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Amine synthesis via iron-catalysed reductive coupling of nitroarenes with alkyl halides

https://doi.org/10.1038/ncomms12494
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Outgoing claims: the papers this work cites, builds on, or argues with.

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Reductive Aminations of Carbonyl Compounds with Borohydride and Borane Reducing Agents
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Amino Group Chemistry
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Modern Synthetic Methods for Copper‐Mediated C(aryl)O, C(aryl)N, and C(aryl)S Bond Formation
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Modern Synthetic Methods for Copper‐Mediated C(aryl)O, C(aryl)N, and C(aryl)S Bond Formation
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Biaryl Phosphane Ligands in Palladium‐Catalyzed Amination
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Hydroaminations of Alkenes: A Radical, Revised, and Expanded Version
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Two‐Dimensional Acetylenic Scaffolding: Extended Donor‐Substituted Perethynylated Dehydroannulenes
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Amine‐bis(phenolate) Iron(III)‐Catalyzed Formal Hydroamination of Olefins
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ChemInform Abstract: REACTIONS OF ANTHRANILIUM SALTS WITH NUCLEOPHILES: ADDUCT FORMATION AND REARRANGEMENT
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ChemInform Abstract: Reductive Amination of Aldehydes and Ketones with Sodium Triacetoxyborohydride. Studies on Direct and Indirect Reductive Amination Procedures.
inferredcites →https://doi.org/10.1002/hc.520020414openalex-snapshot
Sodium arenetellurolate‐catalyzed reduction of nitroalkanes to oximes
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Synthesis of secondary amines
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PD0084430: a non-nucleoside inhibitor of human cytomegalovirus replication in vitro
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Evolution of a Fourth Generation Catalyst for the Amination and Thioetherification of Aryl Halides
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The Lipophilic Bullet Hits the Targets: Medicinal Chemistry of Adamantane Derivatives
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Large-Scale Applications of Transition Metal-Catalyzed Couplings for the Synthesis of Pharmaceuticals
inferredcites →https://doi.org/10.1021/cr500425uopenalex-snapshot
Iron Catalysis in Organic Synthesis
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Benzidine rearrangements. 17. The concerted nature of the one-proton p-semidine rearrangement of 4-methoxyhydrazobenzene
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The Utilization of Aliphatic Nitro Compounds. (I) The Production of Amines and (II) The Production of Oximes
inferredcites →https://doi.org/10.1021/ja037544wopenalex-snapshot
Intramolecular Charge Transfer with the Planarized 4-Aminobenzonitrile 1-tert-Butyl-6-cyano-1,2,3,4-tetrahydroquinoline (NTC6)
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Iron(I) in Negishi Cross-Coupling Reactions
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Rational Ligand Design for the Arylation of Hindered Primary Amines Guided by Reaction Progress Kinetic Analysis
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Preparation, Structure, and Reactivity of Nonstabilized Organoiron Compounds. Implications for Iron-Catalyzed Cross Coupling Reactions
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Z -Selective Olefin Synthesis via Iron-Catalyzed Reductive Coupling of Alkyl Halides with Terminal Arylalkynes
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The Medicinal Chemist’s Toolbox: An Analysis of Reactions Used in the Pursuit of Drug Candidates
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Reactions of anthranilium salts with nucleophiles: adduct formation and rearrangement
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3-Methyl-2,1-benzisoxazolium, benzisothiazolium, and indazolium salts as new active-methyl compounds
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Peracid oxidation of aliphatic amines: general synthesis of nitroalkanes
