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Imidazolium-Based Ionic Liquids Catalyzed Formylation of Amines Using Carbon Dioxide and Phenylsilane at Room Temperature
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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/ange.200704487openalex-snapshot
Hydrogenation of Carbon Dioxide is Promoted by a Task‐Specific Ionic Liquid
inferredcites →https://doi.org/10.1002/anie.200351098openalex-snapshot
Alternatives to Phosgene and Carbon Monoxide: Synthesis of Symmetric Urea Derivatives with Carbon Dioxide in Ionic Liquids
inferredcites →https://doi.org/10.1002/anie.200704487openalex-snapshot
Hydrogenation of Carbon Dioxide is Promoted by a Task‐Specific Ionic Liquid
inferredcites →https://doi.org/10.1002/anie.200806058openalex-snapshot
Conversion of Carbon Dioxide into Methanol with Silanes over N‐Heterocyclic Carbene Catalysts
inferredcites →https://doi.org/10.1002/anie.200904677openalex-snapshot
A Convenient and General Iron‐Catalyzed Reduction of Amides to Amines
inferredcites →https://doi.org/10.1002/anie.201105481openalex-snapshot
Carbon Dioxide Hydrogenation to Formic Acid by Using a Heterogeneous Gold Catalyst
inferredcites →https://doi.org/10.1002/anie.201105516openalex-snapshot
A Diagonal Approach to Chemical Recycling of Carbon Dioxide: Organocatalytic Transformation for the Reductive Functionalization of CO2
inferredcites →https://doi.org/10.1002/anie.201209384openalex-snapshot
Green Carbon Science: Scientific Basis for Integrating Carbon Resource Processing, Utilization, and Recycling
inferredcites →https://doi.org/10.1002/anie.201304529openalex-snapshot
Carbon Dioxide as a C 1 Building Block for the Formation of Carboxylic Acids by Formal Catalytic Hydrocarboxylation
inferredcites →https://doi.org/10.1002/anie.201305630openalex-snapshot
Solvation of Carbon Dioxide in [C4mim][BF4] and [C4mim][PF6] Ionic Liquids Revealed by High‐Pressure NMR Spectroscopy
inferredcites →https://doi.org/10.1002/anie.201400521openalex-snapshot
A Protic Ionic Liquid Catalyzes CO2 Conversion at Atmospheric Pressure and Room Temperature: Synthesis of Quinazoline‐2,4(1H,3H)‐diones
inferredcites →https://doi.org/10.1002/anie.201403711openalex-snapshot
Ruthenium‐Catalyzed Reductive Methylation of Imines Using Carbon Dioxide and Molecular Hydrogen
inferredcites →https://doi.org/10.1002/anie.201407357openalex-snapshot
Carbon Dioxide Reduction to Methylamines under Metal‐Free Conditions
inferredcites →https://doi.org/10.1002/anie.201407689openalex-snapshot
Metal‐Free Catalyst for the Chemoselective Methylation of Amines Using Carbon Dioxide as a Carbon Source
inferredcites →https://doi.org/10.1002/anie.201408151openalex-snapshot
The Formation of Imidazolium Salt Intimate (Contact) Ion Pairs in Solution
inferredcites →https://doi.org/10.1002/cctc.201100016openalex-snapshot
Anion–Cation Cooperative Catalysis by Ionic Liquids
inferredcites →https://doi.org/10.1002/cctc.201200721openalex-snapshot
Mechanistic Insights into the Reduction of Carbon Dioxide with Silanes over N‐Heterocyclic Carbene Catalysts
inferredcites →https://doi.org/10.1002/cctc.201200732openalex-snapshot
Complete Catalytic Deoxygenation of CO2 into Formamidine Derivatives
inferredcites →https://doi.org/10.1002/cssc.200900180openalex-snapshot
Metal‐Free Heterogeneous Catalysis for Sustainable Chemistry
inferredcites →https://doi.org/10.1016/j.molcata.2012.10.014openalex-snapshot
Catalytic synthesis of silyl formates with 1 atm of CO2 and their utilization for synthesis of formyl compounds and formic acid
inferredcites →https://doi.org/10.1016/s0040-4039(03)00384-8openalex-snapshot
Formanilide and carbanilide from aniline and carbon dioxide
inferredcites →https://doi.org/10.1021/ja0647250openalex-snapshot
From Carbon Dioxide to Methane: Homogeneous Reduction of Carbon Dioxide with Hydrosilanes Catalyzed by Zirconium−Borane Complexes
inferredcites →https://doi.org/10.1021/ja103531zopenalex-snapshot
The Catalytic Role of N-Heterocyclic Carbene in a Metal-Free Conversion of Carbon Dioxide into Methanol: A Computational Mechanism Study
inferredcites →https://doi.org/10.1021/ja105320copenalex-snapshot
Tandem Frustrated Lewis Pair/Tris(pentafluorophenyl)borane-Catalyzed Deoxygenative Hydrosilylation of Carbon Dioxide
inferredcites →https://doi.org/10.1021/ja211527qopenalex-snapshot
Recycling of Carbon and Silicon Wastes: Room Temperature Formylation of N–H Bonds Using Carbon Dioxide and Polymethylhydrosiloxane
inferredcites →https://doi.org/10.1021/ol301034jopenalex-snapshot
