| Literature DB >> 32833268 |
Karre Nagaraju1, Dongshun Ni1, Dawei Ma1.
Abstract
Kopsinitarines A-E are complex octacyclic caged Kopsia alkaloids with strained cage skeletons and a unique cyclic hemiaminal bridge that makes total synthesis challenging. Herein, we disclose the first total synthesis of kopsinitarine E. The key synthetic features include a SmI2 -mediated radical cascade cyclization and a subsequent semi-pinacol rearrangement to install the key carbocyclic skeleton, a chemoselective hydrosilyl amide reduction to construct the hemiaminal ether bridge, and an intramolecular Mannich reaction to establish the highly strained cage system.Entities:
Keywords: Mannich reaction; cyclization; indole alkaloids; semi-pinacol rearrangement; total synthesis
Mesh:
Year: 2020 PMID: 32833268 DOI: 10.1002/anie.202011093
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336