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Reductive Amination of Aldehydes and Ketones with Sodium Triacetoxyborohydride. Studies on Direct and Indirect Reductive Amination Procedures 1
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Highly Efficient, General Procedure for the Preparation of Alkylzinc Reagents from Unactivated Alkyl Bromides and Chlorides
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Iron(III)/NaBH4-Mediated Additions to Unactivated Alkenes: Synthesis of Novel 20′-Vinblastine Analogues
inferredcites →https://doi.org/10.1039/c0sc00107dopenalex-snapshot
Diamine ligands in copper-catalyzed reactions
inferredcites →https://doi.org/10.1039/c0sc00331jopenalex-snapshot
Dialkylbiaryl phosphines in Pd-catalyzed amination: a user's guide
inferredcites →https://doi.org/10.1039/c5sc04471eopenalex-snapshot
Chemoselective nitro reduction and hydroamination using a single iron catalyst
inferredcites →https://doi.org/10.1039/jr9390000773openalex-snapshot
160. N-oximino-ethers. Part V. Stereoisomeric N-aryl ethers of oximinophenylacetonitrile
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“Rapid and Inexpensive Method for Reduction of Nitroarenes to Anilines”
inferredcites →https://doi.org/10.1080/00397919908086201openalex-snapshot
A Novel Strategy for N-Alkylation of Primary Amines
inferredcites →https://doi.org/10.1081/scc-200054221openalex-snapshot
Reduction of Nitro‐Aryl Compounds with Zinc in the Presence of Poly[N‐(2‐aminoethyl)acrylamido]trimethylammonium Chloride as a Phase‐Transfer Catalyst
inferredcites →https://doi.org/10.1126/science.aab0245openalex-snapshot
Practical olefin hydroamination with nitroarenes

What points at this work

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

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Light-Switchable N-Alkylation Using Amine-Functionalized Mof
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Transamidation of Carboxamides and Amide Derivatives: Mechanistic Insights, Concepts, and Reactions
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Transition‐Metal‐Free Three‐Component Synthesis of Tertiary Aryl Amines from Nitro Compounds, Boronic Acids, and Trialkyl Phosphites
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Dual Nickel/Photoredox‐Catalyzed Synthesis of N‐formyl N,N’‐Diaryl Ethylenediamines via Multiple C−N/C−C Coupling of Nitroarenes with Trimethylamine
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Iron‐Catalyzed Reductive Deoxygenation of Nitroarenes to Access N ‐Heterocycles
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FeCl 3 ‐Catalyzed Photochemical Reductive Transamidation of Nitroarenes: A Sustainable Approach Using Sacrificial C−H Bonds
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Harnessing Nitroarenes in Streamlined Synthesis of 4‐Quinolones via Reductive C−N Coupling
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Selective Electroreductive N ‐Alkylation of Nitroarenes
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Reversal Reactivity of β‐Alkylnitroalkenes as 1,3‐Binucleophiles: Application to Nitroarenes using Organocatalysis
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Pd‐Catalyzed Mizoroki‐Heck Annulation and Equivalent Aminocarbonylation Reactions Enabled by Mo(CO) 6 ‐Mediated Direct Reduction of Nitro Derivatives
inferred← citeshttps://doi.org/10.1002/ange.201705356openalex-snapshot
Electrophilic Amination with Nitroarenes
inferred← citeshttps://doi.org/10.1002/ange.201804873openalex-snapshot
Cross‐Coupling of Alkyl Redox‐Active Esters with Benzophenone Imines: Tandem Photoredox and Copper Catalysis
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Reductive Molybdenum‐Catalyzed Direct Amination of Boronic Acids with Nitro Compounds
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Catalyst‐Free Reductive Coupling of Aromatic and Aliphatic Nitro Compounds with Organohalides
inferred← citeshttps://doi.org/10.1002/ange.201914851openalex-snapshot
PIII/PV=O Catalyzed Cascade Synthesis of N‐Functionalized Azaheterocycles
inferred← citeshttps://doi.org/10.1002/ange.202012877openalex-snapshot
Light‐Promoted C–N Coupling of Aryl Halides with Nitroarenes
inferred← citeshttps://doi.org/10.1002/ange.202015740openalex-snapshot
Fe‐Catalyzed Anaerobic Mukaiyama‐Type Hydration of Alkenes using Nitroarenes
inferred← citeshttps://doi.org/10.1002/ange.202416126openalex-snapshot
