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首页> 外文期刊>Angewandte Chemie >Gold-Catalyzed Intramolecular Regio- and Enantioselective Cycloisomerization of 1,1-Bis(indolyl)-5-alkynes
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Gold-Catalyzed Intramolecular Regio- and Enantioselective Cycloisomerization of 1,1-Bis(indolyl)-5-alkynes

机译:金催化的1,1-双(吲哚基)-5-炔烃的分子内区域和对映选择性环异构化

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摘要

Indole is one of the most intensively investigated aromatic heterocycle, because its derivatives are abundant in nature and possess various biological activities. Among the large number of indoles, bis(indole) alkaloids, such as hamacan-thins, nortopsentins, and dragmacidins (Scheme 1), are par- ticularly abundant in marine sponges. In bis(indole) alkaloids, two indole moieties are connected to various heterocyclic units. Compounds with 'this structural motif exhibit a wide spectrum of pharmacological activities, including antibacterial, antiviral, and cytotoxic activities, which make bis(indole) alkaloids and their analogues attractive targets for biomedical and synthetic studies.
机译:吲哚是研究最深入的芳香族杂环之一,因为它的衍生物性质丰富且具有多种生物活性。在大量的吲哚中,双(吲哚)生物碱,例如哈马坎-稀,降钙素和降糖药(方案1)在海洋海绵中尤其丰富。在双(吲哚)生物碱中,两个吲哚部分连接至各种杂环单元。具有这种结构基序的化合物具有广泛的药理活性,包括抗菌,抗病毒和细胞毒性活性,这些使双(吲哚)生物碱及其类似物成为生物医学和合成研究的有吸引力的靶标。

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