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Synthesis of Nitrogen Heterocycles through 1,3-Dipolar Cycloaddition Reactions

机译:通过1,3-偶极环加成反应合成氮杂环

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Nitrogen heterocycles represent an extremely vast class of compounds and their importance matches their numbers. From the examples reported in this short review it is clear that the 1,3-DC reaction is one of the most important methods for the construction of nitrogen containing heterocycles. The use of chiral starting material or of chiral auxiliaries has often made it possible to control regioselectivity, endo/exo selectivity, and diastereofacial selectivity in 1,3-DC reactions where one to four new chiral centers are formed. Some examples have been shown of the successful application of these reactions as the key step in the synthesis of optically active target molecules, particularly important in the case of products formed from dipoles, such as nitrones, nitrile oxides, and azomethine ylides. With the increased demand for optically active compounds in the future and with the improvement of asymmetric metal catalysis, the development of new approaches to asymmetric 1,3-DC reactions are to be expected. The development of such reactions might appear as a difficult enough endeavour, but it is by no means an impossible task and it definitely seems worth the effort.
机译:氮杂环代表一类极其庞大的化合物,其重要性与其数量相符。从这篇简短评论中报道的实例中可以明显看出,1,3-DC反应是构建含氮杂环的最重要方法之一。手性原料或手性助剂的使用通常使得在形成1至4个新手性中心的1,3-DC反应中控制区域选择性,内/外选择性和非对面选择性成为可能。已经显示出这些反应的成功应用作为合成光学活性靶分子的关键步骤的一些例子,对于由偶极形成的产物,例如硝酮,腈氧化物和偶氮甲亚胺,这是特别重要的。随着未来对光学活性化合物的需求增加以及不对称金属催化作用的改善,人们有望开发出新的不对称1,3-DC反应方法。这种反应的发展似乎是一项艰巨的努力,但这绝不是一项不可能完成的任务,这显然值得付出努力。

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