872-85-5Relevant articles and documents
TEMPO mediated electrocatalytic oxidation of pyridyl carbinol using palladium nanoparticles dispersed on biomass derived porous nanoparticles
B, Akshaya K.,Bhat, Vinay S.,Hegde, Gurumurthy,Mathew, Agnus T.,S, Supriya,T, Maiyalagan,Varghese, Anitha
, (2020)
Remarkable electrocatalytic property of Pd nanostructures dispersed on CNSareca coated CFP electrode towards TEMPO mediated electrooxidation of pyridyl carbinol was reported for the first time. Carbon nanospheres (CNSs) derived from Areca catechu decorated with Pd nanoparticles were coated on carbon fiber paper (CFP) and was employed for electrooxidation of pyridyl carbinol in aqueous acidic medium. An environmentally benign and economic strategy was utilized for the preparation of CNSs obtained from Areca catechu. The physical characterizations, electronic state and chemical composition of the modified electrode were studied using Fourier transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD) spectroscopy and X-ray photoelectron spectroscopy (XPS). Scanning electron microscopy (SEM), Transmission electron microscopy (TEM) and high resolution transmission electron microscopy (HRTEM) techniques were used for analyzing the morphology of modified electrode. The electrochemical characterizations of the modified electrodes were performed by Cyclic voltammetry (CV) and Electrochemical impedance spectroscopy (EIS). Pd decorated CNSareca dispersed on CFP electrode has exhibited strong electrocatalytic activity towards TEMPO mediated oxidation of pyridyl carbinol.
Zn-doped W/aluminium oxide catalyst: Efficient strategy towards sustainable oxidation of alcohols
An, Yu,Cai, Menglu,Chen, Yingqi,Dai, Liyan,Fang, Yangyang,Li, Jun,Wang, Xiaozhong,Zhang, Ming
, (2020)
Bifunctional catalysts have been considered to have vital importance in catalytic chemical process, but there is still some developing room for convenient materials with dual active sites. These catalysts have a notorious reputation for inhibiting mutual neutralization and controlling the distribution of active sites in order to perform their functions. We tailor a series of W-Zn-Al2O3 catalysts by modulating the doping density of metal species, which can boost the catalytic process of alcohols into corresponding carbonyl compounds in an additive-free-condition. Test results indicate that the proper content of zinc element can promote the overall activities, and subsequent adjustment of doping zinc can dramatically increase the electronic interaction and change the distribution of chemical active sites. Also, a plausible reaction mechanism was proposed to better understand the acid-base bifunctional catalytic process. Theoretical results confirm this system can provide certain references for similar reactants. Present reaction system is a green procedure and features a broad substrate scope, which reveals a sustainable method to process oxidative dehydrogenation reaction.
Samarium-based Grignard-type addition of organohalides to carbonyl compounds under catalysis of CuI
Liu, Chen,Liu, Yongjun,Qi, Yan,Song, Bin,Wang, Liang,Xiao, Shuhuan
supporting information, p. 6169 - 6172 (2021/06/30)
Grignard-type additions were readily achieved under the mediation of CuI (10 mol%) and samarium (2 equiv.) by employing various organohalides,e.g.benzyl, aryl, heterocyclic and aliphatic halides (Cl, Br or I), and diverse carbonyl compounds (e.g.carbonic esters, carboxylic esters, acid anhydrides, acyl chlorides, ketones, aldehydes, propylene epoxides and formamides) to afford alcohols, ketones and aldehydes, respectively, with high efficiency and chemoselectivity, in which the organosamarium intermediate might be involved.
Pyridinium Chlorochromate Supported on Montmorillonite–KSF as a Versatile Oxidant under Ball Milling Conditions
Hosseinzadeh, Rahman,Narimani, Erfan,Mavvaji, Mohammad
, p. 461 - 471 (2021/08/09)
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Combining photo-redox and enzyme catalysis for the synthesis of 4H-pyrimido[2,1-b] benzothiazole derivatives in one pot
Yu, Yuan,Lu, Wei-Fan,Yang, Zeng-Jie,Wang, Na,Yu, Xiao-Qi
supporting information, (2020/12/25)
A novel strategy combining visible-light and enzyme catalysis in one pot for the synthesis of 4H-pyrimido[2,1-b] benzothiazole derivatives from alcohols is described for the first time. Fourteen 4H-pyrimido[2,1-b] benzothiazole derivatives were prepared with yields of up to 98% under mild reaction conditions by a simple operation. The photoorgano catalyst rose Bengal (rB) was employed to oxyfunctionalise alcohols to aldehydes. Compared with aldehydes, alcohols with more stable properties and lower cost, thus we used photocatalysis to oxidize alcohols into aldehydes. Next, the enzyme was used to further catalyze the reaction of Biginelli to produce the target product of 4H-pyrimidine [2,1-b] benzothiazole. Experimental results show that this method provides a more efficient and eco-friendly strategy for the synthesis of 4H-pyrimido[2,1-b] benzothiazole derivatives.