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Synthesis of a novel highly active single-atom nanozyme Cu-N-C with high surface area as a laccase-mimicking catalyst for the efficient catalytic aerobic oxidative synthesis of pyridines and quinazolinones at room temperature

Jan 19, 2026 12:10:13 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Copper catalyzed carbon-selenium bond formation via the coupling reaction of aryl halides, phenylboronic acid and Se

Jan 19, 2026 12:10:13 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Palladium nanoparticles immobilized on magnetic MCM-41 surface modified with aminomethylpyridine: As a recyclable palladium nanocatalyst for carbon-carbon cross-coupling reactions

Jan 19, 2026 12:10:13 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Copper nitrate as a powerful and eco-friendly natural catalyst for mediator-free aerobic oxidation of 2,3-dihydroquinazolinones and 1,4-dihydropyridines under mild conditions

Jan 19, 2026 12:10:13 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
A palladium(0)–threonine complex immobilized on the surface of magnetic mesocellular foam: an efficient, stable, and magnetically separable nanocatalyst for Suzuki, Stille, and Heck cross- coupling reactions

Jan 19, 2026 12:10:13 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Selective indirect electrochemical oxidation of sulfides and thiols using DDQ as an efficient and cost-effective electrocatalys

Jan 19, 2026 12:10:13 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Applications and mechanisms of free and immobilized laccase in detoxification of phenolic compounds - A review

Jan 19, 2026 12:10:13 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Magnetic mesocellular foams with nickel complexes: as efficient and reusable nanocatalysts for the synthesis of symmetrical and asymmetrical diaryl chalcogenides

Jan 19, 2026 12:10:13 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Transition-metal-catalyzed one-pot selenylation of electrophilic arylating agents using triphenyltin chloride/Se as a phenylselenating agent

Jan 19, 2026 12:10:13 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Oxidation/ MCR domino protocol for direct transformation of methyl benzene, alcohol, and nitro compounds to the corresponding tetrazole using a three-functional redox catalytic system bearing TEMPO/Co(III)-porphyrin/ Ni(II) complex

Jan 19, 2026 12:10:13 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
A novel magnetically separable laccase-mediator catalyst system for the aerobic oxidation of alcohols and 2-substituted-2,3-dihydroquinazolin-4(1H)-ones under mild conditions

Jan 19, 2026 12:10:13 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Catalytic oxidation of alcohols and alkyl benzenes to carbonyls using Fe3O4@SiO2@(TEMPO)-co- (Chlorophyll-CoIII) as a bi-functional, self-cooxidant nanocatalyst

Jan 19, 2026 12:10:13 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Aerobic oxidative synthesis of quinazolinones and benzothiazoles in the presence of laccase/DDQ as a bioinspired cooperative catalytic system under mild conditions

Jan 19, 2026 12:10:13 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Fe3O4 as a magnetically reusable Fenton nanocatalyst for the oxidation of thiols to sulfonic acid and sulfides to sulfoxides and sulfones

Jan 19, 2026 12:10:14 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Zeolite nanoparticles (H-ZSM5) as a highly efficient, green, and reusable heterogeneous catalyst for selective oxidation of sulfides to sulfoxides under mild conditions

Jan 19, 2026 12:10:14 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Remediation of heavy metals and enhancement of fertilizing potential of a sewage sludge by the synergistic interaction of woodlice and earthworms

Jan 19, 2026 12:10:14 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Design and synthesis of a versatile cooperative catalytic aerobic oxidation system with co-immobilization of palladium nanoparticles and laccase into the cavities of MCF

Jan 19, 2026 12:10:14 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Magnetic core-shell nanoparticle-supported Sc (III): A novel and robust Lewis acid nanocatalyst for the selective oxidation of sulfides to sulfoxides by H2O2 under solvent-free conditions

Jan 19, 2026 12:10:14 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Chemo-selective oxidation of sulfide to sulfoxides with H2O2 catalyzed by oxo-vanadium/Schiff-base complex immobilized on modified magnetic Fe3O4 nanoparticles as a heterogeneous and recyclable nanocatalyst

Jan 19, 2026 12:10:14 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Application of laccase/DDQ as a new bioinspired catalyst system for the aerobic oxidation of tetrahydroquinazolines and Hantzsch 1,4-dihydropyridines

