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Iron-Catalyzed Asymmetric Aerobic Oxidation: Oxidative Coupling of 2-Naphthols
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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Discovery of Novel Catalysts for Alkene Epoxidation from Metal-Binding Combinatorial Libraries
inferredcites →https://doi.org/10.1002/1521-3765(20020301)8:5<1196::aid-chem1196>3.0.co;2-zopenalex-snapshot
Sulfide Oxidation by Hydrogen Peroxide Catalyzed by Iron Complexes: Two Metal Centers Are Better Than One
inferredcites →https://doi.org/10.1002/adsc.200404008openalex-snapshot
The Current Status and Future Trends in Oxidation Chemistry
inferredcites →https://doi.org/10.1002/adsc.200700519openalex-snapshot
Iron‐Catalyzed Aziridination Reactions
inferredcites →https://doi.org/10.1002/anie.200352635openalex-snapshot
Iron‐Catalyzed Asymmetric Sulfide Oxidation with Aqueous Hydrogen Peroxide
inferredcites →https://doi.org/10.1002/anie.200460108openalex-snapshot
Evidence for the Formation of an Iodosylbenzene(salen)iron Active Intermediate in a (Salen)iron( III )‐Catalyzed Asymmetric Sulfide Oxidation
inferredcites →https://doi.org/10.1002/anie.200460236openalex-snapshot
Highly Enantioselective Iron‐Catalyzed Sulfide Oxidation with Aqueous Hydrogen Peroxide under Simple Reaction Conditions
inferredcites →https://doi.org/10.1002/anie.200600529openalex-snapshot
Chiral Phosphoric Acids: Powerful Organocatalysts for Asymmetric Addition Reactions to Imines
inferredcites →https://doi.org/10.1002/anie.200701235openalex-snapshot
Iron‐Catalyzed Asymmetric Epoxidation of Aromatic Alkenes Using Hydrogen Peroxide
inferredcites →https://doi.org/10.1002/anie.200705061openalex-snapshot
Iron‐Catalyzed Asymmetric Olefin cis‐Dihydroxylation with 97 % Enantiomeric Excess
inferredcites →https://doi.org/10.1002/anie.200800012openalex-snapshot
Sustainable Metal Catalysis with Iron: From Rust to a Rising Star?
inferredcites →https://doi.org/10.1002/chem.200400857openalex-snapshot
Investigations on the Iron‐Catalyzed Asymmetric Sulfide Oxidation
inferredcites →https://doi.org/10.1002/chem.200700566openalex-snapshot
Iron‐Catalyzed Oxidation of Thioethers by Iodosylarenes: Stereoselectivity and Reaction Mechanism
inferredcites →https://doi.org/10.1002/chem.200800595openalex-snapshot
Biomimetic Iron‐Catalyzed Asymmetric Epoxidation of Aromatic Alkenes by Using Hydrogen Peroxide
inferredcites →https://doi.org/10.1002/cssc.200800071openalex-snapshot
Iron‐Catalyzed Hydrogenation, Hydride Transfer, and Hydrosilylation: An Alternative to Precious‐Metal Complexes?
