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Iron catalyzed C N bond formation

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What this work says

Outgoing claims: the papers this work cites, builds on, or argues with.

inferredcites →https://doi.org/10.1002/9781118309872openalex-snapshot
Applications of Transition Metal Catalysis in Drug Discovery and Development
inferredcites →https://doi.org/10.1002/adsc.200700508openalex-snapshot
Iron‐Catalyzed CN Cross‐Coupling of Sulfoximines with Aryl Iodides
inferredcites →https://doi.org/10.1002/adsc.200900066openalex-snapshot
Iron‐Catalyzed Cross‐Coupling Reaction of Vinyl Bromides or Chlorides with Imidazoles in the Absence of Ligands and Additives
inferredcites →https://doi.org/10.1002/adsc.201200324openalex-snapshot
Iron‐Catalyzed CC Bond Cleavage and CN Bond Formation
inferredcites →https://doi.org/10.1002/anie.200602261openalex-snapshot
Regioselective Iron‐Catalyzed Allylic Amination
inferredcites →https://doi.org/10.1002/anie.200603173openalex-snapshot
Efficient Iron/Copper Co‐Catalyzed Arylation of Nitrogen Nucleophiles
inferredcites →https://doi.org/10.1002/anie.200703299openalex-snapshot
Iron‐Catalyzed N‐Arylation of Nitrogen Nucleophiles
inferredcites →https://doi.org/10.1002/anie.200902237openalex-snapshot
On the Role of Metal Contaminants in Catalyses with FeCl 3
inferredcites →https://doi.org/10.1002/anie.201501666openalex-snapshot
Cyclic Hypervalent Iodine Reagents and Iron Catalysts: The Winning Team for Late‐Stage CH Azidation
inferredcites →https://doi.org/10.1002/chem.200800293openalex-snapshot
Iron‐Catalyzed N‐Arylations of Amides
inferredcites →https://doi.org/10.1002/chem.201000581openalex-snapshot
[FeIII(F20‐tpp)Cl] Is an Effective Catalyst for Nitrene Transfer Reactions and Amination of Saturated Hydrocarbons with Sulfonyl and Aryl Azides as Nitrogen Source under Thermal and Microwave‐Assisted Conditions
inferredcites →https://doi.org/10.1007/3418_2015_103openalex-snapshot
Iron-Catalyzed Carbon–Nitrogen, Carbon–Phosphorus, and Carbon–Sulfur Bond Formation and Cyclization Reactions
inferredcites →https://doi.org/10.1007/978-3-642-40546-4openalex-snapshot
Amination and Formation of sp2 C-N Bonds
inferredcites →https://doi.org/10.1007/bf02987557openalex-snapshot
Biologically active natural products: Agrochemicals
inferredcites →https://doi.org/10.1007/s11434-012-5141-zopenalex-snapshot
Recent advances in the iron-catalyzed cycloaddition reactions
inferredcites →https://doi.org/10.1016/j.ica.2010.06.023openalex-snapshot
Copper(I) complexes with Schiff base and 1,2-bis(diphenylphosphino)ethane as ligands: Synthesis, structure and catalytic properties for the amination of aryl halide
inferredcites →https://doi.org/10.1016/j.inoche.2011.05.025openalex-snapshot
Mixed-ligand complexes of copper(I) with Schiff base and triphenylphosphine: Effective catalysts for the amination of aryl halide
inferredcites →https://doi.org/10.1016/j.tet.2012.06.015openalex-snapshot
Chan–Lam coupling reactions: synthesis of heterocycles
inferredcites →https://doi.org/10.1016/j.tet.2014.04.025openalex-snapshot
Iron-catalyzed synthesis of heterocycles
inferredcites →https://doi.org/10.1016/j.tetlet.2007.08.117openalex-snapshot
Solvent-free copper/iron co-catalyzed N-arylation reactions of nitrogen-containing heterocycles with trimethoxysilanes in air
inferredcites →https://doi.org/10.1016/j.tetlet.2007.11.176openalex-snapshot
