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Green and Efficient Synthesis of Sulfonamides Catalyzed by Nano-Ru/Fe3O4

https://doi.org/10.1021/ja807681v
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What this work says

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

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Tuning Catalytic Activity between Homogeneous and Heterogeneous Catalysis: Improved Activity and Selectivity of Free Nano‐Fe2O3 in Selective Oxidations
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The design and synthesis of sulfonamides as caspase-1 inhibitors
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inferredcites →https://doi.org/10.1021/jo971176vopenalex-snapshot
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inferredcites →https://doi.org/10.1021/ol035655uopenalex-snapshot
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inferredcites →https://doi.org/10.1021/om701186uopenalex-snapshot
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inferredcites →https://doi.org/10.1039/b616859kopenalex-snapshot
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inferredcites →https://doi.org/10.1039/c39810000611openalex-snapshot
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inferredcites →https://doi.org/10.1039/dt9920001551openalex-snapshot
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What points at this work

Incoming claims: where this work appears in other papers’ reference lists and arguments.

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inferred← citeshttps://doi.org/10.1016/j.crci.2012.08.010openalex-snapshot
Fe3O4 nanoparticles: As an efficient, green and magnetically reusable catalyst for the one-pot synthesis of 1,8-dioxo-decahydroacridine derivatives under solvent-free conditions
inferred← citeshttps://doi.org/10.1016/j.crci.2013.06.005openalex-snapshot
A one-pot synthesis of 5,5-disubstituted hydantoin derivatives using magnetic Fe3O4 nanoparticles as a reusable heterogeneous catalyst
inferred← citeshttps://doi.org/10.1016/j.dyepig.2024.112042openalex-snapshot
Optical evaluation of dansyl derivatives and their implementation in low-cost and flexible dye-doped PMMA platforms for efficient detection of hazardous chemical vapours
inferred← citeshttps://doi.org/10.1016/j.ejmech.2012.02.045openalex-snapshot
Progresses in the pursuit of aldose reductase inhibitors: The structure-based lead optimization step
inferred← citeshttps://doi.org/10.1016/j.electacta.2021.139223openalex-snapshot
Electrochemical synthesis of new sulfone and sulfonamide derivatives. A green method based on the electrolysis of 2-amino-5-nitrophenol
inferred← citeshttps://doi.org/10.1016/j.foodchem.2020.127376openalex-snapshot
Ultrasensitive determination of sulfathiazole using a molecularly imprinted electrochemical sensor with CuS microflowers as an electron transfer probe and Au@COF for signal amplification
inferred← citeshttps://doi.org/10.1016/j.ijbiomac.2019.08.054openalex-snapshot
Catalytic application of new manganese Schiff-base complex immobilized on chitosan-coated magnetic nanoparticles for one-pot synthesis of 3-iminoaryl-imidazo[1,2-a]pyridines
inferred← citeshttps://doi.org/10.1016/j.jcat.2014.10.013openalex-snapshot
Palladium nanocrystals stabilized by cucurbit[6]uril as efficient heterogeneous catalyst for direct C–H functionalization of polyfluoroarenes
inferred← citeshttps://doi.org/10.1016/j.jcat.2023.01.020openalex-snapshot
Identifying active sites at the Cu/Ce interface for hydrogen borrowing reactions
inferred← citeshttps://doi.org/10.1016/j.jcis.2017.05.044openalex-snapshot
