Copper-Catalyzed Successive C-C bond formations on Indoles or Pyrrole: A Convergent Synthesis of Symmetric and Unsymmetric Hydroxyl Substituted N-H Carbazoles

被引:23
|
作者
Qiao, Yu [1 ]
Wu, Xin-Xing [1 ]
Zhao, Yupeng [1 ]
Sun, Yongqing [1 ]
Li, Baoguo [1 ]
Chen, Shufeng [1 ]
机构
[1] Inner Mongolia Univ, Coll Chem & Chem Engn, Inner Mongolia Key Lab Fine Organ Synth, Hohhot 010021, Peoples R China
基金
中国国家自然科学基金;
关键词
hydroxyl substituted N-H carbazoles; C-C bond formation; copper; indoles; pyrrole; HIGHLY EFFICIENT; SELECTIVE SYNTHESIS; 1ST SYNTHESIS; DERIVATIVES; HYDROACYLATION; BENZANNULATION; ALKALOIDS; MIGRATION; ALKYNES; FACILE;
D O I
10.1002/adsc.201800154
中图分类号
O69 [应用化学];
学科分类号
081704 ;
摘要
A novel copper-catalyzed successive C-Cbond formations on indoles and pyrrole approach for the direct synthesis of hydroxyl substituted N-H carbazoles is described. The current process represents an atom-economical method for the preparation of both symmetric and unsymmetric densely substituted and hydroxyl containing N-H carbazoles from easily accessible starting materials without the need for expensive metals and harsh reaction conditions.
引用
收藏
页码:2138 / 2143
页数:6
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