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学科主题: 金属有机化学
题名: Pd(0)-catalyzed benzylation of indole through eta(3)-benzyl palladium intermediate
其他题名: 经历η3-苄基钯中间体实现钯(0)催化的吲哚苄基化反应
作者: Zhao ZL(赵正乐)1; Gu Q(顾庆)1; Wu XY(伍新燕)1; You SL(游书力)1
通讯作者: 伍新燕 ; 游书力
刊名: Chin. J. Catal.
发表日期: 2015
DOI: 10.1016/S1872-2067(14)60191-1
卷: 36, 期:1, 页:15-18
收录类别: SCI
文章类型: 论文
英文摘要: An efficient method has been developed for the Pd(0)-catalyzed benzylation of indoles, which occurred with exclusive regioselectivity. When this reaction was performed in the presence of Pd(PPh3)(4), it provided access to a broad range of substituted indoles bearing diarylmethanes at their 3-position in 90%-99% yields under mild conditions. (C) 2015, Dalian Institute of Chemical Physics, Chinese Academy of Sciences. Published by Elsevier B.V. All rights reserved.
语种: 英语
相关网址: 查看原文
WOS记录号: WOS:000348274200004
Citation statistics:
内容类型: 期刊论文
URI标识: http://ir.sioc.ac.cn/handle/331003/39560
Appears in Collections:金属有机化学国家重点实验室_期刊论文

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作者单位: 1.华东理工大学
2.中科院上海有机化学研究所, 金属有机化学国家重点实验室

Recommended Citation:
Zhao ZL,Gu Q,Wu XY,et al. Pd(0)-catalyzed benzylation of indole through eta(3)-benzyl palladium intermediate[J]. Chin. J. Catal.,2015,36(1):15-18.
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