Direct (Het)Arylation of Fluorinated Benzothiadiazoles and Benzotriazole with (Het)Aryl Iodides
He CY(贺春阳)1; Wu CZ(吴才智)1; Qing FL(卿凤翎)1; Zhang XG(张新刚)1
刊名J. Org. Chem.
2014
卷号79期号:4页码:1712-1718
其他题名氟代苯丙噻二唑和三氮唑与芳基碘的直接芳基化
通讯作者张新刚
英文摘要A new and controllable method for the preparation of unsymmetrical and symmetrical fluorinated benzothiadiazole (FBT)-arene structures that can be applied in organic optoelectronic materials has been developed. The reaction proceeds under mild reaction conditions with high efficiency and shows excellent functional group compatibility, even toward bromide. Fluorinated benzotriazoles also take part in the reaction.
学科主题氟化学
收录类别SCI
原文出处http://dx.doi.org/10.1021/jo402675v
语种英语
内容类型期刊论文
源URL[http://ir.sioc.ac.cn/handle/331003/38876]  
专题上海有机化学研究所_中科院有机氟化学重点实验室
作者单位1.东华大学
2.中科院上海有机化学研究所
推荐引用方式
GB/T 7714
He CY,Wu CZ,Qing FL,et al. Direct (Het)Arylation of Fluorinated Benzothiadiazoles and Benzotriazole with (Het)Aryl Iodides[J]. J. Org. Chem.,2014,79(4):1712-1718.
APA 贺春阳,吴才智,卿凤翎,&张新刚.(2014).Direct (Het)Arylation of Fluorinated Benzothiadiazoles and Benzotriazole with (Het)Aryl Iodides.J. Org. Chem.,79(4),1712-1718.
MLA 贺春阳,et al."Direct (Het)Arylation of Fluorinated Benzothiadiazoles and Benzotriazole with (Het)Aryl Iodides".J. Org. Chem. 79.4(2014):1712-1718.
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