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Mechanistic Study of Asymmetric Oxidative Biaryl Coupling: Evidence for Self-Processing of the Copper Catalyst to Achieve Control of Oxidase vs Oxygenase Activity
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Oxygen Binding, Activation, and Reduction to Water by Copper Proteins
inferredcites →https://doi.org/10.1002/adsc.200404063openalex-snapshot
Room Temperature Aerobic Copper–Catalysed Selective Oxidation of Primary Alcohols to Aldehydes
inferredcites →https://doi.org/10.1002/anie.200250325openalex-snapshot
Novel Pathways for the Formation of Chiral Binaphthyl Polymers: Oxidative Asymmetric Phenolic Coupling Alone and in Tandem with the Glaser–Hay Coupling
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Efficient, Copper‐Catalyzed, Aerobic Oxidation of Primary Alcohols
inferredcites →https://doi.org/10.1002/anie.200800734openalex-snapshot
Dynamic Stereochemistry Transfer in a Transannular Aldol Reaction: Total Synthesis of Hypocrellin A
inferredcites →https://doi.org/10.1002/chem.200701277openalex-snapshot
Gas‐Phase Study on the CC Coupling of Naphthol Catalyzed by CuII⋅TMEDA: Evidence for the Key Role of Binuclear Clusters
inferredcites →https://doi.org/10.1002/ejic.200601091openalex-snapshot
Ten Years of a Biomimetic Approach to the Copper(II) Radical Site of Galactose Oxidase
inferredcites →https://doi.org/10.1007/s00775-004-0578-4openalex-snapshot
Oxidant types in copper–dioxygen chemistry: the ligand coordination defines the Cu n -O2 structure and subsequent reactivity
inferredcites →https://doi.org/10.1016/0040-4039(95)02063-2openalex-snapshot
Catalytic asymmetric synthesis of binaphthol derivatives by aerobic oxidative coupling of 3-hydroxy-2-naphthoates with chiral diamine-copper complex
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Copper-containing amine oxidases. Biogenesis and catalysis; a structural perspective
inferredcites →https://doi.org/10.1016/j.abb.2004.08.036openalex-snapshot
Mechanism of post-translational quinone formation in copper amine oxidases and its relationship to the catalytic turnover
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Recent advances in copper-catalyzed oxidation of organic compounds
inferredcites →https://doi.org/10.1016/j.tet.2004.07.086openalex-snapshot
Enantioselective oxidative coupling of methyl 3-hydroxy-2-naphthoate using mono-N-alkylated octahydrobinaphthyl-2,2′-diamine ligand
inferredcites →https://doi.org/10.1021/cr020632zopenalex-snapshot
Structure and Spectroscopy of Copper−Dioxygen Complexes
inferredcites →https://doi.org/10.1021/cr020633ropenalex-snapshot
Reactivity of Dioxygen−Copper Systems
inferredcites →https://doi.org/10.1021/ja027745kopenalex-snapshot
General Approach for the Synthesis of Chiral Perylenequinones via Catalytic Enantioselective Oxidative Biaryl Coupling
inferredcites →https://doi.org/10.1021/ja991481topenalex-snapshot
Aerobic Oxidation of Primary Alcohols (Including Methanol) by Copper(II)− and Zinc(II)−Phenoxyl Radical Catalysts
inferredcites →https://doi.org/10.1021/jo00069a010openalex-snapshot
Synthesis of enantiomerically pure binaphthyl derivatives. Mechanism of the enantioselective, oxidative coupling of naphthols and designing a catalytic cycle
inferredcites →https://doi.org/10.1021/jo0340206openalex-snapshot
Enantioselective Oxidative Biaryl Coupling Reactions Catalyzed by 1,5-Diazadecalin Metal Complexes: Efficient Formation of Chiral Functionalized BINOL Derivatives
inferredcites →https://doi.org/10.1021/jo981808topenalex-snapshot
Enantioselective Synthesis of Binaphthol Derivatives by Oxidative Coupling of Naphthol Derivatives Catalyzed by Chiral Diamine·Copper Complexes
inferredcites →https://doi.org/10.1021/ol015595xopenalex-snapshot
Enantioselective Oxidative Biaryl Coupling Reactions Catalyzed by 1,5-Diazadecalin Metal Complexes
inferredcites →https://doi.org/10.1021/ol062468yopenalex-snapshot
Asymmetric Total Synthesis of Nigerone
inferredcites →https://doi.org/10.1021/om020425popenalex-snapshot
Copper(II) Complexes of Novel 1,5-Diaza-cis-decalin Diamine Ligands: An Investigation of Structure and Reactivity
inferredcites →https://doi.org/10.1073/pnas.011602498openalex-snapshot
How many ways to craft a cofactor?
