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重塑现代有机合成:基于连续流添加和非均相催化剂缩合反应的合成策略。

Reworking Organic Synthesis for the Modern Age: Synthetic Strategies Based on Continuous-Flow Addition and Condensation Reactions with Heterogeneous Catalysts.

机构信息

Green & Sustainable Chemistry Cooperation Laboratory, Graduate School of Science, The University of Tokyo, Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.

Department of Chemistry, School of Science, The University of Tokyo, Bunkyo-ku, Tokyo 113-0033, Japan.

出版信息

J Org Chem. 2020 Apr 17;85(8):5132-5145. doi: 10.1021/acs.joc.9b03416. Epub 2020 Mar 2.

Abstract

While organic synthesis carried out in most laboratories uses batch methods, there is growing interest in modernizing fine chemical synthesis through continuous-flow processes. As a synthetic method, flow processes have several advantages over batch systems in terms of environmental compatibility, efficiency, and safety, and recent advances have allowed for the synthesis of several complex molecules, including active pharmaceutical ingredients (APIs). Nevertheless, due to several reasons related to the difficulties arising from byproduct formation during the flow process, such as lower yields, poor selectivities, clogging of columns due to poor solubility, catalyst poisoning, etc., successful examples of continuous-flow synthesis of complex organic molecules are still limited. In order to solve this bottleneck, the development of selective and atom-economical continuous-flow organic transformations are needed. This perspective highlights examples of atom-economical addition and condensation reactions with heterogeneous catalysts under continuous-flow conditions and their applications for the synthesis of complex organic molecules such as natural products and APIs. In order to realize new continuous-flow methodologies, based on addition and condensation reactions, in place of substitution reactions, the development of novel reactions and heterogeneous catalysts is required.

摘要

虽然大多数实验室进行的有机合成都采用分批方法,但通过连续流工艺使精细化学品合成现代化的兴趣日益浓厚。作为一种合成方法,与分批系统相比,流动工艺在环境相容性、效率和安全性方面具有多项优势,最近的进展允许合成包括活性药物成分 (API) 在内的几种复杂分子。然而,由于与流动过程中副产物形成相关的一些原因,例如产率较低、选择性较差、由于溶解度差导致柱堵塞、催化剂中毒等,复杂有机分子的连续流合成的成功实例仍然有限。为了解决这一瓶颈,需要开发选择性和原子经济性的连续流动有机转化。本观点突出了在连续流动条件下使用多相催化剂进行原子经济性加成和缩合反应的实例及其在复杂有机分子(如天然产物和 API)合成中的应用。为了实现基于加成和缩合反应的新型连续流动方法,而不是取代反应,需要开发新的反应和多相催化剂。

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