On the public citation graph

Carbodiimides as catalysts for the reduction of CO 2 with boranes

https://doi.org/10.1039/c8cc02139b
0 signed · 92 inferred · view as graph

Inferred edges come from two machine sources: sweeps of open repository metadata (mostly SSRN and Zenodo), and a bulk OpenAlex citation snapshot. Every row below is labelled with the one it came from. Neither is a complete citation index — absence here is not evidence of absence.

Is this your work? Sign in with ORCID and put your name on the claims that are yours.
Claim with ORCID
Reference health. See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.
See reference health

What this work says

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

inferredcites →https://doi.org/10.1002/9780470516683openalex-snapshot
Chemistry and Technology of Carbodiimides
inferredcites →https://doi.org/10.1002/9783527627806openalex-snapshot
Beyond Oil and Gas: The Methanol Economy
inferredcites →https://doi.org/10.1002/9783527629916openalex-snapshot
Carbon Dioxide as Chemical Feedstock
inferredcites →https://doi.org/10.1002/anie.201000533openalex-snapshot
State‐of‐the‐Art Catalysts for Hydrogenation of Carbon Dioxide
inferredcites →https://doi.org/10.1002/anie.201102010openalex-snapshot
Transformation of Carbon Dioxide with Homogeneous Transition‐Metal Catalysts: A Molecular Solution to a Global Challenge?
inferredcites →https://doi.org/10.1002/anie.201609040openalex-snapshot
Metal‐Free Reduction of CO2 to Methoxyborane under Ambient Conditions through Borondiformate Formation
inferredcites →https://doi.org/10.1002/cctc.201300013openalex-snapshot
Improving the Efficiency of the Hydrogenation of Carbonates and Carbon Dioxide to Methanol
inferredcites →https://doi.org/10.1002/chem.201304376openalex-snapshot
Transition‐Metal‐Free Catalytic Reduction of Carbon Dioxide
inferredcites →https://doi.org/10.1002/chem.201304870openalex-snapshot
Carbene‐9‐BBN Ring Expansions as a Route to Intramolecular Frustrated Lewis Pairs for CO2 Reduction
inferredcites →https://doi.org/10.1002/chem.201400349openalex-snapshot
Metal‐Free Reduction of CO2 with Hydroboranes: Two Efficient Pathways at Play for the Reduction of CO2 to Methanol
inferredcites →https://doi.org/10.1002/chem.201600681openalex-snapshot
Magnesium Catalysis for the Hydroboration of Carbodiimides
inferredcites →https://doi.org/10.1002/chem.201705987openalex-snapshot
Organoactinide‐Catalyzed Monohydroboration of Carbodiimides
inferredcites →https://doi.org/10.1002/cssc.201000447openalex-snapshot
Chemical Technologies for Exploiting and Recycling Carbon Dioxide into the Value Chain
inferredcites →https://doi.org/10.1002/jctb.4229openalex-snapshot
Use of carbon dioxide as feedstock for chemicals and fuels: homogeneous and heterogeneous catalysis
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.ccr.2016.05.005openalex-snapshot
Design principles in frustrated Lewis pair catalysis for the functionalization of carbon dioxide and heterocycles
inferredcites →https://doi.org/10.1016/j.cogsc.2016.11.004openalex-snapshot
Metal-free reduction of CO2
inferredcites →https://doi.org/10.1016/j.jcou.2017.10.023openalex-snapshot
Advances in catalytic homogeneous hydrogenation of carbon dioxide to methanol
inferredcites →https://doi.org/10.1021/acs.accounts.7b00039openalex-snapshot
Reversible Hydrogenation of Carbon Dioxide to Formic Acid and Methanol: Lewis Acid Enhancement of Base Metal Catalysts
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/acscatal.5b00189openalex-snapshot
Hydroboration of Carbon Dioxide Using Ambiphilic Phosphine–Borane Catalysts: On the Role of the Formaldehyde Adduct
inferredcites →https://doi.org/10.1021/acscatal.5b00428openalex-snapshot
Catalytic Hydroboration of Carbonyl Derivatives, Imines, and Carbon Dioxide
inferredcites →https://doi.org/10.1021/acscatal.6b00421openalex-snapshot
