中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Highly Selective gem-Difluoroallylation of Organoborons with Bromodifluoromethylated Alkenes Catalyzed by Palladium

文献类型:期刊论文

作者Min QQ(闵巧桥); Yin ZS(尹增升); Feng Z(冯璋); Guo WH(郭文豪); Zhang XG(张新刚)
刊名J. Am. Chem. Soc.
出版日期2014
卷号136期号:4页码:1230-1233
其他题名钯催化下溴二氟丙烯对有机硼试剂的高选择性偕二氟烯丙基化
通讯作者张新刚
英文摘要A first example of Pd-catalyzed gem-difluoroallylation of organoborons using 3-bromo-3,3-difluoropropene (BDFP) in high efficiency with high alpha/gamma-substitution regioselectivity has been developed. The reaction can also be extended to substituted BDFPs and has advantages of low catalyst loading (0.8 to 0.01 mol %), broad substrate scope, and excellent functional group compatibility, thus providing a facile route for practical application in drug discovery and development.
学科主题氟化学
收录类别SCI
原文出处http://dx.doi.org/10.1021/ja4114825
语种英语
源URL[http://ir.sioc.ac.cn/handle/331003/38875]  
专题上海有机化学研究所_中科院有机氟化学重点实验室
作者单位中科院上海有机化学研究所
推荐引用方式
GB/T 7714
Min QQ,Yin ZS,Feng Z,et al. Highly Selective gem-Difluoroallylation of Organoborons with Bromodifluoromethylated Alkenes Catalyzed by Palladium[J]. J. Am. Chem. Soc.,2014,136(4):1230-1233.
APA 闵巧桥,尹增升,冯璋,郭文豪,&张新刚.(2014).Highly Selective gem-Difluoroallylation of Organoborons with Bromodifluoromethylated Alkenes Catalyzed by Palladium.J. Am. Chem. Soc.,136(4),1230-1233.
MLA 闵巧桥,et al."Highly Selective gem-Difluoroallylation of Organoborons with Bromodifluoromethylated Alkenes Catalyzed by Palladium".J. Am. Chem. Soc. 136.4(2014):1230-1233.

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来源:上海有机化学研究所

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