scholarly journals Synthesis and Catalytic Applications of Ultrasmall Copper Nanoparticles Using Aloe Vera Plant Extract

Author(s):  
Rajagopal Ramkumar ◽  
Shradha Sapru ◽  
Panthalattu Parambil Archana

<div>An extract of <i>Aloe Vera</i> acts as a powerful reducing agent for the synthesis of ultrasmall copper nanoparticles (CuNPs) in water medium. The prepared copper nanoparticles are characterized by XRD, HRTEM and UV-Vis analysis. The diameter of the prepared nanoparticle is less than 5 nm. The catalytic activity of CuNPs has been successfully evaluated for the three-component reaction to synthesize 1,2,3-triazoles and chalcone tethered 1,2,3-triazoles with low catalyst loading and under mild reaction conditions. These triazoles are further utilized for the synthesis of dihydropyrazines.</div>

2020 ◽  
Author(s):  
Rajagopal Ramkumar ◽  
Shradha Sapru ◽  
Panthalattu Parambil Archana

<div>An extract of <i>Aloe Vera</i> acts as a powerful reducing agent for the synthesis of ultrasmall copper nanoparticles (CuNPs) in water medium. The prepared copper nanoparticles are characterized by XRD, HRTEM and UV-Vis analysis. The diameter of the prepared nanoparticle is less than 5 nm. The catalytic activity of CuNPs has been successfully evaluated for the three-component reaction to synthesize 1,2,3-triazoles and chalcone tethered 1,2,3-triazoles with low catalyst loading and under mild reaction conditions. These triazoles are further utilized for the synthesis of dihydropyrazines.</div>


Author(s):  
Long Chen ◽  
Shi-Lu Zheng ◽  
Yun-Xiang Zou ◽  
Zhong Wen ◽  
Jiafu Lin ◽  
...  

Facile synthesis of 2-phosphorylated 2H-chromenes has been accomplished herein via a Y(OTf)3-catalyzed dehydrative coupling of 2H-chromene hemiacetals with P(O)-H compounds. This protocol features low catalyst loading, mild reaction conditions, broad...


2007 ◽  
Vol 85 (3) ◽  
pp. 197-201 ◽  
Author(s):  
Raman Gupta ◽  
Monika Gupta ◽  
Satya Paul ◽  
Rajive Gupta

A novel silica-supported zinc chloride catalyst was prepared and investigated for the Biginelli reaction. The key features of the catalyst include rapid reaction with 100% conversion of aldehyde, good catalyst recyclability, and high stability under the reaction conditions (passes hot filtration test successfully). A low catalyst loading (12 mol% of ZnCl2) was required to achieve a quantitative reaction. Other catalysts such as SiO2–AlCl2, SiO2–AlCl2–ZnCl2 were also prepared and their activity was compared with SiO2–ZnCl2 for the Biginelli reaction.Key words: silica gel, zinc chloride, Biginelli compounds, heterogeneous catalysis, reusability.


2019 ◽  
Vol 9 (13) ◽  
pp. 3398-3407 ◽  
Author(s):  
V. Hung Mai ◽  
Oleg B. Gadzhiev ◽  
Stanislav K. Ignatov ◽  
Georgii I. Nikonov

NHC-supported trihydrides Cp(NHC)RuH3show excellent catalytic activity in the H/D exchange of pyridine and some other N-heterocycles under mild conditions and low catalyst loading.


2019 ◽  
Vol 16 (5) ◽  
pp. 793-800 ◽  
Author(s):  
Mohsen Tazari ◽  
Hamzeh Kiyani

Background: Chromenes and pyran annulated heterocycles are the most common frameworks existing in various biologically active molecules. Due to their beneficial and biological properties, they are eyecatching synthetic targets in the arsenal of organic chemistry. Thus, finding green and efficient methods, as well as searching for a new catalyst for the synthesis of these heterocycles is of interest to organic chemistry researchers. Objective: Sodium malonate as a readily available catalyst was employed aimed at the multicomponent synthesis of numerous 2-amino-4H-chromenes and 2-amino-4H-pyrans in water as a green medium reaction. Methods: The reaction was performed via treatment of aldehydes (1 mmol) with malononitrile/ethyl cyanoacetate (1 mmol) and β-dicarbonyl compounds (1 mmol)/or resorcinol (1 mmol) in water (4 mL) in the presence of sodium malonate (10 mol %) at 70°C. On completion of the reaction (monitored by TLC analysis), the reaction mixture was gradually cooled at room temperature, and the resulting precipitates were collected by filtration, washed with cold ethanol and air-dried to give the corresponding pure products. The solvent was evaporated from the filtrate to recover the catalyst, and the catalyst was reused for subsequent reactions. Results: In the initial stages, we explored the best reaction conditions using three-component reaction of benzaldehyde, malononitrile, and dimedone as the model reaction. The effects of catalyst loading, temperature, and solvents were explored for this reaction. It was found that the best results were obtained for the synthesis of 2-amino-4H-chromenes and 2-amino-4H-pyran when the three-component reaction was carried out with equivalent molar quantities of each of the reactants in water containing 10 mol% sodium malonate at 70°C for 15 min in 96% yield. After finding optimal conditions, these conditions apply to other reactants and the target heterocyclic products were obtained with excellent yields. Conclusion: This study describes an efficient, environmentally benign, and clean one-pot, three-component synthesis of 2-amino-4H-chromenes and 2-amino-4H-pyran-3-carboxylates in the presence of sodium malonate as the commercially available catalyst in an aqueous medium at 70°C. High yields, mild reaction conditions, relatively shorter reaction times, use of simple reagents, and no requirement of the ultrasound, microwave, and ball milling techniques are the salient features and benefits of the present method. In addition, the present process is smooth and green.


