G. Chehardoli

发表

Synthesis of sodium alginate grafted stearate acid (NaAlg-g-St) and evaluation of the polymer as drug release controlling matrix

F. Firozian, G. Chehardoli, H. Bagheri, 2019, Journal of Polymer Research.

Design, synthesis, in vitro, and in silico studies of novel benzylidene 6-methoxy-1-tetralone linked to benzyloxy and benzyl -1,2,3- triazole rings as potential tyrosinase inhibitors

M. Mahdavi, M. Khoshneviszadeh, Mina Saeedi, 2022, Journal of Molecular Structure.

Melamine-(H2SO4)3/Melamine-(HNO3)3 Instead of H2SO4/HNO3: Benign System for Oxidation/Nitration Reactions from in situ NO2+

G. Chehardoli, Seyedeh Bahareh Azimi, 2019, Organic Preparations and Procedures International.

N2O4 Chemisorbed onto n‐Propylsilica Kryptofix 21 and Kriptofix 22 as Two New Functional Polymers for the Fast Oxidation of Urazoles and 1,4‐Dihydropyridines

M. Zolfigol, S. Mallakpour, K. Niknam, 2012 .

Melamine Hydrogen Peroxide (MHP): Novel and Efficient Reagent for the Chemo- and Homoselective and Transition Metal–Free Oxidation of Thiols and Sulfides

M. Zolfigol, G. Chehardoli, 2009 .

Novel tacrine-based acetylcholinesterase inhibitors as potential agents for the treatment of Alzheimer’s disease: Quinolotacrine hybrids

A. Ranjbar, Arezoo Rastegari, T. Akbarzadeh, 2021, Molecular diversity.

Inulin-Grafted Stearate (In-g-St) as the Effective Self-Assembling Polymeric Micelle: Synthesis and Evaluation for the Delivery of Betamethasone

F. Firozian, G. Chehardoli, Parham Norouzian, 2020, Journal of Nanomaterials.

Design, synthesis, molecular modeling and DNA-binding studies of new barbituric acid derivatives

D. Dastan, A. Ebadi, G. Chehardoli, 2022, Journal of the Iranian Chemical Society.

Curcumin-Derived Heterocycles as Anticancer Agents. A Systematic Review.

Asrin Bahmani, G. Chehardoli, Z. Najafi, 2022, Organic Preparations and Procedures International.

Melamine trisulfonic acid (MTSA) as an efficient catalyst for the synthesis of triazolo[1,2-a]indazole-triones and some 2H-indazolo[2,1-b]phthalazine-triones

M. Zolfigol, S. Mallakpour, A. Khazaei, 2013 .

Novel ionic liquid 1,3-disulfonic acid imidazolium hydrogen sulfate {[Dsim] HSO4 } efficiently catalyzed N-boc protection of amines

M. Zolfigol, A. Zare, G. Chehardoli, 2012 .

Simple, Convenient and Heterogeneous Method for Conversion of Urazoles to Triazolinediones Using N,N,N′,N′-Tetrabromobenzene-1,3-disulfonylamide or Trichloromelamine under Mild and Heterogeneous Conditions

M. Zolfigol, S. Mallakpour, G. Chehardoli, 2006 .

H2O2 as a green and environmentally benign reagent for the oxidation of Sulfides in the presence of {[K.18-Crown-6]X3}n (X= Br, I) compared with some other organic tribromides

M. Zolfigol, G. Chehardoli, R. Mohebat, 2020 .

Melamine-(H2SO4)3 and PVP-(H2SO4)n as solid acids: Synthesis and application in the first mono- and di-nitration of bisphenol A and other phenols

M. Zolfigol, G. Chehardoli, Seyedeh Bahareh Azimi, 2011 .

Mild and heterogeneous oxidation of urazoles to their corresponding triazolinediones via in situ generation Cl+ using silica sulfuric acid/KClO3 or silica chloride/oxone system

M. Zolfigol, M. Bagherzadeh, S. Mallakpour, 2007 .

N-nitrosation of secondary amines with [NO+.Crown.H(NO)(3)-2].

