Ali Reza Kiasat
Department of Chemistry, College of Science, Shahid Chamran University of Ahvaz, Ahvaz, Iran.
[ 1 ] - β-Cyclodextrin conjugated imidazolium cation: A neutral, eco-friendly and water-miscible dicationic ionic liquid in the regioselective ring opening of epoxides
The present study, for the first time, presents a feasible protocol for the preparation of β-cyclodextrin/ imidazolium based dicationic ionic liquid, [βCD/Im](OTs)2, and its application as an efficient and eco-friendly microvessel and host ionic liquid system for the regioselective ring opening of the epoxides in water. No evidence for the formation of diol by-products or side reacti...
[ 2 ] - B-podands as efficient catalysts for the ring opening of epoxides in water: A versatile and atom economical method for the synthesis of vicinal azidoalcohols
For the first time B-podands have been studied as an efficient and powerful catalysts in the ring opening of epoxides with azide anion in water. The reaction afforded the corresponding 1,2-azidoalcohols with high regioselectivity under mild reaction conditions and in a highly atom economic fashion.
[ 3 ] - Application of Ytterium Iron Garnet as a Powerful and Recyclable Nanocatalyst for the One-pot Synthesis of Octahydroquinazoline Derivatives under Solvent-free Conditions
In this work, preparation and crystallization of yttrium iron garnet Y3Fe5O12 super-paramagnetic nanoparticle by aqueous sol–gel processes and its application as an effective nano catalyst for esterification and etherification reactions in short reaction time and in high isolated yields. Then this catalist was used for the synthesis of Dihydropyrimidin derivatives is described. The catalyst was...
[ 4 ] - An Effective Green Procedure for the Synthesis of Phenacyl Derivatives Catalyzed by Silica-bound 3-{2-[Poly(ethylene glycol)]ethyl}-substituted 1-Methyl-1H-imidazol-3-ium Bromide as a Recyclable Phase Transfer Catalyst under Aqueous Media
The use of a recyclable phase transfer catalyst, SiO2-PEG-ImBr, is demonstrated in a simple and highly efficient synthesis of phenacyl derivatives by nucleophilic substitution reaction of phenacyl halides with different anions in water. Advantages of this system are easy work-up, moderate to good yields, and recyclable catalyst. The catalyst can be recycled and reused several times with no loss...
[ 5 ] - Biginelli Multicomponent Condensation Reaction Promoted by 4,4ʹ-Bipyridinium Dichloride Ordered Mesoporous Silica Nanocomposite under Solvent Free Conditions
In this paper, 4,4ʹ-bipyridinium dichloride supported SBA-15 (SBA@BiPy2+ 2Cl-) was used for the synthesis of dihydropyrimidinones. The synthesized catalyst was characterized by FT-IR spectroscopy, scanning electron microscopy (SEM), Transmission electron microscopy (TEM) and Thermogravimetric analysis (TGA). This nanocomposite was shown to be an efficient heterogeneous ca...
[ 6 ] - A Simple and Efficient One-Pot Synthesis of 1,4-Dihydropyridine and Polyhydroquinoline Derivatives Using Phosphosulfonic Acid as a Heterogeneous Catalyst under Solvent-Free Conditions
Phosphosulfonic acid (PSA) was found to be an efficient catalyst for the one-pot three-component Hantzsch condensation reaction of arylaldehydes, ethylacetoacetate and ammonium acetate to afford the corresponding 1,4-dihydropyridine and polyhydroquinoline derivatives in high yields. PSA was also applied for the one-pot preparation of polyhydroquinolines via four-component reaction of a...
[ 7 ] - رشد نانولوله‌های کربنی هم راستا به روش نشست بخار شیمیایی کاتالیستی و روش رشد فاز بخار
در این تحقیق، نانولوله‌های کربنی هم‌راستا با روش نشست بخار شیمیایی کاتالیستی و با استفاده از لایه‌نشانی نانوذرات کاتالیستی آهن- مولیبدن بر روی زیر‌لایه‌‌ای از جنس سیلیکون تولید شدند. از گاز استیلن (C2H2) به عنوان منبع کربنی، گاز آرگون(Ar) به عنوان گاز حامل، گاز هیدروژن(H2) برای احیای نانوذرات واز نانوذرات آهن- مولیبدن به عنوان منبع کاتالیستی در دمای℃750 جهترشدنانولوله‌های کربنی استفاده شده است....
