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Yu. A. Mamaev N. G. Yatlukova T. N. Aleksandrova N. M. Litvinova 《Journal of Mining Science》2009,45(2):187-193
The paper generalizes research findings on application of chemical additives to stage-by-stage processing of rebellious gold-bearing
ores. The designed stages of gold extraction intensification are the controlled mineral alteration by preparation, use of
conventional and specific collecting agents to prepare mineral surface to sorption to intensify flotation, creation of selective
collecting agents, and cyanation optimization by introducing additional oxidation agents.
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Translated from Fiziko-Tekhnicheskie Problemy Razrabotki Poleznykh Iskopaemykh, No. 2, pp. 102–109, March–April, 2009. 相似文献
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We report a vinyl cyanation reaction of vinyl triflates and readily available 1,4-dicyanobenzene through a nickel-catalyzed reductive coupling process. The reaction is operated under mild conditions with remarkable functional-group compatibility. Cyclic vinyl triflates with various ring sizes and substituents at different positions all reacted smoothly. The synthetic utility is demonstrated by the derivatization of pharmaceutical and natural compounds, a scale-up synthesis, and various functional group transformations. Preliminary mechanistic studies demonstrate that vinyl triflates are more reactive than 1,4-dicyanobenzene towards the oxidative addition to nickel catalyst. 相似文献
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Thomas Schareina Alexander Zapf Alain Cott Matthias Gotta Matthias Beller 《Advanced Synthesis \u0026amp; Catalysis》2011,353(5):777-780
A novel copper‐catalyzed cyanation of aryl and heteroaryl bromides using acetone cyanohydrin has been developed. 相似文献
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Dr S.M. Islam Paramita Mondal Kazi Tuhina Anupam Singha Roy 《Journal of chemical technology and biotechnology (Oxford, Oxfordshire : 1986)》2010,85(7):999-1010
BACKGROUND: Precise architectures of steric and electronic properties of palladium species play a crucial role in designing highly functionalized catalyst systems responsible for target organic transformations. Pd catalysts supported on polymer materials have been employed extensively as catalysts not only for hydrogenation but also for coupling reactions in the production of fine chemicals. RESULTS: A new polymer‐anchored Pd(II) complex has been synthesized and characterized. The catalyst shows high catalytic activity in the hydrogenation of styrene oxide, Heck cross‐coupling and cyanation reactions of aryl halides. The effect of various reaction parameters were investigated to optimize reaction conditions. The catalytic system shows good activity in the hydrogenation of styrene oxide (conversion 98%) with a selectivity to 2‐phenylethanol (93%) which is higher than its homogeneous analogues. The catalyst also exhibits excellent catalytic activity for the Heck cross‐coupling and cyanation reactions of various substituted and non‐substituted aryl halides. CONCLUSIONS: Results demonstrate that the catalyst is robust and stable and can be recovered quantitatively by simple filtration and reused several times without loss of activity. Copyright © 2010 Society of Chemical Industry 相似文献
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Neeraj Kumar Mishra Taejoo Jeong Satyasheel Sharma Youngmi Shin Sangil Han Jihye Park Joa Sub Oh Jong Hwan Kwak Young Hoon Jung In Su Kim 《Advanced Synthesis \u0026amp; Catalysis》2015,357(6):1293-1298
The rhodium‐catalyzed selective cyanation of C H bonds of indolines and indoles with N‐cyano‐N‐phenyl‐para‐methylbenzenesulfonamide is described. This protocol offers a facile access to C‐7 cyanated indolines and C‐2 cyanated indoles with high site selectivity and excellent functional group tolerance.
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亚铁氰化钾作为氰化试剂具有无毒、廉价和后处理简单等多种优点,逐渐成为研究的热点。由于氰基与铁的结合能力很强,造成氰基很难游离出来,反应常需要昂贵的催化剂和高温等条件,促进亚铁氰化钾中氰基的游离可降低条件、提高产率。研究发现在反应体系中加入水、弱碱或ZnBr2可以促使氰基从亚铁氰化钾中游离,并对其作用机理进行了探析。 相似文献
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以3-氯-4-三氟甲氧基苯胺为原料,经重氮化、甲醛肟化、水解和腈化反应得到纯度≥99.2%(GC)的3-氯-4-三氟甲氧基苯甲腈,总收率为31.5%。中间体及产物结构通过 IR 及元素分析验证。产物色泽好,腈化反应的溶剂可回收使用3次。 相似文献