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

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What this work says

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

inferredcites →https://doi.org/10.1002/9783527616688openalex-snapshot
Industrial Organic Chemistry
inferredcites →https://doi.org/10.1002/ange.201200859openalex-snapshot
N,N‐Dimethylformamid: ein vielseitiger Baustein für die Synthese
inferredcites →https://doi.org/10.1002/ange.201301349openalex-snapshot
A General Catalytic Methylation of Amines Using Carbon Dioxide
inferredcites →https://doi.org/10.1002/ange.201304656openalex-snapshot
Ruthenium‐Catalyzed Direct Methylation of Primary and Secondary Aromatic Amines Using Carbon Dioxide and Molecular Hydrogen
inferredcites →https://doi.org/10.1002/ange.201306850openalex-snapshot
Selective Methylation of Amines with Carbon Dioxide and H2
inferredcites →https://doi.org/10.1002/ange.201407357openalex-snapshot
Carbon Dioxide Reduction to Methylamines under Metal‐Free Conditions
inferredcites →https://doi.org/10.1002/ange.201407689openalex-snapshot
Metal‐Free Catalyst for the Chemoselective Methylation of Amines Using Carbon Dioxide as a Carbon Source
inferredcites →https://doi.org/10.1002/ange.201507921openalex-snapshot
Expanding the Ligand Framework Diversity of Carbodicarbenes and Direct Detection of Boron Activation in the Methylation of Amines with CO2
inferredcites →https://doi.org/10.1002/ange.201702734openalex-snapshot
Betaine Catalysis for Hierarchical Reduction of CO2 with Amines and Hydrosilane To Form Formamides, Aminals, and Methylamines
inferredcites →https://doi.org/10.1002/anie.201200859openalex-snapshot
N,N‐Dimethylformamide: A Multipurpose Building Block
inferredcites →https://doi.org/10.1002/anie.201301349openalex-snapshot
A General Catalytic Methylation of Amines Using Carbon Dioxide
inferredcites →https://doi.org/10.1002/anie.201304656openalex-snapshot
Ruthenium‐Catalyzed Direct Methylation of Primary and Secondary Aromatic Amines Using Carbon Dioxide and Molecular Hydrogen
inferredcites →https://doi.org/10.1002/anie.201306850openalex-snapshot
Selective Methylation of Amines with Carbon Dioxide and H2
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.201507921openalex-snapshot
Expanding the Ligand Framework Diversity of Carbodicarbenes and Direct Detection of Boron Activation in the Methylation of Amines with CO2
inferredcites →https://doi.org/10.1002/anie.201702734openalex-snapshot
Betaine Catalysis for Hierarchical Reduction of CO2 with Amines and Hydrosilane To Form Formamides, Aminals, and Methylamines
inferredcites →https://doi.org/10.1002/chem.201400332openalex-snapshot
Sustainable Heterogeneous Platinum Catalyst for Direct Methylation of Secondary Amines by Carbon Dioxide and Hydrogen
inferredcites →https://doi.org/10.1002/chem.201603688openalex-snapshot
Fluoride‐Catalyzed Methylation of Amines by Reductive Functionalization of CO2 with Hydrosilanes
inferredcites →https://doi.org/10.1002/cssc.201500486openalex-snapshot
Direct Methylation of Amines with Carbon Dioxide and Molecular Hydrogen using Supported Gold Catalysts
inferredcites →https://doi.org/10.1002/cssc.201600521openalex-snapshot
Chemoselective Synthesis of Carbamates using CO2 as Carbon Source
inferredcites →https://doi.org/10.1002/ejoc.201500924openalex-snapshot
Direct [11C]Methylation of Amines from [11C]CO2 for the Synthesis of PET Radiotracers
inferredcites →https://doi.org/10.1016/0022-1902(58)80250-xopenalex-snapshot
