化学
腈
全合成
酰胺
催化加氢
立体化学
组合化学
有机化学
催化作用
作者
Yan Zhang,Yuye Chen,Jing Xu
出处
期刊:Synthesis
[Thieme Medical Publishers (Germany)]
日期:2024-01-12
卷期号:56 (08): 1273-1284
被引量:3
摘要
Abstract Here, we wish to describe our detailed efforts in the total synthesis of three calyciphylline A-type alkaloids, namely (+)-daphlongamine E, (+)-calyciphylline R, and (–)-10-deoxydaphnipaxianine A. Important steps in our approach include a Pt-catalyzed nitrile hydration, a Babler–Dauben rearrangement, a novel selective amide reduction tactic, and an oxidative Nazarov cyclization via an unfunctionalized tertiary divinyl carbinol (TDC).
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