摘要

The synthesis of hymenialdisine has offered challenges that included the formation of the regio-isomers upon monobromination, atom-scrambling in the cyclization step, and low to moderate yields in the last steps. We herein present a short and concise (6 overall steps), high yielding route (44% overall yields) for this biologically interesting natural product that addresses these issues and avoids the use of any protecting groups.

  • 出版日期2015-6-3