The ABCE tetracyclic ring system of daphnicyclidin A was prepared using an intramolecular (4 + 3) cycloaddition of an oxidopyridinium ion as the key step. This route consists of a 10-step synthesis with an overall yield of 20.2%. This result offers support for the use of this strategy for total synthesis of daphnicyclidin A.
Download full-text PDF |
Source |
---|---|
http://dx.doi.org/10.1039/d2ob01246d | DOI Listing |
Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!