An efficient FeCl3-catalyzed amidation reaction of secondary benzylic and allylic alcohols with carboxamides or p-toluenesulfonamide
inferredcites →https://doi.org/10.1016/j.tetlet.2009.02.208openalex-snapshot
FeCl3-catalyzed Ritter reaction. Synthesis of amides
inferredcites →https://doi.org/10.1016/j.tetlet.2009.08.018openalex-snapshot
Iron complex-catalyzed N-arylation of pyrazoles under aqueous medium
inferredcites →https://doi.org/10.1016/j.tetlet.2011.02.050openalex-snapshot
Copper ferrite nanoparticle-mediated N-arylation of heterocycles: a ligand-free reaction
inferredcites →https://doi.org/10.1016/j.tetlet.2015.05.048openalex-snapshot
Iron-catalyzed C–N bond formation via oxidative Csp3–H bond functionalization adjacent to nitrogen in amides and anilines: Synthesis of N-alkyl and N-benzyl azoles
inferredcites →https://doi.org/10.1016/s0040-4039(00)78485-1openalex-snapshot
Regioselective allylic amination catalyzed by iron salts
inferredcites →https://doi.org/10.1021/acs.accounts.5b00020openalex-snapshot
Transition-Metal-Catalyzed C–N Bond Forming Reactions Using Organic Azides as the Nitrogen Source: A Journey for the Mild and Versatile C–H Amination
inferredcites →https://doi.org/10.1021/acs.joc.5b00568openalex-snapshot
Method for the Synthesis of Phenothiazines via a Domino Iron-Catalyzed C–S/C–N Cross-Coupling Reaction
inferredcites →https://doi.org/10.1021/ar800039xopenalex-snapshot
The Promise and Challenge of Iron-Catalyzed Cross Coupling
inferredcites →https://doi.org/10.1021/bk-2013-1141.ch002openalex-snapshot
From the Rainforest to Your Grocery Store and Medicine Cabinet: 50 Years of Natural Products Research
inferredcites →https://doi.org/10.1021/cr040664hopenalex-snapshot
Iron-Catalyzed Reactions in Organic Synthesis
inferredcites →https://doi.org/10.1021/cr100198wopenalex-snapshot
Direct C−H Transformation via Iron Catalysis
inferredcites →https://doi.org/10.1021/cr500425uopenalex-snapshot
Iron Catalysis in Organic Synthesis
inferredcites →https://doi.org/10.1021/cr8002505openalex-snapshot
Copper-Mediated Coupling Reactions and Their Applications in Natural Products and Designed Biomolecules Synthesis
inferredcites →https://doi.org/10.1021/ic900219bopenalex-snapshot
C−H Bond Amination from a Ferrous Dipyrromethene Complex
inferredcites →https://doi.org/10.1021/ja211600gopenalex-snapshot
Iron-Catalyzed Intramolecular Allylic C–H Amination
inferredcites →https://doi.org/10.1021/ja309845kopenalex-snapshot
Iron-Catalyzed Aromatic Amination for Nonsymmetrical Triarylamine Synthesis
inferredcites →https://doi.org/10.1021/ja402082popenalex-snapshot
Enantioselective Iron-Catalyzed Azidation of β-Keto Esters and Oxindoles
inferredcites →https://doi.org/10.1021/ja412521kopenalex-snapshot
Synthesis of Anthranilic Acid Derivatives through Iron-Catalyzed Ortho Amination of Aromatic Carboxamides with N-Chloroamines
inferredcites →https://doi.org/10.1021/ja960088+openalex-snapshot
A Novel Intermediate in Allylic Amination Catalyzed by Iron Salts
inferredcites →https://doi.org/10.1021/ja964006topenalex-snapshot
On the Mechanism of Allylic Amination Catalyzed by Iron Salts
inferredcites →https://doi.org/10.1021/jo000708wopenalex-snapshot
Facile Preparation of Hydrazones by the Treatment of Azides with Hydrazines Catalyzed by FeCl3·6H2O
inferredcites →https://doi.org/10.1021/jo00080a034openalex-snapshot
Iron-catalyzed allylic amination
