Synthesis of the tetracyclic core skeleton of the lundurines by a gold-catalyzed cyclization
Synthesis of the tetracyclic core skeleton of the lundurines by a gold-catalyzed cyclization
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DOI：
10.1016/j.tet.2009.08.067
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发表时间：
2009-10-31
期刊：
影响因子：
2.1
通讯作者：
Echavarren, Antonio M.
中科院分区：
文献类型：
--
作者：
Ferrer, Catalina;Escribano-Cuesta, Ana;Echavarren, Antonio M.
以AuCl3或其他金配合物为催化剂，对烷基吲哚进行8-内环化反应，制备了氟脲类化合物的1h -偶氮基吲哚[5,4-b]骨架。2009爱思唯尔有限公司版权所有。
The 1H-azocino[5,4-b]indole skeleton of the lundurines has been prepared by the 8-endo-dig cyclization of an alkynylindole using AuCl3 or other gold complexes as catalysts. (C) 2009 Elsevier Ltd. All rights reserved.