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.6b00587openalex-snapshot
BH3 Activation by Phosphorus-Stabilized Geminal Dianions: Synthesis of Ambiphilic Organoborane, DFT Studies, and Catalytic CO2 Reduction into Methanol Derivatives
inferredcites →https://doi.org/10.1021/cr00046a004openalex-snapshot
Carbodiimide chemistry: recent advances
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/cr60246a001openalex-snapshot
Advances in the Chemistry of Carbodiimides
inferredcites →https://doi.org/10.1021/ja103982topenalex-snapshot
An Efficient Nickel Catalyst for the Reduction of Carbon Dioxide with a Borane
inferredcites →https://doi.org/10.1021/ja1064153openalex-snapshot
Reactions of Boron Amidinates with CO2 and CO and Other Small Molecules
inferredcites →https://doi.org/10.1021/ja404585popenalex-snapshot
A Highly Active Phosphine–Borane Organocatalyst for the Reduction of CO2 to Methanol Using Hydroboranes
inferredcites →https://doi.org/10.1021/ja5047846openalex-snapshot
Reducing CO2 to Methanol Using Frustrated Lewis Pairs: On the Mechanism of Phosphine–Borane-Mediated Hydroboration of CO2
inferredcites →https://doi.org/10.1021/jacs.5b02905openalex-snapshot
Aromaticity as Stabilizing Element in the Bidentate Activation for the Catalytic Reduction of Carbon Dioxide
inferredcites →https://doi.org/10.1021/jo050392yopenalex-snapshot
Mechanism of Formation of Organic Carbonates from Aliphatic Alcohols and Carbon Dioxide under Mild Conditions Promoted by Carbodiimides. DFT Calculation and Experimental Study
inferredcites →https://doi.org/10.1021/jo801260fopenalex-snapshot
Chemical Recycling of Carbon Dioxide to Methanol and Dimethyl Ether: From Greenhouse Gas to Renewable, Environmentally Carbon Neutral Fuels and Synthetic Hydrocarbons
inferredcites →https://doi.org/10.1021/om5008488openalex-snapshot
Reduction of CO2 to Trimethoxyboroxine with BH3 in THF
inferredcites →https://doi.org/10.1038/ncomms6933openalex-snapshot
Using carbon dioxide as a building block in organic synthesis
inferredcites →https://doi.org/10.1039/b800135aopenalex-snapshot
Catalytic addition of alkyne C–H, amine N–H, and phosphine P–H bonds to carbodiimides: an efficient route to propiolamidines, guanidines, and phosphaguanidines
inferredcites →https://doi.org/10.1039/c3cy00948copenalex-snapshot
Homogeneous catalytic reduction of CO 2 with hydrosilanes
inferredcites →https://doi.org/10.1039/c4cc02103gopenalex-snapshot
Phosphine catalyzed reduction of CO 2 with boranes
inferredcites →https://doi.org/10.1039/c4cc04857aopenalex-snapshot
Lewis base activation of borane–dimethylsulfide into strongly reducing ion pairs for the transformation of carbon dioxide to methoxyboranes
inferredcites →https://doi.org/10.1039/c4cc09239bopenalex-snapshot
Formation of a zwitterionic boronium species from the reaction of a stable carbenoid with borane: CO 2 reduction
inferredcites →https://doi.org/10.1039/c4cc09471aopenalex-snapshot
Towards a methanol economy based on homogeneous catalysis: methanol to H 2 and CO 2 to methanol
inferredcites →https://doi.org/10.1039/c4cs00013gopenalex-snapshot
Guanidines: from classical approaches to efficient catalytic syntheses
inferredcites →https://doi.org/10.1039/c4gc01959hopenalex-snapshot
Sustainable conversion of carbon dioxide: the advent of organocatalysis
inferredcites →https://doi.org/10.1039/c5cc04337aopenalex-snapshot
Organocatalysts with carbon-centered activity for CO 2 reduction with boranes
inferredcites →https://doi.org/10.1039/c7ob00364aopenalex-snapshot
Zwitterionic indenylammonium with carbon-centred reactivity towards reversible CO 2 binding and catalytic reduction
inferredcites →https://doi.org/10.1515/znb-1994-1101openalex-snapshot
Produkte der Carbodiimid-Hydroborierung mit (9H -9-BBN)2 [1] / Hydroboration Products of Carbodiimides with (9H-9-BBN)2 [1]