Copper-Catalyzed Formic Acid Synthesis from CO2 with Hydrosilanes and H2O
inferredcites →https://doi.org/10.1021/om400876jopenalex-snapshot
Nickel-Catalyzed Hydrosilylation of CO2 in the Presence of Et3B for the Synthesis of Formic Acid and Related Formates
inferredcites →https://doi.org/10.1038/ncomms4091openalex-snapshot
Ruthenium-catalysed alkoxycarbonylation of alkenes with carbon dioxide
inferredcites →https://doi.org/10.1038/ncomms6933openalex-snapshot
Using carbon dioxide as a building block in organic synthesis
inferredcites →https://doi.org/10.1039/b008923kopenalex-snapshot
Cycloaddition of carbon dioxide to propylene oxide catalyzed by ionic liquids
inferredcites →https://doi.org/10.1039/b107298fopenalex-snapshot
Metal-free organocatalysis through explicit hydrogen bonding interactions
inferredcites →https://doi.org/10.1039/c0cc00751jopenalex-snapshot
Synthesis of dimethylformamide from CO2, H2 and dimethylamine over Cu/ZnO
inferredcites →https://doi.org/10.1039/c2gc36517kopenalex-snapshot
Cyclization of o-phenylenediamines by CO 2 in the presence of H 2 for the synthesis of benzimidazoles
inferredcites →https://doi.org/10.1039/c3cc41838copenalex-snapshot
Highly efficient catalytic hydrosilylation of carbon dioxide by an N-heterocyclic carbene copper catalyst
inferredcites →https://doi.org/10.1039/c3cc46427jopenalex-snapshot
Amine formylation via carbon dioxide recycling catalyzed by a simple and efficient heterogeneous palladium catalyst
inferredcites →https://doi.org/10.1039/c3cc49365bopenalex-snapshot
Pd/C-catalyzed direct formylation of aromatic iodides to aryl aldehydes using carbon dioxide as a C1 resource
inferredcites →https://doi.org/10.1039/c3cy00375bopenalex-snapshot
Copper-diphosphine complex catalysts for N-formylation of amines under 1 atm of carbon dioxide with polymethylhydrosiloxane
inferredcites →https://doi.org/10.1039/c3gc41467aopenalex-snapshot
Efficient synthesis of quinazoline-2,4(1H,3H)-diones from CO 2 using ionic liquids as a dual solvent–catalyst at atmospheric pressure
inferredcites →https://doi.org/10.1039/c3ra41464gopenalex-snapshot
Sequential covalent bonding activation and general base catalysis: insight into N-heterocyclic carbene catalyzed formylation of N–H bonds using carbon dioxide and silane
inferredcites →https://doi.org/10.1039/c4gc00127copenalex-snapshot
Insights on recyclable catalytic system composed of task-specific ionic liquids for the chemical fixation of carbon dioxide
inferredcites →https://doi.org/10.1039/c4gc00153bopenalex-snapshot
Au catalyzed synthesis of benzimidazoles from 2-nitroanilines and CO2/H2
inferredcites →https://doi.org/10.1039/c4gc01614aopenalex-snapshot
Reductive functionalization of CO 2 with amines: an entry to formamide, formamidine and methylamine derivatives
inferredcites →https://doi.org/10.1039/c4ra12151aopenalex-snapshot
An efficient copper catalyzed formylation of amines utilizing CO 2 and hydrogen
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
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One-Pot Two-Step Reduction of Co2 with Amines and Nabh4 to N-Substituted Compounds at Atmospheric Pressure
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inferred← citeshttps://doi.org/10.1002/9783527838967.ch02openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/adsc.201800140openalex-snapshot
DBU‐Catalyzed Selective N‐Methylation and N‐Formylation of Amines with CO2 and Polymethylhydrosiloxane
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inferred← citeshttps://doi.org/10.1002/adsc.201900906openalex-snapshot
Iron‐Catalyzed Selective N‐Methylation and N‐Formylation of Amines with CO2
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Carboxylate‐Functionalized Zeolitic Imidazolate Framework Enables Catalytic N‐Formylation Using Ambient CO2
inferred← citeshttps://doi.org/10.1002/aic.18493openalex-snapshot
CO2 absorption mechanism and kinetic modeling of mixed amines with ionic liquid activation
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Delineating the Mechanism of Ionic Liquids in the Synthesis of Quinazoline‐2,4(1H,3H)‐dione from 2‐Aminobenzonitrile and CO2
inferred← citeshttps://doi.org/10.1002/ange.201906942openalex-snapshot
Pivotal Role of the Basic Character of Organic and Salt Catalysts in C−N Bond Forming Reactions of Amines with CO2
inferred← citeshttps://doi.org/10.1002/anie.201705438openalex-snapshot
Delineating the Mechanism of Ionic Liquids in the Synthesis of Quinazoline‐2,4(1H,3H)‐dione from 2‐Aminobenzonitrile and CO2