[ 8 ] - تبدیل ناحیه گزین اپوکسیدها به β- استوکسی الکل ها کاتالیز شده با یک کاتالیزگر انتقال فاز جدید سبز و بازیافت پذیر
یک روش ملایم و مؤثر جدید برای باز کردن حلقه اپوکسیدها با آنیون استات در حضور مقادیر کاتالیزوری سیلیکاژل متصل به پلی اتیلن گلیکول استخلاف شده با 1- متیل ایمیدازولیوم برمید (SiO2-PEG-ImBr) به عنوان یک کاتالیزگر انتقال فاز ناهمگن مؤثر در محیط آبی گزارش شده است. β- استوکسی الکل‌های مختلف با راندمان بالا و ناحیه‌گزینی فوق‌العاده، در مدت زمان کوتاهی به دست آمده است. مهم-ترین مزایای این روش عبارتند از...
[ 9 ] - Regioselective conversion of epoxides to vicinal nitrohydrins catalyzed by silica-bound 3-{2-[poly(ethylene glycol)]ethyl}-substituted 1-methyl-1H-imidazol-3-ium bromide as a green and reusable catalyst under aqueous thermal conditions
An environmentally benign procedure for the synthesis of vicinal nitrohydrins via the regioselective ring opening reaction of epoxides with nitrite anion using silica-bound 3-{2-[poly(ethylene glycol)]ethyl}-substituted 1-methyl-1H-imidazol-3-ium bromide as an effective heterogeneous phase transfer catalyst was described. Short reaction time, high yield of products, simple work-up proc...
[ 10 ] - Regioselective conversion of epoxides to vicinal nitrohydrins catalyzed by silica-bound 3-{2-[poly(ethylene glycol)]ethyl}-substituted 1-methyl-1H-imidazol-3-ium bromide as a green and reusable catalyst under aqueous thermal conditions
An environmentally benign procedure for the synthesis of vicinal nitrohydrins via the regioselective ring opening reaction of epoxides with nitrite anion using silica-bound 3-{2-[poly(ethylene glycol)]ethyl}-substituted 1-methyl-1H-imidazol-3-ium bromide as an effective heterogeneous phase transfer catalyst was described. Short reaction time, high yield of products, simple work-up proc...
[ 11 ] - β-Cyclodextrin conjugated imidazolium cation: A neutral, eco-friendly and water-miscible dicationic ionic liquid in the regioselective ring opening of epoxides
The present study, for the first time, presents a feasible protocol for the preparation of β-cyclodextrin/ imidazolium based dicationic ionic liquid, [βCD/Im](OTs)2, and its application as an efficient and eco-friendly microvessel and host ionic liquid system for the regioselective ring opening of the epoxides in water. No evidence for the formation of diol by-products or side reacti...
[ 12 ] - B-podands as efficient catalysts for the ring opening of epoxides in water: A versatile and atom economical method for the synthesis of vicinal azidoalcohols
For the first time B-podands have been studied as an efficient and powerful catalysts in the ring opening of epoxides with azide anion in water. The reaction afforded the corresponding 1,2-azidoalcohols with high regioselectivity under mild reaction conditions and in a highly atom economic fashion.
[ 13 ] - Synthesis and Characterization of γ-Fe2O3@HAp@β-CD Core-Shell Nanoparticles as a Novel Magnetic Nanoreactor and Its Application in the One-Pot Preparation of β-azido Alcohols, β-nitro Alcohols, and β-cyanohydrins
In this study, β-cyclodextrin(β-CD) supported, hydroxyapatite encapsulated γ-Fe2O3 (γ-Fe2O3@HAp@β-CD) was successfully prepared and evaluated as a solid-liquid phase transfer catalyst and also a molecular host system and nanoreactor for the nucleophilic ring-opening of epoxides in water for the preparation of β-azido alcohols, β-nitro alcohols, an...
[ 14 ] - MCM-BP as a Novel Nanomagnetic Reusable Basic Catalyst for the one Pot Solvent-Free Synthesis of Dihydropyridine, Polyhydroquinoline and Polyhydroacridine Derivatives via Hantzsch Multicomponent Condensation Reaction
By the immobilization of bipyridinium chloride onto mesoporous MCM-41encapsulated Fe3O4 nanoparticles via a simple post-synthesis method, a totally new organic-inorganic hybrid nanocomposite was formulated. The heterogeneous hybrid nanomagnetic composite was characterized by <spa...