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/adsc.202400843openalex-snapshot
Magnesium and Calcium Bisguanidinates: Catalytic Activity in the Hydroboration of Unsaturated Molecules
inferred← citeshttps://doi.org/10.1002/ange.202014562openalex-snapshot
Alkyne 1,1‐Hydroboration to a Reactive Frustrated P/B‐H Lewis Pair
inferred← citeshttps://doi.org/10.1002/ange.202112233openalex-snapshot
Selective Catalytic Frustrated Lewis Pair Hydrogenation of CO 2 in the Presence of Silylhalides
inferred← citeshttps://doi.org/10.1002/anie.202014562openalex-snapshot
Alkyne 1,1‐Hydroboration to a Reactive Frustrated P/B‐H Lewis Pair
inferred← citeshttps://doi.org/10.1002/anie.202112233openalex-snapshot
Selective Catalytic Frustrated Lewis Pair Hydrogenation of CO2 in the Presence of Silylhalides
inferred← citeshttps://doi.org/10.1002/asia.202400208openalex-snapshot
Homogeneous and Heterogeneous Frustrated Lewis Pairs for the Activation and Transformation of CO2
inferred← citeshttps://doi.org/10.1002/cctc.201901255openalex-snapshot
Catalytic CO2 Reduction with Boron‐ and Aluminum Hydrides
inferred← citeshttps://doi.org/10.1002/cctc.202000604openalex-snapshot
Frustrated Lewis Pair Catalyzed Reduction of Carbon Dioxide Using Hydroboranes: New DFT Mechanistic Insights
inferred← citeshttps://doi.org/10.1002/cctc.202401179openalex-snapshot
Convenient Partial Reduction of CO2 to a Useful C1 Building Block: Efficient Access to 13C‐Labelled N‐Heterocyclic Carbenes
inferred← citeshttps://doi.org/10.1002/ceur.202500360openalex-snapshot
Establishing Indium in Frustrated Lewis Pair Chemistry: From Synthesis to Catalytic Applications
inferred← citeshttps://doi.org/10.1002/chem.202303380openalex-snapshot
Quo Vadis CO2 Activation: Catalytic Reduction of CO2 to Methanol Using Aluminum and Gallium/Carbon‐based Ambiphiles
inferred← citeshttps://doi.org/10.1002/cjoc.202000521openalex-snapshot
Fe‐Catalyzed Pictet‐Spengler‐Type Cyclization via Selective Four‐Electron Reductive Functionalization of CO2
inferred← citeshttps://doi.org/10.1002/cssc.202002660openalex-snapshot
More Than Just a Reagent: The Rise of Renewable Organohydrides for Catalytic Reduction of Carbon Dioxide
inferred← citeshttps://doi.org/10.1002/cssc.202500594openalex-snapshot
Selective Organocatalytic Synthesis of 3‐Methylindoles and Diindolylmethanes through Reductive Methylation of Indoles with CO2
inferred← citeshttps://doi.org/10.1002/ejoc.202200941openalex-snapshot
Aluminium‐Catalyzed Selective Reduction of Heteroallenes Through Hydroboration: Amide/Thioamide/Selenoamide Bond Construction and C=X (X=O, S, Se) Bond Activation**
inferred← citeshttps://doi.org/10.1002/qua.26512openalex-snapshot
Theoretical designing and understanding of the performances of BH bridged organocatalysts by π‐conjugated molecules in CO2 hydroboration
inferred← citeshttps://doi.org/10.1002/tcr.202100208openalex-snapshot
Reported Catalytic Hydrofunctionalizations that Proceed in the Absence of Catalysts: The Importance of Control Experiments
inferred← citeshttps://doi.org/10.1007/978-981-99-2890-3_1openalex-snapshot
Organocatalytic Reductive Functionalization of Carbon Dioxide
inferred← citeshttps://doi.org/10.1016/bs.adomc.2021.01.003openalex-snapshot
Hydrofunctionalization reactions of heterocumulenes: Formation of C–X (X = B, N, O, P, S and Si) bonds by homogeneous metal catalysts
inferred← citeshttps://doi.org/10.1016/j.ijhydene.2021.02.015openalex-snapshot
Base-assisted transfer hydrogenation of CO2 to formate with ammonia borane in water under mild conditions
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/10.1021/acs.inorgchem.0c01152openalex-snapshot
Ph2PCH2CH2B(C8H14) and Its Formaldehyde Adduct as Catalysts for the Reduction of CO2 with Hydroboranes
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.4c00500openalex-snapshot
Zinc-Catalyzed Hydroboration of Carbon Dioxide Amplified by Borane-Tethered Heteroscorpionate Bis(Pyrazolyl)methane Ligands
