SIOC OpenIR  > 中科院有机氟化学重点实验室
Direct (Het)Arylation of Fluorinated Benzothiadiazoles and Benzotriazole with (Het)Aryl Iodides
Alternative Title氟代苯丙噻二唑和三氮唑与芳基碘的直接芳基化
He CY(贺春阳)1; Wu CZ(吴才智)1; Qing FL(卿凤翎)1; Zhang XG(张新刚)1
2014
Source PublicationJ. Org. Chem.
Volume79Issue:4Pages:1712-1718
AbstractA 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.
Subject Area氟化学
DOI10.1021/jo402675v
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Indexed BySCI
Language英语
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Cited Times:18[WOS]   [WOS Record]     [Related Records in WOS]
Document Type期刊论文
Identifierhttp://ir.sioc.ac.cn/handle/331003/38876
Collection中科院有机氟化学重点实验室
Corresponding AuthorZhang XG(张新刚)
Affiliation1.东华大学
2.中科院上海有机化学研究所
Recommended Citation
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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