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

https://doi.org/10.2139/ssrn.4678615
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Outgoing claims: the papers this work cites, builds on, or argues with.

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The Chemistry of Anilines
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Highly Efficient Ruthenium‐Catalyzed N‐Formylation of Amines with H 2 and CO 2
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Effective Formylation of Amines with Carbon Dioxide and Diphenylsilane Catalyzed by Chelating bis( tz NHC) Rhodium Complexes
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Synthesis of Lithium Boracarbonate Ion Pairs by Copper‐Catalyzed Multi‐Component Coupling of Carbon Dioxide, Diboron, and Aldehydes
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Closing the Loop for Hydrogen Storage: Facile Regeneration of NaBH 4 from its Hydrolytic Product
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Fe‐Catalyzed Pictet‐Spengler‐Type Cyclization via Selective Four‐Electron Reductive Functionalization of CO2
inferredcites →https://doi.org/10.1002/cssc.201801037openalex-extracted
1,4‐Dioxane‐Tuned Catalyst‐Free Methylation of Amines by CO2 and NaBH4
inferredcites →https://doi.org/10.1002/cssc.201903514openalex-extracted
Solvent‐ and Catalyst‐Free Carbon Dioxide Capture and Reduction to Formate with Borohydride Ionic Liquid
inferredcites →https://doi.org/10.1002/ejoc.202001408openalex-extracted
CO2‐Controlled Reductive Amination Reactions with NaBH4
inferredcites →https://doi.org/10.1016/j.cattod.2020.01.030openalex-extracted
Design of Lewis base functionalized ionic liquids for the N-formylation of amines with CO2 and hydrosilane: The cation effects
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Comprehensive Analysis of mRNA Methylation Reveals Enrichment in 3′ UTRs and near Stop Codons
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An one-step approach towards hydrogen production and storage through regeneration of NaBH4
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Reductive formylation of amines with CO 2 using sodium borohydride: A catalyst-free route
inferredcites →https://doi.org/10.1016/j.jpowsour.2017.05.075openalex-extracted
Hydrolysis and regeneration of sodium borohydride (NaBH 4 ) – A combination of hydrogen production and storage
inferredcites →https://doi.org/10.1016/j.rser.2011.07.018openalex-extracted
Sodium borohydride as a fuel for the future
inferredcites →https://doi.org/10.1021/acs.chemrev.7b00435openalex-extracted
Sustainable Conversion of Carbon Dioxide: An Integrated Review of Catalysis and Life Cycle Assessment
inferredcites →https://doi.org/10.1021/acs.inorgchem.0c01152openalex-extracted
Ph2PCH2CH2B(C8H14) and Its Formaldehyde Adduct as Catalysts for the Reduction of CO2 with Hydroboranes
inferredcites →https://doi.org/10.1021/acs.joc.3c00026openalex-extracted
Aminoguanidine-Catalyzed Reductive Cyclization of o-Phenylenediamines with CO2 in the Presence of Triethoxysilane
inferredcites →https://doi.org/10.1021/acs.joc.9b01587openalex-extracted
α-Methylation of 2-Arylacetonitrile by a Trimethylamine-Borane/CO2 System
inferredcites →https://doi.org/10.1021/acs.organomet.7b00497openalex-extracted
Selective Ni-Catalyzed Hydroboration of CO2 to the Formaldehyde Level Enabled by New PSiP Ligation
inferredcites →https://doi.org/10.1021/acs.orglett.1c03023openalex-extracted
Borane–Trimethylamine Complex as a Reducing Agent for Selective Methylation and Formylation of Amines with CO2
inferredcites →https://doi.org/10.1021/acscatal.1c00412openalex-extracted
Selective Reductive Dimerization of CO2 into Glycolaldehyde
inferredcites →https://doi.org/10.1021/acscatal.2c06218openalex-extracted
Autocatalytic O-Formylation of Alcohols Using CO2
inferredcites →https://doi.org/10.1021/acscatal.5b00428openalex-extracted
Catalytic Hydroboration of Carbonyl Derivatives, Imines, and Carbon Dioxide
inferredcites →https://doi.org/10.1021/acscatal.5b01274openalex-extracted
Imidazolium-Based Ionic Liquids Catalyzed Formylation of Amines Using Carbon Dioxide and Phenylsilane at Room Temperature
inferredcites →https://doi.org/10.1021/acscatal.5b02583openalex-extracted