inferredcites →https://doi.org/10.1002/tcr.20001openalex-snapshot
Selective aerobic oxidation of hydroxy compounds catalyzed by photoactivated ruthenium‐salen complexes (selective catalytic aerobic oxidation)
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Synthesis, Structure, and Spectroscopic Properties of a Dinuclear FeIII(μ2‐O)FeIII Complex Using a Strongly Electron‐Donating Ligand: Implications for the Generation of New High‐Valent Species
inferredcites →https://doi.org/10.1007/s10562-006-0162-3openalex-snapshot
An efficient oxidative coupling of naphthols catalyzed by Fe impregnated pillared montmorillonite K10
inferredcites →https://doi.org/10.1016/j.tet.2005.05.044openalex-snapshot
Oxidation of sulfides to sulfoxides. Part 2: Oxidation by hydrogen peroxide
inferredcites →https://doi.org/10.1016/j.tet.2006.06.069openalex-snapshot
Cu(I)-catalyzed asymmetric oxidative cross-coupling of 2-naphthol derivatives
inferredcites →https://doi.org/10.1016/j.tet.2008.01.110openalex-snapshot
Dual activation in oxidative coupling of 2-naphthols catalyzed by chiral dinuclear vanadium complexes
inferredcites →https://doi.org/10.1016/s0040-4039(97)00710-7openalex-snapshot
μ-Oxo diferric complexes as oxidation catalysts with hydrogen peroxide and their potential in asymmetric oxidation
inferredcites →https://doi.org/10.1021/cr020471zopenalex-snapshot
Metal-Catalyzed Epoxidations of Alkenes with Hydrogen Peroxide
inferredcites →https://doi.org/10.1021/cr030011lopenalex-snapshot
The Baeyer−Villiger Reaction: New Developments toward Greener Procedures
inferredcites →https://doi.org/10.1021/cr040664hopenalex-snapshot
Iron-Catalyzed Reactions in Organic Synthesis
inferredcites →https://doi.org/10.1021/ic800335topenalex-snapshot
Molecular and Electronic Structures of Mononuclear Iron Complexes Using Strongly Electron-Donating Ligands and their Oxidized Forms
inferredcites →https://doi.org/10.1021/ja015601kopenalex-snapshot
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inferredcites →https://doi.org/10.1021/ja071916+openalex-snapshot
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inferredcites →https://doi.org/10.1021/ja074322fopenalex-snapshot
Highly Enantioselective Oxidative Couplings of 2-Naphthols Catalyzed by Chiral Bimetallic Oxovanadium Complexes with Either Oxygen or Air as Oxidant
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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/jo00274a007openalex-snapshot
Oxidative coupling reactions of phenols with iron(III) chloride in the solid state
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/jo8021633openalex-snapshot
Iron(III) Chloride Catalyzed Oxidative Coupling of Aromatic Nuclei
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/ol026156gopenalex-snapshot
Catalytic Asymmetric Oxidative Couplings of 2-Naphthols by Tridentate N-Ketopinidene-Based Vanadyl Dicarboxylates
inferredcites →https://doi.org/10.1039/b101670iopenalex-snapshot
Chiral oxovanadium complex catalyzed enantioselective oxidative coupling of 2-naphthols
inferredcites →https://doi.org/10.1039/b303160hopenalex-snapshot
Green oxidation with aqueous hydrogen peroxide
inferredcites →https://doi.org/10.1039/b410307fopenalex-snapshot
Chiral self-dimerization of vanadium complexes on a SiO2 surface: the first heterogeneous catalyst for asymmetric 2-naphthol coupling
inferredcites →https://doi.org/10.1039/b801794hopenalex-snapshot
Iron-catalysed carbon–heteroatom and heteroatom–heteroatom bond forming processes
inferredcites →https://doi.org/10.1039/b804281kopenalex-snapshot
A chiral iron-sexipyridine complex as a catalyst for alkene epoxidation with hydrogen peroxide
inferredcites →https://doi.org/10.1246/bcsj.68.17openalex-snapshot
Recent Advances in Aerobic Oxygenation
inferredcites →https://doi.org/10.5363/tits.14.3_60openalex-snapshot
Green Oxidation with Aqueous Hydrogen Peroxide
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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(R)-2,2′-Dihydroxy-3,3′diphenyl-1,1′-binaphthyl
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Iron‐Catalyzed C C Bond Formation with C H Bond Activation
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Iron‐based Chiral Lewis Acids
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inferred← citeshttps://doi.org/10.1002/ajoc.201900602openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ajoc.202100002openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/ange.200902996openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.200902996openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201409694openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201511007openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201607893openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201608013openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201610168openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201804161openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201805203openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201813887openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201903435openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201903492openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.201904934openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.202004671openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.202007180openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.202008431openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.202014127openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.202301337openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/anie.202519818openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/cctc.201200266openalex-snapshot
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Isothiourea‐Catalysed Regioselective Acylative Kinetic Resolution of Axially Chiral Biaryl Diols
inferred← citeshttps://doi.org/10.1002/chem.201905595openalex-snapshot
Iron‐Catalyzed Oxidative C−C Cross‐Coupling Reaction of Tertiary Anilines with Hydroxyarenes by Using Air as Sole Oxidant**
inferred← citeshttps://doi.org/10.1002/chem.202001662openalex-snapshot
FeIII and FeII Phosphasalen Complexes: Synthesis, Characterization, and Catalytic Application for 2‐Naphthol Oxidative Coupling
inferred← citeshttps://doi.org/10.1002/chem.202203269openalex-snapshot
Atroposelective Synthesis of 2,2′‐Bis(arylamino)‐1,1′‐biaryls by Oxidative Iron(III)‐ and Phosphoric Acid‐Catalyzed C−C Coupling of Diarylamines**
inferred← citeshttps://doi.org/10.1002/chin.200939089openalex-snapshot
ChemInform Abstract: Iron‐Catalyzed Asymmetric Aerobic Oxidation: Oxidative Coupling of 2‐Naphthols.
