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轮烷—从化学奇闻到“爆炸”材料和天然产物。

Propellanes-From a Chemical Curiosity to "Explosive" Materials and Natural Products.

机构信息

Institute of Organic Chemistry (IOC), Karlsruhe Institute of Technology (KIT), Fritz-Haber-Weg 6, 76131, Karlsruhe, Germany.

Institute of Organic and Biomolecular Chemistry, Georg-August Universität Göttingen, Tammannstrasse 2, 37077, Göttingen, Germany.

出版信息

Angew Chem Int Ed Engl. 2017 May 15;56(21):5684-5718. doi: 10.1002/anie.201603951. Epub 2017 Apr 6.

Abstract

Propellanes are a unique class of compounds currently consisting of well over 10 000 representatives, all featuring two more or less inverted tetrahedral carbon atoms that are common to three bridging rings. The central single bond between the two bridgeheads is significantly weakened in the smaller entities, which leads to unusual reactivities of these structurally interesting propeller-like molecules. This Review highlights the synthesis of such propellanes and their occurrence in material sciences, natural products, and medicinal chemistry. The conversion of [1.1.1]propellane into bridgehead derivatives of bicyclo[1.1.1]pentane, including oligomers and polymers with bicyclo[1.1.1]penta-1,3-diyl repeat units, is also featured. A selection of natural products with larger propellane subunits are discussed in detail. Heteropropellanes and inorganic propellanes are also addressed. The historical background is touched in brief to show the pioneering work of David Ginsburg, Günther Snatzke, Kenneth B. Wiberg, Günter Szeimies, and others.

摘要

三叶烷是一类独特的化合物,目前包含超过 10000 种不同的化合物,它们都具有两个或多或少倒置的四面体碳原子,这些碳原子与三个桥环共有。在较小的实体中,两个桥头之间的中心单键显著减弱,导致这些结构有趣的三叶烷样分子具有异常的反应活性。这篇综述重点介绍了这类三叶烷的合成及其在材料科学、天然产物和药物化学中的应用。还介绍了将[1.1.1]三叶烷转化为双环[1.1.1]戊烷的桥接衍生物,包括具有双环[1.1.1]戊-1,3-二基重复单元的低聚物和聚合物。详细讨论了具有较大三叶烷亚基的天然产物的选择。杂三叶烷和无机三叶烷也得到了讨论。简要介绍了历史背景,以展示 David Ginsburg、Günther Snatzke、Kenneth B. Wiberg、Günter Szeimies 等人的开创性工作。

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