Reactions of carbon dioxide with sodium and lithium borohydrides
inferredcites →https://doi.org/10.1016/j.cell.2012.05.003openalex-snapshot
Comprehensive Analysis of mRNA Methylation Reveals Enrichment in 3′ UTRs and near Stop Codons
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/10.1021/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.6b01856openalex-snapshot
Selective Formylation and Methylation of Amines using Carbon Dioxide and Hydrosilane Catalyzed by Alkali-Metal Carbonates
inferredcites →https://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
inferredcites →https://doi.org/10.1021/ar010076fopenalex-snapshot
The Chemistry of Dimethyl Carbonate
inferredcites →https://doi.org/10.1021/ja307924aopenalex-snapshot
Well-Defined Iron Catalyst for Improved Hydrogenation of Carbon Dioxide and Bicarbonate
inferredcites →https://doi.org/10.1021/jacs.5b06077openalex-snapshot
Iron-Catalyzed Reduction of CO 2 into Methylene: Formation of C–N, C–O, and C–C Bonds
inferredcites →https://doi.org/10.1021/jo0511804openalex-snapshot
Electrochemically Promoted C−N Bond Formation from Acetylenic Amines and CO2. Synthesis of 5-Methylene-1,3-oxazolidin-2-ones
inferredcites →https://doi.org/10.1021/om501176uopenalex-snapshot
Selective N-Methylation of Aliphatic Amines with CO2 and Hydrosilanes Using Nickel-Phosphine Catalysts
inferredcites →https://doi.org/10.1038/nature11112openalex-snapshot
Topology of the human and mouse m6A RNA methylomes revealed by m6A-seq
inferredcites →https://doi.org/10.1038/nrg3173openalex-snapshot
Histone methylation: a dynamic mark in health, disease and inheritance
inferredcites →https://doi.org/10.1039/c2ee02774gopenalex-snapshot
Carbon dioxide utilization with C–N bond formation: carbon dioxide capture and subsequent conversion
inferredcites →https://doi.org/10.1039/c3sc22240copenalex-snapshot
CO2 as a C1-building block for the catalytic methylation of amines
inferredcites →https://doi.org/10.1039/c3sc52676copenalex-snapshot
Methylation of amines, nitrobenzenes and aromatic nitriles with carbon dioxide and molecular hydrogen
inferredcites →https://doi.org/10.1039/c4cc05119jopenalex-snapshot
N-Methylation of amine and nitro compounds with CO 2 /H 2 catalyzed by Pd/CuZrO x under mild reaction conditions
inferredcites →https://doi.org/10.1039/c4cy00130copenalex-snapshot
Iron-catalyzed hydrosilylation of CO 2 : CO 2 conversion to formamides and methylamines
inferredcites →https://doi.org/10.1039/c5dt03506fopenalex-snapshot
N-heterocyclic carbene copper( i ) catalysed N-methylation of amines using CO 2
inferredcites →https://doi.org/10.1039/c5gc01386kopenalex-snapshot
B(C 6 F 5 ) 3 -catalyzed methylation of amines using CO 2 as a C1 building block
inferredcites →https://doi.org/10.1039/c5ra20991aopenalex-snapshot
Direct methylation of N-methylaniline with CO 2 /H 2 catalyzed by gold nanoparticles supported on alumina
inferredcites →https://doi.org/10.1039/c6cc09072aopenalex-snapshot
Catalyst-free N-methylation of amines using CO 2
inferredcites →https://doi.org/10.1039/c7gc00484bopenalex-snapshot
Carboxylate-promoted reductive functionalization of CO 2 with amines and hydrosilanes under mild conditions
inferredcites →https://doi.org/10.1039/c7gc03416dopenalex-snapshot
Tungstate catalysis: pressure-switched 2- and 6-electron reductive functionalization of CO 2 with amines and phenylsilane
inferredcites →https://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?
