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Cs2CO3‐Promoted Direct N‐Alkylation: Highly Chemoselective Synthesis of N‐Alkylated Benzylamines and Anilines

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Metal‐Free Reductive Cleavage of CN and SN Bonds by Photoactivated Electron Transfer from a Neutral Organic Donor
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Stereocontrolled Total Synthesis of (+)‐Streptazolin by a Palladium‐Catalyzed Reductive Diyne Cyclization
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Biaryl Phosphane Ligands in Palladium‐Catalyzed Amination
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Selective Amine Cross‐Coupling Using Iridium‐Catalyzed “Borrowing Hydrogen” Methodology
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Metal‐Free Reductive Cleavage of CN and SN Bonds by Photoactivated Electron Transfer from a Neutral Organic Donor
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Synthesis of vinyl fluorides by ring-closing metathesis
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A mild and selective method for N-dealkylation of tertiary amines
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Potassium iodide catalysed monoalkylation of anilines under microwave irradiation
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A mild and highly convenient chemoselective alkylation of thiols using Cs2CO3–TBAI
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Reductive amination of carbonyl compounds using NaBH4 in a Brønsted acidic ionic liquid
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Regioselective synthesis of novel substituted pyrazolo[1,5-a]pyrimidines under solvent-free conditions
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inferredcites →https://doi.org/10.1016/j.tetlet.2014.11.044openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4020(01)00722-0openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0040-4020(01)00989-9openalex-snapshot
N-Alkylation of anilines, carboxamides and several nitrogen heterocycles using CsF–Celite/alkyl halides/CH3CN combination
inferredcites →https://doi.org/10.1021/acs.joc.5b02342openalex-snapshot
Synergistic Effect of the TiCl4/p-TsOH Promoter System on the Aza-Prins Cyclization
inferredcites →https://doi.org/10.1021/acscatal.5b01038openalex-snapshot
Magnesium-Catalyzed Mild Reduction of Tertiary and Secondary Amides to Amines
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Efficient Catalyst-Free Four-Component Synthesis of Novel γ-Aminoethers Mediated by a Mannich Type Reaction
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Highly Reactive, General and Long-Lived Catalysts for Palladium-Catalyzed Amination of Heteroaryl and Aryl Chlorides, Bromides, and Iodides: Scope and Structure–Activity Relationships
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inferredcites →https://doi.org/10.1021/ja304547sopenalex-snapshot
Iridium-Catalyzed Reduction of Secondary Amides to Secondary Amines and Imines by Diethylsilane
inferredcites →https://doi.org/10.1021/ja411911sopenalex-snapshot
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inferredcites →https://doi.org/10.1021/ja5093612openalex-snapshot
Direct Catalytic N-Alkylation of Amines with Carboxylic Acids
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Facile synthesis of amino acid and peptide esters under mild conditions via cesium salts
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Cesium Effect: High Chemoselectivity in Direct N-Alkylation of Amines
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Reaction of Functionalized Anilines with Dimethyl Carbonate over NaY Faujasite. 3. Chemoselectivity toward Mono-N-methylation
inferredcites →https://doi.org/10.1021/jo048076ropenalex-snapshot
Mono-N-methylation of Functionalized Anilines with Alkyl Methyl Carbonates over NaY Faujasites. 4. Kinetics and Selectivity
inferredcites →https://doi.org/10.1021/jo062060eopenalex-snapshot
CuBr/rac-BINOL-Catalyzed N-Arylations of Aliphatic Amines at Room Temperature
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Borrowing Hydrogen Methodology for Amine Synthesis under Solvent-Free Microwave Conditions
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Effective Monoallylation of Anilines Catalyzed by Supported KF
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Mild Nonepimerizing N-Alkylation of Amines by Alcohols without Transition Metals
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Hydroamination of Carbonyl Compounds with Oximes
