On the public citation graph
Cycloaddition of Aziridine with CO2/CS2 Catalyzed by Amidato Divalent Lanthanide Complexes
0 signed · 121 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.
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known work and none has been retracted — and get a dated CiteStamped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.
What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
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/cber.19891221232openalex-snapshot
Regioselective cycloaddition of 1,2‐disubstituted aziridines to heterocumulenes catalyzed by organoantimony halides
inferredcites →https://doi.org/10.1002/cctc.201800148openalex-snapshot
CO 2 Adducts of Carbodicarbenes: Robust and Versatile Organocatalysts for Chemical Transformation of Carbon Dioxide into Heterocyclic Compounds
inferredcites →https://doi.org/10.1002/chem.201103128openalex-snapshot
[11C]Carbon Disulfide: A Versatile Reagent for PET Radiolabelling
inferredcites →https://doi.org/10.1002/chin.200345028openalex-snapshot
Ni(II) Bis(oxazoline)‐Catalyzed Enantioselective Syn Aldol Reactions of N‐Propionylthiazolidinethiones in the Presence of Silyl Triflates.
inferredcites →https://doi.org/10.1002/cjoc.201700810openalex-snapshot
Anionic Copolymerization of Carbonyl Sulfide with Epoxides via Alkali Metal Alkoxides
inferredcites →https://doi.org/10.1002/cssc.201600467openalex-snapshot
N‐Heterocyclic Olefins as Robust Organocatalyst for the Chemical Conversion of Carbon Dioxide to Value‐Added Chemicals
inferredcites →https://doi.org/10.1002/ejoc.200900759openalex-snapshot
A Versatile Synthesis of Various Substituted Taurines from Vicinal Amino Alcohols and Aziridines
inferredcites →https://doi.org/10.1002/ejoc.201600291openalex-snapshot
Synthesis and Characterization of Amidato Divalent Lanthanide Complexes and Their Use in Forming 2,4‐Quinazolidinones from CO2 and 2‐Aminobenzonitriles
inferredcites →https://doi.org/10.1002/ejoc.201601103openalex-snapshot
Synthesis of Thiazolidine‐2‐thiones through a One‐Pot A3‐Coupling–Carbon Disulfide Incorporation Process
inferredcites →https://doi.org/10.1007/s10534-017-0046-6openalex-snapshot
Lipophilic gold(I) complexes with 1,3,4-oxadiazol-2-thione or 1,3-thiazolidine-2-thione moieties: synthesis and their cytotoxic and antimicrobial activities
inferredcites →https://doi.org/10.1007/s11224-013-0218-0openalex-snapshot
Comparative study on the stabilities and properties of heterodimers containing the intermolecular interactions of CF2Cl2 with the isoelectronic and isostructure species of N2O and CO2
inferredcites →https://doi.org/10.1007/s11426-010-4028-6openalex-snapshot
Environmentally benign chemical fixation of CO2 catalyzed by the functionalized ion-exchange resins
inferredcites →https://doi.org/10.1016/j.bmcl.2006.02.060openalex-snapshot
Synthesis and biological evaluation of rhodanine derivatives as PRL-3 inhibitors
inferredcites →https://doi.org/10.1016/j.molcata.2011.10.007openalex-snapshot
Polymer supported diol functionalized ionic liquids: An efficient, heterogeneous and recyclable catalyst for 5-aryl-2-oxazolidinones synthesis from CO2 and aziridines under mild and solvent free condition
inferredcites →https://doi.org/10.1016/j.tet.2008.04.044openalex-snapshot
On the influence of chiral auxiliaries in the stereoselective cross-coupling reactions of titanium enolates and acetals
inferredcites →https://doi.org/10.1016/j.tetlet.2003.09.011openalex-snapshot
Highly efficient chemical fixations of carbon dioxide and carbon disulfide by cycloaddition to aziridine under atmospheric pressure
inferredcites →https://doi.org/10.1016/s0039-6028(01)01639-9openalex-snapshot
Adsorption of CO and CN− on transition metal surfaces: a comparative study of the bonding mechanism
