首页> 外文期刊>Bioorganic and Medicinal Chemistry Letters >Utilizing the intramolecular Fukuyama-Mitsunobu reaction for a flexible synthesis of novel heterocyclic scaffolds for peptidomimetic drug design.
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Utilizing the intramolecular Fukuyama-Mitsunobu reaction for a flexible synthesis of novel heterocyclic scaffolds for peptidomimetic drug design.

机译:利用分子内福山-Mitsunobu反应的灵活合成新型拟肽药物设计的杂环支架。

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摘要

We report the synthesis of the novel scaffolds pyrazino[1,2-b]isoquinoline and pyrrolo[1,2-a]pyrazine displaying the somatostatin pharmacophores. Both classes of compounds contain a pyrazine heterocycle, which can be prepared in a straightforward manner utilizing an intramolecular Fukuyama-Mitsunobu reaction. As both the families derive from amino acids, they can be accessed in high optical purity.
机译:我们报告了新颖的支架吡嗪并[1,2-b]异喹啉和吡咯并[1,2-a]吡嗪的合成,显示了生长抑素药效团。这两类化合物均包含吡嗪杂环,其可以利用分子内福山-光延反应以直接方式制备。由于两个家族均来自氨基酸,因此可以高光学纯度获得它们。

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