inferredcites →https://doi.org/10.1021/jo00123a044openalex-snapshot
Mechanistic aspects of iron-catalyzed allylic amination
inferredcites →https://doi.org/10.1021/jo061234popenalex-snapshot
A General and Efficient FeCl 3 -Catalyzed Nucleophilic Substitution of Propargylic Alcohols
inferredcites →https://doi.org/10.1021/jo200284aopenalex-snapshot
Iron(II)-Catalyzed Amidation of Aldehydes with Iminoiodinanes at Room Temperature and under Microwave-Assisted Conditions
inferredcites →https://doi.org/10.1021/jo201253mopenalex-snapshot
Direct C–N Coupling of Imidazoles and Benzylic Compounds via Iron-Catalyzed Oxidative Activation of C–H Bonds
inferredcites →https://doi.org/10.1021/jo301568eopenalex-snapshot
Iron-Catalyzed N-Alkylation of Azoles via Cleavage of an sp3C–H Bond Adjacent to a Nitrogen Atom
inferredcites →https://doi.org/10.1021/jo400804popenalex-snapshot
Amide Bond Formation through Iron-Catalyzed Oxidative Amidation of Tertiary Amines with Anhydrides
inferredcites →https://doi.org/10.1021/jo900595copenalex-snapshot
Iron-Catalyzed Amidation of Alkynyl Bromides: A Facile Route for the Preparation of Ynamides
inferredcites →https://doi.org/10.1021/jo901095copenalex-snapshot
Recyclable Heterogeneous Iron Catalyst for C−N Cross-Coupling under Ligand-Free Conditions
inferredcites →https://doi.org/10.1021/ol0170105openalex-snapshot
Formation of Aryl−Nitrogen, Aryl−Oxygen, and Aryl−Carbon Bonds Using Well-Defined Copper(I)-Based Catalysts
inferredcites →https://doi.org/10.1021/ol100670mopenalex-snapshot
Iron-Catalyzed N -Alkylation of Azoles via Oxidation of C−H Bond Adjacent to an Oxygen Atom
inferredcites →https://doi.org/10.1021/ol2024357openalex-snapshot
Iron-Catalyzed Oxidative Monoarylation of Primary Amines with Organozinc Reagents
inferredcites →https://doi.org/10.1021/ol402511ropenalex-snapshot
Iron-Catalyzed Ring-Opening Azidation and Allylation of O-Heterocycles
inferredcites →https://doi.org/10.1021/ol500573fopenalex-snapshot
Iron-Catalyzed Hetero-Cross-Dehydrogenative Coupling Reactions of Sulfoximines with Diarylmethanes: A New Route toN-Alkylated Sulfoximines
inferredcites →https://doi.org/10.1021/ol503587nopenalex-snapshot
C–N Bond Formation between Alcohols and Amines Using an Iron Cyclopentadienone Catalyst
inferredcites →https://doi.org/10.1021/ol800593popenalex-snapshot
Efficient Intermolecular Iron-Catalyzed Amidation of C−H Bonds in the Presence of N -Bromosuccinimide
inferredcites →https://doi.org/10.1021/ol801784aopenalex-snapshot
Efficient Iron-Catalyzed N-Arylation of Aryl Halides with Amines
inferredcites →https://doi.org/10.1038/nature14127openalex-snapshot
Metal-catalysed azidation of tertiary C–H bonds suitable for late-stage functionalization
inferredcites →https://doi.org/10.1038/nchembio0606-284openalex-snapshot
Making carbon-nitrogen bonds in biological and chemical synthesis
inferredcites →https://doi.org/10.1039/a807248eopenalex-snapshot
Iron-catalyzed allylic amination by nitroorganics
inferredcites →https://doi.org/10.1039/b402985mopenalex-snapshot
Natural products to drugs: natural product derived compounds in clinical trials
inferredcites →https://doi.org/10.1039/b823407hopenalex-snapshot
Copper catalyzed coupling of aryl chlorides, bromides and iodides with amines and amides
inferredcites →https://doi.org/10.1039/b917010copenalex-snapshot
Ligand-free iron/copper cocatalyzed N-arylations of aryl halides with amines under microwave irradiation
