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Carbon Dioxide Utilisation for the Synthesis of Unsymmetrical Dialkyl and Cyclic Carbonates Promoted by Basic Ionic Liquids

https://doi.org/10.1071/ch17530
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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/adsc.200600525openalex-snapshot
An Efficient Synthesis of Organic Carbonates using Nanocrystalline Magnesium Oxide
inferredcites →https://doi.org/10.1002/asia.201600281openalex-snapshot
Azole‐Anion‐Based Aprotic Ionic Liquids: Functional Solvents for Atmospheric CO2 Transformation into Various Heterocyclic Compounds
inferredcites →https://doi.org/10.1002/cber.19580910223openalex-snapshot
Spezifische Protonenacceptoren als Hilfsbasen bei Alkylierungs‐ und Dehydrohalogenierungsreaktionen
inferredcites →https://doi.org/10.1002/ejic.201301586openalex-snapshot
Immobilization of 1,5,7‐Triazabicyclo[4.4.0]dec‐5‐ene on Magnetic γ‐Fe2O3 Nanoparticles: A Highly Recyclable and Efficient Nanocatalyst for the Synthesis of Organic Carbonates
inferredcites →https://doi.org/10.1002/ejoc.200400888openalex-snapshot
New Highly Active and Selective Heterogeneous Catalytic System for the Synthesis of Unsymmetrical Organic Carbonates: A Green Protocol
inferredcites →https://doi.org/10.1002/ejoc.200500380openalex-snapshot
Lactone Kinetic Resolution by Acylation – Application to the Enantioselective Synthesis of Estrane Derivatives
inferredcites →https://doi.org/10.1006/jcat.2001.3439openalex-snapshot
Catalytic Activity of MCM-41–TBD in the Selective Preparation of Carbamates and Unsymmetrical Alkyl Carbonates from Diethyl Carbonate
inferredcites →https://doi.org/10.1016/j.molcata.2007.01.002openalex-snapshot
Supported and liquid phase task specific ionic liquids for base catalysed Knoevenagel reactions
inferredcites →https://doi.org/10.1016/s0040-4020(00)00671-2openalex-snapshot
Perspectives on Alkyl Carbonates in Organic Synthesis
inferredcites →https://doi.org/10.1016/s0926-860x(96)00402-4openalex-snapshot
Catalysis in the production and reactions of dimethyl carbonate, an environmentally benign building block
inferredcites →https://doi.org/10.1021/acs.joc.6b00441openalex-snapshot
Activation of Benzyl Aryl Carbonates: The Role of Cation−π Interactions
inferredcites →https://doi.org/10.1021/ar010076fopenalex-snapshot
The Chemistry of Dimethyl Carbonate
inferredcites →https://doi.org/10.1021/cr300463yopenalex-snapshot
Frontiers, Opportunities, and Challenges in Biochemical and Chemical Catalysis of CO 2 Fixation
inferredcites →https://doi.org/10.1021/cr4002758openalex-snapshot
Catalysis for the Valorization of Exhaust Carbon: from CO 2 to Chemicals, Materials, and Fuels. Technological Use of CO 2
inferredcites →https://doi.org/10.1021/cr900393dopenalex-snapshot
Organic Carbonates as Solvents in Synthesis and Catalysis
inferredcites →https://doi.org/10.1021/cs5018997openalex-snapshot
Recent Advances in the Catalytic Preparation of Cyclic Organic Carbonates
inferredcites →https://doi.org/10.1021/ie030322mopenalex-snapshot
Synthesis of Modern Synthetic Oils Based on Dialkyl Carbonates
inferredcites →https://doi.org/10.1021/ja01189a040openalex-snapshot
The Preparation of Di-t-butyl Carbonate and t-Butyl Chlorocarbonate1
inferredcites →https://doi.org/10.1021/jo00919a026openalex-snapshot
Noble metal catalysis. III. Preparation of dialkyl oxalates by oxidative carbonylation
inferredcites →https://doi.org/10.1021/jo990520gopenalex-snapshot
Alkyl Carbonates: Efficient Three Component Coupling of Aliphatic Alcohols, CO2, and Alkyl Halides in the Presence of Cs2CO3
inferredcites →https://doi.org/10.1021/om00028a069openalex-snapshot
Palladium-catalyzed generation of O-allylic urethanes and carbonates from amines/alcohols, carbon dioxide, and allylic chlorides
inferredcites →https://doi.org/10.1038/pj.2013.50openalex-snapshot
The anionic ring-opening polymerization of five-membered cyclic carbonates fused to the cyclohexane ring
inferredcites →https://doi.org/10.1039/b316050eopenalex-snapshot
An efficient synthesis of organic carbonates: atom economic protocol with a new catalytic system
inferredcites →https://doi.org/10.1039/b711981jopenalex-snapshot
Electrochemical activation of CO 2 in ionic liquid (BMIMBF 4 ): synthesis of organic carbonates under mild conditions
inferredcites →https://doi.org/10.1039/b9nj00729fopenalex-snapshot
Functionalised ionic liquids: synthesis of ionic liquids with tethered basic groups and their use in Heck and Knoevenagel reactions