inferredcites →https://doi.org/10.1126/science.279.5350.537openalex-snapshot
Catalytic Galactose Oxidase Models: Biomimetic Cu(II)-Phenoxyl-Radical Reactivity
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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inferred← citeshttps://doi.org/10.1021/ol100449copenalex-snapshot
Cu(II)-Mediated Methylthiolation of Aryl C−H Bonds with DMSO
inferred← citeshttps://doi.org/10.1021/ol3001365openalex-snapshot
Enantioselective Total Synthesis of (S)-Bisoranjidiol, an Axially Chiral Bisanthraquinone
inferred← citeshttps://doi.org/10.1021/ol301130uopenalex-snapshot
Copper-Catalyzed Aerobic Oxidative Cross-Dehydrogenative Coupling of Amine and α-Carbonyl Aldehyde: A Practical and Efficient Approach to α-Ketoamides with Wide Substrate Scope
inferred← citeshttps://doi.org/10.1021/ol301583yopenalex-snapshot
Copper-Catalyzed Aerobic Spirocyclization of Biaryl-N-H-imines via 1,4-Aminooxygenation of Benzene Rings
inferred← citeshttps://doi.org/10.1021/ol502197popenalex-snapshot
Aerobic Oxidative Homocoupling of Aryl Amines Using Heterogeneous Rhodium Catalysts
inferred← citeshttps://doi.org/10.1021/ol902571popenalex-snapshot
Synthesis of Spiro Compounds through Tandem Oxidative Coupling and a Framework Rearrangement Reaction
inferred← citeshttps://doi.org/10.1021/om300393mopenalex-snapshot
Copper-Catalyzed Homodimerization of Nitronates and Enolates under an Oxygen Atmosphere
inferred← citeshttps://doi.org/10.1021/om500403kopenalex-snapshot
Aerobic Oxidative Coupling of 2-Naphthol Derivatives Catalyzed by a Hexanuclear Bis(μ-hydroxo)copper(II) Catalyst
inferred← citeshttps://doi.org/10.1038/s41557-022-01095-9openalex-snapshot
Enantioselective synthesis of atropisomeric indoles via iron-catalysed oxidative cross-coupling
inferred← citeshttps://doi.org/10.1039/9781782621966-00092openalex-snapshot
Asymmetric Oxidative Biaryl Coupling Reactions
inferred← citeshttps://doi.org/10.1039/b816707aopenalex-snapshot
Transition metal-catalyzed C–H activation reactions: diastereoselectivity and enantioselectivity
inferred← citeshttps://doi.org/10.1039/b821092fopenalex-snapshot
Total synthesis of chiral biaryl natural products by asymmetric biaryl coupling
inferred← citeshttps://doi.org/10.1039/b915487fopenalex-snapshot
Regioselective copper-catalyzed chlorination and bromination of arenes with O2 as the oxidant
inferred← citeshttps://doi.org/10.1039/c2cc34659aopenalex-snapshot
Copper-mediated oxidative direct C–C (hetero)aromatic cross-coupling
inferred← citeshttps://doi.org/10.1039/c2cs15224jopenalex-snapshot
Recent advances in transition-metal catalyzed reactions using molecular oxygen as the oxidant
inferred← citeshttps://doi.org/10.1039/c2cs15323hopenalex-snapshot
Recent advances in copper-catalyzed dehydrogenative functionalization via a single electron transfer (SET) process
inferred← citeshttps://doi.org/10.1039/c3cc38675aopenalex-snapshot
Heterocoupling of 2-naphthols enabled by a copper–N-heterocyclic carbene complex
inferred← citeshttps://doi.org/10.1039/c3np70077aopenalex-snapshot
Transition metal-promoted biomimetic steps in total syntheses
inferred← citeshttps://doi.org/10.1039/c4cy01676aopenalex-snapshot
In-depth structure–selectivity investigations on asymmetric, copper-catalyzed oxidative biaryl coupling in the presence of 5-cis-substituted prolinamines
inferred← citeshttps://doi.org/10.1039/c4np00050aopenalex-snapshot
Xanthone dimers: a compound family which is both common and privileged
inferred← citeshttps://doi.org/10.1039/c5ob00200aopenalex-snapshot
Copper-catalysed cross-coupling: an untapped potential
inferred← citeshttps://doi.org/10.1039/c8ra09070jopenalex-snapshot
Base-promoted lipase-catalyzed kinetic resolution of atropisomeric 1,1′-biaryl-2,2′-diols
inferred← citeshttps://doi.org/10.1039/c9cc07834gopenalex-snapshot
An enantioselective oxidative coupling reaction of 2-naphthol derivatives catalyzed by chiral diphosphine oxide–iron( ii ) complexes
inferred← citeshttps://doi.org/10.1055/sos-sd-233-00026openalex-snapshot
2.3 Single-Electron-Transfer Oxidation and Reduction Involving Metal Complexes other than Samarium
inferred← citeshttps://doi.org/10.1142/9781848167513_0023openalex-snapshot
Sustainability Trends in Homogeneous Catalytic Oxidations
inferred← citeshttps://doi.org/10.1246/cl.130251openalex-snapshot
MnI2-catalyzed Dimerization of 2-Hydroxyanthracene
inferred← citeshttps://doi.org/10.2174/1570193x15666180418153713openalex-snapshot
Transition Metal Catalyzed Aerobic Asymmetric Coupling of 2-Naphthols
inferred← citeshttps://doi.org/10.26434/chemrxiv.9897818openalex-snapshot
Intermediacy of Copper(I) under Oxidative Conditions in the Aerobic Copper-Catalyzed Decarboxylative Thiolation of Benzoic Acids
inferred← citeshttps://doi.org/10.33774/chemrxiv-2021-zprv7openalex-snapshot
Enantioselective synthesis of atropisomeric indoles via iron catalysed oxidative cross-coupling
inferred← citeshttps://doi.org/10.33774/chemrxiv-2021-zprv7-v2openalex-snapshot
Enantioselective synthesis of atropisomeric indoles via iron catalysed oxidative cross-coupling
inferred← citeshttps://doi.org/10.3390/molecules25040852openalex-snapshot
Enantioselective Iron/Bisquinolyldiamine Ligand-Catalyzed Oxidative Coupling Reaction of 2-Naphthols
inferred← citeshttps://doi.org/10.70675/48de133czb428z472cza6b7zdb6f88641a01openalex-snapshot
Métallation chimiosélective des azobenzènes. Substitution nucléophile aromatique des acides naphtoïques en présence de ligands chiraux
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