Smith Nicole D, Hayashida Joji, Rawal Viresh H
Department of Chemistry, The University of Chicago, 5735 South Ellis Avenue, Chicago, Illinois 60637, USA.
Org Lett. 2005 Sep 29;7(20):4309-12. doi: 10.1021/ol0512740.
[reaction: see text] The tricyclic indeno-tetrahydropyridine core of haouamine A, containing five of the seven rings of the natural product, was constructed by a simple, concise route that features an acid-catalyzed Friedel-Crafts ring closure.
[反应：见正文] 豪胺A的三环茚并四氢吡啶核心结构包含了该天然产物七个环中的五个，它是通过一条简单、简洁的路线构建而成的，该路线的特点是酸催化傅克环化反应。
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