Metalated Mesoporous Poly(triphenylphosphine) with Azo Functionality: Efficient Catalysts for CO2 Conversion
inferredcites →https://doi.org/10.1021/acscatal.6b00421openalex-extracted
Implications of CO2 Activation by Frustrated Lewis Pairs in the Catalytic Hydroboration of CO2: A View Using N/Si+ Frustrated Lewis Pairs
inferredcites →https://doi.org/10.1021/acscatal.7b03834openalex-extracted
Selective Iron-Catalyzed N-Formylation of Amines using Dihydrogen and Carbon Dioxide
inferredcites →https://doi.org/10.1021/acscatal.8b03894openalex-extracted
Controlling Selectivity in the Hydroboration of Carbon Dioxide to the Formic Acid, Formaldehyde, and Methanol Oxidation Levels
inferredcites →https://doi.org/10.1021/cr4002758openalex-extracted
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/ja500708wopenalex-extracted
Ruthenium-Catalyzed Reduction of Carbon Dioxide to Formaldehyde
inferredcites →https://doi.org/10.1021/jacs.5b06077openalex-extracted
Iron-Catalyzed Reduction of CO 2 into Methylene: Formation of C–N, C–O, and C–C Bonds
inferredcites →https://doi.org/10.1038/nature11112openalex-extracted
Topology of the human and mouse m6A RNA methylomes revealed by m6A-seq
inferredcites →https://doi.org/10.1038/ncomms6933openalex-extracted
Using carbon dioxide as a building block in organic synthesis
inferredcites →https://doi.org/10.1038/nrg3173openalex-extracted
Histone methylation: a dynamic mark in health, disease and inheritance
inferredcites →https://doi.org/10.1039/c2gc36517kopenalex-extracted
Cyclization of o-phenylenediamines by CO 2 in the presence of H 2 for the synthesis of benzimidazoles
inferredcites →https://doi.org/10.1039/c3sc22240copenalex-extracted
CO2 as a C1-building block for the catalytic methylation of amines
inferredcites →https://doi.org/10.1039/c4cc02973aopenalex-extracted
Partially reduced iridium oxide clusters dispersed on titania as efficient catalysts for facile synthesis of dimethylformamide from CO 2 , H 2 and dimethylamine
inferredcites →https://doi.org/10.1039/c4cc05119jopenalex-extracted
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/c6gc02243jopenalex-extracted
Synthesis of formamides containing unsaturated groups by N-formylation of amines using CO 2 with H 2
inferredcites →https://doi.org/10.1039/c8cc02139bopenalex-extracted
Carbodiimides as catalysts for the reduction of CO 2 with boranes
inferredcites →https://doi.org/10.1039/c8cs00502hopenalex-extracted
New horizon in C1 chemistry: breaking the selectivity limitation in transformation of syngas and hydrogenation of CO 2 into hydrocarbon chemicals and fuels
inferredcites →https://doi.org/10.1039/c9gc03637gopenalex-extracted
Catalyst-free selective N -formylation and N -methylation of amines using CO 2 as a sustainable C1 source
inferredcites →https://doi.org/10.1039/d0cy00118jopenalex-extracted
Acetate-catalyzed hydroboration of CO 2 for the selective formation of methanol-equivalent products
inferredcites →https://doi.org/10.1039/d0gc02890hopenalex-extracted
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
inferredcites →https://doi.org/10.1039/d1gc01897copenalex-extracted
A substituent- and temperature-controllable NHC-derived zwitterionic catalyst enables CO 2 upgrading for high-efficiency construction of formamides and benzimidazoles
inferredcites →https://doi.org/10.1039/d1gc02815dopenalex-extracted
CO 2 -tuned highly selective reduction of formamides to the corresponding methylamines
inferredcites →https://doi.org/10.1039/d1ra04848aopenalex-extracted
Catalyst free N -formylation of aromatic and aliphatic amines exploiting reductive formylation of CO 2 using NaBH 4
inferredcites →https://doi.org/10.1039/d3cy00401eopenalex-extracted
N-Heterocyclic carbene supported zinc catalysed N -formylation of diverse N–H functionalities with carbon dioxide under ambient conditions
inferredcites →https://doi.org/10.1039/d3qo00058copenalex-extracted
DIC–borane-catalyzed selective methylation of primary amines with CO 2 using boranes as reducing agents
inferredcites →https://doi.org/10.5860/choice.43-0322openalex-extracted
Handbook of industrial chemistry: organic chemicals
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