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生物活性四元酸和四胺酸的多米诺合成

Domino syntheses of bioactive tetronic and tetramic acids.

作者信息

Schobert Rainer

机构信息

Organic Chemistry Laboratory, University of Bayreuth, Universitätsstrasse 30, 95440 Bayreuth, Germany.

出版信息

Naturwissenschaften. 2007 Jan;94(1):1-11. doi: 10.1007/s00114-006-0152-8. Epub 2006 Aug 31.

Abstract

Natural products containing tetronic acid or tetramic acid moieties continue to attract the interest of chemists, biologists, and physicians due to their challenging structures and to the wide range of biological activities they display. This review portrays the structural varieties of tetronic and tetramic acids and the spectrum of possible therapeutically relevant effects in man for exemplary derivatives. Their biosynthetic origin from alpha-amino and alpha-hydroxy acids is briefly discussed as is the relationship between their structures and their modes of interaction with biochemical effectors such as metal cations or enzymes. A short overview of laboratory syntheses of the heterocyclic core structures of tetramic and tetronic acids is provided with an emphasis on those emulating the biosynthesis. A synthesis from the alpha-amino or alpha-hydroxy esters and the cumulated phosphorus ylide Ph(3)PCCO based upon a domino addition-intra-Wittig alkenation sequence is presented with applications to the preparation of the antibiotics reutericyclin and tenuazonic acid, the cytotoxic melophlin B, and the enzyme inhibitor RK-682. Procedural advantages of immobilizing either starting component by attaching it to a resin and its exploitation in the parallel synthesis of libraries of potential drug candidates are described. The basic domino reaction can even be extended by further C-C bond forming steps when starting from suitable alpha-hydroxy or alpha-amino allyl esters. Depending on the chosen reaction conditions, bioactive intermediates of formally three to seven step long cascades can be obtained. Among them, herbicidal 3-alkyltetronic acids and lactone endoperoxides with antiplasmodial activity exceeding that of the natural antimalarial lead artemisinin. Hence, this domino reaction gives access to diversely functionalized derivatives of tetronic and tetramic acids. As it can also be ported to solid phase, it is ideally suited for parallel and combinatorial processing. Future developments might include running such domino sequences in continuous mode in arrays of "labs on microchips".

摘要

含有特窗酸或四胺酸部分的天然产物因其具有挑战性的结构以及所展现出的广泛生物活性,持续吸引着化学家、生物学家和医生的关注。本综述描绘了特窗酸和四胺酸的结构多样性,以及一些示例性衍生物在人体中可能具有的与治疗相关的效应谱。简要讨论了它们由α-氨基酸和α-羟基酸的生物合成起源,以及它们的结构与诸如金属阳离子或酶等生化效应物的相互作用模式之间的关系。提供了四胺酸和特窗酸杂环核心结构的实验室合成的简短概述,重点是那些模拟生物合成的方法。介绍了一种基于多米诺加成-分子内维蒂希烯化序列,由α-氨基或α-羟基酯与累积磷叶立德Ph(3)PCCO合成的方法,并将其应用于制备抗生素罗伊氏菌素和细交链孢菌酮酸、细胞毒性的美洛菲林B以及酶抑制剂RK-682。描述了通过将起始组分连接到树脂上来固定其中任一起始组分的程序优势,以及在潜在药物候选物库的平行合成中对其的利用。当从合适的α-羟基或α-氨基烯丙基酯开始时,基本的多米诺反应甚至可以通过进一步的C-C键形成步骤来扩展。根据所选的反应条件,可以获得形式上为三到七步长的级联反应的生物活性中间体。其中包括具有除草活性的3-烷基特窗酸和抗疟活性超过天然抗疟先导青蒿素的内酯内过氧化物。因此,这种多米诺反应能够得到特窗酸和四胺酸的各种功能化衍生物。由于它也可以移植到固相上,所以非常适合平行和组合处理。未来的发展可能包括在“微芯片实验室”阵列中以连续模式运行此类多米诺序列。

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