Synthesis ◽  
2022 ◽  
Author(s):  
Zhi-Wei Ma ◽  
Chuan-Chuan Wang ◽  
Quan-Jian Lv ◽  
Xiao-Pei Chen ◽  
Ai-Qin Li ◽  
...  

AbstractA new tertiary amine-squaramide organocatalyst has been developed and applied to the asymmetric Michael addition of cyclic diketones to β,γ-unsaturated α-keto esters. The catalyst system performed well with a low catalyst loading of 1 mol% under mild reaction conditions. A series of synthetically and pharmaceutically useful chiral bicyclic compounds were obtained in high yields (up to 97%) with excellent enantioselectivities (up to 99 % ee). Furthermore, this catalytic system can be used efficiently in large-scale reactions with the yields and enantioselectivities being maintained.


2009 ◽  
Vol 87 (5) ◽  
pp. 650-661 ◽  
Author(s):  
Lisa Carosi ◽  
Dennis G. Hall

The use of different organomagnesium reagents in the copper-catalyzed allylic alkylation of 3-chloropropenyl boronates with chiral phosphoramidite ligands produces the desired α-substituted allylic boronate reagents in high regioselectivity and with modest to high enantioselectivities (up to 96% ee). The size of the incoming alkyl substituent from the organomagnesium reagent was found to impact the yield and selectivity of the allylic alkylation. A one-pot procedure for the preparation of these chiral allylic boronates followed by a Lewis acid (BF3) catalyzed addition to aldehydes delivers the desired allylboration products, homoallylic secondary alcohols, in good yields and very high diastereoselectivity. This three-component reaction methodology was applied to the syntheses of two lactone-containing natural products, (–)-massoialactone and (+)-(3R,5R)-3-hydroxy-5-decanolide. The key step of these syntheses involved the one-pot enantioselective copper-catalyzed allylic alkylation/allylboration reaction with a benzylic aldehyde, and afforded the desired product in 87% yield, 92% ee, and high E/Z selectivity in a ratio of 22:1. Remarkably, the allylic alkylation step of this sequential reaction was performed with a low catalyst loading of 2 mol% on a scale of >15 mmol that can provide multiple grams of the three-component product.


2019 ◽  
Vol 6 (1) ◽  
pp. 28-35 ◽  
Author(s):  
Asiyeh Mosallanezhad ◽  
Hamzeh Kiyani

Background: 4-Arylmethylideneisoxazol-5(4H)-ones are a class of organic compounds with a variety of applications in the agriculture, filter dyes, photonic devices, and pharmaceutical industries. They are also used as synthetic precursors for the synthesis of other organic compounds. As a result, efforts are being made to search new and available catalyst and green methods toward their synthesis. Objective: The aim of this work is to investigate the catalytic activity of salicylic acid as an inexpensive, easy to handle, and safe catalyst to synthesis of some derivatives of isoxazole-5(4H)-ones in water medium. Methods: To aqueous solution of equal amounts of aryl/heteroaryl aldehydes, β-ketoesters, and hydroxylamine hydrochloride; salicylic acid (15 mol%) was added and the reaction mixture was stirred at room temperature for a specified periods. The precipitated product was filtered and washed with water to obtain 3-substituted-4-arylmethylideneisoxazol-5(4H)-ones. The reaction conditions were also optimized and extended to synthesis other isoxazol-5(4H)-ones. Results: The salicylic acid is found to possess acceptable catalytic activity for the promotion of three-component cyclocondensation of aryl/heteroaryl aldehydes, β-ketoesters, and hydroxylamine hydrochloride. The three-component reaction led to construction of 3-substituted-4-arylmethylideneisoxazol- 5(4H)-ones in good to high isolated reaction yields. Conclusion: The efficient and environmental friendliness procedure for the synthesis of isoxazol- 5(4H)-ones is introduced. The reaction also carried out smoothly in water as a cost-effective, simple, green, and non-toxic solvent at room temperature without using heating, microwave, and ultrasound sources.


2020 ◽  
Author(s):  
Chenguang Liu ◽  
Mingyang Wang ◽  
Shihan Liu ◽  
Yujie Wang ◽  
Yong Peng ◽  
...  

<p>The first example of non-noble metal-catalyzed asymmetric hydrogenation of aromatic <i>N</i>-heterocycles is reported. A new chiral pincer manganese catalyst showed outstanding catalytic activity in the asymmetric hydrogenation of a wide range of quinolines, affording high yields and excellent enantioselectivities (up to 97% <i>ee</i>). A turnover number of 3840 was reached at a low catalyst loading (S/C=4000), which was competitive with the activity of most effective noble metal catalysts for this reaction. The precise regulation of the enantioselectivity were ensured by a p–p interaction.<u></u></p>


2017 ◽  
Vol 19 (11) ◽  
pp. 2535-2540 ◽  
Author(s):  
Jia-wei Zhang ◽  
Guo-ping Lu ◽  
Chun Cai

An efficient, recyclable Pd–Cu bimetallic nanoparticle catalyst has been prepared, which exhibits superior activity and selectivity toward the hydrosilylation of internal and terminal alkynes under mild reaction conditions with a low catalyst loading.


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