Babak Kaboudin

ORCID: 0000-0003-0495-0006
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About
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Research Areas
  • Organophosphorus compounds synthesis
  • Synthesis and Reactivity of Sulfur-Containing Compounds
  • Sulfur-Based Synthesis Techniques
  • Asymmetric Hydrogenation and Catalysis
  • Chemical Synthesis and Reactions
  • Phosphorus compounds and reactions
  • X-ray Diffraction in Crystallography
  • Chemical Synthesis and Analysis
  • Crystallization and Solubility Studies
  • Multicomponent Synthesis of Heterocycles
  • Synthesis and biological activity
  • Synthesis and Characterization of Heterocyclic Compounds
  • Click Chemistry and Applications
  • Nanomaterials for catalytic reactions
  • Synthesis and Biological Evaluation
  • Ferrocene Chemistry and Applications
  • Catalytic Cross-Coupling Reactions
  • Advanced Photocatalysis Techniques
  • Synthesis of heterocyclic compounds
  • Radical Photochemical Reactions
  • Synthesis and characterization of novel inorganic/organometallic compounds
  • Microwave-Assisted Synthesis and Applications
  • Oxidative Organic Chemistry Reactions
  • Synthesis and Catalytic Reactions
  • Metal complexes synthesis and properties

Institute for Advanced Studies in Basic Sciences
2016-2025

Tokyo University of Pharmacy and Life Sciences
2003-2023

University of Shahrood
2016

University of Zanjan
2012-2016

Bu-Ali Sina University
2016

Indian Institute of Technology Bombay
2001

Shiraz University
1997-1999

We report here on the preparation of an efficient, easily recoverable and reusable Fe3O4 magnetic nanoparticle-supported Cu(II)-β-cyclodextrin complex catalyst for synthesis symmetrical biaryls 1,2,3-triazoles from arylboronic acids. The presented was characterized by TEM, XRD, VSM, TGA, FT-IR spectrometer. By using catalyst, we have developed efficient protocol homocoupling aryl boronic acids biaryls. is also active in via a one-pot reaction acid with sodium azide water followed click...

10.1039/c3gc40753e article EN Green Chemistry 2013-01-01

Abstract We report here the transition‐metal‐catalyzed chemoselective cross‐coupling of arylbroronic acids in high yields without using ligand or base. have developed an efficient copper‐catalyzed protocol for homocoupling and arylboronic acids. The is also suitable aliphatic primary amines with Aminophenols bearing alcoholic substituent on chain were coupled acids, products obtained C–N coupling selectivity. An effective catalyst was Cu 2 –β‐cyclodextrin, which readily available...

10.1002/ejoc.201100994 article EN European Journal of Organic Chemistry 2011-09-19

We report here the one-pot synthesis of 1,2,3-triazoles arylboronic acids in water. An efficient method has been developed for via a reaction an acid with sodium azide presence Cu2–β-CD (CD = Cyclodextrin) as nanocatalyst water followed by click cyclization alkyne at room temperature air without any additives. This is simple, rapid, and high yielding.

10.1039/c2ob25061f article EN Organic & Biomolecular Chemistry 2012-01-01

ABSTRACT Hydrogels containing TiO 2 nanoparticles (NPs) have photocatalytic properties and degrade pollutants under light. In this study, a polyacrylamide (PAAm) hydrogel was synthesized with P25 NPs as the initiator, acrylamide monomer, N,N ′‐methylene bisacrylamide crosslinker in aqueous media sunlight. Fourier transform infrared spectroscopy, thermogravimetric analysis, scanning electron microscopy, transmission microscopy were applied to characterize /PAAm hydrogel. The effects of...

10.1002/app.43386 article EN Journal of Applied Polymer Science 2016-01-28

A simple, efficient, and new method has been developed for the preparation of thiophosphates from benzenethiols. The involves copper(I) iodide catalyzed coupling thiols with <i>H</i>-phosphonates in presence triethylamine. reaction proceeds effectively to afford corresponding moderate good yields via an aerobic dehydrogenative This is easy, rapid, good-yielding synthesis

10.1055/s-0033-1339186 article EN Synthesis 2013-06-25

Alumina-supported phosphorus pentoxide was found to be an efficient reagent for the synthesis of 1,5-benzodiazepine derivatives from phenylenediamine and ketones in solvent-free condition under microwave irradiation.This method is easy, rapid, high-yielding reaction 1, 5-bezodiazepines.Heterocyclic compounds hold a special place among pharmaceutically important natural synthetic materials.The remarkable ability heterocyclic nuclei serve both as biomimetics active pharmacophores has largely...

10.3987/com-01-9253 article EN Heterocycles 2001-01-01

Mononuclear complexes [Pt(ppy)(S∧S)] (1a, S∧S = O,O′-di(cyclohexyl)dithiophosphate (ctp); 2a, O,O′-di(butyl)dithiophosphate (btp)) and [Pt(bzq)(S∧S)] (1b, ctp; 2b, btp) have been prepared by the reaction of precursor [Pt(C∧N)Cl(dmso)], C∧N deprotonated form 2-phenylpyrdine (ppy) 7,8-benzoquinoline (bzq), potassium salt ligands. All were characterized NMR spectroscopy, structure 2b was further identified single crystal X-ray determination. Although are not luminescent in solution at ambient...

10.1021/acs.organomet.7b00054 article EN Organometallics 2017-04-25

Fe3O4 magnetic nanoparticles-supported EDTA–copper(II) complex (Fe3O4-EDTA–Cu(II)) has been prepared and characterized by TEM, SEM, XRD, VSM, TGA, FT-IR spectrometers. The catalyst was applied for the C–N coupling of arylboronic acids with amines preparation N-aryl compounds. Recovery tests confirm that can be easily recovered reused up to eight times without significant loss its catalytic activity.

10.1039/c4ra08137d article EN RSC Advances 2014-09-16

Aim: To induce a safe death to MCF-7 human breast cancer cell line through gene therapy based on iC9 suicide gene. Materials & methods: apoptosis line, was transfected using pyridine-functionalized multi-walled carbon nanotubes. Then, enhance chemotherapy, performed alongside. Results: The results show that the cells were efficiently eliminated in high percentage by this approach. Furthermore, itself/in combination with chemotherapeutic drugs managed pass cycle arrests. Conclusion: We...

10.2217/nnm-2018-0342 article EN Nanomedicine 2019-03-29

Coumarin fused heterocyclic compounds are important materials with wide applications in biological and drug design. We report here a novel condensation-cyclization reaction of 4-chloro-3-formylcoumarin amidoximes. The gave conjunction hybrid compound coumarin pyrimidinones. Condensation-cyclization reactions amidoximes catalyst-free conditions various derivatives pyrimidinones good to excellent yield.

10.1055/a-2529-5234 article EN Synlett 2025-01-30

Hydrophosphorylation of alkynes with dialkylphosphites was investigated under commercially available copper chloride catalyst in the presence ethylene diamine as an efficient ligand.

10.1039/d5ra00300h article EN cc-by-nc RSC Advances 2025-01-01

Abstract Magnesia is found to be an effective catalyst for synthesis of diethyl 1-hydroxyarylmethylphosphonates from aromatic aldehydes and hydrogen phosphite.

10.1080/00397919708003324 article EN Synthetic Communications 1997-02-01
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