Total synthesis of (-)-nakadomarin A
- PMID: 21826301
- DOI: 10.1039/c1cc13665h
Total synthesis of (-)-nakadomarin A
Abstract
A highly diastereoselective bifunctional organocatalyst controlled Michael addition, a nitro-Mannich/lactamization cascade, a furan N-acyliminium cyclisation, a sequential alkyne RCM/syn-reduction and an alkene RCM has allowed a 19 step, highly stereoselective synthesis of (-)-nakadomarin A.
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