Harnessing the Reactivity of Nitroarene Radical Anions to Create Quinoline N ‐Oxides by Electrochemical Reductive Cyclization
inferred← citeshttps://doi.org/10.1002/ange.202416726openalex-snapshot
Photokatalytische PPh3‐vermittelte Synthese von C3‐funktionalisierten Indolen über radikalische Anellierung von Nitroaromaten und Alkenen
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Iron‐Catalyzed Reductive Allylic C─H Amination of Olefin with Nitroarenes via Intermolecular Nitroso Ene Reaction
inferred← citeshttps://doi.org/10.1002/anie.201705356openalex-snapshot
Electrophilic Amination with Nitroarenes
inferred← citeshttps://doi.org/10.1002/anie.201804873openalex-snapshot
Cross‐Coupling of Alkyl Redox‐Active Esters with Benzophenone Imines: Tandem Photoredox and Copper Catalysis
inferred← citeshttps://doi.org/10.1002/anie.201812806openalex-snapshot
Reductive Molybdenum‐Catalyzed Direct Amination of Boronic Acids with Nitro Compounds
inferred← citeshttps://doi.org/10.1002/anie.201814197openalex-snapshot
Catalyst‐Free Reductive Coupling of Aromatic and Aliphatic Nitro Compounds with Organohalides
inferred← citeshttps://doi.org/10.1002/anie.201914851openalex-snapshot
PIII/PV=O Catalyzed Cascade Synthesis of N‐Functionalized Azaheterocycles
inferred← citeshttps://doi.org/10.1002/anie.202012877openalex-snapshot
Light‐Promoted C–N Coupling of Aryl Halides with Nitroarenes
inferred← citeshttps://doi.org/10.1002/anie.202015740openalex-snapshot
Fe‐Catalyzed Anaerobic Mukaiyama‐Type Hydration of Alkenes using Nitroarenes
inferred← citeshttps://doi.org/10.1002/anie.202416126openalex-snapshot
Harnessing the Reactivity of Nitroarene Radical Anions to Create Quinoline N ‐Oxides by Electrochemical Reductive Cyclization
inferred← citeshttps://doi.org/10.1002/anie.202416726openalex-snapshot
Photocatalytic PPh3‐Mediated Synthesis of C3‐Functionalized Indoles via Radical Annulation of Nitroarenes and Alkenes
inferred← citeshttps://doi.org/10.1002/anie.202504750openalex-snapshot
Iron‐Catalyzed Reductive Allylic C─H Amination of Olefin with Nitroarenes via Intermolecular Nitroso Ene Reaction
inferred← citeshttps://doi.org/10.1002/aoc.6444openalex-snapshot
An overview of iron‐catalyzed N‐alkylation reactions
inferred← citeshttps://doi.org/10.1002/cctc.201900230openalex-snapshot
A Free‐Radical Reduction and Cyclization of Alkyl Halides Mediated by FeCl2
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Direct Reductive N‐Functionalization of Aliphatic Nitro Compounds
inferred← citeshttps://doi.org/10.1002/chem.202102000openalex-snapshot
Mo–Catalyzed One‐Pot Synthesis of N‐Polyheterocycles from Nitroarenes and Glycols with Recycling of the Waste Reduction Byproduct. Substituent‐Tuned Photophysical Properties
inferred← citeshttps://doi.org/10.1002/chem.202203807openalex-snapshot
Denitrative Hydroxylation of Unactivated Nitroarenes**
inferred← citeshttps://doi.org/10.1002/chem.202301978openalex-snapshot
Direct Synthesis of Unprotected Indolines Through Intramolecular sp3 C−H Amination Using Nitroarenes as Aryl Nitrene Precursors
inferred← citeshttps://doi.org/10.1002/cjoc.202300493openalex-snapshot
Decarboxylative Amination with Nitroarenes via Synergistic Catalysis †
inferred← citeshttps://doi.org/10.1002/cjoc.70029openalex-snapshot
Light‐Promoted Synthesis of Arylamines from Nitro Compounds and Grignard Reagents
inferred← citeshttps://doi.org/10.1002/cnma.202500038openalex-snapshot
Insights into Heterogeneous Catalysis for the Hydroamination and Hydroaminomethylation Processes of Olefins
inferred← citeshttps://doi.org/10.1002/cssc.202101203openalex-snapshot
Reductive C−N Coupling of Nitroarenes: Heterogenization of MoO3 Catalyst by Confinement in Silica
inferred← citeshttps://doi.org/10.1002/ejoc.202000330openalex-snapshot
Generating Skeletal Diversity and Complexity from Boron‐Substituted 1,3‐Dienes and Enophiles
inferred← citeshttps://doi.org/10.1002/ejoc.202300494openalex-snapshot
Reductive Buchwald‐Hartwig Amination of Nitroarenes with Aryl (pseudo)Halides
inferred← citeshttps://doi.org/10.1002/ejoc.202500293openalex-snapshot
Hypodiboric Acid–Sodium Carbonate Mediated Reductive Cyclization of Nitro(Hetero)Arenes: Synthesis of Imidazopyridines, Benz(oxa/thia)zoles, Benzoxazolones, and Benzoxathiones
inferred← citeshttps://doi.org/10.1002/jhet.3026openalex-snapshot
The Structure ofN‐phenyl‐pyrazoles and Indazoles: Mononitro, Dinitro, and Trinitro Derivatives
