POCl3/Sulfoxide-Promoted Synthesis of Indolizino[8,7-b]indoles

被引:7
作者
Chen, Xiao-Hui [1 ]
Li, Yun-Meng [1 ]
Huang, Xiang [1 ,2 ]
Cui, Hai-Lei [1 ]
机构
[1] Chongqing Univ Arts & Sci, Coll Chem & Environm Engn, Lab Asymmetr Synth, Chongqing 402160, Peoples R China
[2] Chongqing Univ Sci & Technol, Sch Chem & Chem Engn, Chongqing 401331, Peoples R China
基金
中国国家自然科学基金;
关键词
DIMETHYL-SULFOXIDE; DEAROMATIZATION STRATEGIES; POLYCYCLIC INDOLINES; ACID; CATALYST; CASCADE; CONSTRUCTION; BROMINATION; CYCLIZATION; ALKALOIDS;
D O I
10.1021/acs.joc.3c01912
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
A mild chlorocyclization of pyrrole-tethered indoles has been realized using POCl3 as the chlorine source and tetramethylene sulfoxide as the promoter. A variety of chlorinated indolizino-[8,7-b]-indole derivatives have been constructed efficiently under this reaction system in moderate to good yields (19 examples, up to 93% yield).
引用
收藏
页码:16400 / 16409
页数:10
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