首页> 外文期刊>The Journal of Organic Chemistry >A highly diastereoselectrive, tandem mukaiyama aldol-lactonization route to β-Lactones: application to a concise synthesis of the potent pancreatic lipase
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A highly diastereoselectrive, tandem mukaiyama aldol-lactonization route to β-Lactones: application to a concise synthesis of the potent pancreatic lipase

机译:β-内酯的高度非对映选择性,串联mukaiyama aldol-内酯化途径:在强力胰腺脂肪酶的简明合成中的应用

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摘要

β-Lactones (2-oxetanones) have recently emerged as important synthetic targets due to their occurrence in a variety of natural products, their utility as versatile synthetic intermediates, and their use as monomers for the preparation of biodegradable polymers.
机译:β-内酯(2-氧杂环丁烷)由于其在多种天然产物中的存在,它们作为通用合成中间体的用途以及用作制备可生物降解聚合物的单体的用途,最近已成为重要的合成目标。

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