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Editorial [Hot topic: Multicomponent Reaction (Guest Editor: Song Cao)]

机译:社论[热门话题:多组分反应(来宾编辑:曹Ca)]

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After nearly 20 years of extensive study and rapid development, multicomponent reactions have already been an commonly used and powerful tool for the construction of novel and complex target molecules. Up to now, numerous literatures on the development of novel MCRs have been reported and several reviews have summarized the progress on MCRs before the end of 2005 thoroughly. Recently, with the development of new methodologies of organic synthesis, MCRs have penetrated into various aspects of organic synthesis. This special thematic issue includes five reviews which devote to the research on multicomponent reaction of the specific compound classes, new catalysts and the most commonly used green reaction media, respectively.nnThe first review, written by E. J. Yoo and S. Chang, Department of Chemistry, Korea Advanced Institute of Science and Technology, focuses on authors' and other groups' recent progresss on the new type of Cu-catalyzed multicomponent reactions which have been developed relying on the in situ generation of N-sulfonyl- or N-phosphorylketenimine intermediates. They comprehensively summarize this facile and versatile route to ketenimines which has led to the development of a range of highly efficient multicomponent reactions by employing diverse nucleophiles such as amines, alcohols, water, pyrroles, and thiolates.nnAlkynones are versatile three-carbon building blocks in heterocyclic chemistry and are easily prepared by a modified Sonogashira coupling of acid chlorides and terminal alkynes. The second review provided by B. Willy and T. J. J. Muller, Institute of Organic Chemistry and Makromolecular Chemistry, Heinrich-Heine University, is dedicated to their achievements in multicomponent synthesis of heterocycles initiated by Pd-catalyzed generation of alkynones as established (by themselves) within the past years. Thus, isoxazoles, indolizines, pyrazoles, pyridimines, 1,5-benzoheteroazepines, furans, oxazoles and pyrroles are readily accessible by this novel multicomponent reactions under the mild reaction conditions.nnP. J. Tambade, Y. P. Patil and B. M. Bhanage, Department of Chemistry, Institute of Chemical Technology (Autonomous), contribute to the third review, including more than 84 references, which deals with recent development in the fields of multicomponent reactions catalyzed by lanthanides. Some named reactions such as Biginelli, Hantzsch, Ugi, Mannich, and Povarov reaction catalyzed by various lanthanides are dicussed.nnThe combination of water as an environmentally benign solvent for chemical transformations with multicomponent reactions has been receiving much attention. K. Kumaravel and G. Vasuki, Department of Chemistry, Pondicherry University, make a thorough literature survey of multicomponent reactions performed in water or aqueous solutions, are including nearly 108 references.
机译:经过近20年的广泛研究和快速发展,多组分反应已经成为构建新型和复杂目标分子的常用且强大的工具。迄今为止,已报道了许多有关新型MCR的发展的文献,并且有一些综述彻底总结了2005年底之前MCR的进展。近年来,随着有机合成新方法的发展,MCR已渗透到有机合成的各个方面。该专题主题包括五篇综述,分别致力于特定化合物类别,新催化剂和最常用的绿色反应介质的多组分反应研究。nn第一篇评论由化学系Yoo Yoo和S. Chang撰写韩国高级科学技术研究所重点研究作者和其他小组在新型铜催化多组分反应方面的最新进展,这些反应是依赖于原位生成N-磺酰基-或N-磷酰基酮亚胺中间体而开发的。他们全面总结了这种简便而通用的制酮亚胺路线,通过使用多种亲核试剂(如胺,醇,水,吡咯和硫醇盐)开发了一系列高效的多组分反应.nn炔烃是通用的三碳建筑材料杂环化学,可以通过酰基氯和末端炔烃的改良Sonogashira偶联轻松制备。 Heinrich-Heine大学有机化学与分子化学研究所的B.Willy和TJJ Muller提供的第二篇评论致力于他们在Pd催化的炔烃生成中引发的杂环多组分合成中的成就,这一发现是由他们自己建立的。过去的几年。因此,在温和的反应条件下,这种新型的多组分反应很容易获得异恶唑,吲哚嗪,吡唑,嘧啶,1,5-苯并杂氮杂ze,呋喃,恶唑和吡咯。化学技术学院(自治)化学系的J. Tambade,Y。P. Patil和B. M. Bhanage为第三次综述做出了贡献,其中包括84篇参考文献,涉及镧系元素催化的多组分反应领域的最新进展。讨论了由各种镧系元素催化的一些命名的反应,例如Biginelli,Hantzsch,Ugi,Mannich和Povarov反应。nn水作为环境友好的化学转化溶剂与多组分反应的组合受到了广泛关注。朋迪榭里大学化学系的K. Kumaravel和G. Vasuki对在水或水溶液中进行的多组分反应进行了详尽的文献调查,其中包括近108种参考文献。

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  • 来源
    《Current Organic Chemistry》 |2009年第18期|p.1765-1765|共1页
  • 作者

    Song Cao;

  • 作者单位

    Shanghai Key Laboratory of Chemical Biology, School of Pharmacy, East China University of Science and Technology, China.;

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