Application of Pyridinium 1,4-Zwitterionic Thiolates: Synthesis of Benzopyridothiazepines and Benzothiophenes

被引:41
作者
Cheng, Bin [1 ,2 ]
Li, Yuntong [2 ]
Wang, Taimin [1 ]
Zhang, Xinping [2 ]
Li, Hui [2 ]
He, Yixuan [2 ]
Li, Yun [2 ]
Zhai, Hongbin [1 ,2 ,3 ]
机构
[1] Shenzhen Polytech, Inst Marine Biomed, Shenzhen 518055, Peoples R China
[2] Lanzhou Univ, State Key Lab Appl Organ Chem, Coll Chem & Chem Engn, Lanzhou 730000, Peoples R China
[3] Peking Univ, State Key Lab Chem Oncogen, Shenzhen Engn Lab Nano Drug Slow Release, Shenzhen Grad Sch, Shenzhen 518055, Peoples R China
关键词
CATALYZED SYNTHESIS; ARYNES; DERIVATIVES; CYCLOADDITION; SULFUR; ANNULATION; TRIFLATE; CASCADE; ARYL;
D O I
10.1021/acs.joc.0c00374
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Pyridinium 1,4-zwitterionic thiolates, as a novel kind of sulfur-containing synthon, have been applied to the synthesis of 12aH-benzo[f]pyrido [1,2-d] [1,4]thiazepines and benzo[b]thiophenes. Benzopyridothiazepines were produced through a 1,5-dipolar cycloaddition reaction from pyridinium 1,4-zwitterionic thiolates with arynes, whereas benzothiophenes as side products were generated via a [3 + 2] cascade cyclization reaction. The [5 + 2] reaction mode of pyridinium 1,4-zwitterionic thiolates is disclosed for the first time.
引用
收藏
页码:6794 / 6802
页数:9
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