Synthetic studies towards the core structure of nakadomarin A by a thioamide-based strategy
The tricyclic BCD substructure of the marine natural product nakadomarin A has been synthesised. The strategy utilised a key carbon-carbon bond-forming reaction between a furan and an N-acyliminium ion derived from a secondary thiolactam. In addition, a novel three-component coupling reaction betwee...
| Main Authors: | , , , , |
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| Format: | Article |
| Language: | English |
| Published: |
2014-01.
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| Subjects: | |
| Online Access: | Get fulltext |