巴布亚菌素A合成的进展：从硅基烯醇醚选择性形成α-溴代烯酮。
Progress towards the synthesis of Papuaforin A: Selective formation of α-bromoenones from silyl enol ethers.
作者信息
Kraus George A, Jeon Insik
机构信息
Department of Chemistry, Iowa State University, Ames, IA 50011.
出版信息
Tetrahedron Lett. 2008 Jan 7;49(2):286-288. doi: 10.1016/j.tetlet.2007.11.069.
Abstract
The selective one-pot conversion of enol silyl ethers into α-bromoenones allows a direct preparation of a tricyclic intermediate to papuaforin A.
摘要
烯醇硅醚向α-溴代烯酮的选择性一锅法转化使得能够直接制备巴布亚佛林A的三环中间体。
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