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A facile and simple protocol for the 1,3‐dipolar cycloaddition of organic azides with terminal alkynes catalyzed by doped nano‐sized Cu2O on melamine? formaldehyde resin (nano‐Cu2O? MFR) as a new and convenient heterogeneous catalyst is described. In this method, ‘click’ cycloaddition of various structurally diverse β‐azido alcohols and alkynes in the presence of nano‐Cu2O? MFR in H2O/THF 1 : 2 furnished the corresponding 1,4‐disubstituted 1H‐1,2,3‐triazole adducts 1a – 1o in good to excellent yields at room temperature (Scheme and Table 3). The nano‐Cu2O? MFR was characterized by scanning electron microscopy (SEM), X‐ray diffraction (XRD), inductively coupled plasma (ICP) analysis, and FT‐IR. The nano‐Cu2O? MFR could be easily recovered and recycled from the reaction mixture and reused for many consecutive trials without significant decrease in activity (Table 4). The in vitro antibacterial activities of all synthesized compounds were tested on several Gram‐positive and/or Gram‐negative bacteria (Table 5). The results demonstrate the promising antibacterial activity for some of the synthesized compounds.  相似文献   
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The synthesis of bicyclo[3.3.1]nonane systems is reported. The synthesis is based on the tandem 1,3-dinucleophilic addition of 4-hydroxy-2-quinolinone to quinolinium salts.  相似文献   
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A combination of molybdatophosphoric acid and NaNO2 in the presence of wet SiO2 was used as an effective oxidizing agent for the oxidation of 1,2‐dihydroquinolines to their corresponding quinoline derivatives in dichlomethane at room temperature with excellent yields.  相似文献   
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The complex formation reaction of the $ {\text{VO}}_{2}^{ + } $ VO 2 + cation with D-(-)-quinic acid {(1R,3R,4S,5R)-(-)-1,3,4,5-tetrahydroxycyclohexane-1-carboxylic acid} at T = 298 K, I = 0.1 mol·dm?3 of sodium chloride in various aqueous solutions of 1-butyl-3-methylimidazolium tetrafluoroborate, [bmim]BF4, and methanol were studied by using potentiometric and UV spectrophotometric techniques. As far as we know, the calculated stability constants data presented in the current work are the first reported values for [bmim]BF4 and methanol mixed solvents. The Kamlet–Abboud–Taft solvatochromic equation enabled us to interpret the UV data and the stability constants values. The Redlich–Kister equation was applied for the calculation of solvatochromic parameters in the binary water + [bmim]BF4 mixtures. Hydrogen bonding is important for the dissociation constant in both media. In these systems the solvent polarizability and hydrogen-bond donor ability are the main interactions for the stability constants in the aqueous ionic liquid and methanol solutions, respectively.  相似文献   
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KF‐Melamine formaldehyde resin (KF‐MFR) was demonstrated to be a highly efficient heterogenious catalyst for cross‐aldol condensation under microwave irradiation. In this synthesis, various aldehydes and ketones were condensed together in the presence of supported KF on melamine‐formaldehyde resin to afford different chalcone derivatives in good to excellent yields. KF‐MFR proved to have unique termal and chemical resistance and can be reused for many consecutive runs without remarkable loss in catalytic activity.  相似文献   
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In this note, we enumerate all nonisomorphic 3‐factorizations of K10. © 2001 John Wiley & Sons, Inc. J Combin Designs 9: 379–383, 2001  相似文献   
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In this work, magnetic solid-phase extraction based on sodium dodecyl sulfate-coated Fe3O4 nanoparticles has been successfully applied for extraction and preconcentration of trace amounts of nystatin from water and vaccine samples prior to high-performance liquid chromatography–ultraviolet detection. Various experimental parameters affecting extraction and recovery of the analyte, such as the amount of sodium dodecyl sulfate, pH of the sample solution, salt concentration, extraction time, sample volume and desorption conditions, were systematically studied and optimized. Under optimized conditions, nystatin was quantitatively extracted. Proper linear range with good coefficient of determination, (R 2 > 0.99) and limit of detection and quantification (based on signal-to-noise ratios of 3 and 10) of 2.0 and 5.0 µg L?1, over the investigated concentration range (5–700 µg L?1), were obtained, respectively. The intra-day and inter-day relative standard deviations at 50 µg L?1 level of NYS were 1.4 and 4.5% based on six replicate determinations. The accuracy of the method was evaluated by recovery measurements on spiked samples. Suitable recoveries of 96–102 and 26–44% were achieved (at spiked levels of 50, 300 and 500 µg L?1) for water and vaccine samples, respectively.  相似文献   
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