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天然产物全合成中通过关环复分解进行的大环化反应:反应条件及局限性

Macrocyclization by ring-closing metathesis in the total synthesis of natural products: reaction conditions and limitations.

作者信息

Gradillas Ana, Pérez-Castells Javier

机构信息

Departamento de Química, Facultad de Farmacia, Universidad San Pablo-CEU, Urb. Montepríncipe, 28668 Boadilla del Monte, Madrid, Spain.

出版信息

Angew Chem Int Ed Engl. 2006 Sep 18;45(37):6086-101. doi: 10.1002/anie.200600641.

Abstract

The construction of macrocycles by ring-closing metathesis (RCM) is often used as the key step in the synthesis of natural products containing large rings. This reaction is attractive because of its high functional group compatibility and the possibility for further transformations. The finding of suitable reaction conditions is critical for the success of the synthesis. In this Minireview we summarize the efforts of many research groups to develop efficient RCM reactions on their way towards the total synthesis of natural macrocyclic products. Their findings should help in future synthesis to reduce the time-consuming phase of the optimization of the reaction conditions.

摘要

通过关环复分解反应(RCM)构建大环化合物通常被用作合成含大环结构天然产物的关键步骤。该反应具有吸引力,因为它具有高官能团兼容性以及进一步转化的可能性。找到合适的反应条件对于合成的成功至关重要。在这篇微型综述中,我们总结了许多研究小组在全合成天然大环产物过程中为开发高效RCM反应所做的努力。他们的发现应有助于未来的合成减少反应条件优化这一耗时阶段。

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