Magnetic nanoparticles supported Schiff-base/copper complex: An efficient nanocatalyst for preparation of biologically active 3,4-dihydropyrimidinones
inferred← citeshttps://doi.org/10.1016/j.mcat.2021.112011openalex-snapshot
Sustainable synthesis of potential antitumor new derivatives of Abemaciclib and Fedratinib via C-N cross coupling reactions using Pd/Cu-free Co-catalyst
inferred← citeshttps://doi.org/10.1016/j.mencom.2016.11.027openalex-snapshot
Electrochemical synthesis of sulfonamides from arenesulfonohydrazides or sodium p-methylbenzenesulfinate and amines
inferred← citeshttps://doi.org/10.1016/j.micromeso.2018.08.021openalex-snapshot
Phosphosilicate nanosheets for supported palladium nanoparticles as a novel nanocatalyst
inferred← citeshttps://doi.org/10.1016/j.molcata.2013.01.030openalex-snapshot
Thermally responsive gold nanocatalysts based on a modified poly-vinylpyrrolidone
inferred← citeshttps://doi.org/10.1016/j.molcata.2013.11.010openalex-snapshot
Magnetic Fe3O4 nanoparticles: Efficient and recoverable nanocatalyst for the synthesis of polyhydroquinolines and Hantzsch 1,4-dihydropyridines under solvent-free conditions
inferred← citeshttps://doi.org/10.1016/j.molcata.2014.09.009openalex-snapshot
Magnetic Pd/Fe 3 O 4 /reduced-graphene oxide nanohybrid as an efficient and recoverable catalyst for Suzuki–Miyaura coupling reaction in water
inferred← citeshttps://doi.org/10.1016/j.molliq.2024.126787openalex-snapshot
Solvent assisted synthesis, DFT, and ADME investigations of soft sulfonylating reagents and novel adamantane constituted sulfonamides: Realization of environmental challenges
inferred← citeshttps://doi.org/10.1016/j.molstruc.2021.131982openalex-snapshot
Synthesis and characterization of magnetic Fe3O4@Creatinine@Zr nanoparticles as novel catalyst for the synthesis of 5-substituted 1H-tetrazoles in water and the selective oxidation of sulfides with classical and ultrasonic methods
inferred← citeshttps://doi.org/10.1016/j.mtchem.2020.100377openalex-snapshot
Magnetic methylene-based mesoporous organosilica composite-supported IL/Pd: a powerful and highly recoverable catalyst for oxidative coupling of phenols and naphthols
inferred← citeshttps://doi.org/10.1016/j.solidstatesciences.2018.07.010openalex-snapshot
Catalytic performance of tannic acid-SO3H supported on Fe3O4@SiO2 nanoparticles for synthesis of 2,3-dihydroquinazolin-4(1H)-ones
inferred← citeshttps://doi.org/10.1016/j.supflu.2014.11.013openalex-snapshot
ScCO2 assisted preparation of supported metal NPs. Application to catalyst design.
inferred← citeshttps://doi.org/10.1016/j.talanta.2010.04.055openalex-snapshot
β−cyclodextrins-based inclusion complexes of CoFe2O4 magnetic nanoparticles as catalyst for the luminol chemiluminescence system and their applications in hydrogen peroxide detection
inferred← citeshttps://doi.org/10.1016/j.tet.2009.03.065openalex-snapshot
Iridium catalysed C-3 alkylation of oxindole with alcohols under solvent free thermal or microwave conditions
inferred← citeshttps://doi.org/10.1016/j.tet.2009.07.027openalex-snapshot
Iridium catalysed alkylation of 4-hydroxy coumarin, 4-hydroxy-2-quinolones and quinolin-4(1H)-one with alcohols under solvent free thermal conditions
inferred← citeshttps://doi.org/10.1016/j.tet.2011.02.060openalex-snapshot
One-pot synthesis of sulfonamides from methyl sulfinates using ultrasound
inferred← citeshttps://doi.org/10.1016/j.tet.2011.02.075openalex-snapshot
N-Alkylation of poor nucleophilic amines and derivatives with alcohols by a hydrogen autotransfer process catalyzed by copper(II) acetate: scope and mechanistic considerations
