Every reference with a DOI in the deposited reference list resolved to a known
work in Crossref or DataCite at the dated check, and none carried a retraction,
withdrawal, or removal notice.
The 88 checked references that resolve
resolves10.1021/cr8002505Copper-Mediated Coupling Reactions and Their Applications in Natural Products and Designed Biomolecules Synthesis
resolves10.1021/ja00092a058Palladium-catalyzed formation of carbon-nitrogen bonds. Reaction intermediates and catalyst improvements in the hetero cross-coupling of aryl halides and tin amides
resolves10.1021/ja00096a059Palladium-Catalyzed Aromatic Aminations with in situ Generated Aminostannanes
resolves10.1002/anie.200906750Direct Azole Amination: CH Functionalization as a New Approach to Biologically Important Heterocycles
resolves10.1039/c1cs15082kRecent advances in the transition metal-catalyzed twofold oxidative C–H bond activation strategy for C–C and C–N bond formation
resolves10.1039/c005219cRecent advances in transition metal-catalyzed N-atom transfer reactions of azides
resolves10.1002/anie.200601814Recent Advances in Catalytic Enantioselective Intermolecular CH Functionalization
resolves10.1038/nature06485Catalytic C–H functionalization by metal carbenoid and nitrenoid insertion
resolves10.1039/c0cs00142bSelective functionalisation of saturated C–H bonds with metalloporphyrin catalysts
resolves10.1039/C0CS00070ACatalytic C–H functionalization by metalloporphyrins: recent developments and future directions
resolves10.1021/ar200318qMetal-Catalyzed Nitrogen-Atom Transfer Methods for the Oxidation of Aliphatic C–H Bonds
resolves10.1039/C1CS15104ERecent advances in transition metal-catalyzed sp<sup>3</sup>C–H amination adjacent to double bonds and carbonyl groups
resolves10.1002/anie.201208906Enantio‐ and Regioselective Intermolecular Benzylic and Allylic CH Bond Amination
resolves10.1021/cr900005nRhodium-Catalyzed C−C Bond Formation via Heteroatom-Directed C−H Bond Activation
resolves10.1021/cr900184ePalladium-Catalyzed Ligand-Directed C−H Functionalization Reactions
resolves10.1002/chem.201001363Oxidative Coupling of Aromatic Substrates with Alkynes and Alkenes under Rhodium Catalysis
resolves10.1002/anie.201005142Bystanding F<sup>+</sup> Oxidants Enable Selective Reductive Elimination from High‐Valent Metal Centers in Catalysis
resolves10.1039/c1cs15058hTransition metal-catalyzed arylation of unactivated C(sp3)–H bonds
resolves10.1039/c2cs15281aC–C, C–O and C–N bond formation via rhodium(iii)-catalyzed oxidative C–H activation
resolves10.1002/anie.201301451Catalytic Functionalization of C(sp<sup>2</sup>)H and C(sp<sup>3</sup>)H Bonds by Using Bidentate Directing Groups
resolves10.1021/ja312277gPalladium-Catalyzed Picolinamide-Directed Alkylation of Unactivated C(sp<sup>3</sup>)–H Bonds with Alkyl Iodides
resolves10.1021/ja400648wPalladium(0)-Catalyzed Alkynylation of C(sp<sup>3</sup>)–H Bonds
resolves10.1021/ja406484vStereoselective 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
resolves10.1002/anie.201307090An Efficient Palladium‐Catalyzed CH Alkoxylation of Unactivated Methylene and Methyl Groups with Cyclic Hypervalent Iodine (I<sup>3+</sup>) Oxidants
resolves10.1039/c3sc51747kPd(ii)-catalyzed alkylation of unactivated C(sp3)–H bonds: efficient synthesis of optically active unnatural α-amino acids
resolves10.1039/C2SC21162APalladium-catalyzed N-(2-pyridyl)sulfonyl-directed C(sp
<sup>3</sup>
)–H γ-arylation of amino acid derivatives
resolves10.1021/ja411715vNickel-Catalyzed Direct Arylation of C(sp<sup>3</sup>)–H Bonds in Aliphatic Amides via Bidentate-Chelation Assistance
resolves10.1021/ja413131mNickel-Catalyzed Site-Selective Alkylation of Unactivated C(sp<sup>3</sup>)–H Bonds
resolves10.1021/ja106364rPd-Catalyzed Intermolecular <i>ortho</i>-C−H Amidation of Anilides by <i>N</i>-Nosyloxycarbamate
resolves10.1021/ol203046nRhodium(III)-Catalyzed Intermolecular Direct Amination of Aromatic C–H Bonds with <i>N</i>-Chloroamines
resolves10.1021/ol203353aRh[III]-Catalyzed Direct C–H Amination Using <i>N</i>-Chloroamines at Room Temperature
resolves10.1021/ol401569uRhodium(III)-Catalyzed C–H Activation and Amidation of Arenes Using <i>N</i>-Arenesulfonated Imides as Amidating Reagents
resolves10.1021/ol401209fRh[III]-Catalyzed C–H Amidation Using Aroyloxycarbamates To Give <i>N</i>-Boc Protected Arylamines
resolves10.1021/ol401321qExpedient C–H Amidations of Heteroaryl Arenes Catalyzed by Versatile Ruthenium(II) Catalysts
resolves10.1021/ja412521kSynthesis of Anthranilic Acid Derivatives through Iron-Catalyzed Ortho Amination of Aromatic Carboxamides with <i>N</i>-Chloroamines
