分子
全合成
自由基环化
化学
形式综合
组合化学
骨架(计算机编程)
立体化学
计算机科学
有机化学
程序设计语言
作者
Lu-Ning Wang,Zhiqiang Huang,Zhi‐Xiang Yu
标识
DOI:10.1016/j.xcrp.2023.101302
摘要
Many natural products contain compact cis-anti-cis-configurated 5/5/5 and 5/6/4 tricycles, and efficient access to these molecules is posing many hurdles to the synthetic community. Accessing molecules with more strained trans-anti-cis-configurated 5/5/5 tricycles (which are rarely found in nature) was envisioned to be more challenging, and no solution to this has been reported. We describe here a [5+2+1]/epoxidation/transannular radical cyclization strategy to solve the above-mentioned challenges, as demonstrated by the first total synthesis of (+)-antrodiellin B, the asymmetric total synthesis of (−)-hypnophilin, and the formal synthesis of (−)-coriolin, all of which contain a cis-anti-cis-configurated 5/5/5 skeleton, together with the synthesis of compounds with 5/6/4 and trans-anti-cis-configurated 5/5/5 tricycles. The present strategy is helpful for obtaining these and other molecules and their analogs for future downstream studies dependent on synthetic molecules with unusual scaffolds.
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