric transfer hydrogenation of 3-nitroquinolines: facile access to cyclic nitro compounds with two contiguous stereocenters.Pd-catalyzed asymmetric hydrogenation of fluorinated aromatic pyrazol-5-ols via capture of active tautomers.An Enantioselective Approach to 2,3-Disubstituted Indolines through Consecutive Brønsted Acid/Pd-Complex-Promoted Tandem Reactions
P2860
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P2860
Catalytic Asymmetric Hydrogenation of Heteroaromatic Compounds, Indoles
description
im August 2000 veröffentlichter wissenschaftlicher Artikel
@de
wetenschappelijk artikel
@nl
наукова стаття, опублікована в серпні 2000
@uk
name
Catalytic Asymmetric Hydrogenation of Heteroaromatic Compounds, Indoles
@en
Catalytic Asymmetric Hydrogenation of Heteroaromatic Compounds, Indoles
@nl
type
label
Catalytic Asymmetric Hydrogenation of Heteroaromatic Compounds, Indoles
@en
Catalytic Asymmetric Hydrogenation of Heteroaromatic Compounds, Indoles
@nl
prefLabel
Catalytic Asymmetric Hydrogenation of Heteroaromatic Compounds, Indoles
@en
Catalytic Asymmetric Hydrogenation of Heteroaromatic Compounds, Indoles
@nl
P2093
P356
P1476
Catalytic Asymmetric Hydrogenation of Heteroaromatic Compounds, Indoles
@en
P2093
Daisuke Karube
Ryoichi Kuwano
Takashi Kurokawa
Yoshihiko Ito
P304
P356
10.1021/JA001271C
P407
P577
2000-08-01T00:00:00Z