inferred← citeshttps://doi.org/10.1016/j.tet.2011.10.042openalex-snapshot
N-Alkylation of N-arylsulfonyl-α-amino acid methyl esters by trialkyloxonium tetrafluoroborates
inferred← citeshttps://doi.org/10.1016/j.tet.2012.03.008openalex-snapshot
Immobilized palladium on surface-modified Fe3O4/SiO2 nanoparticles: as a magnetically separable and stable recyclable high-performance catalyst for Suzuki and Heck cross-coupling reactions
inferred← citeshttps://doi.org/10.1016/j.tet.2013.11.036openalex-snapshot
Brønsted acid-assisted N-alkylation of sulfonamides using ethers as the alkylation reagents
inferred← citeshttps://doi.org/10.1016/j.tet.2016.05.036openalex-snapshot
Phosphine ligand-free RuCl3-catalyzed reductive N-alkylation of aryl nitro compounds
inferred← citeshttps://doi.org/10.1016/j.tetlet.2009.11.009openalex-snapshot
N-Alkylation of poor nucleophilic amine and sulfonamide derivatives with alcohols by a hydrogen autotransfer process catalyzed by copper(II) acetate
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.02.056openalex-snapshot
Fe(II)-catalyzed N-alkylation of sulfonamides with benzylic alcohols
inferred← citeshttps://doi.org/10.1016/j.tetlet.2010.07.056openalex-snapshot
Direct conversion of thiols and disulfides into sulfonamides
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.01.074openalex-snapshot
Nano Fe3O4 as magnetically recyclable catalyst for the synthesis of α-aminophosphonates in solvent-free conditions
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.03.084openalex-snapshot
Ruthenium-catalyzed direct amination of alcohols with tertiary amines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2011.10.100openalex-snapshot
Heterogeneous bimetallic Pt–Sn/γ-Al2O3 catalyzed direct synthesis of diamines from N-alkylation of amines with diols through a borrowing hydrogen strategy
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.02.009openalex-snapshot
Metal-free synthesis of sulfonamides via iodine-catalyzed oxidative coupling of sulfonyl hydrazides and amines
inferred← citeshttps://doi.org/10.1016/j.tetlet.2016.05.074openalex-snapshot
A highly efficient catalytic α-alkylation of unactivated amides using primary alcohols
inferred← citeshttps://doi.org/10.1016/j.tetlet.2018.10.032openalex-snapshot
Fe-based metal-organic frameworks for the synthesis of N-arylsulfonamides via the reactions of sodium arylsulfinates or arylsulfonyl chlorides with nitroarenes in water
inferred← citeshttps://doi.org/10.1016/j.tgchem.2022.100001openalex-snapshot
Organic solvent-free synthesis of sulfonyl hydrazides in water
inferred← citeshttps://doi.org/10.1016/j.trac.2010.11.008openalex-snapshot
Nanomaterial-amplified chemiluminescence systems and their applications in bioassays
inferred← citeshttps://doi.org/10.1021/acs.chemrev.6b00486openalex-snapshot
Biobased Amines: From Synthesis to Polymers; Present and Future
inferred← citeshttps://doi.org/10.1021/acs.inorgchem.7b01190openalex-snapshot
Tracking the Progress and Mechanism Study of a Solvothermal in Situ Domino N-Alkylation Reaction of Triethylamine and Ammonia Assisted by Ferrous Sulfate
inferred← citeshttps://doi.org/10.1021/acs.joc.0c02263openalex-snapshot
Nanosized CdS as a Reusable Photocatalyst: The Study of Different Reaction Pathways between Tertiary Amines and Aryl Sulfonyl Chlorides through Visible-Light-Induced N-Dealkylation and C–H Activation Processes
inferred← citeshttps://doi.org/10.1021/acs.joc.1c02913openalex-snapshot