inferred← citeshttps://doi.org/10.1002/chir.20843openalex-snapshot
Recent advances in asymmetric oxidative coupling of 2‐naphthol and its derivatives
inferred← citeshttps://doi.org/10.1002/cjoc.202000751openalex-snapshot
Chiral Phosphoric Acid Catalyzed Asymmetric Synthesis of Axially Chiral Compounds†
inferred← citeshttps://doi.org/10.1002/cssc.201902697openalex-snapshot
Cross‐Conjugated Polycatechol Organic Cathode for Aqueous Zinc‐Ion Storage
inferred← citeshttps://doi.org/10.1002/ejoc.201100512openalex-snapshot
Biaryl‐Bridged Salalen Ligands and Their Application in Titanium‐Catalyzed Asymmetric Epoxidation of Olefins with Aqueous H2O2
inferred← citeshttps://doi.org/10.1002/ejoc.201100740openalex-snapshot
Ruthenium‐Catalyzed Oxidative Dearomatization of Phenols to 4‐(tert‐Butylperoxy)cyclohexadienones: Synthesis of 2‐Substituted Quinones from p‐Substituted Phenols
inferred← citeshttps://doi.org/10.1002/ejoc.201201595openalex-snapshot
Cobalt(II)–Porphyrin‐Catalyzed Aerobic Oxidation: Oxidative Coupling of Phenols
inferred← citeshttps://doi.org/10.1002/ejoc.201403512openalex-snapshot
Copper‐Catalyzed Asymmetric Oxidative Cross‐Coupling of 2‐Naphthols with Aryl Methyl Ketones
inferred← citeshttps://doi.org/10.1002/ejoc.201900831openalex-snapshot
Iron and Phenol Co‐Catalysis for Rapid Synthesis of Nitriles under Mild Conditions
inferred← citeshttps://doi.org/10.1002/ejoc.201901583openalex-snapshot
Enantiodivergent Synthesis of Axially Chiral Biphenyls from σ‐Symmetric 1,1'‐Biphenyl‐2,6‐diol Derivatives by Single Lipase‐Catalyzed Acylative and Hydrolytic Desymmetrization
inferred← citeshttps://doi.org/10.1002/ijch.201700050openalex-snapshot
Recent Advances in Iron Catalyzed Oxidation Reactions of Organic Compounds
inferred← citeshttps://doi.org/10.1002/poc.3086openalex-snapshot
Preferential cross‐coupling of naphthol derivatives mediated by copper(II)
inferred← citeshttps://doi.org/10.1002/tcr.201500242openalex-snapshot
Asymmetric Synthesis of Chiral Atropisomeric Bis-Aryl Organophosphorus from Menthyl H-Phosphinate
inferred← citeshttps://doi.org/10.1002/tcr.201900003openalex-snapshot
Efficient Enantioselective Syntheses of Chiral Natural Products Facilitated by Ligand Design
inferred← citeshttps://doi.org/10.1007/128_2011_261openalex-snapshot
Radicals in Transition Metal Catalyzed Reactions? Transition Metal Catalyzed Radical Reactions? A Fruitful Interplay Anyway
inferred← citeshttps://doi.org/10.1007/128_2011_285openalex-snapshot
Radicals in Transition Metal Catalyzed Reactions? Transition Metal Catalyzed Radical Reactions? – A Fruitful Interplay Anyway
inferred← citeshttps://doi.org/10.1007/3418_2015_102openalex-snapshot
Enantioselective Iron Catalysts
inferred← citeshttps://doi.org/10.1007/978-981-10-3421-3_2openalex-snapshot
Metal Catalyzed Synthetic Reactions via Aerobic Oxidation as a Key Step
inferred← citeshttps://doi.org/10.1007/s10562-020-03353-2openalex-snapshot
Accurate Understanding the Catalytic Role of MnO2 in the Oxidative-Coupling of 2-naphthols into 1,1′-bi-2-naphthols
inferred← citeshttps://doi.org/10.1007/s11172-016-1356-5openalex-snapshot
A novel type of catalysts for asymmetric oxidative coupling of 2-naphthol
inferred← citeshttps://doi.org/10.1007/s11426-010-0027-xopenalex-snapshot
Synthesis of substituted benzoxazoles by the iron(III)-catalyzed aerobic oxidation process
inferred← citeshttps://doi.org/10.1007/s11426-021-1003-9openalex-snapshot
