scholarly journals The first efficient biocatalytic route for the synthesis of Kojic acid derivatives in aqueous media

2021 ◽  
Vol 152 ◽  
pp. 106289
Author(s):  
Kiran S. Dalal ◽  
Mangal A. Chaudhari ◽  
Dipak S. Dalal ◽  
Bhushan L. Chaudhari
Keyword(s):  
2016 ◽  
Vol 40 (2) ◽  
pp. 1693-1697 ◽  
Author(s):  
Evgeny A. Kataev ◽  
Mittapalli Ramana Reddy ◽  
Gangarpu Niranjan Reddy ◽  
Vemulapati Hanuman Reddy ◽  
Cirandur Suresh Reddy ◽  
...  

An efficient and green method has been developed for the synthesis of kojic acid derivatives by employing 20 mol% β-cyclodextrin in aqueous media.


2018 ◽  
Vol 42 (8) ◽  
pp. 416-418
Author(s):  
Morteza Miri ◽  
Alireza Hassanabadi

A novel method for oxazine ring formation has been established using the reaction of kojic acid and aromatic aldehydes with methyl carbamate in the presence of p-toluenesulfonic acid in aqueous media to afford 4-aryl-6-hydroxymethyl-1,4-dihydropyrano[3,2-e][1,3] oxazine-2,8-diones in excellent yields. The present method does not involve any hazardous organic solvent. Therefore, this procedure could be classified as green chemistry.


2014 ◽  
Vol 92 (12) ◽  
pp. 1163-1168 ◽  
Author(s):  
Razieh Azimi ◽  
Robabeh Baharfar

A series of spiro-pyranoxindole derivatives were prepared in good yields via a three-component reaction of isatins with activated methylene reagents and kojic acid using 1,4-diazabicyclo[2.2.2]octane (DABCO) immobilized on mesoporous SBA-15 as a heterogenized organocatalyst in aqueous media. The synthesized compounds were evaluated for their antioxidant activity by a 1,1-diphenyl-2-picrylhydrazyl (DPPH) radical scavenging assay.


2020 ◽  
Vol 56 (27) ◽  
pp. 3851-3854 ◽  
Author(s):  
Xiaomin Chai ◽  
Hai-Hua Huang ◽  
Huiping Liu ◽  
Zhuofeng Ke ◽  
Wen-Wen Yong ◽  
...  

A Co-based complex displayed the highest photocatalytic performance for CO2 to CO conversion in aqueous media.


2007 ◽  
Vol 20 (3) ◽  
pp. 227-230 ◽  
Author(s):  
Ana Reverdito ◽  
Mariano García ◽  
Alejandra Salerno ◽  
Oscar Locani ◽  
Isabel Perillo
Keyword(s):  

2003 ◽  
Vol 775 ◽  
Author(s):  
Sung-Hwa Oh ◽  
Ju-Myung Song ◽  
Joon-Seop Kim ◽  
Hyang-Rim Oh ◽  
Jeong-A Yu

AbstractSolution behaviors of poly(styrene-co-sodium methacrylate) were studied by fluorescence spectroscopic methods using pyrene as a probe. The mol% of methacrylate was in the range 3.6–9.4. Water and N,N-dimethylforamide(DMF) mixture was used as a solvent (DMF/water = 0.2 mol %). The critical micelle (or aggregation) concentrations of ionomers and the partition coefficients of pyrene were obtained the temperature range 10–80°C. At room temperature, the values of CMCs (or CACs) were in the range 4.7 ×10-6 5.3 ×10-6 g/mL and we could not find any notable effect of the content of ionic repeat units within the experimental errors. Unlike CMCs, as the ion content increased, partitioning of pyrene between the hydrophobic aggregates and an aqueous media decreased from 1.5 ×105 to 9.4 ×104. As the temperature increased from 10 to 80 °C, the values of CMCs increased less than one order of magnitude. While, the partition coefficients of pyrene decreased one order of magnitude and the effect of the ion content became negligible.


2020 ◽  
Author(s):  
Laurent Sévery ◽  
Jacek Szczerbiński ◽  
Mert Taskin ◽  
Isik Tuncay ◽  
Fernanda Brandalise Nunes ◽  
...  

The strategy of anchoring molecular catalysts on electrode surfaces combines the high selectivity and activity of molecular systems with the practicality of heterogeneous systems. The stability of molecular catalysts is, however, far less than that of traditional heterogeneous electrocatalysts, and therefore a method to easily replace anchored molecular catalysts that have degraded could make such electrosynthetic systems more attractive. Here, we apply a non-covalent “click” chemistry approach to reversibly bind molecular electrocatalysts to electrode surfaces via host-guest complexation with surface-anchored cyclodextrins. The host-guest interaction is remarkably strong and allows the flow of electrons between the electrode and the guest catalyst. Electrosynthesis in both organic and aqueous media was demonstrated on metal oxide electrodes, with stability on the order of hours. The catalytic surfaces can be recycled by controlled release of the guest from the host cavities and readsorption of fresh guest. This strategy represents a new approach to practical molecular-based catalytic systems.


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