1) 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。
2) 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。
3) Sonogashira-coupling reaction
Sonogashira偶合反应
4) 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。
5) 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。
6) Sonogashira reaction
Sonogashira反应
1.
Study on Merrifield Resin-supported Palladium-catalyzed Heck and Sonogashira Reactions in Green Media
Merrifield树脂固载钯催化下绿色介质中的Heck和Sonogashira反应研究
2.
This paper introduces the salt assistance to Pd-catalyzed Suzuki, Heck, Stille and Sonogashira reactions as well as ary- lation of enolate, ortho-arylation of phenol and carbonylation.
介绍了铯盐在钯催化的Suzuki,Heck,Stille,Sonogashira反应,烯醇盐的芳基化,酚类的邻位芳基化以及羰基化反应中的促进作用。
3.
This thesis contains four parts, which mainly described the Sonogashira reactions catalyzed by CuI, Sm system and the cyclic coupling reactions to synthesize biindoles.
本论文分四个部分,主要报道了CuI、Sm粉等体系催化下的Sonogashira反应及通过偶联关环合成联吲哚化合物的反应。
补充资料：加特曼重氮盐偶联反应
分子式：
CAS号：
性质：重氮盐ArN2Cl在酸性溶液中用铜粉处理，放出氮气，发生偶联反应。当芳环上有吸电子基团时，偶联生成联苯型化合物Ar-Ar；当芳环上有给电子基团时，偶联生成偶氮化合物ArN=NAr。是合成这两类化合物常用的方法。 2ArN2Cl+2Cu→Ar-Ar(或ArN=NAr)+N2↑+CuCl2
CAS号：
性质：重氮盐ArN2Cl在酸性溶液中用铜粉处理，放出氮气，发生偶联反应。当芳环上有吸电子基团时，偶联生成联苯型化合物Ar-Ar；当芳环上有给电子基团时，偶联生成偶氮化合物ArN=NAr。是合成这两类化合物常用的方法。 2ArN2Cl+2Cu→Ar-Ar(或ArN=NAr)+N2↑+CuCl2
说明：补充资料仅用于学习参考，请勿用于其它任何用途。
参考词条