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首页> 外文期刊>The Journal of Organic Chemistry >Enantioselective Total Syntheses of (+)-Hostmanin A, (-)-Linderol A, (+)-Methyllinderatin and Structural Reassignment of Adunctin E
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Enantioselective Total Syntheses of (+)-Hostmanin A, (-)-Linderol A, (+)-Methyllinderatin and Structural Reassignment of Adunctin E

机译:(+)-Hostmanin A,(-)-Linderol A,(+)-甲基linderatin的对映选择性总合成和Adunctin E的结构重新分配

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摘要

A one-step protocol has been developed for the enantioselective synthesis of hexahydrodibenzofuran derivatives using a modified Friedel-Crafts reaction. The developed method was applied to the synthesis of a series of natural products including (+)-hostmanin A, (+)-methyllinderatin, and (-)-linderol A. The synthetic and spectroscopic data investigations led to the structural. reassignment of natural product adunctin E, which was further confirmed by single-crystal X-ray analysis.
机译:已开发出一种使用改良的Friedel-Crafts反应对映选择性合成六氢二苯并呋喃衍生物的一步方案。所开发的方法用于合成一系列天然产物,包括(+)-hostmanin A,(+)-甲基linderatin和(-)-linderolA。合成和光谱数据研究得出了结构。天然产物adunctin E的重新分配,这已通过单晶X射线分析进一步证实。

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