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1)  Sonogashira coupling
Sonogashira偶联
1.
Palladium-catalyzed Stille coupling reaction, Sonogashira coupling reaction are the most commonly used carbon-carbon formation reactions in modern organic synthesis.
金属钯催化的Stille偶联、Sonogashira偶联是当今在有机合成工作最常用和非常重要的碳碳偶联反应方式。
2)  Sonogashira coupling reaction
Sonogashira偶联反应
1.
Methods:Sonogashira coupling reaction of terminal alkyne and(E)-β-iodovinyl sulfone was used to synthesis the product.
方法:通过端炔与烯基砜发生了Sonogashira偶联反应,生成含共轭烯炔结构单元的药物前体烯基砜。
3)  Sonogashira cross-coupling reaction
Sonogashira交叉偶联反应
1.
This dissertion mainly describes several organic reactions of alkynes and allenes,including Cu-catalyzed Sonogashira cross-coupling reaction,plladium-catalyzed cyclization of N-arylpropiolamides with arynes,and electrophilic cyclization of allenes.
Cu_2O/PPh_3/TBAB催化体系高效催化Sonogashira交叉偶联反应。
4)  carbonylative Sonogashira coupling reaction
羰基化Sonogashira偶联
5)  Sonogashira-coupling reaction
Sonogashira偶合反应
6)  Sonogashira cross coupling reaction
Sonogashira交联反应
1.
The Sonogashira cross coupling reactions of various aryliodides with terminal alkynes are carried out in good to excellent yields under mild conditions.
研究了离子液体中无膦、无铜、钯催化剂在Sonogashira交联反应中的催化性能。
补充资料:[3-(aminosulfonyl)-4-chloro-N-(2.3-dihydro-2-methyl-1H-indol-1-yl)benzamide]
分子式:C16H16ClN3O3S
分子量:365.5
CAS号:26807-65-8

性质:暂无

制备方法:暂无

用途:用于轻、中度原发性高血压。

说明:补充资料仅用于学习参考,请勿用于其它任何用途。
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