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Autocatalytic O-Formylation of Alcohols Using CO2

https://doi.org/10.1021/acscatal.2c06218

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What this work says

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

inferredcites →https://doi.org/10.1002/14356007openalex-snapshot

Ullmann's Encyclopedia of Industrial Chemistry

inferredcites →https://doi.org/10.1002/9783527821952openalex-snapshot

CO2 as a Building Block in Organic Synthesis

inferredcites →https://doi.org/10.1002/ange.201915988openalex-snapshot

Closing the Loop for Hydrogen Storage: Facile Regeneration of NaBH4 from its Hydrolytic Product

inferredcites →https://doi.org/10.1002/anie.201004263openalex-snapshot

A Well‐Defined Iron Catalyst for the Reduction of Bicarbonates and Carbon Dioxide to Formates, Alkyl Formates, and Formamides

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.201205362openalex-snapshot

Equimolar CO2 Capture by N‐Substituted Amino Acid Salts and Subsequent Conversion

inferredcites →https://doi.org/10.1002/anie.201407357openalex-snapshot

Carbon Dioxide Reduction to Methylamines under Metal‐Free Conditions

inferredcites →https://doi.org/10.1002/cbic.201600684openalex-snapshot

Alkyl Formate Ester Synthesis by a Fungal Baeyer–Villiger Monooxygenase

inferredcites →https://doi.org/10.1002/cctc.201800699openalex-snapshot

Homogeneous Catalytic Reduction of CO 2 with Silicon‐Hydrides, State of the Art

inferredcites →https://doi.org/10.1002/ceat.201400292openalex-snapshot

Thermodynamic Properties of CO2 Conversion by Sodium Borohydride

inferredcites →https://doi.org/10.1002/cssc.201000097openalex-snapshot

Carbon Dioxide as Chemical Feedstock. Edited by Michele Aresta.

inferredcites →https://doi.org/10.1002/cssc.201801037openalex-snapshot

1,4‐Dioxane‐Tuned Catalyst‐Free Methylation of Amines by CO2 and NaBH4

inferredcites →https://doi.org/10.1002/ejoc.201800320openalex-snapshot

Lewis Base Promoted Reduction of CO2 with BH3NH3 into Boryl Formates: CO2 as a Carbon Source in Organic Synthesis Under Mild Conditions

inferredcites →https://doi.org/10.1007/bf01026097openalex-snapshot

Lipase catalysis in organic solvents transesterification of O-formyl esters of secondary alcohols

inferredcites →https://doi.org/10.1007/s11244-013-0195-yopenalex-snapshot

Hydrophobic Formic Acid Esters for Cofactor Regeneration in Aqueous/Organic Two-Liquid Phase Systems

inferredcites →https://doi.org/10.1016/j.ccr.2015.06.003openalex-snapshot

Boron-mediated activation of carbon dioxide

inferredcites →https://doi.org/10.1016/j.chempr.2020.04.008openalex-snapshot

A Bioinspired Multicomponent Catalytic System for Converting Carbon Dioxide into Methanol Autocatalytically

inferredcites →https://doi.org/10.1016/j.jcou.2017.10.007openalex-snapshot

Reductive formylation of amines with CO 2 using sodium borohydride: A catalyst-free route

inferredcites →https://doi.org/10.1016/j.jcou.2021.101759openalex-snapshot

A review on recent developments in N-methylation using CO2

inferredcites →https://doi.org/10.1016/j.molcatb.2014.03.016openalex-snapshot

Lipase-catalyzed transesterification of ethyl formate to octyl formate

inferredcites →https://doi.org/10.1021/acs.accounts.5b00027openalex-snapshot

Hydrogenation and Dehydrogenation Iron Pincer Catalysts Capable of Metal–Ligand Cooperation by Aromatization/Dearomatization

inferredcites →https://doi.org/10.1021/acs.accounts.5b00055openalex-snapshot

Nickel and Iron Pincer Complexes as Catalysts for the Reduction of Carbonyl Compounds