Jan 19, 2026 12:10:14 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Enzymatic regeneration of DDQ in aerobic oxidation of sulfides and oxidative coupling of thiols: New bioinspired cooperative catalytic system

Jan 19, 2026 12:10:14 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Aerobic oxidative aromatization of Hantzsch 1,4‑dihydropyridines via an anomeric‑based oxidation in the presence of Laccase enzyme/4‑Phenyl urazole as a cooperative catalytic oxidation system

Jan 19, 2026 12:10:14 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
NiFe2O4 as a magnetically recoverable nanocatalyst for odourless C–S bond formation via the cleavage of C–O bond in the presence of S8 under mild and green conditions

Jan 19, 2026 12:10:14 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Synthesis of diaryl sulfides via nickel ferrite‐catalysed C─S bond formation in green media

Jan 19, 2026 12:10:14 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Laccase-Based Oxidative Catalytic Systems for the Aerobic Aromatization of Tetrahydroquinazolines and Related N-Heterocyclic Compounds under Mild Conditions

Jan 19, 2026 12:10:14 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Laccase-catalyzed in situ generation and regeneration of Nphenyltriazolinedione for the aerobic oxidative homo-coupling of thiols to disulfides

Jan 19, 2026 12:10:14 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Co(II)-catalyzed regioselective clean and smooth synthesis of 2-(aryl/alkylthio) phenols via sp2 C-H bond activation

Jan 19, 2026 12:10:14 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Laccase-catalyzed, aerobic oxidative coupling of 4-substituted urazoles with sodium arylsulfinates: Green and mild procedure for the synthesis of arylsulfonyl triazolidinediones

Jan 19, 2026 12:10:14 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Laccase-TEMPO as an efficient catalyst system for metal- and halogen-free aerobic oxidation of thioethers to sulfoxides in aqueous media at ambient conditions

Jan 19, 2026 12:10:14 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Graphene oxide/CuFe2O4 nanocomposite as a novel scaffold for the immobilization of laccase and its application as a recyclable nanobiocatalyst for the green synthesis of arylsulfonyl benzenediols

Jan 19, 2026 12:10:14 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Copper-Catalyzed C–S Bond Formation via the Cleavage of C–O Bonds in the Presence of S8 as the Sulfur Source

Jan 19, 2026 12:10:14 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
بررسی اثر عصاره هیدروالکلی گیاه یونجه بر تستهای عملکردی کبد، فاکتورهای بیوشیمیایی خون و سیستم انعقادی در موش صحرایی نر

Jan 19, 2026 12:10:14 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Greener approach for synthesis of monodispersed palladium nanoparticles using aqueous extract of green tea and their catalytic activity for the Suzuki–Miyaura coupling reaction and the reduction of nitroarenes

Jan 19, 2026 12:10:14 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Green and mild laccase-catalyzed aerobic oxidative coupling of benzenediol derivatives with various sodium benzenesulfinates

Jan 19, 2026 12:10:15 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Quantitative Structure–Retention Relationship Modeling of Morphine and Its Derivatives on OV‑1 Column in Gas–Liquid Chromatography Using Genetic Algorithm

Jan 19, 2026 12:10:15 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
A Simple, Robust and Efficient Computational Method for Partition Coefficients of Substituted Aromatic Drugs

Jan 19, 2026 12:10:15 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Magnetic nanoparticle-supported DABCO tribromide: a versatile nanocatalyst for the synthesis of quinazolinones and benzimidazoles and protection/deprotection of hydroxyl groups

Jan 19, 2026 12:10:15 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Efficient and green oxidation of alcohols with tert-butyl hydrogenperoxide catalyzed by a recyclable magnetic core-shell nanoparticle-supported oxo-vanadium ephedrine complex

Jan 19, 2026 12:10:15 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Silica sulfuric acid-coated Fe3O4 nanoparticles as high reusable nanocatalyst for the oxidation of sulfides into sulfoxides, protection and deprotection of hydroxyl groups using HMDS and Ac2O

Jan 19, 2026 12:10:15 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly
Immobilized Sandwich-Type Polyoxometalates [Mn4(XW9O34)2]n− on Tb-Doped TiO2 Nanoparticles as Efficient and Selective Catalysts in the Oxidation of Sulfides and Alcohols

Jan 19, 2026 12:10:15 PM

model.resource.ir.sain.university.scholarly.model.UniversityScholarly

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