Direct asymmetric hydrosilylation of indoles: combined Lewis base and Brønsted acid activation.
about
Catalyst development for organocatalytic hydrosilylation of aromatic ketones and ketimines.Brønsted acid activation strategy in transition-metal catalyzed asymmetric hydrogenation of N-unprotected imines, enamines, and N-heteroaromatic compounds.Enantioselective reduction of ketoimines promoted by easily available (S)-proline derivatives.Highly diastereo- and enantioselective CuH-catalyzed synthesis of 2,3-disubstituted indolinesChiral Indoline Synthesis Via Enantioselective Intramolecular Copper-Catalyzed Alkene Hydroamination.Organocatalytic Transfer Hydrogenation and Hydrosilylation Reactions.Direct, Enantioselective Synthesis of Pyrroloindolines and Indolines From Simple Indole Derivatives.Waste as catalyst: tandem Wittig/conjugate reduction sequence to α-CF3 γ-keto esters that uses Ph3PO as catalyst for the chemoselective conjugate reduction.Asymmetric ruthenium-catalyzed hydrogenation of 2- and 2,9-substituted 1,10-phenanthrolines.Palladium Catalyzed Asymmetric Three-Component Coupling of Boronic Esters, Indoles, and Allylic Acetates.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.Highly efficient asymmetric construction of novel indolines and tetrahydroquinoline derivatives via aza-Barbier/C-N coupling reaction.Kinetic Resolution of 2-Substituted Indolines by N-Sulfonylation using an Atropisomeric 4-DMAP-N-oxide Organocatalyst.Catalytic, Enantioselective, Intramolecular Sulfenoamination of Alkenes with Anilines.Mechanistic investigations of the asymmetric hydrosilylation of ketimines with trichlorosilane reveals a dual activation model and an organocatalyst with enhanced efficiency.A Photoredox-Induced Stereoselective Dearomative Radical (4+2)-Cyclization/1,4-Addition Cascade for the Synthesis of Highly Functionalized Hexahydro-1H-carbazoles.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.Iron-Catalyzed Decarboxylative (4+1) Cycloadditions: Exploiting the Reactivity of Ambident Iron-Stabilized Intermediates.Construction of optically active indolines by formal [4+1] annulation of sulfur ylides and N-(ortho-chloromethyl)aryl amides.Asymmetric Synthesis of Optically Active Spirocyclic Indoline Scaffolds through an Enantioselective Reduction of Indoles.Pd-catalyzed asymmetric hydrogenation of fluorinated aromatic pyrazol-5-ols via capture of active tautomers.Kinetic Resolution of 2-Substituted Indolines by N -Sulfonylation using an Atropisomeric 4-DMAP-N -oxide OrganocatalystCinchona-Derived Picolinamides: Effective Organocatalysts for Stereoselective Imine Hydrosilylation
P2860
Q34273021-EF7C7EFE-2F8A-4B4E-98DA-31602C4DAD72Q34274141-3492C0E9-3439-451F-A664-B769479E3062Q34686772-D1361A32-390F-407D-84EC-53BF6BF4D03CQ35633975-B51238EB-4B7E-4D6E-9FDA-69151D8FCCBCQ36459169-E8CB0A16-2495-4336-9E9F-082657DD584AQ39442487-3D00F6A2-3F09-495A-A0E7-A8B3FC8D4D16Q42599384-DFE05791-48E1-4BDF-B8B4-00908FCE59DEQ43434792-D38B9CC0-CDDC-4726-B51D-660EB74AD0B4Q46229905-C38C8C4B-1169-4FA8-8B44-6C27F1A98AE5Q46382173-0CD0ED1B-915F-4395-92D4-6D65238B76F3Q46806320-0A8DE3AB-4001-4B68-B6C6-72E72C00F5DEQ47262593-DBB5FEE0-4B4F-4228-A428-D33C817C9365Q47566197-D052F1CF-F339-4E0A-AFAA-5F8D52819B57Q48126871-41BE83B4-9FA5-41DA-8D5D-14B195E545FDQ48173126-77951335-74E1-425E-AEF6-297047EF1511Q48373350-9907B1D5-7C16-4102-9B69-D1CF98EAD663Q50439233-247E62EF-BF97-4AA5-B702-9502C13ED530Q50886070-50095F51-C176-482B-B0D3-670F11976E57Q51131087-9A162AB1-B3A4-4A1D-8B1D-2D7B0B7DD5B3Q51162281-ABC0C783-43B0-454E-BE5C-7629406C8421Q51550259-199435AA-2CC2-4CD9-85DC-B995F00969B5Q51812005-9C11AE6B-E17B-4C9E-90B3-9F7035224C89Q53547760-9CFD34AC-B943-4F02-8D45-22B778E0D45FQ54948512-891805A3-B435-4976-8552-827666D6DD09Q56921028-F9750956-C226-42F7-95F0-1EBD4C5D9DFCQ58841891-3677B65A-A9E0-45F2-A6A3-911469D8DEB4
P2860
Direct asymmetric hydrosilylation of indoles: combined Lewis base and Brønsted acid activation.
description
2011 nî lūn-bûn
@nan
2011 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
Direct asymmetric hydrosilylat ...... and Brønsted acid activation.
@ast
Direct asymmetric hydrosilylat ...... and Brønsted acid activation.
@en
Direct asymmetric hydrosilylat ...... and Brønsted acid activation.
@nl
type
label
Direct asymmetric hydrosilylat ...... and Brønsted acid activation.
@ast
Direct asymmetric hydrosilylat ...... and Brønsted acid activation.
@en
Direct asymmetric hydrosilylat ...... and Brønsted acid activation.
@nl
prefLabel
Direct asymmetric hydrosilylat ...... and Brønsted acid activation.
@ast
Direct asymmetric hydrosilylat ...... and Brønsted acid activation.
@en
Direct asymmetric hydrosilylat ...... and Brønsted acid activation.
@nl
P2093
P2860
P356
P1476
Direct asymmetric hydrosilylat ...... and Brønsted acid activation.
@en
P2093
Ying-Chun Chen
You-Cai Xiao
P2860
P304
10661-10664
P356
10.1002/ANIE.201105341
P407
P577
2011-09-20T00:00:00Z