inferredcites →https://doi.org/10.1039/c0ob01102aopenalex-snapshot
An efficient synthesis of benzodiazepinyl phosphonates as clostripain inhibitors via FeCl3 catalyzed four-component reaction
inferredcites →https://doi.org/10.1039/c3ob27128eopenalex-snapshot
Iron-catalyzed N-alkylation using π-activated ethers as electrophiles
inferredcites →https://doi.org/10.1039/c3qo00087gopenalex-snapshot
Iron-catalyzed/mediated oxidative transformation of C–H bonds
inferredcites →https://doi.org/10.1039/c3ra44472dopenalex-snapshot
A green approach for the one-pot multi-component synthesis of N-substituted γ, δ and ε-lactams involving C–N bond formation catalyzed by FeCl3
inferredcites →https://doi.org/10.1039/c4cc01447bopenalex-snapshot
Fe-Catalysed oxidative C–H/N–H coupling between aldehydes and simple amides
inferredcites →https://doi.org/10.1039/c4cc08495kopenalex-snapshot
Synthesis of imidazo[1,2-a]pyridines: a decade update
inferredcites →https://doi.org/10.1039/c4qo00173gopenalex-snapshot
Generation of 1-(trifluoromethyl)isoquinolines via a copper-catalyzed reaction of isoquinoline-N-oxide with Togni reagent
inferredcites →https://doi.org/10.1039/c4qo00350kopenalex-snapshot
Cu- or Fe-catalyzed C–H/C–C bond nitrogenation reactions for the direct synthesis of N-containing compounds
inferredcites →https://doi.org/10.1039/c4ra04037fopenalex-snapshot
Iron-catalysed tandem isomerisation/hydrosilylation reaction of allylic alcohols with amines
inferredcites →https://doi.org/10.1039/c5cc03399copenalex-snapshot
Iron-catalyzed amination of alcohols assisted by Lewis acid
inferredcites →https://doi.org/10.1055/s-0030-1258379openalex-snapshot
Copper-Promoted Carbon-Heteroatom Bond Cross-Coupling with Boronic Acids and Derivatives
inferredcites →https://doi.org/10.1055/s-0034-1379540openalex-snapshot
Iron-Catalyzed C–N Bond Formation via the Beckmann Rearrangement
inferredcites →https://doi.org/10.1055/s-2003-42473openalex-snapshot
Renaissance of Ullmann and Goldberg Reactions - Progress in Copper Catalyzed C-N-, C-O- and C-S-Coupling
inferredcites →https://doi.org/10.1081/scc-100105881openalex-snapshot
2,4-DINITROPHENYLHYDROXYLAMINE: AN EFFICIENT AND MORE GENERAL REAGENT FOR IRON-CATALYZED ALLYLIC AMINATION
inferredcites →https://doi.org/10.1126/science.1233701openalex-snapshot
Complex N-Heterocycle Synthesis via Iron-Catalyzed, Direct C–H Bond Amination
inferredcites →https://doi.org/10.2174/138527208786241556openalex-snapshot
Recent Advances in Iron Catalysis in Organic Synthesis
inferredcites →https://doi.org/10.2174/138527210791317094openalex-snapshot
Recent Uses of Iron Catalysts in Organic Reactions
inferredcites →https://doi.org/10.2174/157017911794407683openalex-snapshot
Recent Progress in Transition-Metal-Catalyzed C-N Cross-Couplings: Emerging Approaches Towards Sustainability
inferredcites →https://doi.org/10.5155/eurjchem.5.4.612-617.1108openalex-snapshot
FeCl3-catalysed C-N coupling reaction between cyclic ethers and heterocyclic amines

What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

inferred← citeshttps://doi.org/10.2139/ssrn.4768767openalex-extracted
Coupling reaction catalyzed by copper(I) complex bearing (E)-4-(((1H-pyrrol-2-yl)methylene)amino)-1,5-dimethyl-2-phenyl-1H-pyrazol-3(2H)-one and triphenylphosphine
inferred← citeshttps://doi.org/10.2139/ssrn.4829364openalex-extracted
