...；膦配体；芳基卤 [gap=1052]ords: organic chemistry; suzuki reaction; palladium chloride; phosphine ligands; aryl halides ...
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卤代芳烃 (Aryl Halides) 指：卤原子直接与芳环相连的化合物： X X 与乙烯式卤相似，不易发生S N 1和S N 2反应 CH 2 X 与烯丙式卤相似，易发生S N 1和S N...
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We have developed a simple and easy-handling procedure for copper-catalyzed cyanation of aryl halides using K4Fe（CN）6 as the cyanide source.
3、使用K4Fe（CN）6作为氰源,我们发展了一个简单并易于操作的铜催化芳卤氰化方法。
参考来源 - Ullmann反应的研究The Suzuki-Miyaura cross-coupling reaction of aryl halides and arylboronic acids has been developed using Pd(OAc)_2/β-Oxo amides as the catalytic system.
发展了醋酸钯/β-羰基胺催化体系高效催化卤代芳烃与芳基硼酸的Suzuki-Miyaura交叉偶联反应。
参考来源 - 钯催化SuzukiPalladium-catalyzed C-H bond activation reactions of N-methyl-1H-imidazole with aryl halides have been developed under solvent-free condition.
5.发展了无溶剂条件下钯催化活化C-H键的芳基卤代烃与氮甲基咪唑的反应。
参考来源 - 铜催化交叉偶联反应研究·2,447,543篇论文数据，部分数据来源于NoteExpress
Cyanation of aryl halides is widely used in the synthesis of liquid crystals but its traditional heating reactions require long time and high temperature.
摘要卤代芳烃的氰化反应在液晶单体合成中广泛应用，但传统的加热方法反应时间长、温度高。
Cyanation of aryl halides is widely used in the synthesis of liquid crystals, but its traditional heating reactions require long time and high temperature.
卤代芳烃的氰化反应在液晶单体合成中广泛应用，但传统的加热方法反应时间长、温度高。
In the chapter 2 of this dissertation, we studied the cross-coupling reaction of aryl halides and vinyl iodides with sodium azide under the catalysis of copper and amino acids.
在本文第二章，我们研究了氨基酸促进的铜催化的芳基卤化物、烯基碘化物与叠氮化钠的交叉偶联反应。
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