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羧酸作为均相催化中的底物。

Carboxylic acids as substrates in homogeneous catalysis.

作者信息

Goossen Lukas J, Rodríguez Nuria, Goossen Käthe

机构信息

FB Chemie-Organische Chemie, TU Kaiserslautern, Erwin-Schrödinger-Strasse Geb. 54, 67663 Kaiserslautern, Germany.

出版信息

Angew Chem Int Ed Engl. 2008;47(17):3100-20. doi: 10.1002/anie.200704782.

Abstract

In organic molecules carboxylic acid groups are among the most common functionalities. Activated derivatives of carboxylic acids have long served as versatile connection points in derivatizations and in the construction of carbon frameworks. In more recent years numerous catalytic transformations have been discovered which have made it possible for carboxylic acids to be used as building blocks without the need for additional activation steps. A large number of different product classes have become accessible from this single functionality along multifaceted reaction pathways. The frontispiece illustrates an important reason for this: In the catalytic cycles carbon monoxide gas can be released from acyl metal complexes, and gaseous carbon dioxide from carboxylate complexes, with different organometallic species being formed in each case. Thus, carboxylic acids can be used as synthetic equivalents of acyl, aryl, or alkyl halides, as well as organometallic reagents. This review provides an overview of interesting catalytic transformations of carboxylic acids and a number of derivatives accessible from them in situ. It serves to provide an invitation to complement, refine, and use these new methods in organic synthesis.

摘要

在有机分子中,羧酸基团是最常见的官能团之一。羧酸的活化衍生物长期以来一直是衍生化和构建碳骨架的通用连接点。近年来,人们发现了许多催化转化反应,使得羧酸无需额外的活化步骤就可作为构建单元使用。通过多方面的反应途径,从这一单一官能团可获得大量不同的产物类别。卷首插图说明了其中一个重要原因:在催化循环中,酰基金属配合物可释放出一氧化碳气体,羧酸盐配合物可释放出二氧化碳气体,每种情况下都会形成不同的有机金属物种。因此,羧酸可作为酰基、芳基或烷基卤化物以及有机金属试剂的合成等效物。本综述概述了羧酸有趣的催化转化反应以及可通过它们原位获得的一些衍生物。它旨在邀请人们在有机合成中补充、完善并使用这些新方法。

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