首页> 外文期刊>Synthesis: International Journal of Methods in Synthetic Organic Chemistry >Advances and Setbacks in the Total Synthesis of the Fungal Metabolite Curvicollide C: Synthesis and Elaboration of Non-Aldol Stereotriads from Gosteli-Type Allyl Vinyl Ethers
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Advances and Setbacks in the Total Synthesis of the Fungal Metabolite Curvicollide C: Synthesis and Elaboration of Non-Aldol Stereotriads from Gosteli-Type Allyl Vinyl Ethers

机译:真菌代谢产物Curvicollide C的总合成方面的进展和挫折:由Gosteli型烯丙基乙烯基醚合成和合成非醛醇立体异构体

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摘要

Advances and setbacks are reported in regard to the asymmetric total synthesis of the fungal metabolite curvicollide C relying on a synthetic strategy that exploits non-aldol stereotriads as chiral building blocks. A catalytic asymmetric Gosteli-Claisen rearrangement, a two-step aldehyde-to-alkyne-homologation, and a Julia-Kocienski olefination served as key C/C-connecting transformations.
机译:据报道,真菌代谢产物curcollcollide C的不对称总合成方面存在进步和挫折,这依赖于利用非醛醇立体三联体作为手性结构单元的合成策略。催化的不对称Gosteli-Claisen重排,两步醛基至炔烃同构反应和Julia-Kocienski烯烃化反应是关键的C / C连接转化。

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