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Synthesis of Medium-Sized Heterocycles by Transition-Metal-Catalyzed Intramolecular Cyclization

机译:通过过渡金属催化的分子分子化合成中尺寸杂环

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摘要

Medium-sized heterocycles (with 8 to 11 atoms) constitute important structural components of several biologically active natural compounds and represent promising scaffolds in medicinal chemistry. However, they are under-represented in the screening of chemical libraries as a consequence of being difficult to access. In particular, methods involving intramolecular bond formation are challenging due to unfavorable enthalpic and entropic factors, such as transannular interactions and conformational constraints. The present review focuses on the synthesis of medium-sized heterocycles by transition-metal-catalyzed intramolecular cyclization, which despite its drawbacks remains a straightforward and attractive synthesis strategy. The obtained heterocycles differ in their nature, number of heteroatoms, and ring size. The methods are classified according to the metal used (palladium, copper, gold, silver), then subdivided according to the type of bond formed, namely carbon–carbon or carbon–heteroatom.
机译:中等杂环(含8至11个原子)构成了几种生物活性天然化合物的重要结构组分,并且代表了药物化学中有前途的支架。然而,由于难以访问的结果,它们在筛选化学文库中被代表。特别地,涉及分子内键形成的方法由于不利的焓和熵因子,例如熵相互作用和构象约束而挑战。本综述专注于通过过渡金属催化的分子内环化合成中型杂环,尽管其缺点仍然是一种简单和有吸引力的合成策略。所得杂环的性质不同,杂原子的数量和环尺寸不同。该方法根据所使用的金属(钯,铜,金,银)进行分类,然后根据形成的粘合剂类型,即碳 - 碳或碳杂原子细分。

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