about
Redox-neutral α-sulfenylation of secondary amines: ring-fused N,S-acetals.Lewis acid-catalyzed redox-neutral amination of 2-(3-pyrroline-1-yl)benzaldehydes via intramolecular [1,5]-hydride shift/isomerization reactionRedox-neutral α-oxygenation of amines: reaction development and elucidation of the mechanism.The Rügheimer-Burrows reaction revisited: Facile preparation of 4-alkylisoquinolines and 3,5-dialkylpyridines from (partially) saturated aminesAsymmetric Redox-Annulation of Cyclic Amines.C-H bond functionalization through intramolecular hydride transfer.Direct metal-catalyzed regioselective functionalization of enamides.The azomethine ylide route to amine C-H functionalization: redox-versions of classic reactions and a pathway to new transformations.Organo- and Organometallic-Catalytic Intramolecular [1,5]-Hydride Transfer/Cyclization Process through C(sp(3) )-H Bond Activation.Redox-Annulation of Cyclic Amines and β-Ketoaldehydes.Hydrogen-Atom Transfer Reactions.C-H functionalisation of cycloalkanes.Intramolecular Redox-Mannich Reactions: Facile Access to the Tetrahydroprotoberberine Core.Metal-free C(sp(3))-H functionalization: oxidative carbo-oxygenation of α-diazo carbonyls via radical dediazotization.Dual C-H functionalization of N-aryl amines: synthesis of polycyclic amines via an oxidative Povarov approach.The redox-Mannich reaction.The Redox-A(3) Reaction.Redox-neutral α,β-difunctionalization of cyclic amines.C-H functionalization of cyclic amines: redox-annulations with α,β-unsaturated carbonyl compounds.Redox-neutral α-arylation of amines.An Ugi Reaction Incorporating a Redox-Neutral Amine C-H Functionalization StepAcetic Acid Promoted Redox Annulations with Dual C-H Functionalization.Intramolecular [3 + 2]-cycloadditions of azomethine ylides derived from secondary amines via redox-neutral C-H functionalization.Redox-Neutral Aromatization of Cyclic Amines: Mechanistic Insights and Harnessing of Reactive Intermediates for Amine α- and β-C-H Functionalization.First principles (DFT) characterization of Rh(I) /dppp-catalyzed C-H activation by tandem 1,2-addition/1,4-Rh shift reactions of norbornene to phenylboronic acid.C(sp3 )-H Bond Activation by Vinylidene Gold(I) Complexes: A Concerted Asynchronous or Stepwise Process?A tandem annulation with a [1,3]-hydride transfer as the key step leading to isochromans.Intermolecular Redox-Neutral Amine C-H Functionalization Induced by the Strong Boron Lewis Acid B(C6 F5 )3 in the Frustrated Lewis Pair Regime.Radical Enantioselective C(sp3 )-H Functionalization.Iterative direct C(sp3)-H functionalization of amines: diastereoselective divergent syntheses of α,α'-disubstituted alicyclic amines.Classical-Reaction-Driven Stereo- and Regioselective C(sp(3) )-H Functionalization of Aliphatic Amines.Asymmetric tandem 1,5-hydride shift/ring closure for the synthesis of chiral spirooxindole tetrahydroquinolines.Hf(OTf)4-Catalyzed highly diastereoselective synthesis of 1,3-disubstituted tetralin derivatives via benzylic C(sp3)-H bond functionalization.Yttrium-Catalyzed Intramolecular Hydroalkoxylation/Claisen Rearrangement Sequence: Efficient Synthesis of Medium-Sized Lactams.Copper-catalyzed redox-neutral C-H amination with amidoximes.The functionalization of a cascade of C(sp(2))-H/C(sp(3))-H bonds: synthesis of fused dihydropyrazoles via visible-light photoredox catalysis.Iron-Catalyzed Regioselective Transfer Hydrogenative Couplings of Unactivated Aldehydes with Simple Alkenes.Rhodium-Catalyzed Intramolecular C-H Bond Activation with Triazoles: Preparation of Stereodefined Pyrrolidines and Other Related Cyclic Compounds.Synthesis of Polycyclic Imidazolidinones via Amine Redox-Annulation.Regio- and Diastereoselective and Enantiospecific Metal-Free C(sp(3) )-H Arylation: Facile Access to Optically Active 5-Aryl 2,5-Disubstituted Pyrrolidines.
P2860
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P2860
description
2013 nî lūn-bûn
@nan
2013年の論文
@ja
2013年学术文章
@wuu
2013年学术文章
@zh
2013年学术文章
@zh-cn
2013年学术文章
@zh-hans
2013年学术文章
@zh-my
2013年学术文章
@zh-sg
2013年學術文章
@yue
2013年學術文章
@zh-hant
name
The redox-neutral approach to C-H functionalization.
@en
The redox-neutral approach to C-H functionalization.
@nl
type
label
The redox-neutral approach to C-H functionalization.
@en
The redox-neutral approach to C-H functionalization.
@nl
prefLabel
The redox-neutral approach to C-H functionalization.
@en
The redox-neutral approach to C-H functionalization.
@nl
P2860
P356
P1476
The redox-neutral approach to C-H functionalization.
@en
P2093
P2860
P304
13274-13287
P356
10.1002/CHEM.201301522
P407
P50
P577
2013-09-11T00:00:00Z