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1.
The halohydrin reaction of chiral N-enoyl-2-oxazolidinones 1 by halogen (Br2/I2) and water were efficiently carried out in aqueous organic solvent promoted by silver(I) with high anti- and regioselectivity and moderate to good diastereoselectivities. The alkenoyl, cinnamoyl and electron-deficient cinnamoyl substrates smoothly underwent bromohydrin reaction in aqueous acetone but no iodohydrin reaction, where as electron-rich cinnamoyl substrates preferred to undergo iodohydrin reaction in aqueous acetone with moderate diastereoselectivity and enhanced diastereoselectivity was observed in aqueous THF.  相似文献   
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Chloramphenicol and thiamphenicol have been enantioselectively synthesized using an asymmetric halohydrin reaction as a key step. In particular, halomethoxylation reaction was used, where O-methyl functions as a hydroxyl protecting group and eliminates an additional protection step.  相似文献   
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This article describes the analysis of autofluorescence of advanced glycation end products of hemoglobin (Hb-AGE). Formed as a result of slow, spontaneous and non-enzymatic glycation reactions, Hb-AGE possesses a characteristic autofluorescence at 308/345 nm (lambda(ex)/lambda(em)). Even in the presence of heme as a quenching molecule, the surface presence of the glycated adduct gave rise to autofluorescence with the quantum yield of 0.19. The specificity of monoclonal antibody developed against common AGE structure with Hb-AGE was demonstrated using reduction in fluorescence polarization value due to increased molecular volume while binding. The formation of fluorescent adduct in hemoglobin in the advanced stage of glycation and the non-fluorescent HbA(1c) will be of major use in distinguishing and to know the past status of diabetes mellitus. While autofluorescence correlated highly with HbA(1c) value under in vivo condition (r = 0.85), it was moderate in the clinical samples (r = 0.55). The results suggest a non-linear relation between glycemia and glycation, indicating the application of Hb-AGE as a measure of susceptibility to glycation rather than glycation itself.  相似文献   
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3,4-Diaroylfuroxans 1 react with various dipolarophiles 3 under microwave activation to afford the cycloadduct 4 instead of the expected isoxazole 5 in good yields in the absence of solvent.  相似文献   
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This paper presents the fabrication of a negative-channel metal–oxide–semiconductor (NMOS) inverter based on quantum dot gate field-effect transistors (QDG-FETs). A QDG-FET produces one intermediate state in its transfer characteristic. NMOS inverters based on a QDG-FET produce three states in their transfer characteristic. The generation of the third state in the inverter characteristic makes this a promising circuit element for multivalued logic implementation. A circuit simulation result based on the Berkley simulation (BSIM) circuit model of the QDG-FET is also presented in this paper, predicting the fabricated device characteristic.  相似文献   
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The lifetime of a sensor network is influenced by the efficient utilization of the resource constrained sensor nodes. The tree-based data gathering offers good quality of service (QoS) for the running applications. However, data gathering at the sink reduces the network lifetime due to a fast failure of highly loaded nodes. Loss of connectivity and sensing coverage affect the performance of the applications that demand critical QoS. In this paper, a data gathering tree management scheme has been proposed to deal with arbitrary node failures in delay-sensitive sensor networks. A load-balanced distributed BFS tree construction procedure has been introduced for an efficient data gathering. Based on the initial tree construction, a tree maintenance scheme and an application message handler have been designed to ensure the reliable delivery of the application messages. The correctness of the proposed scheme has been verified both theoretically and with the help of simulation. The proposed scheme offers low overhead, enhanced network lifetime and good QoS in terms of delay and reliability of the application messages.  相似文献   
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The kinetics of the substitution reactions of [Pt(dach)(H2O)2]2+ and [Pt(en)(H2O)2]2+ (where ‘dach’ and ‘en’ are cis-1,2-diaminocyclohexane and ethylenediamine, respectively) with excess N,N′-diethylthiourea have been studied in aqueous solution by UV–Vis spectrophotometry. The effect of different N–N spectator ligands on the reactivity of platinum(II) complexes was investigated by studying the water lability of the reactant complexes. The kinetic study has been substantiated by product isolation, IR, NMR and ESI-MS spectral analysis and DFT calculations. The reactions follow normal square-planar substitution mainly in an associative way. Rate parameters have been evaluated under different conditions. The substitution rates of the complexes studied can be tuned through the nature of the N–N chelates, which is important in the development of new active compounds for cancer therapy.  相似文献   
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