化学
生物催化
环加成
天然产物
发散合成
氧化磷酸化
组合化学
对映选择合成
化学合成
有机化学
立体化学
有机合成
氨基酸
立体异构
脚手架
仿生合成
酶
反应条件
作者
Zhili Wang,Delin Tang,Haibo Feng,Rui Tong,Mengfei Long,Xia Meng,Yang Han,Luqi Huang,Ping Su,Xi Zhang
摘要
The asymmetric construction of highly congested polycyclic architectures remains a formidable challenge in chemical synthesis. Biocatalysis offers exquisite stereocontrol, yet the repertoire of enzyme-catalyzed cycloadditions remains notably limited. Here, we elucidate the intriguing oxidative [3 + 2] cycloaddition capability of a flavoenzyme CpaO and develop it as a robust biocatalyst for asymmetric construction of the pentacyclic scaffold of (-)-α-Cyclopiazonic acid ((-)-α-CPA), a nanomolar inhibitor of sarco/endoplasmic reticulum calcium(II)-dependent ATPase. This work presents not only the most concise, scalable, and fully asymmetric synthesis of (-)-α-CPA to date but also unlocks the collective access to its highly oxidized, structurally diverse family members, thereby enriching the scenarios of enzyme-catalyzed bonding strategies in natural product synthesis.
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