【摘 要】
：
Transition-metal-catalyzed decarboxylative coupling reactions was one of the highlights for the formation of carbon-carbon bond,which have shown great potential in synthetic organic chemistry.
【出 处】
：
第十九届全国金属有机化学学术讨论会
论文部分内容阅读
Transition-metal-catalyzed decarboxylative coupling reactions was one of the highlights for the formation of carbon-carbon bond,which have shown great potential in synthetic organic chemistry.
其他文献
自然界中含量丰富的五环三萜化合物具有抗炎、抗癌、抗病毒等多种生物活性[1].基于独特的手性刚性骨架和多个可修饰位点的特点,此类化合物的聚集性质和在超分子组装方面的应用已经引起关注[2].
Pillararene-based pseudo[2]rotaxanes could be achieved by pillararenes with three different types of guest molecules:(Ⅰ) electropositive guests,1(Ⅱ) neutral guests,2 and(Ⅲ) electronegative guests.
Developing multifunctional gene/drug delivery systems with the merit of storage stability,low cytotoxicity,high gene/drug loading capacity,as well as controllable gene/drug releasing features,has attr
Palladium-catalyzed organic reactions has emerged as one of the most powerful method of organic synthesis,in particular for carbon-carbon bond formations.
3-Arylpyridazine is a ubiquitous structural motif found in pharmaceuticals,[1] ligands,[2] and functional materials.[3] Over the past years,the synthesis of 3-arylpyridazine derivatives has attracted
T Azetidine derivatives are one of the most important building blocks in pharmaceutical research.[1] The typical procedure for direct alkylation of azetidines is the Ni-catalyzed or Pd-catalyzed Suzuk
Palladium-catalyzed cross-coupling reactions are most powerful and utilized tools for the construction of C-C bond formation.The properties of such palladium catalysts can be tuned by changing the str
C-H bond activation has recently attracted great attention owing to its advantages of environmental friendly and atom economy,which has been widely applied to the syntheses of natural products,drug mo
Recently,photoredox catalysis has emerged as a robust and reliable tool in green chemistry,making the reaction under lower energy consumption and milder conditions(usually at room temperature).
During recent years,with the emergence of a large number of studies on transition-metal-catalyzed C-H bond activation,C-H bond functionalization has also become an appealing and convenient tool to con