On the public citation graph

A comparative DFT study of TBD-catalyzed reactions of amines with CO 2 and hydrosilane: the effect of solvent polarity on the mechanistic preference and the origins of chemoselectivities

0 signed · 55 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 See whether every reference in this work resolves to a known work and none has been retracted — and get a dated CiteStamped badge you can embed.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/anie.201001035openalex-snapshot

An Isolated CO2 Adduct of a Nitrogen Base: Crystal and Electronic Structures

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.201702734openalex-snapshot

Betaine Catalysis for Hierarchical Reduction of CO2 with Amines and Hydrosilane To Form Formamides, Aminals, and Methylamines

inferredcites →https://doi.org/10.1016/j.jorganchem.2013.04.060openalex-snapshot

Understanding the mechanism of CuI-catalyzed N–H carboxylation of heterocyclic rings with CO2 from a theoretical point of view

inferredcites →https://doi.org/10.1021/acscatal.5b00734openalex-snapshot

Bridging Amines with CO2: Organocatalyzed Reduction of CO2 to Aminals

inferredcites →https://doi.org/10.1021/acscatal.6b02715openalex-snapshot

Utilization of CO2 as a C1 Building Block for Catalytic Methylation Reactions

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/acssuschemeng.8b02352openalex-snapshot

Waste Recycling: Ionic Liquid-Catalyzed 4-Electron Reduction of CO2 with Amines and Polymethylhydrosiloxane Combining Experimental and Theoretical Study

inferredcites →https://doi.org/10.1021/ja068215hopenalex-snapshot

An Unexpected Role of a Trace Amount of Water in Catalyzing Proton Transfer in Phosphine-Catalyzed (3 + 2) Cycloaddition of Allenoates and Alkenes

inferredcites →https://doi.org/10.1021/jacs.5b03651openalex-snapshot

The Real Role of N-Heterocyclic Carbene in Reductive Functionalization of CO2: An Alternative Understanding from Density Functional Theory Study

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/ol061095yopenalex-snapshot

Theoretical Rationale for Regioselection in Phosphine-Catalyzed Allenoate Additions to Acrylates, Imines, and Aldehydes

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

Using carbon dioxide as a building block in organic synthesis

inferredcites →https://doi.org/10.1039/c39880000602openalex-snapshot

Reversible homogeneous catalysis of carbon dioxide hydrogenation/reduction at room temperature and low pressures

inferredcites →https://doi.org/10.1039/c3ra41464gopenalex-snapshot

Sequential covalent bonding activation and general base catalysis: insight into N-heterocyclic carbene catalyzed formylation of N–H bonds using carbon dioxide and silane

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/c7cc06795jopenalex-snapshot

A DFT study unveils the secret of how H 2 is activated in the N-formylation of amines with CO 2 and H 2 catalyzed by Ru( ii ) pincer complexes in the absence of exogenous additives

inferredcites →https://doi.org/10.1039/c7gc00199aopenalex-snapshot

Efficient, selective and sustainable catalysis of carbon dioxide

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?

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.4658689openalex-extracted

Aminolysis of Five-Membered Cyclic Carbonate Catalyzed by Guanidines: Solvent Effects on the Formation of Guanidine Dimers

inferred← citeshttps://doi.org/10.1002/adsc.201900906openalex-snapshot

Iron‐Catalyzed Selective N‐Methylation and N‐Formylation of Amines with CO2

inferred← citeshttps://doi.org/10.1002/adsu.202100380openalex-snapshot

Carboxylate‐Functionalized Zeolitic Imidazolate Framework Enables Catalytic N‐Formylation Using Ambient CO2

inferred← citeshttps://doi.org/10.1002/ange.201906942openalex-snapshot

Pivotal Role of the Basic Character of Organic and Salt Catalysts in C−N Bond Forming Reactions of Amines with CO2

inferred← citeshttps://doi.org/10.1002/anie.201906942openalex-snapshot

Pivotal Role of the Basic Character of Organic and Salt Catalysts in C−N Bond Forming Reactions of Amines with CO2

inferred← citeshttps://doi.org/10.1002/chem.201901686openalex-snapshot

Delineation of the Critical Parameters of Salt Catalysts in the N‐Formylation of Amines with CO2

inferred← citeshttps://doi.org/10.1002/chem.201904359openalex-snapshot

Redox‐Neutral Metal‐Free Three‐Component Carbonylative Dearomatization of Pyridine Derivatives with CO2

inferred← citeshttps://doi.org/10.1002/chem.202202210openalex-snapshot

Mechanism of BPh3‐Catalyzed N‐Methylation of Amines with CO2 and Phenylsilane: Cooperative Activation of Hydrosilane

inferred← citeshttps://doi.org/10.1016/b978-0-12-824419-7.00013-3openalex-snapshot

Catalytic upgrading of CO2 to N-formamides

inferred← citeshttps://doi.org/10.1016/b978-0-323-85585-3.00010-9openalex-snapshot

Organic base-mediated fixation of CO2 into value-added chemicals

inferred← citeshttps://doi.org/10.1016/b978-0-443-15181-1.00009-2openalex-snapshot