inferred← citeshttps://doi.org/10.1002/slct.201900460openalex-snapshot
Sustainable Amine Synthesis: Iron Catalyzed Reactions of Hydrosilanes with Imines, Amides, Nitroarenes and Nitriles
inferred← citeshttps://doi.org/10.1002/tcr.202400108openalex-snapshot
The Progress of Reductive Coupling Reaction by Iron Catalysis
inferred← citeshttps://doi.org/10.1007/s11426-021-1170-2openalex-snapshot
Visible-light-mediated tungsten-catalyzed C-H amination of unactivated alkanes with nitroarenes
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Recent Advances in the Synthesis of Piperidines: Functionalization of Preexisting Ring Systems
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Activated carbon supported bimetallic catalysts with combined catalytic effects for aromatic nitro compounds hydrogenation under mild conditions
inferred← citeshttps://doi.org/10.1016/j.apcatb.2019.118100openalex-snapshot
In situ coupled amorphous cobalt nitride with nitrogen-doped graphene aerogel as a trifunctional electrocatalyst towards Zn-air battery deriven full water splitting
inferred← citeshttps://doi.org/10.1016/j.apcatb.2024.123924openalex-snapshot
Light-Switchable N-Alkylation Using Amine-Functionalized MOF
inferred← citeshttps://doi.org/10.1016/j.cclet.2023.108303openalex-snapshot
Iron/B2pin2 catalytic system enables the generation of alkyl radicals from inert alkyl C-O bonds for amine synthesis
inferred← citeshttps://doi.org/10.1016/j.chempr.2018.04.008openalex-snapshot
Remote sp3 C–H Amination of Alkenes with Nitroarenes
inferred← citeshttps://doi.org/10.1016/j.jcat.2017.05.026openalex-snapshot
One-pot reductive amination of carbonyl compounds with nitro compounds with CO/H2O as the hydrogen donor over non-noble cobalt catalyst
inferred← citeshttps://doi.org/10.1016/j.jcat.2025.116050openalex-snapshot
Nickel-catalyzed C N bond formation of diarylamine between nitroarenes and aryl Grignard reagents
inferred← citeshttps://doi.org/10.1016/j.surfin.2025.107162openalex-snapshot
Cu-N-C supported on Al2O3 catalyzes N, N-dimethylation reaction of nitroarenes with methanol
inferred← citeshttps://doi.org/10.1016/j.talanta.2021.122919openalex-snapshot
Distribution visualization of the chlorinated disinfection byproduct of diazepam in zebrafish with desorption electrospray ionization mass spectrometry imaging
inferred← citeshttps://doi.org/10.1016/s1872-2067(20)63561-6openalex-snapshot
Intermediate formation enabled regioselective access to amide in the Pd-catalyzed reductive aminocarbonylation of olefin with nitroarene
inferred← citeshttps://doi.org/10.1021/acs.accounts.1c00115openalex-snapshot
Copper-Catalyzed Carbonylative Coupling of Alkyl Halides
inferred← citeshttps://doi.org/10.1021/acs.chemmater.2c02993openalex-snapshot
In Situ Construction of Single-Site Ti Active Centers on Carbon Nitride for Photocatalytic Chemoselective Hydrogen Transfer Reduction
inferred← citeshttps://doi.org/10.1021/acs.chemrev.8b00547openalex-snapshot
Reduction of Nitro Compounds Using 3d-Non-Noble Metal Catalysts
inferred← citeshttps://doi.org/10.1021/acs.iecr.7b03887openalex-snapshot
Mild and Selective Synthesis of Secondary Amines Direct from the Coupling of Two Aldehydes with Ammonia
inferred← citeshttps://doi.org/10.1021/acs.joc.2c01253openalex-snapshot
Palladium-Catalyzed Intramolecular Heck/Aminocarbonylation of Alkene-Tethered Iodobenzenes with Nitro Compounds: Synthesis of Carbamoyl-Substituted Benzoheterocycles
inferred← citeshttps://doi.org/10.1021/acs.joc.4c00591openalex-snapshot
B2(OH)4-Mediated Reductive Ring-Opening of N-Tosyl Aziridines by Nitroarenes: A Green and Regioselective Access to Vicinal Diamines
inferred← citeshttps://doi.org/10.1021/acs.joc.4c00673openalex-snapshot
Ruthenium-Catalyzed Selective Mono N-Ethylation of Arylamines and Tandem Reduction/N-Ethylation of Nitroarenes Using Triethylamine and Formic Acid
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00736openalex-snapshot
Nitrone Synthesis via Pair Electrochemical Coupling of Nitro-Compounds with Benzyl Alcohol Derivatives
inferred← citeshttps://doi.org/10.1021/acs.joc.9b01084openalex-snapshot
Copper-Catalyzed Cyanoalkylation of Amines via C–C Bond Cleavage: An Approach for C(sp3)–N Bond Formations
inferred← citeshttps://doi.org/10.1021/acs.joc.9b02068openalex-snapshot
Direct Amidation of Carboxylic Acids with Nitroarenes
inferred← citeshttps://doi.org/10.1021/acs.oprd.1c00410openalex-snapshot