inferredcites →https://doi.org/10.1021/acs.inorgchem.7b00107openalex-snapshot
Recyclable Single-Component Rare-Earth Metal Catalysts for Cycloaddition of CO2 and Epoxides at Atmospheric Pressure
inferredcites →https://doi.org/10.1021/acs.jmedchem.5b00863openalex-snapshot
Discovery of Novel DNA Gyrase Inhibiting Spiropyrimidinetriones: Benzisoxazole Fusion with N-Linked Oxazolidinone Substituents Leading to a Clinical Candidate (ETX0914)
inferredcites →https://doi.org/10.1021/acs.jmedchem.7b00718openalex-snapshot
Quest for Novel Chemical Entities through Incorporation of Silicon in Drug Scaffolds
inferredcites →https://doi.org/10.1021/acs.orglett.8b02186openalex-snapshot
Stereocontrolled, Divergent, Al(lll)-Catalyzed Coupling of Chiral N-Aryl Epoxy Amines and CO2
inferredcites →https://doi.org/10.1021/acscatal.5b00194openalex-snapshot
Combining Low-Pressure CO2 Capture and Hydrogenation To Form Methanol
inferredcites →https://doi.org/10.1021/acscatal.7b03370openalex-snapshot
Utilization of CO2 as a C1 Building Block in a Tandem Asymmetric A3 Coupling-Carboxylative Cyclization Sequence to 2-Oxazolidinones
inferredcites →https://doi.org/10.1021/acsmedchemlett.7b00263openalex-snapshot
Design, Synthesis, and Antibacterial Evaluation of Oxazolidinones with Fused Heterocyclic C-Ring Substructure
inferredcites →https://doi.org/10.1021/cs501124dopenalex-snapshot
Acid–Base Bifunctional Periodic Mesoporous Metal Phosphonates for Synergistically and Heterogeneously Catalyzing CO2 Conversion
inferredcites →https://doi.org/10.1021/ic101709qopenalex-snapshot
Reactivity of Bis(2,2,5,5-tetramethyl-2,5-disila-1-azacyclopent-1-yl)tin with CO2, OCS, and CS2 and Comparison to That of Bis[bis(trimethylsilyl)amido]tin
inferredcites →https://doi.org/10.1021/ja00212a037openalex-snapshot
Asymmetric Diels-Alder cycloaddition reactions with chiral .alpha.,.beta.-unsaturated N-acyloxazolidinones
inferredcites →https://doi.org/10.1021/ja00275a082openalex-snapshot
Highly diastereoselective alkylation onto 4-acetoxy-2-azetidinones employing tin(II) enolates of 3-acyl C-4-chiral 1,3-thiazolidine-2-thiones
inferredcites →https://doi.org/10.1021/ja035509jopenalex-snapshot
Ni(II) Bis(oxazoline)-Catalyzed Enantioselective Syn Aldol Reactions of N-Propionylthiazolidinethiones in the Presence of Silyl Triflates
inferredcites →https://doi.org/10.1021/jo001387ropenalex-snapshot
Asymmetric Aldol Additions: Use of Titanium Tetrachloride and (−)-Sparteine for the Soft Enolization of N-Acyl Oxazolidinones, Oxazolidinethiones, and Thiazolidinethiones
inferredcites →https://doi.org/10.1021/jo201561topenalex-snapshot
Three-Component, One-Flask Synthesis of Rhodanines (Thiazolidinones)
inferredcites →https://doi.org/10.1021/jo800269vopenalex-snapshot
Quaternary Ammonium Bromide Functionalized Polyethylene Glycol: A Highly Efficient and Recyclable Catalyst for Selective Synthesis of 5-Aryl-2-oxazolidinones from Carbon Dioxide and Aziridines Under Solvent-Free Conditions
inferredcites →https://doi.org/10.1021/jo801703hopenalex-snapshot
Tributylphosphine-Catalyzed Cycloaddition of Aziridines with Carbon Disulfide and Isothiocyanate
inferredcites →https://doi.org/10.1021/ol025553oopenalex-snapshot
Magnesium Halide-Catalyzed Anti-Aldol Reactions of Chiral N-Acylthiazolidinethiones
inferredcites →https://doi.org/10.1021/ol049689topenalex-snapshot
(Salen)chromium(III)/DMAP: An Efficient Catalyst System for the Selective Synthesis of 5-Substituted Oxazolidinones from Carbon Dioxide and Aziridines
inferredcites →https://doi.org/10.1021/ol401013sopenalex-snapshot
A Practical Method for the Synthesis of Highly Enantioenriched trans-1,2-Amino Alcohols
inferredcites →https://doi.org/10.1021/ol701563eopenalex-snapshot
Phosphine-Catalyzed Construction of Sulfur Heterocycles