inferred← citeshttps://doi.org/10.1002/anie.201906942openalex-snapshot
Pivotal Role of the Basic Character of Organic and Salt Catalysts in C−N Bond Forming Reactions of Amines with CO2
inferred← citeshttps://doi.org/10.1002/asia.202400497openalex-snapshot
Homogeneous Catalysis in N‐Formylation/N‐Methylation Utilizing Carbon Dioxide as the C1 Source
inferred← citeshttps://doi.org/10.1002/cctc.201500651openalex-snapshot
Solvent‐Free Iridium‐Catalyzed Reactivity of CO2 with Secondary Amines and Hydrosilanes
inferred← citeshttps://doi.org/10.1002/cctc.201601027openalex-snapshot
Carbon Dioxide Based N‐Formylation of Amines Catalyzed by Fluoride and Hydroxide Anions
inferred← citeshttps://doi.org/10.1002/cctc.201601682openalex-snapshot
Heterogeneous Cobalt‐Catalyzed Direct N‐Formylation of Isoquinolines with CO2 and H2
inferred← citeshttps://doi.org/10.1002/cctc.201700069openalex-snapshot
Pd Nanoparticles Decorated on Hypercrosslinked Microporous Polymer: A Highly Efficient Catalyst for the Formylation of Amines through Carbon Dioxide Fixation
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A Titanium Dioxide Supported Gold Nanoparticle Catalyst for the Selective N‐Formylation of Functionalized Amines with Carbon Dioxide and Hydrogen
inferred← citeshttps://doi.org/10.1002/cctc.201800185openalex-snapshot
Ru@PsIL‐Catalyzed Synthesis of N‐Formamides and Benzimidazole by using Carbon Dioxide and Dimethylamine Borane
inferred← citeshttps://doi.org/10.1002/cctc.201800699openalex-snapshot
Homogeneous Catalytic Reduction of CO 2 with Silicon‐Hydrides, State of the Art
inferred← citeshttps://doi.org/10.1002/cctc.201801086openalex-snapshot
Controllable Homogeneity/Heterogeneity Switch of Imidazolium Ionic Liquids for CO2 Utilization
inferred← citeshttps://doi.org/10.1002/cctc.201801963openalex-snapshot
Modified Graphene Oxide Based Zinc Composite: an Efficient Catalyst for N‐formylation and Carbamate Formation Reactions Through CO2 Fixation
inferred← citeshttps://doi.org/10.1002/cctc.201901687openalex-snapshot
Mechanistic Insights on the Functionalization of CO2 with Amines and Hydrosilanes Catalyzed by a Zwitterionic Iridium Carboxylate‐Functionalized Bis‐NHC Catalyst
inferred← citeshttps://doi.org/10.1002/cctc.201901962openalex-snapshot
Highly Efficient Binuclear Copper‐catalyzed Oxidation of N,N‐Dimethylanilines with O2
inferred← citeshttps://doi.org/10.1002/cctc.202001572openalex-snapshot
Homogeneous and Heterogeneous Ionic Liquid System: Promising “Ideal Catalysts” for the Fixation of CO2 into Cyclic Carbonates
inferred← citeshttps://doi.org/10.1002/cctc.202201351openalex-snapshot
Effective N‐formylation of Amines with CO2 in Anaerobic Fermentation Gas Catalyzed by Triply Synergistic Effect of Ionic Porous Organic Polymer
inferred← citeshttps://doi.org/10.1002/chem.201601006openalex-snapshot
Selective Metal‐Free Hydrosilylation of CO 2 Catalyzed by Triphenylborane in Highly Polar, Aprotic Solvents
inferred← citeshttps://doi.org/10.1002/chem.201603688openalex-snapshot
Fluoride‐Catalyzed Methylation of Amines by Reductive Functionalization of CO2 with Hydrosilanes
inferred← citeshttps://doi.org/10.1002/chem.201701420openalex-snapshot
Reductive Coupling of CO2, Primary Amine, and Aldehyde at Room Temperature: A Versatile Approach to Unsymmetrically N,N‐Disubstituted Formamides
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Mechanistic Insights on the Reduction of CO2 to Silylformates Catalyzed by Ir‐NSiN Species
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Porous Organic Polymers with Built‐in N‐Heterocyclic Carbenes: Selective and Efficient Heterogeneous Catalyst for the Reductive N‐Formylation of Amines with CO2
inferred← citeshttps://doi.org/10.1002/chem.201901686openalex-snapshot
Delineation of the Critical Parameters of Salt Catalysts in the N‐Formylation of Amines with CO2
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Recent Advances in Homogeneous Carbonylation Using CO2 as CO Surrogate
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Recent advances in organic synthesis with CO2
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N-formylation of amines using phenylsilane and CO2 over ZnO catalyst under mild condition
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Efficient photocatalytic CO2 N-formylation of amines over Pd/Bi-ZnOx without extra reductant
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inferred← citeshttps://doi.org/10.1016/j.cej.2024.151102openalex-snapshot
