Abstract
The first total synthesis of hamigerans D, G, L, and N–Q has been accomplished. A convergent approach was used to build the basic tricarbocyclic ring system bearing a 5-6-6 structure. A sequence of oxidative cleavage, homologation, and ring regeneration provided access to the 5-7-6 skeleton of hamigeran G. Based on the biogenetic hypothesis, elegant and highly efficient biomimetic transformations of hamigeran G into hamigerans D, N–Q, and L were achieved.
| Original language | English |
|---|---|
| Pages (from-to) | 9942-9946 |
| Number of pages | 5 |
| Journal | Angewandte Chemie - International Edition |
| Volume | 55 |
| Issue number | 34 |
| DOIs | |
| State | Published - 16 Aug 2016 |
Keywords
- biomimetic synthesis
- cross-couplings
- heterocycles
- natural products
- total synthesis