Abstract
The first total syntheses of sarcophytonolide H and the originally proposed and correct structures of isosarcophytonolide D have been achieved via transannular ring-closing metathesis (RCM). These total syntheses culminated in the stereostructural confirmation of sarcophytonolide H and the reassignment of isosarcophytonolide D, respectively. The antifouling activity of the synthetic sarcophytonolide H and its analogues was also evaluated.
Original language | English |
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Pages (from-to) | 2110-2113 |
Number of pages | 4 |
Journal | Organic Letters |
Volume | 18 |
Issue number | 9 |
DOIs | |
Publication status | Published - May 6 2016 |
ASJC Scopus subject areas
- Biochemistry
- Physical and Theoretical Chemistry
- Organic Chemistry