Coupling reaction catalyzed by copper(I) complex bearing (E)-4-(((1H-pyrrol-2-yl)methylene)amino)-1,5-dimethyl-2-phenyl-1H-pyrazol-3(2H)-one and triphenylphosphine
inferred← citeshttps://doi.org/10.1002/9783527809080.cataz03739openalex-snapshot
C‐N bond formation
inferred← citeshttps://doi.org/10.1002/adsc.201700833openalex-snapshot
A Simple and Efficient Method for the Preparation of α‐Halogenated Ketones Using Iron(III) Chloride and Iron(III) Bromide as Halogen Sources with Phenyliodonium Diacetate as Oxidant
inferred← citeshttps://doi.org/10.1002/adsc.201701183openalex-snapshot
Ligand‐free Iron(II)‐Catalyzed N‐Alkylation of Hindered Secondary Arylamines with Non‐activated Secondary and Primary Alcohols via a Carbocationic Pathway
inferred← citeshttps://doi.org/10.1002/adsc.202100081openalex-snapshot
Catalytic Formal Hydroamination of Allylic Alcohols Using Manganese PNP‐Pincer Complexes
inferred← citeshttps://doi.org/10.1002/ajoc.202400337openalex-snapshot
“Novel Metal‐Free Porphyrin with Ionic Liquid and Sulphonic Acid Moieties for Visible Light Assisted Photocatalytic C−N Coupling of Heterocyclic Compounds with Aryl Halides”
inferred← citeshttps://doi.org/10.1002/ange.202013687openalex-snapshot
Efficient Amination of Activated and Non‐Activated C(sp3)−H Bonds with a Simple Iron–Phenanthroline Catalyst
inferred← citeshttps://doi.org/10.1002/anie.202013687openalex-snapshot
Efficient Amination of Activated and Non‐Activated C(sp3)−H Bonds with a Simple Iron–Phenanthroline Catalyst
inferred← citeshttps://doi.org/10.1002/chem.201704401openalex-snapshot
Iron‐Catalyzed Hydroborylative Cyclization of 1,6‐Enynes
inferred← citeshttps://doi.org/10.1002/eom2.12273openalex-snapshot
3D hierarchical porous carbon foams as high‐performance free‐standing anodes for microbial fuel cells
inferred← citeshttps://doi.org/10.1002/hlca.202100173openalex-snapshot
Pd/Gorlos‐Phos‐Catalyzed Chemoselective Amination of Bromophenyl Chlorides with Primary Arylamines
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/slct.201902617openalex-snapshot
A Novel Recyclable Ni/Cu/Fe Termetallic Nanocatalyst for the Synthesis of Propargylamines through the A 3 ‐Coupling Reactions
inferred← citeshttps://doi.org/10.1016/bs.aihch.2019.01.003openalex-snapshot
The literature of heterocyclic chemistry, part XVII, 2017
inferred← citeshttps://doi.org/10.1016/j.est.2024.113050openalex-snapshot
Iron-assisted synthesis of nitrogen-doped carbon material for sodium-ion batteries
inferred← citeshttps://doi.org/10.1016/j.jorganchem.2024.123169openalex-snapshot
A highly efficient N-rich Cu-MOF heterogeneous catalyst based on N,N-bis(1H-tetrazole- 5-yl)amine for the A3 coupling reaction
inferred← citeshttps://doi.org/10.1016/j.poly.2022.115869openalex-snapshot
Copper complexes bearing tridentate salicylaldimine Schiff-base ligands: Synthesis, characterizations and catalytic performance in the oxidation reaction of alcohols
inferred← citeshttps://doi.org/10.1016/j.tet.2017.10.045openalex-snapshot
Synthesis of polysubstituted phenyl acetates via FeCl 3 -mediated domino reaction of 2-(aryl(piperidin-1-yl)methyl)phenols and 1,3-diketones
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.01.058openalex-snapshot
Iron-catalyzed aerobic oxidative cross-coupling amidation of N,N-dimethylanilines
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00988openalex-snapshot
