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Devdutt Chaturvedi Nisha Mishra Amit K. Chaturvdi Virendra Mishra 《Phosphorus, sulfur, and silicon and the related elements》2013,188(3):550-558
A quick and efficient, one-pot synthesis of dithiocarbazates was accomplished in high yields by the reaction of various alcoholic tosylates of primary, secondary, and tertiary alcohols, with substituted hydrazines using an Amberlite IRA 400 (basic resin)/CS 2 system. The reaction conditions are mild with simpler work-up procedures than previously reported methods. 相似文献
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A quick, efficient, one-pot synthesis of dithiocarbazates was accomplished in high yields by the reaction of various tosylates of primary, secondary, and tertiary alcohols with a variety of substituted hydrazines using the benzyl–trimethylammonium hydroxide (Triton-B)/CS2 system. The reaction conditions are mild with simpler workup procedures than the reported methods. 相似文献
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电极过程自由基中间体的ESR研究——取代苯基重氮盐的电解还原 总被引:2,自引:0,他引:2
本文用自由基捕捉剂苯亚甲基叔丁基氮氧化物(PBN)与ESR相结合的方法研究了十种取代苯基重氮盐RC6H4N2+BF4-(R=F,Cl,Br,NO2,OCH3及CH3)在乙腈中电解还原产生的活泼自由基。结果表明:1.RC6H4N2+BF4-电解还原时产生RC6H4自由基,并能被捕捉剂PBN所捕捉,以形成稳定的自由基加合物[RC6H4-PBN]·。2.由[RC6H4-PBN]·ESR谱的超精细裂分常数算出的二面角θβ值大小与处于不同位置的给定取代基R的关系为:θβ(O-R) < θβ(m-R) < θβ(P-R) 相似文献
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Palladium‐catalyzed decarboxylative coupling of α,β‐unsaturated carboxylic acids with aryl tosylates
We report a general method for selective cross‐coupling of α,β‐unsaturated carboxylic acids with aryl tosylates enabled by versatile Pd(II) complexes. This method features the general cross‐coupling of ubiquitous α,β‐unsaturated carboxylic acids by decarboxylation. The transformation is characterized by its operational simplicity, the use of inexpensive, air‐stable Pd(II) catalysts, scalability and wide substrate scope. The reaction proceeds with high trans selectivity to furnish valuable (E)‐1,2‐diarylethenes. 相似文献
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Olga L. Mezentseva Galina B. Slepchenko Elena V. Dorozhko Eugenia S. Moiseeva Vladimir P. Kryukovskiy Nikolay K. Zaycev 《Electroanalysis》2023,35(4):e202200252
A highly sensitive electrochemical sensor based on arenediazonium tosylates was designed to detect meldonium in urine. The effect of the concentration of ArN2+OTs− arenediazonium tosylate modifier and various substituents was studied. Basic operating parameters for voltammetric meldonium detection were established and the procedure for urine sample preparation was developed. The following values were obtained: limit of detection (LOD) 0.005 mg ⋅ L−1 (P=0.95) and limit of quantification (LOQ) 0.01 mg ⋅ L−1. The relationship between the analytical signal and meldonium concentration in the solution ranging from 0.01 to 400 mg ⋅ L−1 was described by a linear function. The meldonium concentration error did not exceed 18 %. The analysis time for a single urine sample was reduced to 15 minutes. 相似文献
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This review analyses the principal approaches to the synthesis of the cinnoline nucleus, used as synthetic precursors of arenediazonium
salts, arylhydrazones, and arylhydrazines, and also reductive methods for the synthesis of polycondensed derivatives of cinnoline.
The mechanisms of the transformations and the possibilities and limitations of the various methods are discussed. Special
attention is paid to methods based on the cyclization of derivatives of arenediazonium salts, which have been developed substantially
in recent years.
In memory of A. A. Potekhin
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Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 5, pp. 643–667, May, 2008. 相似文献
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