Synthesis of structurally diversified BINOLs and NOBINs via palladium-catalyzed C-H arylation with diazoquinones
inferred← citeshttps://doi.org/10.1007/s11426-022-1246-8openalex-snapshot
Asymmetric synthesis of binaphthyls through photocatalytic cross-coupling and organocatalytic kinetic resolution
inferred← citeshttps://doi.org/10.1007/s11426-025-2577-7openalex-snapshot
Chiral phosphoric acid-catalyzed atroposelective oxidative coupling of carbazoles
inferred← citeshttps://doi.org/10.1016/b978-0-08-097742-3.00318-9openalex-snapshot
3.13 Oxidative Coupling of Phenols and Phenol Ethers
inferred← citeshttps://doi.org/10.1016/b978-0-08-097774-4.00619-7openalex-snapshot
Application of Nontoxic Iron Salts in Oxidative CC Coupling Reactions
inferred← citeshttps://doi.org/10.1016/b978-0-08-097774-4.00620-3openalex-snapshot
Iron Complexes as Substitutes for Toxic Metals in Asymmetric Synthesis
inferred← citeshttps://doi.org/10.1016/b978-0-32-390644-9.00028-7openalex-snapshot
Oxidation: Asymmetric Oxidative Dearomatization
inferred← citeshttps://doi.org/10.1016/b978-0-32-390644-9.00119-0openalex-snapshot
Carbon–Carbon Bond Formation by Asymmetric Iron- and Cobalt-Catalyzed Reactions
inferred← citeshttps://doi.org/10.1016/b978-0-443-15680-9.00007-7openalex-snapshot
Homogeneous polymerization under green conditions
inferred← citeshttps://doi.org/10.1016/bs.acat.2024.06.001openalex-snapshot
Chiral iron complexes for asymmetric catalysis
inferred← citeshttps://doi.org/10.1016/j.catcom.2017.10.025openalex-snapshot
Highly efficient asymmetric aerobic oxidative coupling of 2-naphthols in the presence of bioinspired iron aminopyridine complexes
inferred← citeshttps://doi.org/10.1016/j.ccr.2015.07.006openalex-snapshot
Synthesis of axially chiral biaryl compounds by asymmetric catalytic reactions with transition metals
inferred← citeshttps://doi.org/10.1016/j.ccr.2018.11.001openalex-snapshot
Building molecular complexity through transition-metal-catalyzed oxidative annulations/cyclizations: Harnessing the utility of phenols, naphthols and 1,3-dicarbonyl compounds
inferred← citeshttps://doi.org/10.1016/j.gresc.2022.06.003openalex-snapshot
Construction of axially chiral compounds via catalytic asymmetric radical reaction
inferred← citeshttps://doi.org/10.1016/j.jece.2020.104268openalex-snapshot
Gold nanoparticle supported on mesoporous vanadium oxide for photo-oxidation of 2-naphthol with hydrogen peroxide and aerobic oxidation of benzyl alcohols
inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.139056openalex-snapshot
An overview of the synthesis, structures and magnetic properties of dinuclear iron complexes with salen type Schiff base ligands
inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.146736openalex-snapshot
Chiral Cu-Box-catalyzed asymmetric oxidative coupling of 2‑naphthols for the synthesis of 3,3′-disubstituted BINOLs
inferred← citeshttps://doi.org/10.1016/j.mtchem.2020.100377openalex-snapshot
Magnetic methylene-based mesoporous organosilica composite-supported IL/Pd: a powerful and highly recoverable catalyst for oxidative coupling of phenols and naphthols
inferred← citeshttps://doi.org/10.1016/j.poly.2016.03.023openalex-snapshot
Oxidative coupling of 2-naphthol catalyzed by a new methoxido bridged dinuclear oxidovanadium(V) complex
inferred← citeshttps://doi.org/10.1016/j.tet.2017.03.094openalex-snapshot
