2-Aryl-Indenylphosphine Ligands Design, Synthesis and Application in Pd-Catalyzed Cross-Coupling Rea

来源 :中国化学会第十三届全国有机合成化学学术研讨会 | 被引量 : 0次 | 上传用户:faxiwe88730
下载到本地 , 更方便阅读
声明 : 本文档内容版权归属内容提供方 , 如果您对本文有版权争议 , 可与客服联系进行内容授权或下架
论文部分内容阅读
  Pd-catalyzed C-C cross-coupling reactions play a vital role in modern organic synthesis.Due to the high cost of Pd as well as environmental and product safety issues,the development of highly active Pd catalytic system is crucial to the industrial applications of these coupling reactions.The ligand structure defines the steric and electronic properties of the palladium catalyst and therefore plays a crucial role in the efficiency of the cross-coupling reaction.The aryl substituted indenyl phosphine ligands developed by our group have been widely used in Suzuki-Miyaura,Sonogashira and Buchwald-Hartwig cross-coupling reactions in water.
其他文献
  Chirality is one of the most important fundamental features in nature.Most biological molecules are chiral,and many important biological processes involve s
  In the past decades,a great deal of effort has been devoted to the development of aminocarbonylation reactions due to the significant role amide played in b
  Our group is interested in organoselenium catalyzed reactions because of their green processes that generate no wastes,and because of the possibility to rec
  Paeoveitol,a pair of norditerpene enantiomers,were isolated by Chen from the root of Paeonia veitchii (Chuan-Chi-Shao),which has a long history of using as
  Organic reactions that involve transition metal-catalyzed direct functionalization of non-activated C(sp2)-H bonds represent one of the attractive transform
  The selective α-oxygenation ofcarbonyl compounds constitutes an important reactivity mode in organic synthesis,as the resultant α-oxygenated carbonyl moie
  由于CF2基团的特点,在分子中引入CF2有可能明显性质或者增强生理活性,因此在分子中引入CF2基团是提高药物性能的一种可选途径,通常的引入CF2的方法有直接氟化法和含氟砌
  M(por) (M =Rh and Co) (por =porphyrinato dianion) reacted selectively with isopropyl ketones at the carbon(CO)-carbon(α) bond under room temperature to giv
  近年来,过渡金属催化的烯块环化反应取得了巨大的进展,提供了一类高效、实用的合成官能团化的环状有机化合物的合成方法.1目前发展的过渡金属催化的烯炔环化反应具有以下
  Diversity oriented synthesis (DOS) constitute one of the two major directions of modem organic synthesis.Electron deficient enamines such as enaminones and