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.4c01241openalex-snapshot
Boron Complexes with Propiolamidinato Ligands: Synthesis, Structure, and Photophysical Properties
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.5c04011openalex-snapshot
Controlling Selectivity in Carbon Dioxide Hydroboration to Formic Acid and Methanol Levels Regulated by Lewis Acid: A Computational Mechanistic Study
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.5c05408openalex-snapshot
Optimized Reductivity of the NaBH 4 /ZrCl 4 System for Converting Carbon Dioxide into Methanol under Ambient Conditions without a Catalyst
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.6c01255openalex-snapshot
Magnesium-Catalyzed CO 2 Reduction to Formic Acid or Methanol: Solvent or No Solvent Settles the Selectivity
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.8b01068openalex-snapshot
Selective Three-Component Coupling for CO2 Chemical Fixation to Boron Guanidinato Compounds
inferred← citeshttps://doi.org/10.1021/acs.jpca.9b11648openalex-snapshot
Formation of Formic Acid Derivatives through Activation and Hydroboration of CO 2 by Low-Valent Group 14 (Si, Ge, Sn, Pb) Catalysts
inferred← citeshttps://doi.org/10.1021/acs.organomet.3c00126openalex-snapshot
Pitfalls for POCOP-Type Palladium Pincer Complexes in Catalytic Reduction of CO2 with Catecholborane
inferred← citeshttps://doi.org/10.1021/acscatal.5c06417openalex-snapshot
Designing the Future of Advancing Catalysis: Structural Trends in Metal-Free Systems for CO 2 Conversion
inferred← citeshttps://doi.org/10.1021/acscatal.8b03894openalex-snapshot
Controlling Selectivity in the Hydroboration of Carbon Dioxide to the Formic Acid, Formaldehyde, and Methanol Oxidation Levels
inferred← citeshttps://doi.org/10.1021/jacs.9b08342openalex-snapshot
Selective Conversion of Carbon Dioxide to Formaldehyde via a Bis(silyl)acetal: Incorporation of Isotopically Labeled C1 Moieties Derived from Carbon Dioxide into Organic Molecules
inferred← citeshttps://doi.org/10.1039/c8dt03951hopenalex-snapshot
Hydroboration of carbon dioxide with catechol- and pinacolborane using an Ir–CNP* pincer complex. Water influence on the catalytic activity
inferred← citeshttps://doi.org/10.1039/c9cc00593eopenalex-snapshot
9-Borabicyclo[3.3.1]nonane: a metal-free catalyst for the hydroboration of carbodiimides
inferred← citeshttps://doi.org/10.1039/c9cs00478eopenalex-snapshot
Carbodiimide-based synthesis of N-heterocycles: moving from two classical reactive sites to chemical bond breaking/forming reaction
inferred← citeshttps://doi.org/10.1039/d0cy00118jopenalex-snapshot
Acetate-catalyzed hydroboration of CO 2 for the selective formation of methanol-equivalent products
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/d2dt00691jopenalex-snapshot
Ferrocene tethered boramidinate frustrated Lewis pairs: stepwise capture of CO 2 and CO
inferred← citeshttps://doi.org/10.1039/d2qo00504bopenalex-snapshot
A tandem reduction of primary amines, carbonyl compounds, CO 2 , and boranes catalyzed by in situ formed frustrated Lewis pairs
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/10.1039/d4cy01327aopenalex-snapshot
DMSO-catalyzed CO 2 reduction with 9-BBN: selective formation of either formoxy- or methoxyborane under mild conditions and C -methylenation of indoles
inferred← citeshttps://doi.org/10.1039/d4sc02888kopenalex-snapshot
Four-electron reduction of CO 2 : from formaldehyde and acetal synthesis to complex transformations
inferred← citeshttps://doi.org/10.70675/00a2969fz1377z4015za503z6cd318c8267eopenalex-snapshot
Selective 4e- reduction of CO2 to bis(boryl)acetal and implication of this product as a reagent for C2 carbohydrate synthesis
Editorial review for independent work. ICSAC — the Institute for Complexity Science and Advanced Computing — runs a structured editorial panel for researchers publishing outside journals, and publishes on CiteStamp rails. Submission is free and goes through ORCID: icsacinstitute.org/submit.