Ligand-Enabled Stereoselective β-C(sp(3))-H Fluorination: Synthesis of Unnatural Enantiopure anti-β-Fluoro-α-amino Acids.
about
Facile Access to Fluoroaromatic Molecules by Transition-Metal-Free C-F Bond Cleavage of Polyfluoroarenes: An Efficient, Green, and Sustainable Protocol.Palladium-Catalyzed Transformations of Alkyl C-H Bonds.Ligand-Enabled Arylation of γ-C-H Bonds.Palladium-catalyzed directing group-assisted C8-triflation of naphthalenes.Identification of monodentate oxazoline as a ligand for copper-promoted ortho-C-H hydroxylation and aminationLigand-Promoted C(sp(3) )-H Olefination en Route to Multi-functionalized Pyrazoles.Enantioselective Palladium-Catalyzed Oxidative β,β-Fluoroarylation of α,β-Unsaturated Carbonyl Derivatives.Ketones as directing groups in photocatalytic sp3 C-H fluorination.Ligand-Enabled Pd(II)-Catalyzed Bromination and Iodination of C(sp3)-H Bonds.Highly Versatile β-C(sp3)-H Iodination of Ketones Using a Practical Auxiliary.Complementary Strategies for Directed C(sp3 )-H Functionalization: A Comparison of Transition-Metal-Catalyzed Activation, Hydrogen Atom Transfer, and Carbene/Nitrene Transfer.Selective Palladium(II)-Catalyzed Carbonylation of Methylene β-C-H Bonds in Aliphatic Amines.Stereoselective Sulfinyl Aniline-Promoted Pd-Catalyzed C-H Arylation and Acetoxylation of Aliphatic Amides.Catalytic Oxidative Trifluoromethoxylation of Allylic C-H Bonds Using a Palladium Catalyst.Enantiopure Sulfinyl Aniline as a Removable and Recyclable Chiral Auxiliary for Asymmetric C(sp3 )-H Bond Activation.Bulky α-diimine palladium complexes: highly efficient for direct C-H bond arylation of heteroarenes under aerobic conditions.Selective Synthesis of Fluorine-Containing Cyclic β-Amino Acid Scaffolds.Ag-Catalyzed difluorohydration of β-alkynyl ketones for diastereoselective synthesis of 1,5-dicarbonyl compounds.Site-selective 18F fluorination of unactivated C-H bonds mediated by a manganese porphyrin.A Convenient Late-Stage Fluorination of Pyridylic C-H Bonds with N-Fluorobenzenesulfonimide.Ligand-enabled ortho-C-H olefination of phenylacetic amides with unactivated alkenes.A comprehensive overview of directing groups applied in metal-catalysed C-H functionalisation chemistryLigand-Assisted Palladium(II)/(IV) Oxidation forsp3CH Fluorination
P2860
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P2860
Ligand-Enabled Stereoselective β-C(sp(3))-H Fluorination: Synthesis of Unnatural Enantiopure anti-β-Fluoro-α-amino Acids.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年論文
@yue
2015年論文
@zh-hant
2015年論文
@zh-hk
2015年論文
@zh-mo
2015年論文
@zh-tw
2015年论文
@wuu
2015年论文
@zh
2015年论文
@zh-cn
name
Ligand-Enabled Stereoselective β-C
@nl
Ligand-Enabled Stereoselective ...... e anti-β-Fluoro-α-amino Acids.
@en
type
label
Ligand-Enabled Stereoselective β-C
@nl
Ligand-Enabled Stereoselective ...... e anti-β-Fluoro-α-amino Acids.
@en
prefLabel
Ligand-Enabled Stereoselective β-C
@nl
Ligand-Enabled Stereoselective ...... e anti-β-Fluoro-α-amino Acids.
@en
P2093
P2860
P356
P1476
Ligand-Enabled Stereoselective ...... e anti-β-Fluoro-α-amino Acids.
@en
P2093
Gen-Cheng Li
Hai-Yan Fu
Keita Tanaka
P2860
P304
P356
10.1021/JACS.5B04088
P407
P577
2015-05-27T00:00:00Z