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161.
A flexible approach for total syntheses of possible multiplolide A diastereomers establishing the relative and absolute configuration is documented. The adopted strategy features ring-closing metathesis (RCM) as the key reaction and screening of a set of substrates for the feasibility of RCM in general and for the requisite E-configuration of ring olefin in particular. Selective protecting groups manipulation prior to the assembly of the central macrocyclic core was instrumental in installing the epoxide functionality on a fully deprotected nonenolide at the end of the synthesis.  相似文献   
162.
We have developed a rapid and sensitive method for immunomagnetic separation (IMS) of Salmonella along with their real time detection via PCR. Silica-coated magnetic nanoparticles were functionalized with carboxy groups to which anti-Salmonella antibody raised against heat-inactivated whole cells of Salmonella were covalently attached. The immuno-captured target cells were detected in beverages like milk and lemon juice by multiplex PCR and real time PCR with a detection limit of 104 cfu.mL?1 and 103 cfu.mL?1, respectively. We demonstrate that IMS can be used for selective concentration of target bacteria from beverages for subsequent use in PCR detection. PCR also enables differentiation of Salmonella typhi and Salmonella paratyphi A using a set of four specific primers. In addition, IMS—PCR can be used as a screening tool in the food and beverage industry for the detection of Salmonella within 3–4 h which compares favorably to the time of several days that is needed in case of conventional detection based on culture and biochemical methods.
The method uses silica coated magnetic nanoparticles immobilized with anti-Salmonella antibody for immunomagnetic separation of Salmonella from beverages followed by detection by multiplex PCR (mPCR) and real time PCR (qPCR). This methodology contributes to rapid screening and accurate detection of Salmonella contaminations in beverages.  相似文献   
163.
A simple, reliable, trace determination of selenomethionine (Semet) based on a direct hydride generation atomic absorption spectrometric method was developed using sodium tetrahydroborate (0.3% in 0.2% NaOH) and hydrochloric acid (3 M). The method excluded any chemical pretreatment prior to hydride generation (HG). The optimized HG system was successfully coupled with the HPLC system. The detection limit (3σ of blank; n=5), reproducibility (R.S.D. of three successive analyses/day, performed on three different days), and repeatability (R.S.D. of three successive analyses) of the method were 1.08 ng ml−1, 9.8% for 9.04 ng ml−1 and 2.1–9.5% for 30.0–1.27 ng ml−1 Semet as Se (standards prepared in Milli-Q water). Calibration graph was linear up to 30 ng ml−1. This HPLC-HG-AAS method is very promising and successfully determined Semet (spiked) in human urine.  相似文献   
164.
An unsteady two-dimensional numerical simulation is performed to investigate the forced convection heat transfer for flow past a long heated equilateral triangular cylinder in an unconfined medium for the low Reynolds number laminar regime. The Reynolds number considered in this study ranges from 50 to 250 with three different values of Prandtl number (Pr?=?0.71, 7 and 100). Fictitious confining boundaries are chosen on the lateral sides of the computational domain that makes the blockage ratio β?=?5?% in order to make the problem computationally feasible. An unstructured triangular mesh is used for the computational domain discretization and the simulation is carried out with the commercial CFD solver Fluent. The flow and heat transfer characteristics are analyzed with the streamline and isotherm patterns at various Reynolds numbers. The dimensionless frequency of vortex shedding (Strouhal number), drag coefficient and Nusselt numbers are presented and discussed. The results obtained are in good agreement with the available results in the literature.  相似文献   
165.
166.
Abstract

Selective interpolymer complexation has been studied between methacrylic acid-methacrylamide copolymer and some complementary polymers such as poly(methacrylamide), poly(vinyl pyrrolidone), and poly(ethylene oxide). The relative order of complexation ability of the various nonionic polymers has been interpreted on the basis of the nature of interactions between different units of polymers. Configurational environment and neighboring group influences seem to affect interpolymer complex formation.  相似文献   
167.
[reaction: see text] We report highly efficient two-step procedures for the synthesis of 1,3-oxazole-, thiazole-, and imidazole-containing peptides on solid phase from dipeptides composed of C-terminal threonine, serine, cysteine, or diaminopropionic acid by using different cyclodehydration procedures followed or preceded by oxidation. The methods are compatible with Fmoc solid-phase peptide synthesis conditions and with N-Fmoc, N-Boc, N-Cbz, and N-Alloc protecting groups.  相似文献   
168.
[reaction: see text] A highly stereoselective surfactant-catalyzed intramolecular nitrone (formed by dehydration in water) cycloaddition in aqueous media leading to exclusive formation of a single isomer is reported. Either oxepane or pyran is formed from 3-O-allyl furanoside derivatives, which constitute the framework of a large number of biologically active compounds. Therefore, the environmentally friendly, efficient, and highly stereoselective syntheses of these chiral intermediates are still a meaningful pursuit.  相似文献   
169.
A new, convenient, ecofriendly synthesis of 3,5-diarylisoxazoles is reported from α,β-unsaturated ketoximes. Similarly, a novel synthesis of isoxazole carboxylic acids is also reported. Both the methods use efficient, environmentally friendly, and nontoxic iodoxybenzoic acid (IBX) as an oxidative cyclizing reagent. Easy procedure, environmentally benign reaction conditions, and nontoxicity are advantages to the methodology.  相似文献   
170.
    
The Fe(III) complex, [FeIII(HQS)3] (HQS = 8-hydroxyquinoline-5-sulfonic acid), is found to effect sensitization of the large band gap semiconductor, TiO2. The role of interfacial electron transfer in sensitization of TiO2 nanoparticles by surface adsorbed [FeIII(HQS)3] was studied using femtosecond time scale transient absorption spectroscopy. Electron injection has been confirmed by direct detection of the electron in the conduction band. A TiO2-based dye-sensitized solar cell (DSSC) was fabricated using [FeIII(HQS)3] as a sensitizer, and the resulting DSSC exhibited an open-circuit voltage value of 425 mV. The value of the short-circuit photocurrent was found to be 2.5 mA/cm2. The solar to electric power conversion efficiency of the [FeIII(HQS)3] sensitized TiO2-based DSSC device was 0.75 %. The results are discussed in the context of sensitization of TiO2 by other Fe(II)-dye complexes.  相似文献   
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