中国科学院机构知识库网格
Chinese Academy of Sciences Institutional Repositories Grid
Palladium-Catalyzed Difluoroalkylation of Isocyanides: Access to Difluoroalkylated Phenanthridine Derivatives

文献类型:期刊论文

作者Gu JW(顾继伟); Zhang XG(张新刚)
刊名Org. Lett.
出版日期2015
卷号17期号:21页码:5384-5387
其他题名钯催化下异氰的二氟烷基化
通讯作者张新刚
英文摘要An efficient and general method for the synthesis of difluoroalkylated phenanthridine derivatives through palladium-catalyzed reaction of difluoroalkyl bromides with isocyanides is described. The reaction can also be extended to perfluoroalkyl iodides. Mechanistic studies reveal that a difluoroalkyl radical via a single-electron-transfer pathway is involved 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/acs.orglett.5b02739
语种英语
WOS记录号WOS:000364434900060
源URL[http://ir.sioc.ac.cn/handle/331003/39753]  
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, 有机氟化学重点实验室
推荐引用方式
GB/T 7714
Gu JW,Zhang XG. Palladium-Catalyzed Difluoroalkylation of Isocyanides: Access to Difluoroalkylated Phenanthridine Derivatives[J]. Org. Lett.,2015,17(21):5384-5387.
APA 顾继伟,&张新刚.(2015).Palladium-Catalyzed Difluoroalkylation of Isocyanides: Access to Difluoroalkylated Phenanthridine Derivatives.Org. Lett.,17(21),5384-5387.
MLA 顾继伟,et al."Palladium-Catalyzed Difluoroalkylation of Isocyanides: Access to Difluoroalkylated Phenanthridine Derivatives".Org. Lett. 17.21(2015):5384-5387.

入库方式: OAI收割

来源:上海有机化学研究所

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