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inferred← citeshttps://doi.org/10.1016/j.mcat.2019.110507openalex-snapshot
Mild and efficient synthesis of secondary aromatic amines by one-pot stepwise reductive amination of arylaldehydes with nitroarenes promoted by reusable nickel nanoparticles
inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.145647openalex-snapshot
N-Benzylation of 3-(Methylthio)-1H-1,2,4-triazol-5-amine Governed by Solvent-Stabilized Tautomerism: Crystallographic and DFT Insights
inferred← citeshttps://doi.org/10.1016/j.molstruc.2026.147489openalex-snapshot
Immobilization of zwitterion-functionalized ionic liquids on covalent organic frameworks for efficient CO2 fixation towards carbamate synthesis and N-formylation
inferred← citeshttps://doi.org/10.1016/j.rechem.2024.101986openalex-snapshot
Synthesis, in silico and antimicrobial activity study of substituted aromatic imines and their corresponding amines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2019.151122openalex-snapshot
Regioselective single-step synthesis of 2-aminoimidazole derivatives
inferred← citeshttps://doi.org/10.1021/acs.accounts.2c00302openalex-snapshot
Chiral Amines via Enantioselective π-Allyliridium-C,O-Benzoate-Catalyzed Allylic Alkylation: Student Training via Industrial–Academic Collaboration
inferred← citeshttps://doi.org/10.1021/acs.iecr.4c03657openalex-snapshot
Efficient N-Alkylation of Secondary Amines to Prepare N-Butyl-1,2-benzisothiazolin-3-one Based on Cs Ion Effect with Cs/LTA Zeolite Catalysts
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.4c02314openalex-snapshot
Alloxazine-Based Ligands and Their Ruthenium Complexes as NADH Oxidation Catalysts and G4 Binders
inferred← citeshttps://doi.org/10.1021/acs.jnatprod.0c00031openalex-snapshot
Antineoplastic Agents. 607. Emetine Auristatins
inferred← citeshttps://doi.org/10.1021/acs.joc.6b02431openalex-snapshot
6-(Aryldiazenyl)pyrazolo[1,5-a]pyrimidines as Strategic Intermediates for the Synthesis of Pyrazolo[5,1-b]purines
inferred← citeshttps://doi.org/10.1021/acs.joc.7b00290openalex-snapshot
Room-Temperature CuI-Catalyzed Amination of Aryl Iodides and Aryl Bromides
inferred← citeshttps://doi.org/10.1021/acs.joc.7b02471openalex-snapshot
One-Step Synthesis of Fully Functionalized Pyrazolo[3,4-b]pyridines via Isobenzofuranone Ring Opening
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01571openalex-snapshot
3-Formylpyrazolo[1,5-a]pyrimidines as Key Intermediates for the Preparation of Functional Fluorophores
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02862openalex-snapshot
Palladium-Catalyzed Carbonylative Synthesis of Isoindolinones from Benzylamines with TFBen as the CO Source
inferred← citeshttps://doi.org/10.1021/acs.oprd.6c00330openalex-snapshot
Economical, Practical, and Scalable Synthetic Process Development for the Antiglaucoma Drug Omidenepag Isopropyl
inferred← citeshttps://doi.org/10.1021/acs.organomet.1c00552openalex-snapshot
Nickel Complexes Bearing N,N,O-Tridentate Salicylaldiminato Ligand: Efficient Catalysts for Imines Formation via Dehydrogenative Coupling of Primary Alcohols with Amines
inferred← citeshttps://doi.org/10.1021/acs.organomet.4c00328openalex-snapshot
Unveiling the Potential of SNS-Ni Complex for Establishing C–N Bonds: An Approach toward Chemoselectivity
inferred← citeshttps://doi.org/10.1021/acs.orglett.9b02990openalex-snapshot
General Synthesis of N-Alkylation of Amines with Secondary Alcohols via Hydrogen Autotransfer
inferred← citeshttps://doi.org/10.1021/acscatal.2c00470openalex-snapshot
Kinetic, ESI–CID–MS, and Computational Studies of π-AllyliridiumC,O-Benzoate-Catalyzed Allylic Amination: Understanding the Effect of Cesium Ion
inferred← citeshttps://doi.org/10.1021/acschemneuro.2c00140openalex-snapshot
Advances in Sulfonamide Kappa Opioid Receptor Antagonists: Structural Refinement and Evaluation of CNS Clearance
inferred← citeshttps://doi.org/10.1021/acsomega.0c04592openalex-snapshot
Water-Compatible Synthesis of 1,2,3-Triazoles under Ultrasonic Conditions by a Cu(I) Complex-Mediated Click Reaction
inferred← citeshttps://doi.org/10.1021/acsomega.9b04169openalex-snapshot
Cs2CO3-Mediated Rapid Room-Temperature Synthesis of 3-Amino-2-aroyl Benzofurans and Their Copper-Catalyzed N -Arylation Reactions
inferred← citeshttps://doi.org/10.1021/jacs.9b08746openalex-snapshot
Anti-Markovnikov Hydroamination of Unactivated Alkenes with Primary Alkyl Amines
inferred← citeshttps://doi.org/10.1038/s41598-021-03446-xopenalex-snapshot
Environmental and molecular approach to dye industry waste degradation by the ascomycete fungus Nectriella pironii
