Total synthesis of conosilane A via a site-selective C–H functionalization strategy†
Abstract
The first total synthesis of conosilane A, a densely oxygenated nonisoprenoid sesquiterpene, has been achieved through stereoselective intramolecular radical cyclization and double utilization of site-selective C–H functionalization as key steps, thus simplifying the synthetic endeavors in natural product synthesis.
- This article is part of the themed collection: Natural product synthesis