Efficient diastereoselective synthesis of trifarane-type sesquiterpenes, trifarienols A and B.

Efficient diastereoselective synthesis of trifarane-type sesquiterpenes, trifarienols A and B.
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三呋烷型倍半萜、三呋烯醇 A 和 B 的高效非对映选择性合成。

DOI:
10.1021/jo900369t
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发表时间:
2009
期刊:
The Journal of organic chemistry
影响因子:
--
通讯作者:
T. Honda
T. Honda
中科院分区:
--
文献类型:
--
作者:
Kazunori Takahashi;Ryuichi Akao;T. Honda

文献摘要

被引文献

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通过醛的分子内 Hosomi-Sakurai 反应,实现了三法烯醇 A 和 B(从马来西亚 Cheilolejeunea trifaria 中分离出的三法烷型倍半萜)的非对映选择性全合成,一步构建了具有目标化合物外亚甲基部分的取代双环[3.3.1]壬烷骨架。
Diastereoselective total synthesis of trifarienols A and B, trifarane-type sesquiterpenes isolated from the Malaysian Cheilolejeunea trifaria, was achieved via an intramolecular Hosomi-Sakurai reaction of the aldehyde to construct a substituted bicyclo[3.3.1]nonane skeleton having the exo-methylene moiety of the target compounds in one step.