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Drimenol: A versatile synthon for compounds with trans-drimane skeleton

机译:Drimenol:适用于具有反式-drimane骨架的化合物的通用合成子

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摘要

Several reviews have been published on sesquiterpenes, and on drimane-type sesquiterpenes, going through drimenol and related compounds among others. However, to our knowledge, this is the first review exclusively on drimenol. Although, the main focus is on drimenol as a synthon for other drimane-type compounds, synthetic routes to obtain racemic and (-)-drimenol are summarized, as well as its isolation and determination of its configuration, in the early fifties. The reviewed synthetic routes start from natural (-)-drimenol as chiral synthon in most of cases, nevertheless total syntheses are considered as well. The strategies where racemic drimenol is involved begin with biomimetic cyclization of trans-farnesol. Microbiological procedures to functionalize the A ring of drimenol are also commented. The revision is classified according to the chemical structure of the final product, which mainly correspond to structures of natural occurrence, although other related derivatives are also analyzed.
机译:关于倍半萜烯和drimane型倍半萜烯的研究已经发表了一些评论,其中涉及到了drimenol和相关化合物。然而,据我们所知,这是专门针对drimenol的第一篇评论。尽管主要侧重于drimenol作为其他drimane型化合物的合成子,但在五十年代初总结了获得外消旋和(-)-drimenol的合成途径,以及其分离和结构确定。在大多数情况下,已综述的合成路线从天然(-)-门甲酸作为手性合成子开始,但是也考虑了总合成。涉及外消旋烯丙二醇的策略始于反式法尼醇的仿生环化。还评论了使drimenol的A环功能化的微生物程序。该修订版根据最终产品的化学结构进行分类,该化学结构主要对应于天然结构,尽管还分析了其他相关衍生物。

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