Ru Doped Hydrotalcite Catalyzed Borrowing Hydrogen-Mediated N-Alkylation of Benzamides, Sulfonamides, and Dehydrogenative Synthesis of Quinazolinones
inferred← citeshttps://doi.org/10.1021/acs.joc.2c00402openalex-snapshot
Direct Synthesis of Amides from Benzonitriles and Benzylic Alcohols via a KOt-Bu-Mediated MPV-type Hydrogen Transfer Process
inferred← citeshttps://doi.org/10.1021/acs.joc.5b00130openalex-snapshot
Iron-Catalyzed N -Arylsulfonamide Formation through Directly Using Nitroarenes as Nitrogen Sources
inferred← citeshttps://doi.org/10.1021/acs.joc.7b00622openalex-snapshot
Mitsunobu Reaction Using Basic Amines as Pronucleophiles
inferred← citeshttps://doi.org/10.1021/acs.joc.8b02886openalex-snapshot
Iron-Catalyzed C(sp2)–C(sp3) Cross-Coupling of Chlorobenzenesulfonamides with Alkyl Grignard Reagents: Entry to Alkylated Aromatics
inferred← citeshttps://doi.org/10.1021/acs.joc.9b00203openalex-snapshot
Manganese-Catalyzed N -Alkylation of Sulfonamides Using Alcohols
inferred← citeshttps://doi.org/10.1021/acs.joc.9b02816openalex-snapshot
Boron-Catalyzed N-Alkylation of Arylamines and Arylamides with Benzylic Alcohols
inferred← citeshttps://doi.org/10.1021/acs.jpcc.9b08352openalex-snapshot
Modifying Ligand Chemistry To Enhance Reusability of pH-Responsive Colloidal Gold Nanoparticle Catalyst
inferred← citeshttps://doi.org/10.1021/acs.langmuir.7b00870openalex-snapshot
pH Triggered Recovery and Reuse of Thiolated Poly(acrylic acid) Functionalized Gold Nanoparticles with Applications in Colloidal Catalysis
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b00824openalex-snapshot
Effective Recognition of Different Types of Amino Groups: From Aminobenzenesulfonamides to Amino-(N-alkyl)benzenesulfonamides via Iridium-Catalyzed N-Alkylation with Alcohols
inferred← citeshttps://doi.org/10.1021/acs.orglett.5b02685openalex-snapshot
Direct Alkylation of Amines with Alcohols Catalyzed by Base
inferred← citeshttps://doi.org/10.1021/acs.orglett.6b01412openalex-snapshot
I2/TBHP Mediated C–N and C–H Bond Cleavage of Tertiary Amines toward Selective Synthesis of Sulfonamides and β-Arylsulfonyl Enamines: The Solvent Effect on Reaction
inferred← citeshttps://doi.org/10.1021/acscatal.8b02030openalex-snapshot
Reaction Route and Mechanism of the Direct N-Alkylation of Sulfonamides on Acidic Mesoporous Zeolite β-Catalyst
inferred← citeshttps://doi.org/10.1021/acscentsci.1c00125openalex-snapshot
Borrowing Hydrogen for Organic Synthesis
inferred← citeshttps://doi.org/10.1021/acsomega.2c01107openalex-snapshot
Magnetically Recoverable Silica-Decorated Ferromagnetic-Nanoceria Nanocatalysts and Their Use withO- andN-Butyloxycarbonylation Reaction via Solvent-Free Condition
inferred← citeshttps://doi.org/10.1021/cc100047jopenalex-snapshot
Synthesis of 2,3-Dihydroquinazolin-4(1H)-ones by Three-Component Coupling of Isatoic Anhydride, Amines, and Aldehydes Catalyzed by Magnetic Fe3O4 Nanoparticles in Water
inferred← citeshttps://doi.org/10.1021/cr9002159openalex-snapshot
Hydrogen Autotransfer in the N -Alkylation of Amines and Related Compounds using Alcohols and Amines as Electrophiles
inferred← citeshttps://doi.org/10.1021/cs500460mopenalex-snapshot
Highly Active, Selective, and Reusable RuO2/SWCNT Catalyst for Heck Olefination of Aryl Halides
inferred← citeshttps://doi.org/10.1021/ic201608jopenalex-snapshot
pH-Sensitive Gold Nanoparticle Catalysts for the Aerobic Oxidation of Alcohols
inferred← citeshttps://doi.org/10.1021/jo100325eopenalex-snapshot
Impregnated Copper on Magnetite as Recyclable Catalyst for the Addition of Alkoxy Diboron Reagents to C−C Double Bonds
inferred← citeshttps://doi.org/10.1021/jo200559hopenalex-snapshot