Recent Advances in Nonprecious Metal Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c00183openalex-snapshot
Sequential C–S and S–N Coupling Approach to Sulfonamides
inferred← citeshttps://doi.org/10.1021/acs.orglett.0c03006openalex-snapshot
Photochemical Decarboxylative C(sp3)–X Coupling Facilitated by Weak Interaction of N-Heterocyclic Carbene
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c01654openalex-snapshot
NaI/PPh3-Mediated Photochemical Reduction and Amination of Nitroarenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.1c03343openalex-snapshot
Visible-Light- and PPh3-Mediated Direct C–N Coupling of Nitroarenes and Boronic Acids at Ambient Temperature
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c00781openalex-snapshot
Molybdenum-Mediated Reductive Hydroamination of Vinylcyclopropanes with Nitroarenes: Synthesis of Homoallylamines
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c01167openalex-snapshot
P(III)-Promoted Reductive Coupling of Aromatic and Aliphatic Nitro Compounds with Grignard Reagents
inferred← citeshttps://doi.org/10.1021/acs.orglett.3c01694openalex-snapshot
Nickel/Photoredox-Catalyzed Direct Amidation of Aldehydes with Nitroarenes via Fully Catalytic Process
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c02513openalex-snapshot
Metal and Photocatalyst-Free Amide Synthesis via Decarbonylative Condensation of Alkynes and Photoexcited Nitroarenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c03778openalex-snapshot
Molybdenum-Mediated Reductive ortho-Alkylation of Nitroarenes with Alcohols
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c04792openalex-snapshot
Cathodic Deoxygenative Alkylation of Nitro(hetero)arenes with Organic Halides
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c00624openalex-snapshot
Mo-Mediated Reductive Cyclization/Allylation of 2-Alkynyl Nitroarenes with 1,3-Dienes: Synthesis of 3-Allylindoles
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c00964openalex-snapshot
Copper-Catalyzed Reductive Hydroamination of Inactive Diarylacetylenes with Nitroarenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.5c04214openalex-snapshot
Asymmetric Synthesis of 2-Benzyl-2-arylindolin-3-ones by Iron-Catalyzed Reductive Benzylation of 2-Aryl-3 H -indole-3-ones
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c00890openalex-snapshot
Photoexcited Nitroarenes: A Workhorse for Strategic Synthesis of N -Heterocycles via Reductive C–N Coupling/Cyclization Cascade
inferred← citeshttps://doi.org/10.1021/acs.orglett.6c01492openalex-snapshot
Diaryl-Pyrazole Phosphine Ligand Design Enables Palladium-Catalyzed Denitrative C–H Arylation of N -Fused Azaheterocycles with Nitroarenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b00908openalex-snapshot
N-Trifluoromethylation of Nitrosoarenes with Sodium Triflinate
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b00813openalex-snapshot
A Strategy to Aminate Pyridines, Diazines, and Pharmaceuticals via Heterocyclic Phosphonium Salts
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b02109openalex-snapshot
Palladium-Catalyzed Carbonylative Synthesis of α,β-Unsaturated Amides from Styrenes and Nitroarenes
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b00191openalex-snapshot
Intramolecular Reductive Cyclization of o-Nitroarenes via Biradical Recombination
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b01849openalex-snapshot
CuH-Catalyzed Synthesis of 3-Hydroxyindolines and 2-Aryl-3H-indol-3-ones from o-Alkynylnitroarenes, Using Nitro as Both the Nitrogen and Oxygen Source
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02534openalex-snapshot
Cobalt(II)-Catalyzed Alkoxycarbonylation of Aliphatic Amines via C–N Bond Activation
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b04092openalex-snapshot
Synergistic Copper-Catalyzed Reductive Aminocarbonylation of Alkyl Iodides with Nitroarenes
inferred← citeshttps://doi.org/10.1021/acscatal.3c06351openalex-snapshot
Aminations of Aryl Halides Using Nitroaromatics as Coupling Partners: Overcoming the Hydrodehalogenation Pathway under a Hydrogen Atmosphere in Water
inferred← citeshttps://doi.org/10.1021/acscatal.4c04404openalex-snapshot
Molybdenum-Catalyzed Reductive Ortho-Allylation of Nitroarenes with 1,3-Dienes
inferred← citeshttps://doi.org/10.1021/acscatal.7b02859openalex-snapshot
Nickel-Catalyzed Reductive Transamidation of Secondary Amides with Nitroarenes
