中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Nickel-Catalyzed Reductive Cross-Coupling of (Hetero)Aryl Iodides with Fluorinated Secondary Alkyl Bromides

文献类型:期刊论文

作者Li XF(李学飞)1; Feng Z(冯璋)1; Jiang ZX(江中兴)1; Zhang XG(张新刚)1
刊名Org. Lett.
出版日期2015
卷号17期号:22页码:5570-5573
其他题名镍催化下(杂)芳基碘代物与氟代二级溴代烷烃的还原偶联反应
通讯作者江中兴 ; 张新刚
英文摘要A mild and efficient nickel-catalyzed reductive cross-coupling between fluorinated secondary alkyl bromides and (hetero)aryl iodides is described. The use of FeBr2 as an additive successfully overcomes the hydrodebromination and beta-fluorine elimination of fluorinated substrates and allows the efficient synthesis of a wide range of trifluoromethyl and difluoroalkyl containing aliphatic compounds with a fluoroalkyl substituted tertiary carbon center. The notable features of this protocol are the synthetic and operational simplicity without preparation of moisture sensitive organometallic reagents and excellent functional group compatibility, even toward active proton containing substrates.
学科主题氟化学
收录类别SCI
原文出处http://dx.doi.org/10.1021/acs.orglett.5b02716
语种英语
WOS记录号WOS:000365462900015
源URL[http://ir.sioc.ac.cn/handle/331003/39763]  
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.武汉大学
2.中科院上海有机化学研究所, 有机氟化学重点实验室
推荐引用方式
GB/T 7714
Li XF,Feng Z,Jiang ZX,et al. Nickel-Catalyzed Reductive Cross-Coupling of (Hetero)Aryl Iodides with Fluorinated Secondary Alkyl Bromides[J]. Org. Lett.,2015,17(22):5570-5573.
APA 李学飞,冯璋,江中兴,&张新刚.(2015).Nickel-Catalyzed Reductive Cross-Coupling of (Hetero)Aryl Iodides with Fluorinated Secondary Alkyl Bromides.Org. Lett.,17(22),5570-5573.
MLA 李学飞,et al."Nickel-Catalyzed Reductive Cross-Coupling of (Hetero)Aryl Iodides with Fluorinated Secondary Alkyl Bromides".Org. Lett. 17.22(2015):5570-5573.

入库方式: OAI收割

来源:上海有机化学研究所

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