Iron-catalyzed selective oxidative arylation of phenols and biphenols
inferred← citeshttps://doi.org/10.1016/j.tet.2019.02.021openalex-snapshot
Oxidative phenol-arene and phenol-phenol cross-coupling using periodic acid
inferred← citeshttps://doi.org/10.1016/j.tet.2020.131645openalex-snapshot
Chiral vanadium complex-catalyzed oxidative coupling of arenols
inferred← citeshttps://doi.org/10.1016/j.tet.2025.134495openalex-snapshot
Copper–amine-complex-catalyzed highly selective oxidative cross-coupling of 2-naphthols: Synthesis of C-Symmetric BINOLs
inferred← citeshttps://doi.org/10.1016/j.tetasy.2010.01.023openalex-snapshot
Synthesis of salan (salalen) ligands derived from binaphthol for titanium-catalyzed asymmetric epoxidation of olefins with aqueous H2O2
inferred← citeshttps://doi.org/10.1016/j.tetasy.2010.05.050openalex-snapshot
The synthesis of novel tetradentate ligands derived from salen and their application in enantioselective silylcyanation of aldehydes
inferred← citeshttps://doi.org/10.1016/j.tetasy.2012.07.011openalex-snapshot
Asymmetric cyanohydrin synthesis using an aluminium(salan) complex
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.05.074openalex-snapshot
Iron-catalyzed Michael reactions revisited: a synthetically useful process for the preparation of tri-carbonyl compounds and chiral warfarin
inferred← citeshttps://doi.org/10.1016/j.tetlet.2012.11.109openalex-snapshot
An efficient oxidative coupling method for synthesis of novel diastereomeric biaryl diols derived from estrone
inferred← citeshttps://doi.org/10.1016/j.tetlet.2015.01.182openalex-snapshot
Convenient and rapid strategies towards 6-(hetero)aryl pyridylmethylamines: first catalytic issues
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.03.027openalex-snapshot
Cu-mediated C2-dehydrogenative homocoupling of indoles via C–H activation assisted by a removable N-pyrimidyl group
inferred← citeshttps://doi.org/10.1016/j.tetlet.2024.154929openalex-snapshot
Chemoselective synthesis of bridged benzo[no]tetraphen-8-one via copper-catalyzed radical dimerization of 1-alkynylnaphthols
inferred← citeshttps://doi.org/10.1021/acs.accounts.2c00545openalex-snapshot
Atroposelective Synthesis of C–C Axially Chiral Compounds via Mono- and Dinuclear Vanadium Catalysis
inferred← citeshttps://doi.org/10.1021/acs.chemrev.0c01306openalex-snapshot
Recent Advances in Catalytic Asymmetric Construction of Atropisomers
inferred← citeshttps://doi.org/10.1021/acs.chemrev.4c00132openalex-snapshot
Regioselective Substitution of BINOL
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00567openalex-snapshot
Oxidative C–H/C–H Coupling Reactions between Two (Hetero)arenes
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6c00255openalex-snapshot
Earth-Abundant 3d Transition Metal-Catalyzed Enantioselective C–H Functionalization
inferred← citeshttps://doi.org/10.1021/acs.jafc.4c07615openalex-snapshot
Streamlined Synthesis of Ellagitannins: Site-Selective Functionalization of the Glucose Core and Stereodivergent Construction of the Hexahydroxydiphenoic Groups
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00874openalex-snapshot
Mechanistic Insights into the FeCl3-Catalyzed Oxidative Cross-Coupling of Phenols with 2-Aminonaphthalenes
inferred← citeshttps://doi.org/10.1021/acs.joc.1c01406openalex-snapshot
Cr-Catalyzed Direct ortho-Aminomethylation of Phenols