Impregnated Ruthenium on Magnetite as a Recyclable Catalyst for the N-Alkylation of Amines, Sulfonamides, Sulfinamides, and Nitroarenes Using Alcohols as Electrophiles by a Hydrogen Autotransfer Process
inferred← citeshttps://doi.org/10.1021/jo200862popenalex-snapshot
Discovery and Mechanistic Studies of a General Air-Promoted Metal-Catalyzed Aerobic N-Alkylation Reaction of Amides and Amines with Alcohols
inferred← citeshttps://doi.org/10.1021/jo300706bopenalex-snapshot
Direct Substitution of Hydroxy Group of π-Activated Alcohols with Electron-Deficient Amines Using Re2O7 Catalyst
inferred← citeshttps://doi.org/10.1021/jo4011798openalex-snapshot
Formal Substitution of Bromocyclopropanes with Nitrogen Nucleophiles
inferred← citeshttps://doi.org/10.1021/jp202473yopenalex-snapshot
Porous Fe3O4/Carbon Core/Shell Nanorods: Synthesis and Electromagnetic Properties
inferred← citeshttps://doi.org/10.1021/ol1002434openalex-snapshot
Simple and Versatile Catalytic System for N-Alkylation of Sulfonamides with Various Alcohols
inferred← citeshttps://doi.org/10.1021/ol1020527openalex-snapshot
Ruthenium-Catalyzed Tertiary Amine Formation from Nitroarenes and Alcohols
inferred← citeshttps://doi.org/10.1021/ol200202gopenalex-snapshot
Synthesis and Cross-Coupling of Sulfonamidomethyltrifluoroborates
inferred← citeshttps://doi.org/10.1021/ol202582copenalex-snapshot
Manganese Dioxide Catalyzed N-Alkylation of Sulfonamides and Amines with Alcohols under Air
inferred← citeshttps://doi.org/10.1021/op100024jopenalex-snapshot
Borrowing Hydrogen in Water and Ionic Liquids: Iridium-Catalyzed Alkylation of Amines with Alcohols
inferred← citeshttps://doi.org/10.1021/sc400147ropenalex-snapshot
Nanoporous Titania-Supported Gold Nanoparticle-Catalyzed Green Synthesis of 1,2,3-Triazoles in Aqueous Medium
inferred← citeshttps://doi.org/10.1038/s41598-019-38544-4openalex-snapshot
A tunable pair electrochemical strategy for the synthesis of new benzenesulfonamide derivatives
inferred← citeshttps://doi.org/10.1038/s41598-020-74733-2openalex-snapshot
A new electrochemical strategy for the synthesis of a new type of sulfonamide derivatives
inferred← citeshttps://doi.org/10.1039/b910145dopenalex-snapshot
New catalytic properties of iron complexes: dehydration of amides to nitriles
inferred← citeshttps://doi.org/10.1039/b917923bopenalex-snapshot
Impregnated copper on magnetite: an efficient and green catalyst for the multicomponent preparation of propargylamines under solvent free conditions
inferred← citeshttps://doi.org/10.1039/b918382popenalex-snapshot
Iron, ruthenium, osmium
inferred← citeshttps://doi.org/10.1039/b921171copenalex-snapshot
Green chemistry by nano-catalysis
inferred← citeshttps://doi.org/10.1039/c0cy00069hopenalex-snapshot
Superparamagnetic nanoparticles for asymmetric catalysis—a perfect match
inferred← citeshttps://doi.org/10.1039/c0ob01144dopenalex-snapshot
A novel acid-catalyzed C5-alkylation of oxindoles using alcohols
inferred← citeshttps://doi.org/10.1039/c1cc10604jopenalex-snapshot
Regioselective N-alkylation of 2-aminobenzothiazoles with benzylic alcohols
inferred← citeshttps://doi.org/10.1039/c1cc12760hopenalex-snapshot
Direct substitution of the hydroxy group with highly functionalized nitrogen nucleophiles catalyzed by Au(iii)
inferred← citeshttps://doi.org/10.1039/c1cc14861copenalex-snapshot
Direct N-alkylation of amino-azoles with alcohols catalyzed by an iridium complex/base system
inferred← citeshttps://doi.org/10.1039/c2cc34178fopenalex-snapshot
Au/Ag–Mo nano-rods catalyzed reductive coupling of nitrobenzenes and alcohols using glycerol as the hydrogen source