M. Shamsipur, M. Zolfigol, S. Salehzadeh, 2001, The Journal of organic chemistry.

1,3,5-Triazine-2,4,6-triyltrisulfamic acid (TTSA): A new organic solid acid for the nitrosation of secondary amines and oxidation of urazoles in the presence of NaNO2 under mild and heterogeneous conditions

M. Zolfigol, S. Mallakpour, A. Ghorbani‐Choghamarani, 2009 .

N-Bromo Reagent Mediated Oxidation of Urazoles to Their Corresponding Triazolinediones under Mild and Heterogeneous Conditions

M. Zolfigol, S. Mallakpour, K. Niknam, 2008 .

{[K.18 -Crown -6]Br3}n : a unique tribromide-type and columnar nanotube-like structure for the oxidative coupling of thiols and bromination of some aromatic compounds

M. Ward, M. Zolfigol, H. Adams, 2007 .

The first report on the catalytic oxidation of urazoles to their corresponding triazolinediones via in situ catalytic generation of Br+ using periodic acid or oxone ®/KBr system

M. Zolfigol, M. Bagherzadeh, S. Mallakpour, 2007 .

A new crystal engineering approach for the synthesis of {[K.18-Crown-6]I3}n as a nanotube-Like and recyclable catalyst for the chemoselective silylation of alcohols

M. Zolfigol, S. Salehzadeh, K. Niknam, 2011 .

A catalytic and transition metal-free method for the chemoselective oxidation of alcohols to their corresponding carbonyl compounds using periodic acid or iodic acid in the presence of a catalytic amount of KBr

M. Zolfigol, F. Shirini, G. Chehardoli, 2007 .

Uronium Hydrogen Sulfate/Urea-Hydrogen Peroxide as a Green and Metal-Free Catalytic System for the Efficient, Chemo-, and Homoselective Oxidation of Sulfides to Sulfoxides

M. Zolfigol, A. Hasaninejad, G. Chehardoli, 2011 .

Synthesis and Crystal Structure Determination of [H2‐cryptand 222](Br3)2: A Unique Tribromide Catalyst for the Catalytic Chemoselective N‐Boc Protection of Amines

M. Zolfigol, N. Hall, G. Chehardoli, 2011 .

Novel tacrine-based acetylcholinesterase inhibitors as potential agents for the treatment of Alzheimer’s disease: Quinolotacrine hybrids

A. Ranjbar, Arezoo Rastegari, T. Akbarzadeh, 2021, Molecular Diversity.

The role of crown ethers in drug delivery

Asrin Bahmani, G. Chehardoli, 2019, Supramolecular Chemistry.

Tribromoisocyanuric Acid and DABCO-Br as Efficient Catalysts for the Silylation of Hydroxyl Groups with Hexamethyldisilazane

M. Zolfigol, K. Niknam, G. Chehardoli, 2008 .

Silica Sulfuric Acid and Al(HSO4)3: As Efficient Catalysts for the Formylation of Alcohols by Using Ethyl Formate under Heterogeneous Conditions

M. Zolfigol, K. Niknam, F. Shirini, 2008 .

Melamine-(H2SO4)3/melamine-(HNO3)3 instead of H2SO4/HNO3: a safe system for the fast oxidation of thiols and sulfides under solvent-free conditions

M. Zolfigol, G. Chehardoli, 2015 .

Epoxidation of aromatic α,β-unsaturated ketones using PVP–H2O2 under mild and heterogeneous conditions

M. Zolfigol, M. Shiri, G. Chehardoli, 2007 .

Silica Sulfuric Acid/NaNO2 as a Novel Heterogeneous System for the Oxidation of Urazoles Under Mild Conditions

S. Mallakpour, M. Ali Zolfigol, G. Chehardoli, 2003 .

OXIDATION OF URAZOLES UNDER MILD AND HETEROGENEOUS CONDITIONS WITH KHSO5 AND NaNO2

M. Zolfigol, M. Bagherzadeh, S. Mallakpour, 2001 .

Ultrasound-assisted synthesis of kojic acid-1,2,3-triazole based dihydropyrano[3,2-b]pyran derivatives using Fe3O4@CQD@CuI as a novel nanomagnetic catalyst

M. Khoshneviszadeh, S. Babaee, T. Akbarzadeh, 2022, Scientific Reports.

Design, Synthesis, and Molecular Docking of Some Novel Tacrine Based Cyclopentapyranopyridine‐ and Tetrahydropyranoquinoline‐Kojic Acid Derivatives as Anti‐Acetylcholinesterase Agents

M. Zolfigol, M. Mahdavi, S. Babaee, 2021, Chemistry & biodiversity.

H2O2 as green and environmentally benign reagent for the oxidation of TMS ethers, THP ethers, and alcohols in the presence of {[K.18-Crown-6]Br3}n

