| Literature DB >> 31115973 |
Ken-Ichi Takao1, Hirotaka Kai1, Ai Yamada1, Yuuki Fukushima1, Daisuke Komatsu1, Akihiro Ogura1, Keisuke Yoshida2.
Abstract
The short, efficient total synthesis of (+)-aquatolide was achieved by a biomimetic transannular [2+2] photocycloaddition, and provides the first example of constructing a 5/5/4/8-ring system from asteriscunolides. Furthermore, the reaction leading to a 5/4/4/7-ring system, the originally proposed structure of aquatolide, was also developed. This strategy achieved syntheses of five more humulanolides, (-)-asteriscunolides A, C, D, and I, and (+)-tetradehydroasteriscanolide.Entities:
Keywords: biomimetic synthesis; cycloaddition; metathesis; terpenoids; total synthesis
Year: 2019 PMID: 31115973 DOI: 10.1002/anie.201904404
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336