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Convergent total synthesis of (−)-dactylolide
Tetrahedron Letters ( IF 1.8 ) Pub Date : 2018-01-13 , DOI: 10.1016/j.tetlet.2018.01.034
Tokihiro Tanaka , Yuto Murai , Takayuki Kishi , Hiroyoshi Takamura , Isao Kadota

A convergent total synthesis of (−)-dactylolide is described. Constructing the 2,6-disubstituted exo-methylene THP moiety was achieved by the intramolecular allylation of α-acetoxy ether. The cyclization precursor was prepared from two segments, an alcohol and carboxylic acid derivatives, by esterification followed by reductive acetylation.



中文翻译:

(-)-半乳糖苷的聚合全合成

描述了(-)-癸二酰肼的会聚全合成。通过α-乙酰氧基醚的分子内烯丙基化来构建2,6-二取代的-亚甲基THP部分。环化前体由两个部分(醇和羧酸衍生物)制备,先进行酯化反应,然后进行还原性乙酰化反应。

更新日期:2018-01-13
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