inferred← citeshttps://doi.org/10.1021/acscatal.9b03604openalex-snapshot
Iron-Catalyzed Reductive Coupling of Nitroarenes with Olefins: Intermediate of Iron–Nitroso Complex
inferred← citeshttps://doi.org/10.1021/acscatal.9b05049openalex-snapshot
Reductive Cleavage of Azoarene as a Key Step in Nickel-Catalyzed Amidation of Esters with Nitroarenes
inferred← citeshttps://doi.org/10.1021/acsomega.9b01608openalex-snapshot
Synthesis of Mono- N -Methyl Aromatic Amines from Nitroso Compounds and Methylboronic Acid
inferred← citeshttps://doi.org/10.1021/jacs.0c01666openalex-snapshot
An Improved PIII/PV═O-Catalyzed Reductive C–N Coupling of Nitroaromatics and Boronic Acids by Mechanistic Differentiation of Rate- and Product-Determining Steps
inferred← citeshttps://doi.org/10.1021/jacs.0c08035openalex-snapshot
P(III)/P(V)-Catalyzed Methylamination of Arylboronic Acids and Esters: Reductive C–N Coupling with Nitromethane as a Methylamine Surrogate
inferred← citeshttps://doi.org/10.1021/jacs.2c01487openalex-snapshot
Enabling Reductive C–N Cross-Coupling of Nitroalkanes and Boronic Acids by Steric Design of P(III)/P(V)═O Catalysts
inferred← citeshttps://doi.org/10.1021/jacs.2c12450openalex-snapshot
Tandem C/N-Difunctionalization of Nitroarenes: Reductive Amination and Annulation by a Ring Expansion/Contraction Sequence
inferred← citeshttps://doi.org/10.1021/jacs.3c04647openalex-snapshot
Reductive Arylation of Nitroarenes with Chloroarenes: Reducing Conditions Enable New Reactivity from Palladium Catalysts
inferred← citeshttps://doi.org/10.1021/jacs.5c11470openalex-snapshot
Iron-Catalyzed Asymmetric Reductive Cross-Coupling of Ketimines with Alkyl Iodides
inferred← citeshttps://doi.org/10.1021/jacs.6c06427openalex-snapshot
Electrochemical Strain-Release Difunctionalization of Azabicyclo-[1.1.0]butanes with Nitroarenes
inferred← citeshttps://doi.org/10.1021/jacs.6c11412openalex-snapshot
General Synthesis of γ-Arylamino Alcohols via Difunctionalization of Terminal Alkenes Using a Supported Cobalt Single-Atom Catalyst
inferred← citeshttps://doi.org/10.1021/jacs.7b05279openalex-snapshot
Practical Singly and Doubly Electrophilic Aminating Agents: A New, More Sustainable Platform for Carbon–Nitrogen Bond Formation
inferred← citeshttps://doi.org/10.1021/jacs.8b03739openalex-snapshot
Manganese-Mediated Reductive Transamidation of Tertiary Amides with Nitroarenes
inferred← citeshttps://doi.org/10.1021/jacs.8b10769openalex-snapshot
Intermolecular Reductive C–N Cross Coupling of Nitroarenes and Boronic Acids by P III /P V ═O Catalysis
inferred← citeshttps://doi.org/10.1038/ncomms13776openalex-snapshot
Erratum: Amine synthesis via iron-catalysed reductive coupling of nitroarenes with alkyl halides
inferred← citeshttps://doi.org/10.1038/ncomms14878openalex-snapshot
Direct amidation of esters with nitroarenes
inferred← citeshttps://doi.org/10.1038/s41467-021-26767-xopenalex-snapshot
SET activation of nitroarenes by 2-azaallyl anions as a straightforward access to 2,5-dihydro-1,2,4-oxadiazoles
inferred← citeshttps://doi.org/10.1038/s41467-022-30176-zopenalex-snapshot
Decarboxylative tandem C-N coupling with nitroarenes via SH2 mechanism
inferred← citeshttps://doi.org/10.1038/s41467-024-50596-3openalex-snapshot
Electrochemical deoxygenative amination of stabilized alkyl radicals from activated alcohols
inferred← citeshttps://doi.org/10.1038/s41929-017-0023-zopenalex-snapshot
Decarboxylative C(sp3)–N cross-coupling via synergetic photoredox and copper catalysis
inferred← citeshttps://doi.org/10.1039/c7sc03950fopenalex-snapshot
Amide synthesis via nickel-catalysed reductive aminocarbonylation of aryl halides with nitroarenes
inferred← citeshttps://doi.org/10.1039/c8cc08470jopenalex-snapshot
Metal free direct C(sp 2 )–H arylaminations using nitrosoarenes to 2-hydroxy-di(het)aryl amines as multifunctional Aβ-aggregation modulators
inferred← citeshttps://doi.org/10.1039/c8ob01172aopenalex-snapshot
Synthesis of N -arylsulfonamides via Fe-promoted reaction of sulfonyl halides with nitroarenes in an aqueous medium
inferred← citeshttps://doi.org/10.1039/c8qo01405aopenalex-snapshot
Manganese-mediated reductive amidation of esters with nitroarenes
inferred← citeshttps://doi.org/10.1039/c9cc06638aopenalex-snapshot
Direct amide synthesis via Ni-mediated aminocarbonylation of arylboronic acids with CO and nitroarenes