inferredcites →https://doi.org/10.1021/om400949mopenalex-snapshot
NHC–Gold(I) Complexes as Effective Catalysts for the Carboxylative Cyclization of Propargylamines with Carbon Dioxide
inferredcites →https://doi.org/10.1039/c0gc00070aopenalex-snapshot
Equimolar CO2 capture by imidazolium-based ionic liquids and superbase systems
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/c1gc15581dopenalex-snapshot
Protic onium salts-catalyzed synthesis of 5-aryl-2-oxazolidinones from aziridines and CO2 under mild conditions
inferredcites →https://doi.org/10.1039/c4gc01709aopenalex-snapshot
Mesoporous zirconium phosphonates as efficient catalysts for chemical CO 2 fixation
inferredcites →https://doi.org/10.1039/c4gc02200aopenalex-snapshot
Carboxylation of terminal alkynes with CO 2 catalyzed by bis(amidate) rare-earth metal amides
inferredcites →https://doi.org/10.1039/c4ra08902bopenalex-snapshot
Efficient pyrrolidine catalyzed cycloaddition of aziridines with isothiocyanates, isoselenocyanates and carbon disulfide “on water”
inferredcites →https://doi.org/10.1039/c5gc00948kopenalex-snapshot
CO 2 , COS and CS 2 adducts of N-heterocyclic olefins and their application as organocatalysts for carbon dioxide fixation
inferredcites →https://doi.org/10.1039/c5gc02761fopenalex-snapshot
Cooperative calcium-based catalysis with 1,8-diazabicyclo[5.4.0]-undec-7-ene for the cycloaddition of epoxides with CO 2 at atmospheric pressure
inferredcites →https://doi.org/10.1039/c6gc00511jopenalex-snapshot
Cooperative rare earth metal–zinc based heterometallic catalysts for copolymerization of CO 2 and cyclohexene oxide
inferredcites →https://doi.org/10.1039/c6sc00419aopenalex-snapshot
Palladium-catalyzed incorporation of atmospheric CO 2 : efficient synthesis of functionalized oxazolidinones
inferredcites →https://doi.org/10.1039/c7cc04776bopenalex-snapshot
Selective α-arylation of α,β-unsaturated imides mediated by a visible light photoredox catalyst
inferredcites →https://doi.org/10.1039/c7gc01458aopenalex-snapshot
Activation of (salen)CoI complex by phosphorane for carbon dioxide transformation at ambient temperature and pressure
inferredcites →https://doi.org/10.1039/c7gc03534aopenalex-snapshot
Ni-Catalyzed chemoselective alcoholysis of N -acyloxazolidinones
inferredcites →https://doi.org/10.1039/c7ob02915bopenalex-snapshot
Synthesis of thiazolidine-thiones, imino-thiazolidines and oxazolidines via the base promoted cyclisation of epoxy-sulfonamides and heterocumulenes
inferredcites →https://doi.org/10.1055/s-0033-1338446openalex-snapshot
Addition of Terminal Alkynes to Aromatic Nitriles Catalyzed by Divalent Lanthanide Amides Supported by Amidates: Synthesis of Ynones
inferredcites →https://doi.org/10.1055/s-0037-1609966openalex-snapshot
Stereoselective Oxidation of Titanium(IV) Enolates with Oxygen
inferredcites →https://doi.org/10.1080/17415993.2015.1079635openalex-snapshot
Electrochemically generated base synthesis of thiazolidine-2-thiones
inferredcites →https://doi.org/10.3390/molecules16065207openalex-snapshot
Synthesis and Characterization of (Z)-5-Arylmethylidene-rhodanines with Photosynthesis-Inhibiting Properties
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.4769597openalex-extracted
Heteronuclear Bicentric Ionic Liquids Tailored for Mild Catalytic Conversion of Co2 into Cyclic Carbonates
inferred← citeshttps://doi.org/10.1002/adsc.202200514openalex-snapshot
Regio‐ and Stereospecific Desulfinylative Chlorination of Spiroaziridine Oxindoles at Spiro‐Center for Formal [3+2]‐Cycloaddition with CS2: Sequential One‐Pot Synthesis of (−)‐Spirobrassinin
inferred← citeshttps://doi.org/10.1002/adsc.202201253openalex-snapshot