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02435openalex-snapshot
Iron-Catalyzed Oxidative Cross-Coupling of Phenols and Tyrosine Derivatives with 3-Alkyloxindoles
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02485openalex-snapshot
Pd(II)-Catalyzed Azine-Assisted Enantioselective Oxidative C–H/C–H Cross-Coupling of Ferrocenes with Various Heteroarenes
inferred← citeshttps://doi.org/10.1021/acs.joc.3c02020openalex-snapshot
Decarboxylative Iodination and Suzuki-Miyaura Coupling Reactions to Access Chiral 3,3′-Diaryl-1,1′-bi-2-naphthols
inferred← citeshttps://doi.org/10.1021/acs.joc.4c01421openalex-snapshot
An Axially Chiral Quinoline-2-Carboxylic Acid-Cu Catalyst for Enantioselective Synthesis of C2- and C1-Symmetric BINOLs
inferred← citeshttps://doi.org/10.1021/acs.joc.5c01856openalex-snapshot
Chiral Copper Complex-Catalyzed Enantioselective Oxidative Cross-Coupling of 2-Naphthols for Synthesis of C 1 -Symmetric BINOLs
inferred← citeshttps://doi.org/10.1021/acs.joc.5c01897openalex-snapshot
Synthesis of 8-Aza- and 8,8′-Diaza-BINOL Derivatives through Cu(II)-TMEDA-Catalyzed Aerobic Oxidative Coupling
inferred← citeshttps://doi.org/10.1021/acs.joc.5c02152openalex-snapshot
Fe-BPsalan Complex-Catalyzed Asymmetric 1,3-Dipolar [3 + 2] Cycloaddition of Nitrones with α,β-Unsaturated Acyl Imidazoles
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02083openalex-snapshot
Enantioselective Vanadium-Catalyzed Oxidative Coupling: Development and Mechanistic Insights
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02494openalex-snapshot
Chiral Dinuclear Vanadium Complex-Mediated Oxidative Coupling of Resorcinols
inferred← citeshttps://doi.org/10.1021/acs.joc.8b03084openalex-snapshot
Selective Oxidative Phenol Coupling by Iron Catalysis
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00822openalex-snapshot
Cobalt(II)[salen]-Catalyzed Selective Aerobic Oxidative Cross-Coupling between Electron-Rich Phenols and 2-Naphthols
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c00048openalex-snapshot
Ruthenium-Catalyzed Cross-Selective Asymmetric Oxidative Coupling of Arenols
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02256openalex-snapshot
Cu-Catalyzed Site-Selective and Enantioselective Ring Opening of Cyclic Diaryliodoniums with 1,2,3-Triazoles
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02830openalex-snapshot
Catalytic Asymmetric Synthesis of Atropisomeric Nitrones: Versatile Intermediate for Axially Chiral Biaryls
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c01053openalex-snapshot
Nickel-Catalyzed Ring-Opening C–O Functionalization of peri-Xanthenoxanthenes for 8-Substituted Binaphthol Synthesis
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c00479openalex-snapshot
Novel Axially Chiral Ligand-Enabled Copper-Catalyzed Asymmetric Oxidative Coupling of 2-Naphthols for the Synthesis of 6,6′-Disubstituted BINOLs
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c00968openalex-snapshot
Rhodium-Catalyzed Atroposelective C–H Arylation of (Hetero)Arenes Using Carbene Precursors as Arylating Reagents
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c01355openalex-snapshot
Pd-Catalyzed Dynamic Kinetic Asymmetric Cross-Coupling of Heterobiaryl Bromides with N-Tosylhydrazones
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c00378openalex-snapshot
Biomimetic Total Synthesis of Bimagnolignan: A Natural Anti-Breast Cancer Agent
