Abstract
AbstractHere, 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).
Funder
Guangdong Provincial Key Laboratory of Catalysis
Ed. Dep. Guangdong Prov., Key Research Proj. in Colleges and Universities in Guangdong Province
Shenzhen Science, Technology and Innovation Commission
Innovative Team of Universities in Guangdong Province
National Natural Science Foundation of China
Shenzhen Key Laboratory of Small Molecule Drug Discovery and Synthesis