inferred← citeshttps://doi.org/10.1039/c9ob01751hopenalex-snapshot
Functionalization of activated methylene C–H bonds with nitroarenes and sulfur for the synthesis of thioamides
inferred← citeshttps://doi.org/10.1039/c9ob02457copenalex-snapshot
Brønsted acid/visible-light-promoted Markovnikov hydroamination of vinylarenes with arylamines
inferred← citeshttps://doi.org/10.1039/d0cc00826eopenalex-snapshot
Metal free amination of congested and functionalized alkyl bromides at room temperature
inferred← citeshttps://doi.org/10.1039/d0cc03098hopenalex-snapshot
Direct N -formylation of nitroarenes with CO 2
inferred← citeshttps://doi.org/10.1039/d0cc03258aopenalex-snapshot
Step and redox efficient nitroarene to indole synthesis
inferred← citeshttps://doi.org/10.1039/d0cc04062bopenalex-snapshot
Deaminative carbonylative coupling of alkylamines with styrenes under transition-metal-free conditions
inferred← citeshttps://doi.org/10.1039/d0cc06023bopenalex-snapshot
Radical chemistry of nitrosoarenes: concepts, synthetic applications and directions
inferred← citeshttps://doi.org/10.1039/d0nj04673fopenalex-snapshot
Sustainable route for the synthesis of flower-like Ni@N-doped carbon nanosheets from bagasse and its catalytic activity towards reductive amination of nitroarenes with bio-derived aldehydes
inferred← citeshttps://doi.org/10.1039/d0qo00563kopenalex-snapshot
Recent advances in nitro-involved radical reactions
inferred← citeshttps://doi.org/10.1039/d0qo01479fopenalex-snapshot
Deaminative carbonylative thioesterification of activated alkylamines with thiophenols under transition-metal-free conditions
inferred← citeshttps://doi.org/10.1039/d0ra09639copenalex-snapshot
Highly economical and direct amination of sp 3 carbon using low-cost nickel pincer catalyst
inferred← citeshttps://doi.org/10.1039/d0ra10868eopenalex-snapshot
Fe-mediated synthesis of N -aryl amides from nitroarenes and acyl chlorides
inferred← citeshttps://doi.org/10.1039/d1qo00386kopenalex-snapshot
Iron- and zinc-mediated reductive coupling of styrenes and alkyl bromides: mechanistic investigation using DFT calculations
inferred← citeshttps://doi.org/10.1039/d1qo01269jopenalex-snapshot
Ruthenium-catalysed chemoselective alkylation of nitroarenes with alkanols
inferred← citeshttps://doi.org/10.1039/d2qo00010eopenalex-snapshot
Palladium-catalyzed denitrative N -arylation of nitroarenes with pyrroles, indoles, and carbazoles
inferred← citeshttps://doi.org/10.1039/d2qo00576jopenalex-snapshot
Arylations with nitroarenes for one-pot syntheses of triaryl-methanols and tetraarylmethanes
inferred← citeshttps://doi.org/10.1039/d2qo00706aopenalex-snapshot
Copper-promoted cross-coupling of nitroarenes with 4-alkyl-1,4-dihydropyridines using a peroxide-driven radical reductive strategy
inferred← citeshttps://doi.org/10.1039/d2qo00928eopenalex-snapshot
Manganese-mediated reductive N , N -dialkylation of nitroarenes: a dramatic NiI 2 effect
inferred← citeshttps://doi.org/10.1039/d2qo01700hopenalex-snapshot
Exploring visible light for carbon–nitrogen and carbon–oxygen bond formation via nickel catalysis
inferred← citeshttps://doi.org/10.1039/d2sc03047kopenalex-snapshot
Photomediated reductive coupling of nitroarenes with aldehydes for amide synthesis
inferred← citeshttps://doi.org/10.1039/d3gc01544kopenalex-snapshot
Visible-light-induced iron-catalyzed synthesis of N -aryl amides from nitroarenes and chloroalkanes
inferred← citeshttps://doi.org/10.1039/d3ob01728aopenalex-snapshot
Reductive transamidation of tertiary amides with nitroarenes enabled by magnesium and chlorosilane
inferred← citeshttps://doi.org/10.1039/d3qo01124kopenalex-snapshot
Nickel-catalyzed reductive coupling of nitroarenes and phosphine oxides to access phosphinic amides
inferred← citeshttps://doi.org/10.1039/d3ra05100eopenalex-snapshot
Reductive coupling of nitro compounds with boronic acid derivatives: an overview
inferred← citeshttps://doi.org/10.1039/d3sc06618eopenalex-snapshot
Dual role of nitroarenes as electrophiles and arylamine surrogates in Buchwald–Hartwig-type coupling for C–N bond construction
inferred← citeshttps://doi.org/10.1039/d4cc02582bopenalex-snapshot
Shining light on the nitro group: distinct reactivity and selectivity
inferred← citeshttps://doi.org/10.1039/d4ob00656aopenalex-snapshot
Visible light-induced reductive aza-6π electrocyclization access to phenanthridines