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c01582openalex-snapshot
Chiral α-Aminophosphonates as Ligands in Copper-Catalyzed Asymmetric Oxidative Coupling of 2-Naphthols
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c02482openalex-snapshot
Cu(I)-Catalyzed Atropselective Heterobiaryl Coupling Employing Umpoled Indoles
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c02927openalex-snapshot
Enantioselective Synthesis of 3-Iodo-4-arylcoumarinyl Atropisomers via Cu-Catalyzed Asymmetric Ring-Opening of Cyclic Hetero Diaryliodoniums
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c03491openalex-snapshot
Fe(III)-Catalyzed Highly Efficient Oxidative Cross-Coupling of 2-Naphthols and 2,6-Dihydroxynaphthalene with Furans
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c01760openalex-snapshot
Iron-Catalyzed Aerobic Oxidative Aromatic Coupling of Unprotected Primary Arylamines
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01152openalex-snapshot
Iron Phosphate Catalyzed Asymmetric Cross-Dehydrogenative Coupling of 2-Naphthols with β-Ketoesters
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01734openalex-snapshot
Reversal of Enantioselectivity Approach to BINOLs via Single and Dual 2-Naphthol Activation Modes
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b02552openalex-snapshot
Asymmetric Oxidative Coupling of Phenols and Hydroxycarbazoles
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b00800openalex-snapshot
Stereoselective Synthesis of Optically Pure 2-Amino-2′-hydroxy-1,1′-binaphthyls
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b02477openalex-snapshot
Cu-Catalyzed Enantioselective Atropisomer Synthesis via Thiolative Ring Opening of Five-Membered Cyclic Diaryliodoniums
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00927openalex-snapshot
Cascade Approach to Highly Functionalized Biaryls by a Nucleophilic Aromatic Substitution with Arylhydroxylamines
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02267openalex-snapshot
Copper-Catalyzed Enantioselective Ring-Opening of Cyclic Diaryliodoniums and O-Alkylhydroxylamines
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02425openalex-snapshot
NHC-Catalyzed Atroposelective Acylation of Phenols: Access to Enantiopure NOBIN Analogs by Desymmetrization
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b04555openalex-snapshot
Enantioselective Synthesis of Axially Chiral Biaryls via Copper-Catalyzed Thiolation of Cyclic Diaryliodonium Salts
inferred← citeshttps://doi.org/10.1021/acscatal.2c00318openalex-snapshot
Catalytic Oxidative Coupling of Phenols and Related Compounds
inferred← citeshttps://doi.org/10.1021/acscatal.4c00726openalex-snapshot
Axially Chiral Copper Catalyst for Asymmetric Synthesis of Valuable Diversely Substituted BINOLs
inferred← citeshttps://doi.org/10.1021/acscatal.4c01839openalex-snapshot
Aerobic Oxidative Coupling of 2-Aminonaphthalenes by Homogenous Nonheme Iron Catalysts
inferred← citeshttps://doi.org/10.1021/acscatal.5c04562openalex-snapshot
Enantioselective Synthesis of Axially Chiral Biphenols via Oxygen-Triggered Kinetic Resolution by Peptide-Phosphonium Salt Catalysis
inferred← citeshttps://doi.org/10.1021/acscatal.6c05589openalex-snapshot
Access to Atropisomeric Biaryls by Harnessing C−H Activation and Ring Opening of Cyclic Diaryliodonium Salts
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