inferredcites →https://doi.org/10.1039/c0gc00065eopenalex-snapshot
Synthesis of cyclic carbonates from epoxides and CO2
inferredcites →https://doi.org/10.1039/c0gc00765jopenalex-snapshot
Organotin-oxomolybdate coordination polymer as catalyst for synthesis of unsymmetrical organic carbonates
inferredcites →https://doi.org/10.1039/c2gc35191aopenalex-snapshot
TBD catalysis with dimethyl carbonate: a fruitful and sustainable alliance
inferredcites →https://doi.org/10.1039/c3gc40790jopenalex-snapshot
Synthesis of cyclic carbonates with carbon dioxide and cesium carbonate
inferredcites →https://doi.org/10.1039/c3nj00640aopenalex-snapshot
Non-symmetrical dialkyl carbonate synthesis promoted by 1-(3-trimethoxysilylpropyl)-3-methylimidazolium chloride
inferredcites →https://doi.org/10.1039/c4cc08510hopenalex-snapshot
Structurally simple complexes of CO 2
inferredcites →https://doi.org/10.1039/c4cs00374hopenalex-snapshot
Recent advances in dialkyl carbonates synthesis and applications
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/c4gc01754dopenalex-snapshot
Fixation of CO 2 into cyclic carbonates catalyzed by ionic liquids: a multi-scale approach
inferredcites →https://doi.org/10.1039/c5cc04088dopenalex-snapshot
A facile one-step synthesis of star-shaped alkynyl carbonates from CO 2
inferredcites →https://doi.org/10.1039/c5py00625bopenalex-snapshot
Unveiling the hyperbolic thermal behaviour of poly(p-phenylene alkylene)s
inferredcites →https://doi.org/10.1039/c5ra07290eopenalex-snapshot
Synthesis of 6-membered cyclic carbonates from 1,3-diols and low CO 2 pressure: a novel mild strategy to replace phosgene reagents
inferredcites →https://doi.org/10.1039/c5sc00040hopenalex-snapshot
Task-specific ionic liquid and CO 2 -cocatalysed efficient hydration of propargylic alcohols to α-hydroxy ketones
inferredcites →https://doi.org/10.1039/c6cc02853eopenalex-snapshot
Tuning the basicity of ionic liquids for efficient synthesis of alkylidene carbonates from CO 2 at atmospheric pressure
inferredcites →https://doi.org/10.1039/c6cc05730fopenalex-snapshot
Synthesis of cyclic carbonates from diols and CO 2 catalyzed by carbenes
inferredcites →https://doi.org/10.1039/c6dt02755eopenalex-snapshot
Three powerful dinuclear metal–organic catalysts for converting CO 2 into organic carbonates
inferredcites →https://doi.org/10.1039/c6gc00413jopenalex-snapshot
A dual-walled cage MOF as an efficient heterogeneous catalyst for the conversion of CO 2 under mild and co-catalyst free conditions
inferredcites →https://doi.org/10.1039/c6ra04084eopenalex-snapshot
Efficient fixation and conversion of CO 2 into dimethyl carbonate catalyzed by an imidazolium containing tri-cationic ionic liquid/super base system

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.4769597openalex-extracted
Heteronuclear Bicentric Ionic Liquids Tailored for Mild Catalytic Conversion of Co2 into Cyclic Carbonates
inferred← citeshttps://doi.org/10.1002/9783527838967.ch02openalex-snapshot
Ionic Liquid–Catalyzed Transformation of Carbon Dioxide to Chemicals Under Metal‐free Conditions
inferred← citeshttps://doi.org/10.1002/slct.202300436openalex-snapshot
Zinc‐Catalyzed Synthesis of Carbonate Derivatives
inferred← citeshttps://doi.org/10.1007/s11426-018-9396-3openalex-snapshot
Basic ionic liquids promoted chemical transformation of CO2 to organic carbonates
inferred← citeshttps://doi.org/10.1007/s41981-022-00216-2openalex-snapshot
Continuous flow organocatalyzed methoxycarbonylation of benzyl alcohol derivatives with dimethyl carbonate
inferred← citeshttps://doi.org/10.1016/j.jcou.2020.01.003openalex-snapshot
The coupling of CO2 with diols promoted by organic dual systems: Towards products divergence via benchmarking of the performance metrics
inferred← citeshttps://doi.org/10.1016/j.jcou.2022.101930openalex-snapshot
Design and synthesis of pyridinamide functionalized ionic liquids for efficient conversion of carbon dioxide into cyclic carbonates
inferred← citeshttps://doi.org/10.1016/j.mcat.2024.114227openalex-snapshot
Heteronuclear bicentric ionic liquids tailored for moderate catalytic conversion of CO2 into cyclic carbonates
inferred← citeshttps://doi.org/10.3390/catal12020124openalex-snapshot
En Route to CO2-Based (a)Cyclic Carbonates and Polycarbonates from Alcohols Substrates by Direct and Indirect Approaches
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