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在高级环烯醚萜前体合成中的环加成和一碳同系化研究。

Cycloaddition and one-carbon homologation studies in the synthesis of advanced iridoid precursors.

作者信息

Stevens Anne T, Caira Mino R, Bull James R, Chibale Kelly

机构信息

Department of Chemistry, University of Cape Town, Rondebosch, 7701, South Africa.

出版信息

Org Biomol Chem. 2009 Sep 7;7(17):3527-36. doi: 10.1039/b902452b. Epub 2009 Jul 8.

Abstract

A Diels-Alder cycloaddition approach to the sweroside aglycone intermediate of iridoids was explored using silylated butenolides and levoglucosenone as dienophiles under both Lewis acid and thermal conditions. Results of this study reveal no evidence that using less sterically demanding derivatives compromise the diastereofacial selectivity of the cycloaddition using silylated butenolides. Further chemistry performed on cycloadducts concentrated on the identification and management of methodologies suitable for its conversion into sweroside aglycone. During the course of these studies, a dehydrative cyclisation onto a preformed tetrahydrofuran ring to a bis-tetrahydrofuranoid moiety was unravelled. In addition studies on levoglucosenone-derived cycloadducts provide extensive insight into the conformational behaviour and reactivity. Further, the X-ray crystal structure of an alcohol intermediate from one-carbon homologation studies provided the first structural evidence confirming the diastereoselectivity of the cycloaddition procedure.

摘要

利用硅烷基化丁烯内酯和左旋葡聚糖酮作为亲双烯体,在路易斯酸和热条件下,探索了一种用于环烯醚萜类化合物獐牙菜苷苷元中间体的狄尔斯-阿尔德环加成方法。该研究结果表明,没有证据表明使用空间位阻较小的衍生物会损害使用硅烷基化丁烯内酯进行环加成的非对映面选择性。对环加成产物进行的进一步化学研究集中于确定和开发适合将其转化为獐牙菜苷苷元的方法。在这些研究过程中,揭示了一种在预先形成的四氢呋喃环上脱水环化生成双四氢呋喃类部分的反应。此外,对左旋葡聚糖酮衍生的环加成产物的研究提供了对其构象行为和反应性的深入了解。此外,来自一碳同系化研究的醇中间体的X射线晶体结构提供了首个结构证据,证实了环加成过程的非对映选择性。

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