Ionic liquid-based advanced porous organic hyper-crosslinked polymers (ILHCPs) for CO2 capture and conversion
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Highly selective visible-light-driven CO2 formylation of benzylamine over PtNi/ZnO photocatalyst
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Metal-free reduction of CO2
inferred← citeshttps://doi.org/10.1016/j.cogsc.2016.11.006openalex-snapshot
Recent advances in organic synthesis with CO2 as C1 synthon
inferred← citeshttps://doi.org/10.1016/j.fuel.2022.125074openalex-snapshot
Protophilic solvent-impelled quasi-catalytic CO2 valorization to formic acid and N-formamides
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Cationic quaternary ammonium-stabilized Nb oxoclusters catalyze reductive amination of carbon dioxide with hydrosilane
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Protic vs aprotic ionic liquid for CO2 fixation: A simulation study
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UiO-66 as an efficient catalyst for N-formylation of amines with CO2 and dimethylamine borane as a reducing agent
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Synthesis of carbonates and related compounds incorporating CO2 using ionic liquid-type catalysts: State-of-the-art and beyond
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CO 2 absorption behavior of azole-based protic ionic liquids: Influence of the alkalinity and physicochemical properties
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Theoretical investigations on the methylation of N H bond using CO 2 and hydrosilane catalyzed by Zinc II complexes: Mechanism and ligand effect
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Reductive formylation of amines with CO 2 using sodium borohydride: A catalyst-free route
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Fixation of CO2 in structurally diverse quinazoline-2,4(1H,3H)-diones under ambient conditions
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A polymeric ionic liquid catalyst for the N-formylation and N-methylation of amines using CO2/PhSiH3
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Efficient DMF-assisted synthesis of formamides from amines using CO2 catalyzed by heterogeneous metal-free imidazolium-hypercrosslinked polymers
inferred← citeshttps://doi.org/10.1016/j.jcou.2024.102741openalex-snapshot
One-pot two-step reduction of CO2 with amines and NaBH4 to N-substituted compounds at atmospheric pressure
inferred← citeshttps://doi.org/10.1016/j.mcat.2022.112600openalex-snapshot
Metal−free catalysis of the reductive amination of aldehydes using a phosphonium−doped porous aromatic framework
inferred← citeshttps://doi.org/10.1016/j.mcat.2025.114896openalex-snapshot
Highly efficient NiCo alloy catalyst fabricated by MOFs-templated strategy for N-formylation reaction of amines with CO2 and phenylsilane
inferred← citeshttps://doi.org/10.1016/j.molliq.2020.114503openalex-snapshot
Effect of supramolecular polymeric aggregation in room temperature ionic liquids (RTILs) on catalytic activity in the synthesis of 4H-chromene derivatives and Knoevenagel condensation
inferred← citeshttps://doi.org/10.1016/j.molstruc.2023.136247openalex-snapshot
Reductive functionalization of CO2 under mild reaction conditions for the catalytic synthesis of N-formamides by Mannich base based Cobalt (III) complex
inferred← citeshttps://doi.org/10.1016/j.msec.2018.05.038openalex-snapshot
Synthesis and tribological behavior of fatty acid constituted tetramethylguanidinium (TMG) ionic liquids for a steel/steel contact
inferred← citeshttps://doi.org/10.1016/j.mtsust.2025.101160openalex-snapshot
A review on the evolution of ionic liquids: Sustainable synthesis, applications, and future prospects
inferred← citeshttps://doi.org/10.1016/j.nanoen.2025.110673openalex-snapshot
Pt1In single atom alloy for visible-light-driven CO2 formylation of benzylamine
inferred← citeshttps://doi.org/10.1016/j.scp.2021.100495openalex-snapshot
Enhancement of CO2 adsorption on natural zeolite, modified clinoptilolite with cations, amines and ionic liquids
inferred← citeshttps://doi.org/10.1016/j.tet.2017.05.003openalex-snapshot
Synthesis of benzothiazoles from 2-aminobenzenethiols in the presence of a reusable polythiazolium precatalyst under atmospheric pressure of carbon dioxide
inferred← citeshttps://doi.org/10.1016/s1872-2067(17)62802-xopenalex-snapshot
Transformation of carbon dioxide into valuable chemicals over bifunctional metallosalen catalysts bearing quaternary phosphonium salts