Hydrogen bond promotion for CO2 activation in homogeneous catalytic systems

inferred← citeshttps://doi.org/10.1016/j.apenergy.2020.115557openalex-snapshot

Towards highly efficient electrochemical CO2 reduction: Cell designs, membranes and electrocatalysts

inferred← citeshttps://doi.org/10.1016/j.cattod.2020.01.030openalex-snapshot

Design of Lewis base functionalized ionic liquids for the N-formylation of amines with CO2 and hydrosilane: The cation effects

inferred← citeshttps://doi.org/10.1016/j.jcou.2020.101240openalex-snapshot

A polymeric ionic liquid catalyst for the N-formylation and N-methylation of amines using CO2/PhSiH3

inferred← citeshttps://doi.org/10.1016/j.jcou.2024.102874openalex-snapshot

Mechanistic insight into C−S bond construction using CO2 as a carbon source: Synthesis of benzothiazoles from 2-aminothiophenols in imidazolium acetate

inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.140299openalex-snapshot

Aminolysis of five-membered cyclic carbonate catalyzed by guanidines: Solvent effects on the formation of guanidine dimers

inferred← citeshttps://doi.org/10.1016/j.molstruc.2024.140802openalex-snapshot

Synthesis, mechanistic insights, and anticancer evaluation of novel 2-aroylbenzo[b]thiophen-3-ols: A DFT and Hirshfeld surface analysis

inferred← citeshttps://doi.org/10.1021/acs.joc.0c02032openalex-snapshot

Hydrosilane-Assisted Synthesis of Urea Derivatives from CO2 and Amines

inferred← citeshttps://doi.org/10.1021/acs.joc.2c02179openalex-snapshot

Advancements and Challenges in Reductive Conversion of Carbon Dioxide via Thermo-/Photocatalysis

inferred← citeshttps://doi.org/10.1021/acs.joc.4c00130openalex-snapshot

DFT Study of Functional Reduction of CO2 with BH3NMe3: The Real Role of Organic Catalyst TBD

inferred← citeshttps://doi.org/10.1021/acs.joc.4c02854openalex-snapshot

Mechanistic Insights into the Methylation and Formylation of Amines with CO2: Exploring Diverse CO2 Activation Models

inferred← citeshttps://doi.org/10.1021/acs.joc.4c03189openalex-snapshot

Copper-PMHS System-Enabled Reductive Cyclization of o-Aminobenzamides with CO2 as a Single-Carbon Synthon

inferred← citeshttps://doi.org/10.1021/acs.orglett.0c02963openalex-snapshot

Reductive CO2 Fixation via the Selective Formation of C–C Bonds: Bridging Enaminones and Synthesis of 1,4-Dihydropyridines

inferred← citeshttps://doi.org/10.1021/acscatal.0c03795openalex-snapshot

A NHC-Silyliumylidene Cation for Catalytic N-Formylation of Amines Using Carbon Dioxide

inferred← citeshttps://doi.org/10.1021/acssuschemeng.0c02325openalex-snapshot

Insights into Naturally Occurring Compound Catalyzed Formylation and Methylation Reactions of Amines with CO2: The Origins of Chemoselectivity

inferred← citeshttps://doi.org/10.1021/acssuschemeng.4c03464openalex-snapshot

Phosphonium-Salt-Catalyzed N-Methylation and N-Formylation of Amines with CO2

inferred← citeshttps://doi.org/10.1039/c8gc03929aopenalex-snapshot

Organocatalyzed carboxylative cyclization of propargylic amides with atmospheric CO 2 towards oxazolidine-2,4-diones

inferred← citeshttps://doi.org/10.1039/d0cc01371dopenalex-snapshot

Synthesis of silyl formates, formamides, and aldehydes via solvent-free organocatalytic hydrosilylation of CO 2

inferred← citeshttps://doi.org/10.1039/d0gc02890hopenalex-snapshot

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

inferred← citeshttps://doi.org/10.1039/d0gc03009kopenalex-snapshot

Highly effective capture and subsequent catalytic transformation of low-concentration CO 2 by superbasic guanidines

inferred← citeshttps://doi.org/10.1039/d0ra05858kopenalex-snapshot

Recent advances in liquid hydrosilane-mediated catalytic N -formylation of amines with CO 2

inferred← citeshttps://doi.org/10.1039/d3cy00682dopenalex-snapshot

Theoretical study of reductive CO 2 functionalization with amines and phenylsilanes: what kind of solvents can be used as catalysts?

inferred← citeshttps://doi.org/10.1039/d5gc00942aopenalex-snapshot

Deoxygenative dual CO 2 conversions: methylenation and switchable N -formylation/ N -methylation of tryptamines

inferred← citeshttps://doi.org/10.1039/d6ob00185hopenalex-snapshot

DFT investigation of the 2-aminothiazole-catalyzed five-component reaction of CO 2 /amines/aldehydes: multi-species synergistic activation and chemoselective control in N -methylation

inferred← citeshttps://doi.org/10.2174/1570179418666211022160149openalex-snapshot

Sustainable Catalyst-free N-formylation using CO2 as a Carbon Source

inferred← citeshttps://doi.org/10.3390/catal16040334openalex-snapshot

Efficient S-Formylation of Thiols with CO2 Catalyzed by Carboxylate Salt Compounds

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.