A5000136014- Chemical Synthesis and Reactions
- Synthesis and biological activity
- Multicomponent Synthesis of Heterocycles
- Sulfur-Based Synthesis Techniques
- Synthesis and Characterization of Heterocyclic Compounds
- Curcumin's Biomedical Applications
- Alzheimer's disease research and treatments
- Oxidative Organic Chemistry Reactions
- Synthesis and Biological Evaluation
- Enzyme function and inhibition
- Chemical Synthesis and Analysis
- Natural Antidiabetic Agents Studies
- Cholinesterase and Neurodegenerative Diseases
- Synthesis of Organic Compounds
- Microwave-Assisted Synthesis and Applications
- Click Chemistry and Applications
- Synthesis of heterocyclic compounds
- Computational Drug Discovery Methods
- Biochemical effects in animals
- Metal complexes synthesis and properties
- Vanadium and Halogenation Chemistry
- X-ray Diffraction in Crystallography
- Electrochemical sensors and biosensors
- Antibiotic Resistance in Bacteria
- Chemical Reactions and Mechanisms
Kermanshah University of Medical Sciences
2016-2025
INTI International University
2024-2025
The University of Queensland
2023
Imam Khomeini International University
2023
Pharmaceutical Sciences Research Center
2017
Tarbiat Modares University
2011
Islamic Azad University, Tehran
2011
Kerman University of Medical Sciences
2009
In-Q-Tel
2008
Isfahan University of Technology
2000-2004
The present study aims to evaluate the α-amylase and α-glucosidase inhibitory activity of 26 polyphenols using molecular docking virtual screening studies.
Abstract Herein, we present an interesting role of tungstate-decorated amphiphilic carbon quantum dots (A-CQDs/W) in the selective oxidative cleavage alkenes to aldehydes. In this work, for first time, disclose unprecedented tungstate-based system incorporating A-CQDs as a bridge homogeneous catalyst and efficient wide substrate scope into The A-CQDs/W were synthesized via one-step hydrothermal synthesis approach using 1-aminopropyl-3-methyl-imidazolium chloride stearic acid surface...
Chiral CQDs hold significant promise for enantioselective detection in the pharmaceutical industry.
Benzyltriphenylphosphonium peroxymonosulfate could be used for selective oxidation of aromatic and aliphatic sulfides thiols to their corresponding sulfoxides disulfides under nonaqueous aprotic conditions without catalyst.
Abstract Iron(III) trifluoroacetate was used as an efficient and nonhygroscopic catalyst for the alcoholysis, hydrolysis, acetolysis of epoxides. The addition chloride, bromide, iodide, nitrate ions to epoxides produce corresponding 2-halo 2-nitratoalkanols also conversion acetonides thiiranes were performed efficiently in presence this catalyst.
Wet silica-supported potassium permanganate was used as an inexpensive and efficient reagent for conversion of semicarbazones phenylhydrazones to the corresponding carbonyl compounds under solid-state conditions.
Abstract This paper describes the oxidation of alcohols under solvent-free conditions using benzyltriphenylphosphonium peroxymonosulfate, which has been prepared by mixing an aqueous solution chloride with oxone® at room temperature. reagent is stable white powder, may be stored for months without loss its activity. compound readily soluble in organic solvents such as acetonitrile, chloroform, and dichloromethane slightly carbon tetrachloride, ether, hexane.
The first class of carbonic anhydrase inhibitors (CAIs) discovered was sulfonamides, but their clinical use is limited due to side effects caused by inhibition multiple CA isoforms. To overcome this, researchers have focused on developing isoform-selective CAIs. This study involved the synthesis and characterization novel carboxylic acid/sulfonamide derivatives. We investigated interaction between these compounds human II (hCA II) isoform using spectroscopic computational methods....