inferred← citeshttps://doi.org/10.1016/s1872-2067(17)62877-8openalex-snapshot
Zinc phthalocyanine as an efficient catalyst for halogen-free synthesis of formamides from amines via carbon dioxide hydrosilylation under mild conditions
inferred← citeshttps://doi.org/10.1016/s1872-2067(21)63841-xopenalex-snapshot
Improving the performance of metal-organic frameworks for thermo-catalytic CO2 conversion: Strategies and perspectives
inferred← citeshttps://doi.org/10.1016/s1872-5813(22)60055-0openalex-snapshot
Recent advances on oxazolidinones synthesize from carbon dioxide
inferred← citeshttps://doi.org/10.1021/acs.accounts.1c00251openalex-snapshot
Ionic-Liquid-Catalyzed Approaches under Metal-Free Conditions
inferred← citeshttps://doi.org/10.1021/acs.chemrev.3c00391openalex-snapshot
Energy Applications of Ionic Liquids: Recent Developments and Future Prospects
inferred← citeshttps://doi.org/10.1021/acs.chemrev.4c00696openalex-snapshot
Ionic Liquids Promoted Transformation of Carbon Dioxide
inferred← citeshttps://doi.org/10.1021/acs.chemrev.5c00329openalex-snapshot
Frontiers of Ionic Liquids in Carbon Dioxide Separation and Valorization
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.1c01104openalex-snapshot
A Porous Copper–Organic Framework Assembled by [Cu 12 ] Nanocages: Highly Efficient CO 2 Capture and Chemical Fixation and Theoretical DFT Calculations
inferred← citeshttps://doi.org/10.1021/acs.joc.4c03034openalex-snapshot
Three-Component Synthesis of Oxazolidinones via Phosphine-Catalyzed Fixation of Carbon Dioxide and Mechanistic Investigation in Mass Spectrometry
inferred← citeshttps://doi.org/10.1021/acs.joc.5c00965openalex-snapshot
The DMSO-Catalyzed CO 2 Reduction with 9-BBN as a Source for the Selective N-Formylation, Room Temperature N-Methylation of Amines, N-Hydroxymethylation of Heterocycles, and C–N Couplings
inferred← citeshttps://doi.org/10.1021/acs.joc.8b01555openalex-snapshot
Copper-Catalyzed N-Formylation of Amines through Tandem Amination/Hydrolysis/Decarboxylation Reaction of Ethyl Bromodifluoroacetate
inferred← citeshttps://doi.org/10.1021/acs.jpca.6b11610openalex-snapshot
New Insight into the Formation Mechanism of Imidazolium-Based Ionic Liquids from N-Alkyl Imidazoles and Halogenated Hydrocarbons: A Polar Microenvironment Induced and Autopromoted Process
inferred← citeshttps://doi.org/10.1021/acs.orglett.7b01906openalex-snapshot
Reductive CO2 Fixation via Tandem C–C and C–N Bond Formation: Synthesis of Spiro-indolepyrrolidines
inferred← citeshttps://doi.org/10.1021/acsami.8b14671openalex-snapshot
Zwitterionic Covalent Organic Frameworks as Catalysts for Hierarchical Reduction of CO 2 with Amine and Hydrosilane
inferred← citeshttps://doi.org/10.1021/acsami.9b14509openalex-snapshot
Metal-Free N-Formylation of Amines with CO2 and Hydrosilane by Nitrogen-Doped Graphene Nanosheets
inferred← citeshttps://doi.org/10.1021/acscatal.0c03795openalex-snapshot
A NHC-Silyliumylidene Cation for Catalytic N-Formylation of Amines Using Carbon Dioxide
inferred← citeshttps://doi.org/10.1021/acscatal.5b01874openalex-snapshot
Ionic Liquid-Catalyzed C–S Bond Construction using CO2 as a C1 Building Block under Mild Conditions: A Metal-Free Route to Synthesis of Benzothiazoles
inferred← citeshttps://doi.org/10.1021/acscatal.6b01856openalex-snapshot
Selective Formylation and Methylation of Amines using Carbon Dioxide and Hydrosilane Catalyzed by Alkali-Metal Carbonates
inferred← citeshttps://doi.org/10.1021/acscatal.7b01422openalex-snapshot
Tetrabutylphosphonium-Based Ionic Liquid Catalyzed CO2 Transformation at Ambient Conditions: A Case of Synthesis of α-Alkylidene Cyclic Carbonates
inferred← citeshttps://doi.org/10.1021/acscatal.7b04108openalex-snapshot
Guanidine-Catalyzed Reductive Amination of Carbon Dioxide with Silanes: Switching between Pathways and Suppressing Catalyst Deactivation
inferred← citeshttps://doi.org/10.1021/acscatal.8b03274openalex-snapshot
Mechanistic Study of the N-Formylation of Amines with Carbon Dioxide and Hydrosilanes
inferred← citeshttps://doi.org/10.1021/acsomega.7b00618openalex-snapshot
N-Alkylated 1,4-Diazabicyclo[2.2.2]octane–Polyethylene Glycol Melt as Deep Eutectic Solvent for the Synthesis of Fisher Indoles and 1 H -Tetrazoles
inferred← citeshttps://doi.org/10.1021/acssuschemeng.0c07903openalex-snapshot
Ionic Liquid-Promoted Formylation of N(sp2)-Heteroarenes with CO2/H2 over Pd/C
inferred← citeshttps://doi.org/10.1021/acssuschemeng.2c01162openalex-snapshot
