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101.
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103.
We have developed simple, greener, safer multicomponent synthesis series of 4-arylidene-2-phenyl-5(4H) oxazolones 4(a-r) catalyzed by Bronsted acid ionic liquid as triethylammonium hydrogen sulfate [Et3NH][HSO4] and catalytic amount of acetic anhydride and sodium acetate with excellent yields (90–99%). The protocol offers economical, environmentally benign, solvent-free conditions, and recycle–reuse of the catalyst and easily available starting as benzoyl chloride 1, amino acid 2 and a variety of aldehydes 3. The cyclization followed by condensation of benzoyl chloride, amino acid, and a variety of aldehydes catalyzed by ILs [Et3NH][HSO4] and catalytic amount of acetic anhydride and sodium acetate. The final products were confirmed by their characterization data such as FTIR, 1H-NMR, 13C-NMR, Mass, high-resolution mass spectra and were compared with its reported method. 相似文献
104.
Sanjay Jadhav Gajanan Rashinkar Rajashri Salunkhe Arjun Kumbhar 《Tetrahedron letters》2017,58(33):3201-3204
A simple, efficient and metal-free route for the synthesis of dissymmetric ketones through Suzuki type cross-coupling reaction has been established. This strategy signifies an attractive, cost-effective and operationally convenient tool for the synthesis of a wide range of dissymmetric ketones. Although conventional routes for the synthesis of ketones have been widely used, the potential challenge with these methods is functional group tolerance. The reported metal-free method represents a reaction with moderate functional group tolerance. The procedure is operationally convenient and shows broad substrate scope with good to excellent product yields. 相似文献
105.
碳-氧键氢解是生物质呋喃基化合物制备交通燃料常见的模型反应,其中5-羟甲基糠醛(HMF)转化为汽油添加剂2,5-二甲基呋喃(DMF)尤为引人关注.本文采用CeO2,ZrO2和Al2O3负载的Cu-Co双金属催化剂用于HMF选择性氢解制DMF的反应中.采用X射线衍射、N2吸附-脱附、投射电镜、H2-程序升温还原、氨-程序升温脱附和元素分析表征了新鲜的和使用过催化剂的结构,并将其与催化活性相关联.Cu-Co/CeO2催化剂通过在大的Cu颗粒上还原C=O键生成了最多的2,5双(羟甲基呋喃)(BHMF).但Cu-Co/Al2O3催化剂具有高度分散的Cu,Cu-Co复合氧化物和大量的弱酸位,因而生成DMF的选择性最高.Cu-Co/ZrO2催化剂则由于存在强酸位,DMF选择性较低,生成了各种过度氢解产物,如2,5而甲基四氢呋喃和5,5-二(亚甲基)双(2-甲基呋喃).因此,考察了Cu-Co/Al2O3催化剂上的反应路径,以及温度、氢气压力和时间等操作条件的影响,使其具有较优的HMF转化率和DMF选择性. 相似文献
106.
Sanjay K. Bharti Saurabh K. Patel Gopal Nath Ragini Tilak Sushil K. Singh 《Transition Metal Chemistry》2010,35(8):917-925
Six Cu(II) complexes of Schiff base ligands of arylidene-2-(4-(4-bromo/methoxy-phenyl)thiazol-2-yl) hydrazines have been synthesized,
characterized and screened for DNA cleavage and antimicrobial activities. The chemical structures of the complexes were deduced
by physicochemical and spectroscopic methods. Elemental analyses indicated that the stoichiometry of the complexes is CuL2 (L = Schiff base ligand). The DNA cleavage activities of the complexes were evaluated by agarose gel electrophoresis in the
presence and absence of oxidant (H2O2) and free radical scavenger (DMSO). All the six complexes showed significant nuclease activity in the presence of H2O2, and two of the complexes showed moderate nuclease activity even in the absence of oxidant. The complexes did not show nuclease
activity in the presence of free radical scavenger. The compounds were tested for activity against selected bacteria and fungi. 相似文献
107.