resolves10.1021/ja9054959Allylic C−H Amination for the Preparation of <i>syn</i>-1,3-Amino Alcohol Motifs
resolves10.1002/anie.200902761Direct, Chemoselective <i>N</i>‐<i>tert</i>‐Prenylation of Indoles by CH Functionalization
resolves10.1021/ja1030936Scope and Mechanism of Allylic C−H Amination of Terminal Alkenes by the Palladium/PhI(OPiv)<sub>2</sub>Catalyst System: Insights into the Effect of Naphthoquinone
resolves10.1002/anie.200903035Palladium‐Catalyzed Amidation of Unactivated C(sp<sup>3</sup>)H Bonds: from Anilines to Indolines
resolves10.1021/ja210660gHighly Efficient Syntheses of Azetidines, Pyrrolidines, and Indolines via Palladium Catalyzed Intramolecular Amination of C(sp<sup>3</sup>)–H and C(sp<sup>2</sup>)–H Bonds at γ and δ Positions
resolves10.1002/anie.201305615Use of a Readily Removable Auxiliary Group for the Synthesis of Pyrrolidones by the Palladium‐Catalyzed Intramolecular Amination of Unactivated γ C(sp<sup>3</sup>)H Bonds
resolves10.1002/anie.201306625Stereoselective Synthesis of Chiral α‐Amino‐β‐Lactams through Palladium(II)‐Catalyzed Sequential Monoarylation/Amidation of C(sp<sup>3</sup>)H Bonds
resolves10.1021/ja3113565Iron(II) Bromide-Catalyzed Intramolecular C–H Bond Amination [1,2]-Shift Tandem Reactions of Aryl Azides
resolves10.1021/ja062856vIntermolecular Amidation of Unactivated sp<sup>2</sup> and sp<sup>3</sup> C−H Bonds via Palladium-Catalyzed Cascade C−H Activation/Nitrene Insertion
resolves10.1039/b905820fCatalytic C–H amination: recent progress and future directions
resolves10.1002/chem.200902374Functionalization of Organic Molecules by Transition‐Metal‐Catalyzed C(sp<sup>3</sup>)H Activation
resolves10.1002/anie.200903957Silver‐Mediated Direct Amination of Benzoxazoles: Tuning the Amino Group Source from Formamides to Parent Amines
resolves10.1002/anie.201005922Cobalt‐ and Manganese‐Catalyzed Direct Amination of Azoles under Mild Reaction Conditions and the Mechanistic Details
resolves10.1021/ja111652vIntramolecular Oxidative C−N Bond Formation for the Synthesis of Carbazoles: Comparison of Reactivity between the Copper-Catalyzed and Metal-Free Conditions
resolves10.1021/ja207296yIntermolecular Oxidative C–N Bond Formation under Metal-Free Conditions: Control of Chemoselectivity between Aryl sp<sup>2</sup> and Benzylic sp<sup>3</sup> C–H Bond Imidation
resolves10.1021/ja303527mRhodium-Catalyzed Intermolecular Amidation of Arenes with Sulfonyl Azides via Chelation-Assisted C–H Bond Activation
resolves10.1002/anie.201205723Rhodium‐Catalyzed Direct CH Amination of Benzamides with Aryl Azides: A Synthetic Route to Diarylamines
resolves10.1002/chem.201301025Ruthenium‐Catalyzed Direct CH Amidation of Arenes Including Weakly Coordinating Aromatic Ketones
resolves10.1021/ja406383hIr(III)-Catalyzed Mild C–H Amidation of Arenes and Alkenes: An Efficient Usage of Acyl Azides as the Nitrogen Source
resolves10.1021/jo4019683Iridium-Catalyzed Direct Arene C–H Bond Amidation with Sulfonyl- and Aryl Azides
resolves10.15227/orgsyn.091.0052Rhodium-Catalyzed Direct Amination of Arene C-H Bonds Using Azides as the Nitrogen Source
resolves10.1021/ja4118472Hydrogen-Bond-Assisted Controlled C–H Functionalization via Adaptive Recognition of a Purine Directing Group
resolves10.1002/anie.201310544Iridium‐Catalyzed Direct CH Amidation with Weakly Coordinating Carbonyl Directing Groups under Mild Conditions
resolves10.1021/ja411072aMechanistic Studies of the Rhodium-Catalyzed Direct C–H Amination Reaction Using Azides as the Nitrogen Source
resolves10.1021/ja303529zTotal Synthesis of the Potent cAMP Signaling Agonist (−)-Alotaketal A
resolves10.1021/ja046831cPalladium-Catalyzed Oxygenation of Unactivated sp<sup>3</sup> C−H Bonds
resolves10.1007/s00044-008-9138-8Design, synthesis, antifungal activity, and ADME prediction of functional analogues of terbinafine
resolves10.1039/c1cs15013hRecent developments in natural product synthesis using metal-catalysed C–H bond functionalisation
resolves10.1002/anie.201201666CH Bond Functionalization: Emerging Synthetic Tools for Natural Products and Pharmaceuticals
resolves10.1039/C39900000327The generation and use of a masked α-acyl cation in aromatic substitution reactions; Ag
<sup>+</sup>
induced reactions of 3-(bromomethyl)-5,6-dihydro-1,4,2-dioxazine derivatives
resolves10.1021/ja3082186Catalytic Functionalization of Unactivated sp<sup>3</sup> C–H Bonds via <i>exo</i>-Directing Groups: Synthesis of Chemically Differentiated 1,2-Diols
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