A practical Cu(I)-catalyzed domino approach to 1,2-disubstituted indoles and its application for the assembly of indolophenanthridines

被引:8
作者
Gao, Jilong [1 ]
Xu, Bingqing [1 ]
Zhu, Jiaqi [1 ]
Shao, Yingying [1 ]
Chen, Lubin [1 ]
Zhu, Jiaoyan [1 ]
Wang, Xiaxia [1 ]
Lv, Xin [1 ]
机构
[1] Zhejiang Normal Univ, Coll Chem & Life Sci, Dept Chem, Jinhua 321004, Peoples R China
基金
中国国家自然科学基金;
关键词
Copper; cross-coupling; domino reactions; indoles; fused phenanthridines; ONE-POT SYNTHESIS; C-N; SUBSTITUTED INDOLES; EFFICIENT SYNTHESIS; MODULAR SYNTHESIS; ROOM-TEMPERATURE; ARYL HALIDES; H ARYLATION; COPPER; PALLADIUM;
D O I
10.3998/ark.5550190.p009.387
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A facile and efficient approach to 1,2-disubstituted indoles has been developed using a novel Cu(I)-catalyzed cascade coupling/cyclization reaction of 2-alkynylanilines with aryl iodides. Facilitated by CuI/t-BuOK without any ligand or CuI/Cs2CO3/1,10-phenanthroline, a variety of 1,2-disubstituted indoles were conveniently generated in one pot with good to excellent yields. Furthermore, a series of indolo[1,2-f] phenanthridines were successfully assembled from the tandem reactions of 2-alkynylanilines with o-dihaloarenes through copper-catalyzed coupling / cyclization followed by palladium-catalyzed intramolecular direct C(sp(2))-H arylation.
引用
收藏
页码:1 / 14
页数:14
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