Acidic Ionic Liquids as Metal-Free and Recyclable Catalysts for Direct Reduction of Aromatic Allylic Alcohol in Dimethyl Carbonate via Hydrogen Transfer
inferred← citeshttps://doi.org/10.1021/acssuschemeng.2c03904openalex-snapshot
Recyclable Metallic Imidazolium-Based Ionic Liquid-Catalyzed Selective Mono- and Double-Hydroboration in Water
inferred← citeshttps://doi.org/10.1021/acssuschemeng.5c09672openalex-snapshot
Tri(alkylamino)cyclopropenium Acetate Ion Pair Catalysis for Reductive Functionalization of CO 2 with Amines and Hydrosilane to N -Formamides and N -Methylamines
inferred← citeshttps://doi.org/10.1021/acssuschemeng.6b02865openalex-snapshot
N-Formylation of Amines with CO2 and H2 Using Pd–Au Bimetallic Catalysts Supported on Polyaniline-Functionalized Carbon Nanotubes
inferred← citeshttps://doi.org/10.1021/acssuschemeng.7b00363openalex-snapshot
Hydroxyl Group-Regulated Active Nano-Pd/C Catalyst Generation via in Situ Reduction of Pd(NH3)xCly/C for N-Formylation of Amines with CO2/H2
inferred← citeshttps://doi.org/10.1021/acssuschemeng.7b01287openalex-snapshot
Natural Product Glycine Betaine as an Efficient Catalyst for Transformation of CO2 with Amines to Synthesize N-Substituted Compounds
inferred← citeshttps://doi.org/10.1021/acssuschemeng.8b02352openalex-snapshot
Waste Recycling: Ionic Liquid-Catalyzed 4-Electron Reduction of CO2 with Amines and Polymethylhydrosiloxane Combining Experimental and Theoretical Study
inferred← citeshttps://doi.org/10.1021/acssuschemeng.8b03245openalex-snapshot
Renewable and Biocompatible Lecithin as an Efficient Organocatalyst for Reductive Conversion of CO2 with Amines to Formamides and Methylamines
inferred← citeshttps://doi.org/10.1038/nprot.2016.175openalex-snapshot
N-formylation and N-methylation of amines using metal-free N-heterocyclic carbene catalysts and CO2 as carbon source
inferred← citeshttps://doi.org/10.1038/s41467-023-39089-xopenalex-snapshot
A porous metal-organic cage liquid for sustainable CO2 conversion reactions
inferred← citeshttps://doi.org/10.1039/c6cc01234eopenalex-snapshot
Solvent-promoted catalyst-free N-formylation of amines using carbon dioxide under ambient conditions
inferred← citeshttps://doi.org/10.1039/c6cc03058kopenalex-snapshot
Immobilization of ionic liquids to covalent organic frameworks for catalyzing the formylation of amines with CO 2 and phenylsilane
inferred← citeshttps://doi.org/10.1039/c6dt04893eopenalex-snapshot
Transition metal free catalytic hydroboration of aldehydes and aldimines by amidinato silane
inferred← citeshttps://doi.org/10.1039/c6gc01038eopenalex-snapshot
A route for direct transformation of aryl halides to benzyl alcohols via carbon dioxide fixation reaction catalyzed by a (Pd@N-GMC) palladium nanoparticle encapsulated nitrogen doped mesoporous carbon material
inferred← citeshttps://doi.org/10.1039/c6gc01455kopenalex-snapshot
Biomass-derived γ-valerolactone as an efficient solvent and catalyst for the transformation of CO 2 to formamides
inferred← citeshttps://doi.org/10.1039/c6gc02243jopenalex-snapshot
Synthesis of formamides containing unsaturated groups by N-formylation of amines using CO 2 with H 2
inferred← citeshttps://doi.org/10.1039/c6ra05199eopenalex-snapshot
Copper-catalyzed N -formylation of amines with CO 2 under ambient conditions
inferred← citeshttps://doi.org/10.1039/c7cc03860gopenalex-snapshot
Catalyst-free N-formylation of amines using BH 3 NH 3 and CO 2 under mild conditions
inferred← citeshttps://doi.org/10.1039/c7cc03948dopenalex-snapshot
Metal free mild and selective aldehyde cyanosilylation by a neutral penta-coordinate silicon compound
inferred← citeshttps://doi.org/10.1039/c7cy00772hopenalex-snapshot
Reduction of carbon dioxide and organic carbonyls by hydrosilanes catalysed by the perrhenate anion
inferred← citeshttps://doi.org/10.1039/c7gc00484bopenalex-snapshot
Carboxylate-promoted reductive functionalization of CO 2 with amines and hydrosilanes under mild conditions
inferred← citeshttps://doi.org/10.1039/c7gc03416dopenalex-snapshot
Tungstate catalysis: pressure-switched 2- and 6-electron reductive functionalization of CO 2 with amines and phenylsilane
inferred← citeshttps://doi.org/10.1039/c7ra04245kopenalex-snapshot
Imidazolium-based ionic liquid-catalyzed hydrosilylation of imines and reductive amination of aldehydes using hydrosilane as the reductant
inferred← citeshttps://doi.org/10.1039/c7sc00824dopenalex-snapshot
Formylation or methylation: what determines the chemoselectivity of the reaction of amine, CO 2 , and hydrosilane catalyzed by 1,3,2-diazaphospholene?
