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通过战略利用环 closing metathesis 设计和合成多环、杂环和大环。

Design and Synthesis of Polycycles, Heterocycles, and Macrocycles via Strategic Utilization of Ring-Closing Metathesis.

机构信息

Department of Chemistry, Indian Institute of Technology Bombay, Powai, Mumbai-, 400 076, India.

出版信息

Chem Rec. 2018 Nov;18(11):1613-1632. doi: 10.1002/tcr.201800025. Epub 2018 Jun 19.

Abstract

In this perspective, we summarize new synthetic approaches for the construction of various polycyclic compounds involving ring-closing metathesis as a key step. In this regard, we used ring-closing metathesis in combination with other popular reactions like Suzuki-Miyaura coupling, Claisen rearrangement, Fischer indolization, Grignard addition, Diels-Alder reaction, and [2+2] cycloaddition reaction etc. To this end, a variety of functional molecules such as α-amino acids, cyclophanes, heterocycles, propellanes, spirocycles, and macrocycles have been prepared. The strategies developed and the molecules prepared here play a key role in designing new materials and also act as lead compounds in drug design. The strategies and tactics developed here are useful to design polycycles, macrocycles, and heterocycles of diverse ring systems.

摘要

在这个视角下,我们总结了新的合成方法,用于构建各种多环化合物,其中包括作为关键步骤的闭环复分解反应。在这方面,我们将闭环复分解反应与其他流行的反应(如 Suzuki-Miyaura 偶联反应、Claisen 重排反应、Fischer 吲哚化反应、格氏加成反应、Diels-Alder 反应和 [2+2] 环加成反应等)结合使用。为此,我们制备了各种功能分子,如α-氨基酸、环芳烷、杂环、丙二烯、螺环和大环。这里开发的策略和制备的分子在设计新材料方面发挥着关键作用,并且作为药物设计中的先导化合物。这里开发的策略和战术对于设计各种环系的多环、大环和杂环化合物非常有用。

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