Construction of indoloquinolinones via Pd(II)-catalyzed tandem C-C/C-N bond formation: application to the total synthesis of isocryptolepine
Construction of indoloquinolinones via Pd(II)-catalyzed tandem C-C/C-N bond formation: application to the total synthesis of isocryptolepine
复制标题
通过 Pd(II) 催化串联 C-C/C-N 键形成构建吲哚喹啉酮：在异隐托品全合成中的应用
DOI：
10.1016/j.tetlet.2014.11.008
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发表时间：
2014-12-17
影响因子：
1.8
通讯作者：
Lin, Aijun
中科院分区：
文献类型：
--
作者：
Chen, Xuebing;Sun, Peng;Lin, Aijun
通过Pd催化的串联C-C/C-N键的形成，已经以中等至良好的产率实现了吲哚并喹啉酮骨架的构建。该方法已应用于生物活性天然产物异隐草碱的全合成，总收率较高。(C)2014爱思唯尔有限公司版权所有。
Construction of indoloquinolinone skeleton via Pd-catalyzed tandem C-C/C-N bond formation has been achieved in moderate to good yields. The method was applied toward the total synthesis of the bioactive natural product isocryptolepine in good overall yields. (C) 2014 Elsevier Ltd. All rights reserved.