B−N Coordinated Phenanthroimidazole‐Based Zinc‐Salen as a Photocatalyst for the Synthesis of Oxazolidinones using Carbon Dioxide as a C1 Source under Mild Reaction Conditions
inferred← citeshttps://doi.org/10.1002/asia.202400688openalex-snapshot
Ammonium Zincates as Catalysts for the Microwave‐Enhanced Synthesis of Symmetric Piperazines by Regioselective Opening of Aziridines
inferred← citeshttps://doi.org/10.1002/cctc.202500710openalex-snapshot
Additive‐Free Synthesis of Cyclic Carbamates From Aziridines and CO2 Catalyzed by IER Supported Iron(III) Halides
inferred← citeshttps://doi.org/10.1002/chem.202500933openalex-snapshot
Recent Advances in the Fixation of CO2 to Form N‐Containing Heterocyclic Compounds
inferred← citeshttps://doi.org/10.1002/cssc.201901171openalex-snapshot
Synthesis of Oxazolidinones by using Carbon Dioxide as a C 1 Building Block and an Aluminium‐Based Catalyst
inferred← citeshttps://doi.org/10.1002/cssc.202001823openalex-snapshot
Bypassing the Inertness of Aziridine/CO 2 Systems to Access 5‐Aryl‐2‐Oxazolidinones: Catalyst‐Free Synthesis Under Ambient Conditions
inferred← citeshttps://doi.org/10.1002/ejoc.202100124openalex-snapshot
4‐Aryl‐2‐Imino‐1,3‐Dithiolanes from the Room Temperature Coupling of Sodium Dithiocarbamates with Sulfonium Salts
inferred← citeshttps://doi.org/10.1002/ejoc.202400616openalex-snapshot
Non‐Reductive CO2 Valorization into Oxazolidinones via Cycloaddition to Aziridines: A Personal Insight
inferred← citeshttps://doi.org/10.1007/s11426-021-1006-9openalex-snapshot
Eco-friendly co-catalyst-free cycloaddition of CO2 and aziridines activated by a porous MOF catalyst
inferred← citeshttps://doi.org/10.1007/s40242-024-3253-zopenalex-snapshot
Metal Acetylacetonates as Robust Catalysts for the Synthesis of Oxazolidinone from CO2 and Aziridine Under Atmospheric Pressure
inferred← citeshttps://doi.org/10.1016/b978-0-323-89812-6.00011-0openalex-snapshot
Five-membered ring systems with O and N atoms
inferred← citeshttps://doi.org/10.1016/b978-0-323-91198-6.00005-xopenalex-snapshot
Functional polymers from CO2 as feedstock
inferred← citeshttps://doi.org/10.1016/b978-0-443-31482-7.00046-1openalex-snapshot
Functions Containing a Thiocarbonyl Group and at Least one Halogen; Also at Least one Chalcogen and no Halogen
inferred← citeshttps://doi.org/10.1016/j.cattod.2020.01.031openalex-snapshot
Optimizing the performance of porous pyridinium frameworks for carbon dioxide transformation
inferred← citeshttps://doi.org/10.1016/j.ccr.2022.214419openalex-snapshot
Lanthanide-containing clusters for catalytic water splitting and CO2 conversion
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2021.06.123openalex-snapshot
A comprehensive survey upon diverse and prolific applications of chitosan-based catalytic systems in one-pot multi-component synthesis of heterocyclic rings
inferred← citeshttps://doi.org/10.1016/j.inoche.2025.114218openalex-snapshot
Beyond the norm: Exploring the unusual oxidation states of lanthanides (+1, +II, +IV and +V) and their potential applications
inferred← citeshttps://doi.org/10.1016/j.jcou.2021.101595openalex-snapshot
Sustainable synthesis of five-membered heterocycles using carbon dioxide and Fe-iminopyridine catalysts
inferred← citeshttps://doi.org/10.1016/j.jmst.2026.07.115openalex-snapshot
Rationally designing cluster-based MOF catalysts to achieve high-efficiency CS2 green conversion via quadruple synergistic effect
inferred← citeshttps://doi.org/10.1016/j.mcat.2024.114227openalex-snapshot
Heteronuclear bicentric ionic liquids tailored for moderate catalytic conversion of CO2 into cyclic carbonates
inferred← citeshttps://doi.org/10.1016/j.tetlet.2026.155960openalex-snapshot
Ring-opening ring-closing strategy towards construction of aza-heterocycles from aziridines
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.4c00659openalex-snapshot