inferred← citeshttps://doi.org/10.1039/c8dt02346hopenalex-snapshot
Current advances in the catalytic conversion of carbon dioxide by molecular catalysts: an update
inferred← citeshttps://doi.org/10.1039/c8gc03549kopenalex-snapshot
Eco-friendly acetylcholine-carboxylate bio-ionic liquids for controllable N -methylation and N -formylation using ambient CO 2 at low temperatures
inferred← citeshttps://doi.org/10.1039/c8ta00823jopenalex-snapshot
Function-oriented ionic polymers having high-density active sites for sustainable carbon dioxide conversion
inferred← citeshttps://doi.org/10.1039/c9gc00827fopenalex-snapshot
Conversion of CO 2 to value-added products mediated by ionic liquids
inferred← citeshttps://doi.org/10.1039/c9gc01137dopenalex-snapshot
Mild and facile synthesis of formamide: reduction and functionalization of CO 2 using NaBH(OAc) 3 under atmospheric pressure
inferred← citeshttps://doi.org/10.1039/c9gc03637gopenalex-snapshot
Catalyst-free selective N -formylation and N -methylation of amines using CO 2 as a sustainable C1 source
inferred← citeshttps://doi.org/10.1039/c9gc04342jopenalex-snapshot
Catalytic transformation of CO 2 into C1 chemicals using hydrosilanes as a reducing agent
inferred← citeshttps://doi.org/10.1039/c9qo00691eopenalex-snapshot
A novel chiral DMAP–thiourea bifunctional catalyst catalyzed enantioselective Steglich and Black rearrangement reactions
inferred← citeshttps://doi.org/10.1039/d0cc03098hopenalex-snapshot
Direct N -formylation of nitroarenes with CO 2
inferred← citeshttps://doi.org/10.1039/d0gc00493fopenalex-snapshot
Synthesis of bioderived polycarbonates with adjustable molecular weights catalyzed by phenolic-derived ionic liquids
inferred← citeshttps://doi.org/10.1039/d0gc01440kopenalex-snapshot
One-pot synthesis of bio-based polycarbonates from dimethyl carbonate and isosorbide under metal-free condition
inferred← citeshttps://doi.org/10.1039/d0gc01741hopenalex-snapshot
Tetracoordinate borates as catalysts for reductive formylation of amines with carbon dioxide
inferred← citeshttps://doi.org/10.1039/d0gc01804jopenalex-snapshot
Efficient synthesis of bio-derived polycarbonates from dimethyl carbonate and isosorbide: regulating exo -OH and endo -OH reactivity by ionic liquids
inferred← citeshttps://doi.org/10.1039/d0gc02890hopenalex-snapshot
Selective N -formylation/ N -methylation of amines and N -formylation of amides and carbamates with carbon dioxide and hydrosilanes: promotion of the basic counter anions of the zinc catalyst
inferred← citeshttps://doi.org/10.1039/d0ra05858kopenalex-snapshot
Recent advances in liquid hydrosilane-mediated catalytic N -formylation of amines with CO 2
inferred← citeshttps://doi.org/10.1039/d0sc03528aopenalex-snapshot
From CO 2 activation to catalytic reduction: a metal-free approach
inferred← citeshttps://doi.org/10.1039/d1cy01824hopenalex-snapshot
Acylamido-based anion-functionalized ionic liquids for efficient synthesis of poly(isosorbide carbonate)
inferred← citeshttps://doi.org/10.1039/d1gc01897copenalex-snapshot
A substituent- and temperature-controllable NHC-derived zwitterionic catalyst enables CO 2 upgrading for high-efficiency construction of formamides and benzimidazoles
inferred← citeshttps://doi.org/10.1039/d1gc04485kopenalex-snapshot
Hydrogen-bonding and acid cooperative catalysis for benzylation of arenes with benzyl alcohols over ionic liquids
inferred← citeshttps://doi.org/10.1039/d1ob00755fopenalex-snapshot
Carbon dioxide based methodologies for the synthesis of fine chemicals
inferred← citeshttps://doi.org/10.1039/d2cc04643aopenalex-snapshot
In situ activation of COOH-functionalized ZIF-90-enabled reductive CO 2 N -formylation
inferred← citeshttps://doi.org/10.1039/d3cy00401eopenalex-snapshot
N-Heterocyclic carbene supported zinc catalysed N -formylation of diverse N–H functionalities with carbon dioxide under ambient conditions
inferred← citeshttps://doi.org/10.1039/d3nj00097dopenalex-snapshot