inferredcites →https://doi.org/10.1021/acs.accounts.9b00324openalex-snapshot

Integrated CO2 Capture and Conversion to Formate and Methanol: Connecting Two Threads

inferredcites →https://doi.org/10.1021/acs.chemrev.5b00197openalex-snapshot

CO2 Hydrogenation to Formate and Methanol as an Alternative to Photo- and Electrochemical CO2 Reduction

inferredcites →https://doi.org/10.1021/acs.organomet.5b00190openalex-snapshot

Revisiting CO2 Reduction with NaBH4 under Aprotic Conditions: Synthesis and Characterization of Sodium Triformatoborohydride

inferredcites →https://doi.org/10.1021/acscatal.0c05681openalex-snapshot

CO2-Promoted Reactions: An Emerging Concept for the Synthesis of Fine Chemicals and Pharmaceuticals

inferredcites →https://doi.org/10.1021/acscatal.7b01729openalex-snapshot

Manganese-Catalyzed Direct Deoxygenation of Primary Alcohols

inferredcites →https://doi.org/10.1021/cr068357uopenalex-snapshot

Transformation of Carbon Dioxide

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/ncomms5017openalex-snapshot

Direct synthesis of formic acid from carbon dioxide by hydrogenation in acidic media

inferredcites →https://doi.org/10.1038/ncomms6933openalex-snapshot

Using carbon dioxide as a building block in organic synthesis

inferredcites →https://doi.org/10.1039/a608150iopenalex-snapshot

Highly active ruthenium complexes with bidentate phosphine ligands for the solvent-free catalytic synthesis of N,N-dimethylformamide and methyl formate

inferredcites →https://doi.org/10.1039/c0cs00129eopenalex-snapshot

Transition-metal-catalyzed C–C bond formation through the fixation of carbon dioxide

inferredcites →https://doi.org/10.1039/c1ee02156gopenalex-snapshot

CO2 capture and activation by superbase/polyethylene glycol and its subsequent conversion

inferredcites →https://doi.org/10.1039/c1ob06064copenalex-snapshot

Formate dehydrogenase - a biocatalyst with novel applications in organic chemistry

inferredcites →https://doi.org/10.1039/c3cy00948copenalex-snapshot

Homogeneous catalytic reduction of CO 2 with hydrosilanes

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/c5gc01008jopenalex-snapshot

CHEM21 selection guide of classical- and less classical-solvents

inferredcites →https://doi.org/10.1039/c6gc00611fopenalex-snapshot

Updating and further expanding GSK's solvent sustainability guide

inferredcites →https://doi.org/10.1039/c7cc03860gopenalex-snapshot

Catalyst-free N-formylation of amines using BH 3 NH 3 and CO 2 under mild conditions

inferredcites →https://doi.org/10.1039/c9gc01897bopenalex-snapshot

Converting H + from coordinated water into H − enables super facile synthesis of LiBH 4

inferredcites →https://doi.org/10.1039/c9gc03637gopenalex-snapshot

Catalyst-free selective N -formylation and N -methylation of amines using CO 2 as a sustainable C1 source

inferredcites →https://doi.org/10.1039/c9se01141bopenalex-snapshot

Methanol production from CO 2 via an integrated, formamide-assisted approach

inferredcites →https://doi.org/10.1039/c9ta00769eopenalex-snapshot

Realizing facile regeneration of spent NaBH 4 with Mg–Al alloy

inferredcites →https://doi.org/10.1073/pnas.1821029116openalex-snapshot

Climate change mitigation potential of carbon capture and utilization in the chemical industry

inferredcites →https://doi.org/10.1201/9781439847503openalex-snapshot

Fenaroli's Handbook of Flavor Ingredients

inferredcites →https://doi.org/10.1557/s43577-022-00316-3openalex-snapshot

Complex hydrides for CO2 reduction

inferredcites →https://doi.org/10.3390/biom10010070openalex-snapshot

Novel and Efficient Synthesis of Phenethyl Formate via Enzymatic Esterification of Formic Acid

