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Bidentate, Monoanionic Auxiliary-Directed Functionalization of Carbon–Hydrogen Bonds

https://doi.org/10.1021/ar5004626
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The 72 checked references that resolve
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Nickel-Catalyzed Direct Arylation of C(sp<sup>3</sup>)–H Bonds in Aliphatic Amides via Bidentate-Chelation Assistance
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β-Arylation of Carboxamides via Iron-Catalyzed C(sp<sup>3</sup>)–H Bond Activation
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Auxiliary-Assisted Palladium-Catalyzed Arylation and Alkylation of sp<sup>2</sup> and sp<sup>3</sup> Carbon−Hydrogen Bonds
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Scope and Limitations of Auxiliary-Assisted, Palladium-Catalyzed Arylation and Alkylation of sp<sup>2</sup> and sp<sup>3</sup> C–H Bonds
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Nonnatural Amino Acid Synthesis by Using Carbon–Hydrogen Bond Functionalization Methodology
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Synthesis of Highly Branched Polyethylene Using “Sandwich” (8-<i>p</i>-Tolyl naphthyl α-diimine)nickel(II) Catalysts
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Novel Acetoxylation and C−C Coupling Reactions at Unactivated Positions in α-Amino Acid Derivatives
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Total Synthesis of Celogentin C by Stereoselective CH Activation
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Stereoselective Synthesis of β-Alkylated α-Amino Acids via Palladium-Catalyzed Alkylation of Unactivated Methylene C(sp<sup>3</sup>)–H Bonds with Primary Alkyl Halides
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Experimental and computational studies on the mechanism of the Pd-catalyzed C(sp <sup>3</sup> )–H γ-arylation of amino acid derivatives assisted by the 2-pyridylsulfonyl group
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Pd(ii)-catalyzed alkylation of unactivated C(sp3)–H bonds: efficient synthesis of optically active unnatural α-amino acids
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Site-Selective C(sp<sup>3</sup>)–H Functionalization of Di-, Tri-, and Tetrapeptides at the N-Terminus
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1,2,3-Triazoles as versatile directing group for selective sp2 and sp3 C–H activation: cyclization vs substitution
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Iron‐Catalyzed C(sp<sup>2</sup>)H and C(sp<sup>3</sup>)H Arylation by Triazole Assistance
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Palladium‐Catalyzed Direct Functionalization of 2‐Aminobutanoic Acid Derivatives: Application of a Convenient and Versatile Auxiliary
resolves10.1021/ja209205x
Total Synthesis and Structural Revision of the Piperarborenines via Sequential Cyclobutane C–H Arylation
resolves10.1002/anie.201203897
Sequential CH Arylation and Olefination: Total Synthesis of the Proposed Structure of Pipercyclobutanamide A
resolves10.1021/jo4027148
Applications of C–H Functionalization Logic to Cyclobutane Synthesis
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Ruthenium-catalyzed ortho-C–H bond alkylation of aromatic amides with α,β-unsaturated ketones via bidentate-chelation assistance
resolves10.1002/1521-3773(20020816)41:16<2991::AID-ANIE2991>3.0.CO;2-6
Aryl CbH Activation by CuII To Form an Organometallic Aryl–CuIII Species: A Novel Twist on Copper Disproportionation This research was supported by MICYT of Spain through project PBQ2000-0548 and with the grant SGR-3102-UG-01 as well as the Distinction award from from CIRIT Generalitat de Catalunya (Spain). An FI doctoral grant from CIRIT to X.R. and financial support from the National Institutes of Health (USA; T.D.P.S. GM-50730; K.O.H. RR-01209) are also acknowledged. SSRL operations are funded by the Department of Energy, Basic Energy Sciences, and the SSRL Structural Molecular Biology Program is supported by the NIH NCRR BTP and the DOE OBER.
resolves10.1021/ja802123p
Carbon−Nitrogen Bond Formation Involving Well-Defined Aryl−Copper(III) Complexes
resolves10.1021/ja1045378
Copper-Catalyzed Aerobic Oxidative Functionalization of an Arene C−H Bond: Evidence for an Aryl-Copper(III) Intermediate
resolves10.1021/ja2058567
Nucleophilic Aryl Fluorination and Aryl Halide Exchange Mediated by a Cu<sup>I</sup>/Cu<sup>III</sup> Catalytic Cycle
resolves10.1021/ja412521k
Synthesis of Anthranilic Acid Derivatives through Iron-Catalyzed Ortho Amination of Aromatic Carboxamides with <i>N</i>-Chloroamines
resolves10.1021/ja412880r
Cu(II)-Mediated C–H Amidation and Amination of Arenes: Exceptional Compatibility with Heterocycles
resolves10.1021/ja4026424
Divergence between Organometallic and Single-Electron-Transfer Mechanisms in Copper(II)-Mediated Aerobic C–H Oxidation
resolves10.1021/ja061715q
Cu(II)-Catalyzed Functionalizations of Aryl C−H Bonds Using O<sub>2</sub> as an Oxidant
resolves10.1039/c39890001633
Synthesis and X-ray structure of bis(trifluoromethyl)(N,N-diethyldithiocarbamato)-copper; a remarkably stable perfluoroalkylcopper(III) complex
resolves10.1021/ja3092278
Copper-Promoted Sulfenylation of sp<sup>2</sup> C–H Bonds
resolves10.1002/anie.201300135
Directed Amination of Non‐Acidic Arene CH Bonds by a Copper–Silver Catalytic System
resolves10.1021/ol402904d
Copper-Catalyzed Etherification of Arene C–H Bonds
resolves10.1021/ja4047125
Copper-Catalyzed, Directing Group-Assisted Fluorination of Arene and Heteroarene C–H Bonds
resolves10.1021/ja5008432
Pyrroloindolone Synthesis via a Cp*Co<sup>III</sup>-Catalyzed Redox-Neutral Directed C–H Alkenylation/Annulation Sequence
resolves10.1021/ja00291a073
Implications of three-center, two-electron M--H--C bonding for related alkyl migration reactions: design and study of an ethylene polymerization catalyst
resolves10.1002/anie.201404579
Cobalt‐Catalyzed, Aminoquinoline‐Directed C(sp<sup>2</sup>)H Bond Alkenylation by Alkynes
resolves10.1021/ol502005g
Cobalt-Catalyzed, Aminoquinoline-Directed Coupling of sp<sup>2</sup> C–H Bonds with Alkenes
resolves10.1021/ol502007t
Cobalt-Catalyzed Direct Carbonylation of Aminoquinoline Benzamides
resolves10.1021/ja0701614
Palladium-Catalyzed Methylation and Arylation of sp<sup>2</sup> and sp<sup>3</sup> C−H Bonds in Simple Carboxylic Acids
resolves10.1021/ja016280f
Selective Functionalization of Amino Acids in Water: A Synthetic Method via Catalytic C−H Bond Activation
resolves10.1038/nature13389
Palladium-catalysed C–H activation of aliphatic amines to give strained nitrogen heterocycles
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