Total synthesis of (-)-nakadomarin A

[摘要]：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.

[全文传递流程]：

一般上传文献全文的时限在1个工作日内