inferred← citeshttps://doi.org/10.1039/c2nr31929bopenalex-snapshot
Magnetically recyclable nanocatalysts (MRNCs): a versatile integration of high catalytic activity and facile recovery
inferred← citeshttps://doi.org/10.1039/c2ra20418eopenalex-snapshot
A green, mild and efficient one-pot method for the synthesis of sulfonamides from thiols and disulfides in water
inferred← citeshttps://doi.org/10.1039/c3cs35480fopenalex-snapshot
Nano-magnetite (Fe3O4) as a support for recyclable catalysts in the development of sustainable methodologies
inferred← citeshttps://doi.org/10.1039/c3gc41101jopenalex-snapshot
Nanoparticle catalyzed reaction (NPCR): ZnO-NP catalyzed Ugi-reaction in aqueous medium
inferred← citeshttps://doi.org/10.1039/c3gc42640hopenalex-snapshot
Journey on greener pathways: from the use of alternate energy inputs and benign reaction media to sustainable applications of nano-catalysts in synthesis and environmental remediation
inferred← citeshttps://doi.org/10.1039/c3ob27128eopenalex-snapshot
Iron-catalyzed N-alkylation using π-activated ethers as electrophiles
inferred← citeshttps://doi.org/10.1039/c3ra40872hopenalex-snapshot
Iodine-catalyzed oxidative system for cyclization of primary alcohols with o-aminobenzamides to quinazolinones using DMSO as the oxidant in dimethyl carbonate
inferred← citeshttps://doi.org/10.1039/c3ra43823fopenalex-snapshot
Triflic acid mediated functionalization of α-hydroxyphosphonates: route for sulfonamide phosphonates
inferred← citeshttps://doi.org/10.1039/c4cs00496eopenalex-snapshot
Substitution of alcohols by N-nucleophiles via transition metal-catalyzed dehydrogenation
inferred← citeshttps://doi.org/10.1039/c4cy01170hopenalex-snapshot
Heterogeneous catalysis for the direct synthesis of chemicals by borrowing hydrogen methodology
inferred← citeshttps://doi.org/10.1039/c4gc00164hopenalex-snapshot
Magnetic nanomaterials in catalysis: advanced catalysts for magnetic separation and beyond
inferred← citeshttps://doi.org/10.1039/c4gc00418copenalex-snapshot
Bare magnetic nanoparticles: sustainable synthesis and applications in catalytic organic transformations
inferred← citeshttps://doi.org/10.1039/c4gc00558aopenalex-snapshot
Magnetically recyclable magnetite–palladium (Nanocat-Fe–Pd) nanocatalyst for the Buchwald–Hartwig reaction
inferred← citeshttps://doi.org/10.1039/c4gc02115kopenalex-snapshot
Synthesis of sulfonamides via I 2 -mediated reaction of sodium sulfinates with amines in an aqueous medium at room temperature
inferred← citeshttps://doi.org/10.1039/c4nj01155dopenalex-snapshot
Green fabrication of ferromagnetic Fe 3 O 4 nanoparticles and their novel catalytic applications for the synthesis of biologically interesting benzoxazinone and benzthioxazinone derivatives
inferred← citeshttps://doi.org/10.1039/c4ra14797aopenalex-snapshot
Ruthenium( ii ) complexes containing a phosphine-functionalized thiosemicarbazone ligand: synthesis, structures and catalytic C–N bond formation reactions via N-alkylation
inferred← citeshttps://doi.org/10.1039/c5cc00321kopenalex-snapshot
A novel rhodium-catalyzed domino-hydroformylation-reaction for the synthesis of sulphonamides
inferred← citeshttps://doi.org/10.1039/c5dt01260kopenalex-snapshot
Excellent catalytic activity of magnetically recoverable Fe 3 O 4 –graphene oxide nanocomposites prepared by a simple method
inferred← citeshttps://doi.org/10.1039/c6nj01623eopenalex-snapshot
Porous Ru/RuO x /LDH as highly active heterogeneous catalysts for the aerobic oxidation of alcohols
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