Sanjay S. Latthe Hiroaki Imai V. Ganesan Charles Kappenstein A. Venkateswara Rao 《Journal of Sol-Gel Science and Technology》2010,53(2):208-215
Optically transparent silica films were prepared at room temperature (~27°C) by keeping the molar ratio of TEOS:MeOH:H2O (0.001 M NH4F) constant at 1:19.29:6.20, respectively. A surface chemical modification of the films was done with alkylchlorosilanes at
different concentrations from 0 to 1 vol. % and aging times varied from half to 2 h. The DMCS and TMCS surface modified silica
films showed the static water contact angle of 146° and 162°, respectively. When the DMCS and TMCS modified films were cured
at temperatures higher than 240 and 275°C, respectively, the films became superhydrophilic. Further, the humidity study was
carried out at a relative humidity of 90% at 30°C temperature over 60 days. We characterized the water repellent silica films
by Fourier transform infrared spectroscopy, scanning electron microscopy, atomic force microscopy, % of optical transmission,
humidity tests and contact angle measurements. 相似文献
108.
Madhukar N. Jachak Maruti G. Ghagare Dilip R. Birari Ramhari V. Rote Muddassar A. Kazi Sanjay M. Jachak Raghunath B. Toche 《Monatshefte für Chemie / Chemical Monthly》2010,46(3):569-576
Abstract
A novel synthesis of pyrazole-4-carboxamides is reported. The reaction of N-(3-(dimethylamino)-2-formylacryloyl)formamide, an intermediate obtained by Vilsmeier–Haack formylation of acetonitrile, with hydrazine hydrate or monosubstituted hydrazines provides such compounds in good yields. This method has advantages over other methods for construction of such ring systems previously described in the literature. 相似文献109.
Banerjee K Dasgupta S Jadhav MR Naik DG Ligon AP Oulkar DP Savant RH Adsule PG 《Journal of AOAC International》2010,93(6):1957-1964
An analytical method is reported for residue analysis of the fungicide meptyldinocap in different fruit matrixes that involves extraction with ethyl acetate, hydrolysis of the residues with ethanolamine, and determination by LC/MS/MS. The method involves extraction of 10 g sample with 10 mL ethyl acetate; evaporation of the ethyl acetate phase to dryness, and subsequent hydrolysis of the residues to 4,6-dinitro-2-(1-methylheptyl) phenol on reaction with 1% ethanolamine. The pH of this hydrolyzed product was neutralized with formic acid and analyzed by LC/MS/MS. The hydrolysis reaction followed pseudo-first-order kinetics, and the reaction product was spectroscopically confirmed as 2-(1-methylheptyl)-4,6-dinitrophenol. The method offered > 80% recoveries at an LOQ of 10 ng/g for grape and mango, 25 ng/g for pomegranate with intralaboratory Horwitz ratio < 0.5, and measurement uncertainties < 10% at LOQ levels. Considering first-order rate kinetics, activation energy, enthalpy of activation, and entropy of activation varied as solvent > mango > grape > pomegranate. Free energy of activation at 298 K was higher than at 280 K and was similar for solvent and three matrixes at both temperatures. 相似文献
110.
Sandip R. Sabale D. V. Jadhav B. S. Mohite 《Journal of Radioanalytical and Nuclear Chemistry》2010,283(2):273-278
A simple and efficient column chromatographic method has been developed for the sequential separation of U(VI), Th(IV) and
Ce(III) using poly[dibenzo-18-crown-6] as stationary phase and l-arginine as a counter ion. The different elution patterns with various eluting agents were observed for individual element.
The capacity of poly[dibenzo-18-crown-6] for U(VI), Th(IV) and for Ce(III) was found to be 0.96, 0.86 and 1.49 (±0.01) mmol/g
of crown polymer, respectively. The method is efficient to separate the elements in multicomponent mixtures and has good recovery.
The method is extended to determine the U(VI), Th(IV) and Ce(III) from monazite sand. The method is simple, rapid and selective
having good reproducibility (~±2%). 相似文献