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立体选择性芳环形成羟醛缩合反应:催化剂控制的轴向手性化合物的合成。

Stereoselective Arene-Forming Aldol Condensation: Catalyst-Controlled Synthesis of Axially Chiral Compounds.

作者信息

Witzig Reto M, Lotter Dominik, Fäseke Vincent C, Sparr Christof

机构信息

Department of Chemistry, University of Basel, 4056, Basel, Switzerland.

出版信息

Chemistry. 2017 Sep 21;23(53):12960-12966. doi: 10.1002/chem.201702471. Epub 2017 Sep 5.

Abstract

The fundamental role that aldol chemistry adopts in various disciplines, such as stereoselective catalysis or the biosynthesis of aromatic polyketides, illustrates its exceptional versatility. On the one hand, numerous aldol addition reactions reliably transfer the stereochemical information from catalysts into various valuable products. On the other hand, countless aromatic polyketide natural products are produced by an ingenious biosynthetic machinery based on arene-forming aldol condensations. With the aim of complementing aldol methodology that controls stereocenter configuration, we recently combined these two tenets by investigating small-molecule-catalyzed aldol condensation reactions that stereoselectively form diverse axially chiral compounds through the construction of a new aromatic ring.

摘要

羟醛化学在各种学科中所起的基础作用,如立体选择性催化或芳香族聚酮化合物的生物合成,体现了其非凡的通用性。一方面,众多羟醛加成反应能可靠地将立体化学信息从催化剂传递到各种有价值的产物中。另一方面,无数芳香族聚酮天然产物是由基于芳烃形成的羟醛缩合反应的精巧生物合成机制产生的。为了补充控制立体中心构型的羟醛方法,我们最近将这两个原则结合起来,研究了通过构建新的芳香环立体选择性地形成各种轴向手性化合物的小分子催化羟醛缩合反应。

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