Hydrogen bonding-catalyzed synthesis of 1,4-dioxanes from dehydrative cyclization of vicinal diols in ionic liquids
inferred← citeshttps://doi.org/10.1039/d3qo00058copenalex-snapshot
DIC–borane-catalyzed selective methylation of primary amines with CO 2 using boranes as reducing agents
inferred← citeshttps://doi.org/10.1063/5.0176219openalex-snapshot
DABCO-PEG ionic liquid catalyzed synthesis, single-crystal structure, and antioxidant activity of a flavanone derivative
inferred← citeshttps://doi.org/10.1126/sciadv.abg0396openalex-snapshot
Hydrogen-bond donor and acceptor cooperative catalysis strategy for cyclic dehydration of diols to access O-heterocycles
inferred← citeshttps://doi.org/10.1134/s1070363223010231openalex-snapshot
N-Methyl-N-arylformamides: Synthesis and Interaction of with Carbonic Anhydrase (PDB: 3FW3) and Nuclease (PDB: 6O70) Enzymes via In Silico Molecular Docking
inferred← citeshttps://doi.org/10.1134/s1990793119080062openalex-snapshot
Cyclization of o-Phenylenediamine and o-Substituted Anilines with Supercritical Carbon Dioxide
inferred← citeshttps://doi.org/10.1140/epjp/i2017-11627-1openalex-snapshot
Plant-mediated green synthesis of ZnO nanoparticles using Garcinia gummi-gutta seed extract: Photoluminescence, screening of their catalytic activity in antioxidant, formylation and biodiesel production
inferred← citeshttps://doi.org/10.1246/cl.230153openalex-snapshot
Silver-catalyzed Reductive Formylation of Amines with Carbon Dioxide
inferred← citeshttps://doi.org/10.1360/n032017-00220openalex-snapshot
Recent progress in CO2 catalytic reduction to high value-added chemicals
inferred← citeshttps://doi.org/10.1360/ssc-2021-0102openalex-snapshot
Research progress on ionic liquid mediated chemical reactions
inferred← citeshttps://doi.org/10.1515/pac-2017-0304openalex-snapshot
DMF-promoted reductive functionalization of CO2 with secondary amines and phenylsilane to methylamines
inferred← citeshttps://doi.org/10.2174/2405461505666200316121735openalex-snapshot
Synthesis of Nano ZnO: A Catalyst for N-formylation of Aromatic Amines and Biodiesel Application
inferred← citeshttps://doi.org/10.24200/sci.2017.4491openalex-snapshot
Synthesis of Nα-protected formamides from amino acids using MgO nano catalyst: Study of molecular docking and antibacterial activity
inferred← citeshttps://doi.org/10.3389/fchem.2018.00462openalex-snapshot
Ionic Liquids Catalysis for Carbon Dioxide Conversion With Nucleophiles
inferred← citeshttps://doi.org/10.3390/catal14080492openalex-snapshot
N-Formylation of Carbon Dioxide and Amines with EDTA as a Recyclable Catalyst under Ambient Conditions
inferred← citeshttps://doi.org/10.3390/catal8080304openalex-snapshot
Ionic Liquids as Bifunctional Cosolvents Enhanced CO2 Conversion Catalysed by NADH-Dependent Formate Dehydrogenase
inferred← citeshttps://doi.org/10.3390/catal9020163openalex-snapshot
Supramolecular Chemistry and Self-Organization: A Veritable Playground for Catalysis
inferred← citeshttps://doi.org/10.3390/molecules24071241openalex-snapshot
Cu(I)/Ionic Liquids Promote the Conversion of Carbon Dioxide into Oxazolidinones at Room Temperature
inferred← citeshttps://doi.org/10.3390/molecules26226963openalex-snapshot
Rational Design of Simple Organocatalysts for the HSiCl3 Enantioselective Reduction of (E)-N-(1-Phenylethylidene)aniline
inferred← citeshttps://doi.org/10.3390/molecules29040870openalex-snapshot
CO2-Driven N-Formylation/N-Methylation of Amines Using C-Scorpionate Metal Complexes
inferred← citeshttps://doi.org/10.3390/nano16120727openalex-snapshot
Research Progress of Ionic Liquids Hybridized with Porous Materials for CO2 Capture: From Bulk to Confinement-Enhanced Adsorbents
inferred← citeshttps://doi.org/10.58837/chula.the.2018.111openalex-snapshot
Hybrid materials from covalent organic frameworks and ionic liquids
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