M. Zolfigol, G. Chehardoli, M. Rasouli, 2017 .

{[[K.18-Crown-6]Br3}n: A tribromide catalyst for the catalytic protection of amines and alcohols

M. Zolfigol, G. Chehardoli, Fatemeh Derakhshan-Panah, 2013 .

Acid/NaNO2: An Efficient System for the Oxidation of Urazoles and Bis-Urazoles under Mild and Heterogeneous Conditions

M. Zolfigol, G. Chehardoli, M. Rasouli, 2014 .

Organic Solid Acid/NaNO2: An Efficient System for the Oxidation of Urazoles and Bis-Urazoles under Mild and Heterogeneous Conditions

M. Zolfigol, S. Mallakpour, G. Chehardoli, 2011 .

Oxidation of urazoles via in situ generation of Cl+ by using N,N,2,3,4,5,6-heptachloroaniline or a UHP/MCln system under mild conditions †

M. Zolfigol, M. Bagherzadeh, S. Mallakpour, 2001 .

An efficient method for the oxidation of urazoles with [NO+·crown·H(NO3)2−]

M. Shamsipur, M. Zolfigol, S. Mallakpour, 2001 .

OXIDATION OF URAZOLES TO THEIR CORRESPONDING TRIAZOLINEDIONES UNDER MILD AND HETEROGENEOUS CONDITIONS VIA IN SITU GENERATION OF NO+IOX −

M. Zolfigol, S. Mallakpour, H. Nasr‐Isfahani, 2001 .

Synthetic strategies, SAR studies, and computer modeling of indole 2 and 3-carboxamides as the strong enzyme inhibitors: a review

Asrin Bahmani, G. Chehardoli, 2020, Molecular Diversity.

Poly(N‐Bromobenzene‐1,3‐Disulfonylamide), N,N,N′,N′‐Tetrabromobenzene‐1,3‐Disulfonylamide and DABCO‐Bromine Complex: As Novel Reagents for the Oxidative Coupling of Thiols to Disulfides

M. Zolfigol, G. Chehardoli, Nadiya Koukabi, 2007 .

N‐Nitrosation of Secondary Amines with [NO+×Crown×H (NO3)2‐].

M. Shamsipur, M. Zolfigol, S. Salehzadeh, 2001 .

Synthesis of Gadolinium Complexes Using Medicinal Plant Extracts

D. Dastan, G. Chehardoli, M. Ghavam, 2021, Avicenna Journal of Pharmaceutical Research.

Molybdatophosphoric acid as an efficient catalyst for the catalytic and chemoselective oxidation of sulfides to sulfoxides using urea hydrogen peroxide as a commercially available oxidant

M. Zolfigol, A. Hasaninejad, G. Chehardoli, 2010 .

Designing A Bacterial Biosensor For Arsenic Detection In Water Solutions

A. Roointan, M. Saidijam, A. Rahmani, 2014 .

Electrochemical detection of sulfite in food samples

Yasser Fakri Mustafa, G. Chehardoli, S. Habibzadeh, 2022, Journal of Electrochemical Science and Engineering.

6‐Methoxy‐1‐tetralone Derivatives Bearing an N‐Arylpyridinium Moiety as Cholinesterase Inhibitors: Design, Synthesis, Biological Evaluation, and Molecular Docking Study

M. Mahdavi, M. Khoshneviszadeh, Mina Saeedi, 2022, ChemistrySelect.

Synthesis and molecular modeling of new 2‐benzylidenethiobarbituric acid derivatives as potent tyrosinase inhibitors agents

M. Hajimahmoodi, G. Chehardoli, Z. Najafi, 2022, Journal of the Chinese Chemical Society.

Novel indolotacrine hybrids as acetylcholinesterase inhibitors: design, synthesis, biological evaluation, and molecular docking studies

M. Zolfigol, M. Faramarzi, M. Mahdavi, 2023, Journal of the Iranian Chemical Society.

A Quick Overview of Recent Approaches to the Synthesis and Design of New Drugs

Asrin Bahmani, G. Chehardoli, 2020, Avicenna Journal of Pharmaceutical Research.

Fused 1,4‐Dihydropyridines and Their Corresponding Pyridines: Synthesis, Molecular Modeling and Cholinesterase Inhibition

Asrin Bahmani, Roshanak Hariri, T. Akbarzadeh, 2023, ChemistrySelect.