Synthesis of fused N-heterocycles via tandem C-H activation
Synthesis of fused N-heterocycles via tandem C-H activation
复制标题
通过串联 C-H 活化合成稠合 N-杂环
DOI：
10.1039/c2cc34158a
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发表时间：
2012-01-01
影响因子：
4.9
通讯作者：
Guo, Hai-Ming
中科院分区：
文献类型：
--
作者：
Meng, Ge;Niu, Hong-Ying;Guo, Hai-Ming
利用嘌呤或苯并咪唑的分子内环化反应合成稠合N-杂环化合物。准备了一系列中环和大环。
The synthesis of fused N-heterocycles has been developed using an intramolecular cyclisation of purines or benzimidazoles. A range of medium and large rings were prepared.