Enantioselective Dinuclear Zinc-Catalyzed Michael Addition Reaction of Pyrazolin-5-ones to Nitroalke

来源 :中国化学会全国第十二届有机合成化学学术研讨会 | 被引量 : 0次 | 上传用户:seraph_gigi
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
  Pyrazolones and Pyrazolone derivatives have been widely applied to the synthesis of many drugs.[1] For example,edaravone(3-methyl-1-phenyl-2-pyrazolin-5-one)has been developed as a medical drug for brain ischrmia.[2] Due to the importance of biological activities of Pyrazolone compounds,the development of asymmetric methods to synthesize Pyrazolonederivatives is very interesting.[3] In recent years,different research groups have developed asymmetric synthesis methods of Pyrazolone derivatives.[1,3] However,the catalystic system for this kind of reaction is organocatalysis,few metal catalytic system has been developed.Our labouratory mainly researches asymmetric reactions,which are catalysted by dinuclear zinc catalyst.[4] Herein,the asymmetric Michael addition reaction of 5-Methyl-2-phenyl-1,2-dihydropyrazol-3-one to nitroalkenes is catalysted by dinuclear zinc catalyst.It gives the corresponding products in good yield with general diastereoselectivity and enantioseletivity.
其他文献
Previously we have achieved an one-pot tandem Wittig-cyanosilylation sequence,in which the by-product Ph3PO from the Wittig step were internally recycled as indispensable co-catalysts for the followin
The preparation of ethers is one of the most fundamental and frequently used important reactions in synthetic organic chemistry.The first example of the formation of carbon-oxygen single bonds,the Wil
Since being introduced by Schmalz et al,1 alkynylcyclopropane(ACP)ketone has recently been proved to be a versatile building block in organic synthesis.As a novel type of donor-acceptor cyclopropane,A
Sulfonamides are extensively employed as artificial antifolic agents for the prevention and cure of bacterial infections in human biological systems and a large amount of their heterocyclic derivative
Transition-metal-catalyzed C-H bond functionalization has attracted widespread attention due to its high efficiency and atom economy.However,most of these transformations have been accomplished with t
1,5-Benzodiazepine and its derivatives have attracted considerable attention as an important class of heterocyclic compounds in the field of drugs and pharmaceuticals [1].These compounds are widely us
4-hydroxy-6-methyl-2-pyrone is an important class of compounds found in a variety of natural products and bioactive molecules and is used as versatile intermediates in organic and natural-product synt
Optically active α-hydroxy phosphonates[1] are an important class of compounds because of their biological and medical activities.Although asymmetric hydrogenation of β-keto phosphonates,α-and β-keto
钯催化的C-H 活化反应是近年来的一个研究热点.吲哚是一类重要的杂环类化合物.长期以来,吲哚类化合物的官能化一直是研究热点,它作为一类重要化合物在药物化学和天然产物合成上具有重要用途1.近几年来,文献中对于吲哚实现直接官能团化已有一些成功的报道2.Stille 偶联反应最早由Eaborn 和Kosugi 小组于1976-1977 年提出3,已经越来越为人们所关注,在医药以及天然产物合成中得到了广泛
Indole is a privileged compound in pharmaceutical fragrance,agrochemicals,pigment and material scienceand over the past few years,[1] indole-based derivatives have been reported as highly potent agent