inferredcites →https://doi.org/10.5860/choice.43-0322openalex-snapshot
Handbook of industrial chemistry: organic chemicals

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/10.1002/9783527831883.ch26openalex-snapshot
Methylation Reactions with CO 2
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/asia.202400497openalex-snapshot
Homogeneous Catalysis in N‐Formylation/N‐Methylation Utilizing Carbon Dioxide as the C1 Source
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/cctc.202401260openalex-snapshot
Pd/PVP‐ Catalyzed Formylation of Amines and Nitroarenes to N‐Formamides with CO2 and Dimethylamine Borane: The Influence of CO2 on the Formation of Azoxyarenes
inferred← citeshttps://doi.org/10.1002/cssc.201802757openalex-snapshot
A Highly Effective Route to Si−O−Si Moieties through O‐Silylation of Silanols and Polyhedral Oligomeric Silsesquioxane Silanols with Disilazanes
inferred← citeshttps://doi.org/10.1002/cssc.202301120openalex-snapshot
Borohydride Ionic Liquids as Reductants of CO2 in the Selective N‐formylation of Amines
inferred← citeshttps://doi.org/10.1002/ejic.202000401openalex-snapshot
Lithium Organoaluminate Complexes as Catalysts for the Conversion of CO2 into Cyclic Carbonates
inferred← citeshttps://doi.org/10.1002/ejoc.202001408openalex-snapshot
CO2‐Controlled Reductive Amination Reactions with NaBH4
inferred← citeshttps://doi.org/10.1002/slct.202201727openalex-snapshot
Triethylamine Catalyzed Reductive CO 2 to Form N‐Formylation of Amines and Hydrazides
inferred← citeshttps://doi.org/10.1002/slct.202304621openalex-snapshot
Catalysis‐Controlled Selective N ‐mono or N ‐di‐methylation of Anilines: A Review on Synthesis of N ‐methyl or N , N ‐dimethyl anilines
inferred← citeshttps://doi.org/10.1007/s10311-020-01121-7openalex-snapshot
Catalyst-free fixation of carbon dioxide into value-added chemicals: a review
inferred← citeshttps://doi.org/10.1007/s11426-023-1804-4openalex-snapshot
Bimolecular reduction of carbon dioxide: double synthons for alkynes trifunctionalization
inferred← citeshttps://doi.org/10.1016/j.jcou.2020.101155openalex-snapshot
Imidazolium hydrogen carbonate ionic liquids: Versatile organocatalysts for chemical conversion of CO2 into valuable chemicals
inferred← citeshttps://doi.org/10.1016/j.jcou.2021.101590openalex-snapshot
Catalyst-free hierarchical reduction of CO2 with BH3N(C2H5)3 for selective N-methylation and N-formylation of amines
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.jscs.2022.101421openalex-snapshot
Platinum nanoparticles as recyclable heterogeneous catalyst for selective methylation of amines and imines with formic acid: Indirect utilization of CO2
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.joc.5c03245openalex-snapshot
Solvent-Tuned Selective N -Ethylation and N -Acetylation of Amines Using NaBH(OAc) 3
inferred← citeshttps://doi.org/10.1021/acs.joc.9b01180openalex-snapshot
Reduction of CO2 with NaBH4/I2 for the Conversion of Thiophenols to Aryl Methyl Sulfides
inferred← citeshttps://doi.org/10.1021/acs.joc.9b01587openalex-snapshot
α-Methylation of 2-Arylacetonitrile by a Trimethylamine-Borane/CO2 System
inferred← citeshttps://doi.org/10.1021/acs.organomet.9b00712openalex-snapshot
Cp2TiCl2-Catalyzed Carboxylation of Aryl Chlorides with Carbon Dioxide in the Presence of n-BuMgCl
inferred← citeshttps://doi.org/10.1021/acs.orglett.8b02730openalex-snapshot
Reduction of CO2 into Methylene Coupled with the Formation of C–S Bonds under NaBH4/I2 System
inferred← citeshttps://doi.org/10.1021/acscatal.2c06218openalex-snapshot
Autocatalytic O-Formylation of Alcohols Using CO2
inferred← citeshttps://doi.org/10.1021/acssuschemeng.3c04457openalex-snapshot
Catalyst-Free N-Formylation of Amines Using Formic Acid as a Sustainable C1 Source
inferred← citeshttps://doi.org/10.1039/c9gc03277kopenalex-snapshot
Biomass-derived N-doped porous carbon: an efficient metal-free catalyst for methylation of amines with CO 2
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/d0nj02798gopenalex-snapshot
Triazinetriamine-derived porous organic polymer-supported copper nanoparticles (Cu-NPs@TzTa-POP): an efficient catalyst for the synthesis of N -methylated products via CO 2 fixation and primary carbamates from alcohols and urea
inferred← citeshttps://doi.org/10.1039/d1gc02815dopenalex-snapshot
CO 2 -tuned highly selective reduction of formamides to the corresponding methylamines
inferred← citeshttps://doi.org/10.1039/d2ra03134eopenalex-snapshot
Catalyst-free reductive cyclization of bis(2-aminophenyl) disulfide with CO 2 in the presence of BH 3 NH 3 to synthesize 2-unsubstituted benzothiazole derivatives
inferred← citeshttps://doi.org/10.1039/d3nj03341dopenalex-snapshot
Ruthenium/HI-catalyzed direct hydromethylation of indoles and quinolines in DME
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/10.6023/cjoc202405049openalex-snapshot
Boron-Promoted Co-Catalyzed N-Methylation of Secondary Aromatic Amines with CO2 and H2
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