inferred← citeshttps://doi.org/10.1039/bk9781837672615-00026openalex-snapshot
Synthetic Methods for Alkyl Amines
inferred← citeshttps://doi.org/10.1039/c7cy02488fopenalex-snapshot
Mechanistic studies on the N -alkylation of amines with alcohols catalysed by iridium( i ) complexes with functionalised N-heterocyclic carbene ligands
inferred← citeshttps://doi.org/10.1039/c7nj02727copenalex-snapshot
Environmentally friendly synthesis of secondary amines via one-pot reductive amination over a heterogeneous Co–N x catalyst
inferred← citeshttps://doi.org/10.1039/c7ra04336hopenalex-snapshot
Simple access toward 3-halo- and 3-nitro-pyrazolo[1,5-a]pyrimidines through a one-pot sequence
inferred← citeshttps://doi.org/10.1039/c8cy00859kopenalex-snapshot
Direct access to N -alkylated amines and imines via acceptorless dehydrogenative coupling catalyzed by a cobalt( ii )-NNN pincer complex
inferred← citeshttps://doi.org/10.1039/c8ob00601fopenalex-snapshot
Cp*Rh( iii ) catalyzed ortho -halogenation of N -nitrosoanilines by solvent-controlled regioselective C–H functionalization
inferred← citeshttps://doi.org/10.1039/c9qo00544gopenalex-snapshot
A pincer ligand enabled ruthenium catalyzed highly selective N -monomethylation of nitroarenes with methanol as the C1 source
inferred← citeshttps://doi.org/10.1039/c9ra04682hopenalex-snapshot
Pyrazolo-fused 4-azafluorenones as key reagents for the synthesis of fluorescent dicyanovinylidene-substituted derivatives
inferred← citeshttps://doi.org/10.1039/d0dt01244kopenalex-snapshot
Copper( ii ) and zinc( ii ) complexes of mono- and bis-1,2,3-triazole-substituted heterocyclic ligands
inferred← citeshttps://doi.org/10.1039/d0qi01374aopenalex-snapshot
Cobalt mediated N -alkylation of amines by alcohols: role of hydrogen bonding pocket
inferred← citeshttps://doi.org/10.1039/d0qo00785dopenalex-snapshot
The present and future synthetic strategies of structural modifications of sinomenine
inferred← citeshttps://doi.org/10.1039/d1nj01654gopenalex-snapshot
Biorenewable carbon-supported Ru catalyst for N -alkylation of amines with alcohols and selective hydrogenation of nitroarenes
inferred← citeshttps://doi.org/10.1039/d3ra05736dopenalex-snapshot
One-pot reductive amination of carbonyl compounds and nitro compounds via Ir-catalyzed transfer hydrogenation
inferred← citeshttps://doi.org/10.1039/d4cy00161copenalex-snapshot
Highly dispersed ruthenium capsulated in UiO-66-NH 2 for hydrogen-borrowing-mediated N -alkylation reactions
inferred← citeshttps://doi.org/10.1039/d4sc03916eopenalex-snapshot
Modular synthesis of α-branched secondary alkylamines via visible-light-mediated carbonyl alkylative amination
inferred← citeshttps://doi.org/10.1039/d5dt01716eopenalex-snapshot
Synthesis of N -alkylated amines via alcohol dehydrogenation catalyzed by a bis-azo-diamido coordinated ruthenium( iii ) complex
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/10.1055/a-1898-9675openalex-snapshot
Synthesis of 7-Arylpurines from Substituted Pyrimidines
inferred← citeshttps://doi.org/10.1142/s2251237324400082openalex-snapshot
Green Synthesis of Novel Acridone Fused Tetracyclic Analogues via Microwave-Promoted Fast, Solvent-Free Benzylation and Their DFT Studies
inferred← citeshttps://doi.org/10.1155/2023/3740956openalex-snapshot
Performance of Plastic Waste-Based Polyionic Liquid toward the Dehydration of Crude Oil Emulsions
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2669666/v1openalex-snapshot
Synthesis and Anti-microbial activity of Isoxazole derivates via Nitrile Oxide, 1,3-Dipolar Cycloaddition Reaction
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2669666/v2openalex-snapshot
Synthesis and Anti-microbial activity of Isoxazole derivates via Nitrile Oxide, 1,3-Dipolar Cycloaddition Reaction
inferred← citeshttps://doi.org/10.3390/m1196openalex-snapshot
3-(tert-Butyl)-N-(4-methoxybenzyl)-1-methyl-1H-pyrazol-5-amine
inferred← citeshttps://doi.org/10.3390/m1215openalex-snapshot
Synthesis, Characterization, and DFT Studies of N-(3,5-Bis(trifluoromethyl)benzyl)stearamide
inferred← citeshttps://doi.org/10.3987/com-21-14610openalex-snapshot
A New and Convenient Synthetic Method for 4-Aminoquinoline-3-carbonitrile and Its Derivatives
inferred← citeshttps://doi.org/10.6023/cjoc202412019openalex-snapshot
N-Alkylation of Aliphatic Alcohol Amine Catalyzed by Tridentate P Ligand Ruthenium Complex
inferred← citeshttps://doi.org/10.70675/e25465cez1f3cz49a3za6e2zbf71deeda99dopenalex-snapshot
Modifications chimiques d’extraits naturels de plantes alpines : approche orientée vers la diversité
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