Metal Hydrogen-Bonded Organic Frameworks as Open Lewis Acid Catalysts for Two Types of CO2 Transformations
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.4c05062openalex-snapshot
Green CS2 Conversion Catalyzed by a Three-Dimensional Porous Cerium-Organic Framework
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.9b01169openalex-snapshot
Synthesis of Homo- and Heteronuclear Rare-Earth Metal Complexes Stabilized by Ethanolamine-Bridged Bis(phenolato) Ligands and Their Application in Catalyzing Reactions of CO2 and Epoxides
inferred← citeshttps://doi.org/10.1021/acs.joc.0c00877openalex-snapshot
Enantioselective Hydroboration of Ketones Catalyzed by Rare-Earth Metal Complexes Containing Trost Ligands
inferred← citeshttps://doi.org/10.1021/acs.joc.3c00690openalex-snapshot
Synthesis of Oxazolidines and Dihydroxazines via Cyclization of α-Aminated Ketones
inferred← citeshttps://doi.org/10.1021/acs.joc.4c01907openalex-snapshot
Fe(II)-Iminopyridine Catalyst for the Regioselective Synthesis of Oxazolidinones Using Carbon Dioxide
inferred← citeshttps://doi.org/10.1021/acs.joc.4c03034openalex-snapshot
Three-Component Synthesis of Oxazolidinones via Phosphine-Catalyzed Fixation of Carbon Dioxide and Mechanistic Investigation in Mass Spectrometry
inferred← citeshttps://doi.org/10.1021/acs.joc.5c01639openalex-snapshot
Stereoselective Synthesis of 4,5-Disubstituted Oxazolidin-2-ones via Tandem Lossen Rearrangement and Ring Closure of Asymmetric Aldol Adducts
inferred← citeshttps://doi.org/10.1021/acs.joc.6c01591openalex-snapshot
CAN-Promoted Boc2O-Mediated Cascade Conversion of Aziridines to Oxazolidinones
inferred← citeshttps://doi.org/10.1021/acs.organomet.9b00657openalex-snapshot
Mechanism for CO2 Fixation with Aziridines Synergistically Catalyzed by HKUST-1 and TBAB: A DFT Study
inferred← citeshttps://doi.org/10.1021/acs.orglett.2c01987openalex-snapshot
Activation of CS2 with the 2H-Phosphindole Complex to Construct P,S-Polycycles
inferred← citeshttps://doi.org/10.1021/acs.orglett.4c00157openalex-snapshot
Regioselective Addition of Sulfur and Amine Nucleophiles To Assemble S═C–S, S–N, and Umpolung C–N Bonds: Exploration of the −CBr3 Group as a Synthetic Equivalent of S═C–S
inferred← citeshttps://doi.org/10.1021/acsami.2c19614openalex-snapshot
Highly Efficient Conversion of Aziridines and CO2 Catalyzed by Microporous [Cu12] Nanocages
inferred← citeshttps://doi.org/10.1021/acssuschemeng.0c01736openalex-snapshot
Conversion of CO 2 into Cyclic Carbonates under Ambient Conditions Catalyzed by Rare-Earth Metal Complexes Bearing Poly(phenolato) Ligand
inferred← citeshttps://doi.org/10.1039/c9cs00047jopenalex-snapshot
Advances in the use of CO 2 as a renewable feedstock for the synthesis of polymers
inferred← citeshttps://doi.org/10.1039/c9nj05831aopenalex-snapshot
Lanthanide clusters as highly efficient catalysts regarding carbon dioxide activation
inferred← citeshttps://doi.org/10.1039/d0dt00183jopenalex-snapshot
A designed and potentially decadentate ligand for use in lanthanide( iii ) catalysed biomass transformations: targeting diastereoselective trans -4,5-diaminocyclopentenone derivatives
inferred← citeshttps://doi.org/10.1039/d0nj02154gopenalex-snapshot
Photoswitchable Cu( ii )/Cu( i ) catalyses assisted by enzyme-like non-covalent interactions in Cu( ii )–melamine coordination polymers for installing CO 2 /CS 2 and CF 3 groups in heterocycles
inferred← citeshttps://doi.org/10.1039/d0nj05228kopenalex-snapshot
Asymmetric epoxidation of α,β-unsaturated ketones catalyzed by rare-earth metal amides RE[N(SiMe 3 ) 2 ] 3 with chiral TADDOL ligands
inferred← citeshttps://doi.org/10.1039/d0ra00693aopenalex-snapshot
Bifunctional phase-transfer catalysts for synthesis of 2-oxazolidinones from isocyanates and epoxides
