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3-Cyanocarbazoles, key-intermediates in the total synthesis of pyrido [4,3-b] carbazoles, have been obtained starting from easily available materials and involving the cyclization of diarylamines. The first step of the preparation consists in a SNAr reaction between a para substituted aniline and a chloro- (or bromo)-dinitrobenzene. This nucleophilic substitution has been found to be hindered by the steric effect of a methyl group, explained in terms of inhibition of resonance and confirmed by X-ray determination. 相似文献
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Fernández P Durand JS Pérez-Conde C Paniagua G 《Analytical and bioanalytical chemistry》2003,375(8):1020-1023
This paper reports a new flow-through fluoroimmunosensor, the function of which is based on antibodies immobilized on an inmunoreactor of controlled-pore glass (CPG), for determination of digoxin, used in the treatment of congestive heart failure and artery disease. The immunosensor has a detection limit of 1.20 microg L(-1) and provides high reproducibility (RSD=4.5% for a concentration of 0.0025 mg L(-1), and RSD=6.7% for 0.01 mg L(-1)). The optimum working concentration range was found to be 1.2 x 10(-3)-4.0 x 10(-2) mg L(-1). The lifetime of the immunosensor was about 50 immunoassays; if stored unused its lifetime can be extended to three months. A sample speed of about 10-12 samples per hour can be attained. Possible interference from substances with structures similar to digoxin (morphine, heroin, tebaine, codeine, pentazocine and narcotine) was investigated. No cross-reactivity was seen at the highest digoxin: interferent ratio studied (1:100). The proposed fluoroimmunosensor was successfully used to determine digoxin concentrations in human serum samples. 相似文献
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Victorin N. Mallet Monique Duguay Marc Bernier Natalie Trottier 《International journal of environmental analytical chemistry》2013,93(3):271-279
Abstract In this study isocratic high performance liquid chromatography in the reversed-phase mode (RP-8 or RP-18 column) with UV-detection (254 nm), was evaluated for the analysis, directly or after extraction, of organophosphorous pesticides in environmental water. Fifteen pesticides were studied and good resolution was obtained for eight by direct analysis of a multi-residue water sample. Reproducibility in terms of retention times was found to be very good. Linear calibration curves were obtained down to 0.5ng/μL (3 ng injected) with a coefficient of variation near 10%. The limit of quantitation for direct analysis was found to be 0.5mg/L (3ng) in water. However, by extraction with methylene chloride or ethyl acetate and concentration of the extract some of the pesticides could be determined at 0.5 μg/L (ppb) in water. 相似文献
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Foundations of Computational Mathematics - We introduce some general tools to design exact splitting methods to compute numerically semigroups generated by inhomogeneous quadratic differential... 相似文献
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