inferred← citeshttps://doi.org/10.1039/d4ob01654hopenalex-snapshot
Recent advances in the synthetic applications of nitrosoarene chemistry
inferred← citeshttps://doi.org/10.1039/d4ob01714eopenalex-snapshot
Visible-light-induced aerobic oxidative cyclization of nitroarenes with triethylamine using an organophotocatalyst
inferred← citeshttps://doi.org/10.1039/d4ob01928hopenalex-snapshot
Transformative reactions in nitroarene chemistry: C–N bond cleavage, skeletal editing, and N–O bond utilization
inferred← citeshttps://doi.org/10.1039/d4qo00059eopenalex-snapshot
Recent progress in the synthesis of N -substituted arylamines by reductive cross-coupling of nitroarenes
inferred← citeshttps://doi.org/10.1039/d4qo00687aopenalex-snapshot
Silacarboxylic acid-mediated photoredox Z -stereoselective fluoroalkylation of alkynes
inferred← citeshttps://doi.org/10.1039/d4qo00956hopenalex-snapshot
Molybdenum-mediated reductive deuteration of nitroarenes with D 2 O: synthesis of ortho - and para -deuterated anilines
inferred← citeshttps://doi.org/10.1039/d4qo01692kopenalex-snapshot
A domino reaction strategy for facile and modular construction of synthetically challenging functionalized ortho -fluoroanilines
inferred← citeshttps://doi.org/10.1039/d5ma00711aopenalex-snapshot
Selective and sustainable nitro reduction and reductive N -alkylation using a recyclable V 2 O 5 /TiO 2 catalyst for amine synthesis
inferred← citeshttps://doi.org/10.1039/d5qo00019jopenalex-snapshot
Synthesis of carbazoles: light-promoted tandem coupling of nitroarenes with Grignard reagents
inferred← citeshttps://doi.org/10.1039/d5qo01269dopenalex-snapshot
Electrochemically driven reductive coupling of nitroarenes with alkyl bromides
inferred← citeshttps://doi.org/10.1039/d6cc03378dopenalex-snapshot
Emerging ground-state and photoexcited-state reactivity of the nitro group
inferred← citeshttps://doi.org/10.1039/d6qo00188bopenalex-snapshot
Rotating magnetic field-enhanced PPh 3 -mediated deoxygenative C–N coupling of nitroarenes with boronic acids
inferred← citeshttps://doi.org/10.1039/d6qo01036aopenalex-snapshot
Photoexcited nitroarene-catalyzed aliphatic C–H functionalization via direct hydrogen atom transfer in flow
inferred← citeshttps://doi.org/10.1055/a-1792-6579openalex-snapshot
Recent Advances to Mediate Reductive Processes of Nitroarenes Using Single-Electron Transfer, Organomagnesium, or Organozinc Reagents
inferred← citeshttps://doi.org/10.1055/a-1817-0882openalex-snapshot
DBU- and DABCO-Promoted Selective Access to 2,5-Diarylnitrobenzoates and Cyclohexenones via One-Pot Reactions
inferred← citeshttps://doi.org/10.1055/s-0042-1751503openalex-snapshot
Direct Reductive Coupling of Nitro Compounds for the Synthesis of Advanced Amines
inferred← citeshttps://doi.org/10.14233/ajchem.2019.21857openalex-snapshot
Unusual Cleavage of N-N Bond of 1-Arylamino-1,2,3-triazole Derivatives: A Simple and Alternate Approach to 4,5-Disubstituted-1H-1,2,3-triazoles
inferred← citeshttps://doi.org/10.21203/rs.3.rs-9897056/v1openalex-snapshot
Direct and Diverse Synthesis of γ‑Amino Alcohols via Difunctionalization of Terminal Alkenes Using a Supported Cobalt Single‑Atom Catalyst
inferred← citeshttps://doi.org/10.2174/1385272826666220509142255openalex-snapshot
The Coupling of Carbon and Nitrogen Substituents with Nitroarenes: Vicarious Nucleophilic Substitution of Hydrogen in Nitroarenes
inferred← citeshttps://doi.org/10.3390/molecules25020410openalex-snapshot
Cross-Linked Cyclodextrins Bimetallic Nanocatalysts: Applications in Microwave-Assisted Reductive Aminations
inferred← citeshttps://doi.org/10.52396/justc-2022-0119openalex-snapshot
Nickel-catalyzed alkene ipso-selective reductive hydroamination with nitroarenes
inferred← citeshttps://doi.org/10.6023/cjoc202109037openalex-snapshot
Photochemical Reduction of Nitroaromatics Mediated by p-Toluenethiol/PCy3
inferred← citeshttps://doi.org/10.6023/cjoc202502017openalex-snapshot
Recent Progress on Radical-Mediated Activation of Nitroarenes
inferred← citeshttps://doi.org/10.70675/0380b41fz3c31z4ef1zb15az10065f5c9181openalex-snapshot
Development of novel heterogeneous selective catalysts for the direct amination of alcohols
inferred← citeshttps://doi.org/10.70675/504f874cz5e55z40a3za31bz4b4466e207d1openalex-snapshot
Utilisation d’organoboranes fonctionnalisés pour la construction de structures polycycliques
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