inferred← citeshttps://doi.org/10.1039/d1cc01865eopenalex-snapshot
An uncommon multicentered Zn I –Zn I bond-based MOF for CO 2 fixation with aziridines/epoxides
inferred← citeshttps://doi.org/10.1039/d1dt00525aopenalex-snapshot
Non-precious metal carbamates as catalysts for the aziridine/CO 2 coupling reaction under mild conditions
inferred← citeshttps://doi.org/10.1039/d1ob00458aopenalex-snapshot
Diethylammonium iodide as catalyst for the metal-free synthesis of 5-aryl-2-oxazolidinones from aziridines and carbon dioxide
inferred← citeshttps://doi.org/10.1039/d1ob00755fopenalex-snapshot
Carbon dioxide based methodologies for the synthesis of fine chemicals
inferred← citeshttps://doi.org/10.1039/d1qi01643aopenalex-snapshot
Metal-assisted synthesis of salen-based porous organic polymer for highly efficient fixation of CO 2 into cyclic carbonates
inferred← citeshttps://doi.org/10.1039/d1qo00458aopenalex-snapshot
Aziridine used as a vinylidene unit in palladium-catalyzed [2 + 2 + 1] domino annulation
inferred← citeshttps://doi.org/10.1039/d1ta10522aopenalex-snapshot
Highly effective CS 2 conversion with aziridines catalyzed by novel [Dy 24 ] nano-cages in MOFs under mild conditions
inferred← citeshttps://doi.org/10.1039/d2gc03879jopenalex-snapshot
Tandem electrocatalytic aziridination – ring expansion of simple aromatic olefins using ammonia and carbon dioxide
inferred← citeshttps://doi.org/10.1039/d2nj05479eopenalex-snapshot
From CO 2 to CS 2 : a theoretical investigation of the cycloaddition to aziridines mediated by metal-free porphyrin-based catalytic systems
inferred← citeshttps://doi.org/10.1039/d2qo00583bopenalex-snapshot
Amine-catalyzed site- and stereo-selective coupling of epoxy amines and carbon dioxide to construct oxazolidinones
inferred← citeshttps://doi.org/10.1039/d4cc02894eopenalex-snapshot
Chemical fixation of CO 2 /CS 2 to access iodoallenyl oxazolidinones and allenyl thiazolidine-thiones
inferred← citeshttps://doi.org/10.1039/d4cy00246fopenalex-snapshot
Magnesium-porphyrin as an efficient photocatalyst for the transformation of CO 2 to cyclic carbonates and oxazolidinones under ambient conditions
inferred← citeshttps://doi.org/10.1039/d4gc04541fopenalex-snapshot
High-efficiency green catalytic conversion for waste CS 2 by non-noble metal cage-based MOFs: an access pathway to high-value thiazolidine-2-thione
inferred← citeshttps://doi.org/10.1039/d4qi02101kopenalex-snapshot
A review on framework (MOF/COF/POP)-based materials for efficient conversion of CO 2 to bio-active oxazolidinones
inferred← citeshttps://doi.org/10.1039/d5nj03189copenalex-snapshot
Activating harmful small molecules under mild conditions: theoretical insights into cinchonine-based valorization of CO 2 , CS 2 , and COS
inferred← citeshttps://doi.org/10.1055/a-1372-1619openalex-snapshot
Tandem Alkylation/Michael Addition Reaction of Dithiocarbamic Acids with Alkyl γ-Bromocrotonates: Access to Functionalized 1,3-Thiazolidine-2-thiones
inferred← citeshttps://doi.org/10.3390/catal9060511openalex-snapshot
Recent Advances in the Chemical Fixation of Carbon Dioxide: A Green Route to Carbonylated Heterocycle Synthesis
inferred← citeshttps://doi.org/10.3390/inorganics11030091openalex-snapshot
Adding Diversity to Diiron Aminocarbyne Complexes with Amine Ligands
inferred← citeshttps://doi.org/10.3390/molecules27185751openalex-snapshot
Aziridination Reactivity of a Manganese(II) Complex with a Bulky Chelating Bis(Alkoxide) Ligand
inferred← citeshttps://doi.org/10.3390/molecules28010242openalex-snapshot
Novel MCM-41 Supported Dicationic Imidazolium Ionic Liquids Catalyzed Greener and Efficient Regioselective Synthesis of 2-Oxazolidinones from Aziridines and Carbon Dioxide
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.