inferredcites →https://doi.org/10.5860/choice.44-5067openalex-snapshot

Greene's protective groups in organic synthesis

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.4678615openalex-extracted

One-Pot Two-Step Reduction of Co2 with Amines and Nabh4 to N-Substituted Compounds at Atmospheric Pressure

inferred← citeshttps://doi.org/10.1002/ajoc.202300097openalex-snapshot

Research Progress on Carbon Dioxide Reduction Coupled with the Formation of C−O Bonds to Oxygenated Compounds

inferred← citeshttps://doi.org/10.1002/ange.9277722openalex-snapshot

CO 2 as a Redox Shuttle Enables Photocatalytic Dehydrogenative Decarbonylation of Biomass‐Derived Alcohols to Light Alkanes

inferred← citeshttps://doi.org/10.1002/anie.9277722openalex-snapshot

CO 2 as a Redox Shuttle Enables Photocatalytic Dehydrogenative Decarbonylation of Biomass‐Derived Alcohols to Light Alkanes

inferred← citeshttps://doi.org/10.1002/cctc.202300510openalex-snapshot

Frustrated Lewis Pairs Catalyse the Solvent‐Assisted Synthesis of Azoles from ortho‐Substituted Anilines, CO2 and H2

inferred← citeshttps://doi.org/10.1002/cctc.202300905openalex-snapshot

Autocatalysis and CO2: Carbon Capture and Utilization (CCU) Meets Natural Processes

inferred← citeshttps://doi.org/10.1002/cctc.202401834openalex-snapshot

CO2‐Promoted Reactions: A Prosperous Strategy for Conversion of Functional Group in Organic Synthesis

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.jece.2026.125131openalex-snapshot

Covalent immobilization of thiolate-based ionic liquids on 2-chlorotrityl chloride resin: A versatile metal- and halogen-free catalyst for CO2 valorization

inferred← citeshttps://doi.org/10.1021/acs.joc.4c00437openalex-snapshot

CO2-Promoted and Copper-Catalyzed Dehydroxylative Coupling of Benzylic Alcohols by the NaBH4/I2 System

inferred← citeshttps://doi.org/10.1021/acs.orglett.4c01147openalex-snapshot

Silver-Catalyzed Coupling of Ethynylbenziodoxolones with CO2 and Amines to Afford O-β-Oxoalkyl Carbamates

inferred← citeshttps://doi.org/10.1021/acs.orglett.5c00677openalex-snapshot

Iridium-Catalyzed, Copper-Induced Reductive Cyclization of NO2-Pyrrolarenes with CO2 as a Single-Carbon Source

inferred← citeshttps://doi.org/10.1021/acssuschemeng.3c02935openalex-snapshot

Perspectives from the 2022 Cohort of the American Chemical Society Summer School on Green Chemistry & Sustainable Energy

inferred← citeshttps://doi.org/10.1038/s41467-023-40306-wopenalex-snapshot

Enhancing polyol/sugar cascade oxidation to formic acid with defect rich MnO2 catalysts

inferred← citeshttps://doi.org/10.1038/s41467-023-43289-wopenalex-snapshot

Straightforward synthesis of functionalized γ-Lactams using impure CO2 stream as the carbon source

inferred← citeshttps://doi.org/10.1039/d4sc03665dopenalex-snapshot

Aluminium porphyrins catalyse the hydrogenation of CO 2 with H 2

inferred← citeshttps://doi.org/10.1039/d4su00305eopenalex-snapshot

Establishing ultraporous permanently polarized hydroxyapatite as a green and highly efficient catalyst for carbon dioxide conversion in continuous flow under mild conditions

inferred← citeshttps://doi.org/10.1039/d5su00739aopenalex-snapshot

First sustainable synthesis of biobased ethyl and methyl formates by ecocatalysis

inferred← citeshttps://doi.org/10.1039/d6ob00632aopenalex-snapshot

From one to two CO 2 molecules: controllable divergent synthesis of formate esters and carbonates

inferred← citeshttps://doi.org/10.20517/cs.2025.13openalex-snapshot

Reductive O-formylation of carbon dioxide and alcohols over porous phenanthroline-based polymer supported single iridium atom catalyst

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