Gold-Catalyzed Hydroamination of Propargylic Alcohols: Controlling Divergent Catalytic Reaction Pathways To Access 1,3-Amino Alcohols, 3-Hydroxyketones, or 3-Aminoketones
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b03160openalex-snapshot
Iron-Catalyzed Nitrene Transfer Reaction of 4-Hydroxystilbenes with Aryl Azides: Synthesis of Imines via C═C Bond Cleavage
inferred← citeshttps://doi.org/10.1021/acscatal.2c05293openalex-snapshot
Merging Photoinduced Iron-Catalyzed Decarboxylation with Copper Catalysis for C–N and C–C Couplings
inferred← citeshttps://doi.org/10.1021/acscatal.8b01879openalex-snapshot
Bisphosphines: A Prominent Ancillary Ligand Class for Application in Nickel-Catalyzed C–N Cross-Coupling
inferred← citeshttps://doi.org/10.1039/c7ob02124kopenalex-snapshot
FeCl 3 /ZnI 2 -Catalyzed regioselective synthesis of angularly fused furans
inferred← citeshttps://doi.org/10.1039/d0mh01088jopenalex-snapshot
Magnetically supported ionic liquids: a sustainable catalytic route for organic transformations
inferred← citeshttps://doi.org/10.1039/d0nj01610aopenalex-snapshot
N -Arylation of (hetero)arylamines using aryl sulfamates and carbamates via C–O bond activation enabled by a reusable and durable nickel(0) catalyst
inferred← citeshttps://doi.org/10.1039/d0ob01241fopenalex-snapshot
Fe( iii )-Catalyzed synthesis of steroidal imidazoheterocycles as potent antiproliferative agents
inferred← citeshttps://doi.org/10.1039/d0ra06518hopenalex-snapshot
Progress and prospects in copper-catalyzed C–H functionalization
inferred← citeshttps://doi.org/10.1039/d3ra06358eopenalex-snapshot
Clay based heterogeneous catalysts for carbon–nitrogen bond formation: a review
inferred← citeshttps://doi.org/10.1070/rcr4999openalex-snapshot
Metal-catalyzed reactions for the C(sp2)–N bond formation: achievements of recent years
inferred← citeshttps://doi.org/10.1080/00958972.2024.2443569openalex-snapshot
Copper(I) complex with (E)-4-(((1H-pyrrol-2-yl)methylene)amino)-1,5-dimethyl-2-phenyl-1H-pyrazol-3(2H) one and triphenylphosphine: an efficient catalyst for C-N coupling
inferred← citeshttps://doi.org/10.1134/s1068162024604622openalex-snapshot
Design, Synthesis, Antioxidant, Antitubercular Activity, and In Silico Studies of Novel α-Amino Phosphonates of Vanillin, a Potent Bioactive Molecule
inferred← citeshttps://doi.org/10.14233/ajchem.2022.23704openalex-snapshot
Recent Advances Review on Iron Complexes as Catalyst in Oxidation Reactions of Organic Compounds
inferred← citeshttps://doi.org/10.3389/fchem.2020.580086openalex-snapshot
Microwave-Assisted Synthesis of Quinazolines and Quinazolinones: An Overview
inferred← citeshttps://doi.org/10.3390/molecules24061145openalex-snapshot
Base-Promoted SNAr Reactions of Fluoro- and Chloroarenes as a Route to N-Aryl Indoles and Carbazoles
inferred← citeshttps://doi.org/10.3390/molecules28010356openalex-snapshot
Metal-Free Aerobic C–N Bond Formation of Styrene and Arylamines via Photoactivated Electron Donor–Acceptor Complexation
inferred← citeshttps://doi.org/10.70675/15ff0925z0144z46a6z8f4ez4f83c36576a8openalex-snapshot
Les réactions d'amination C(sp³)–H catalytiques par transfert de nitrènes : diversité moléculaire et éco-compatibilité
inferred← citeshttps://doi.org/10.70675/656eb804ze63bz48a6z84b3z2178c6efbcbfopenalex-snapshot
(Bi)metallic nanoparticles in glycerol : synthesis, characterization and catalytic aplications
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