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Pd(0)-catalyzed benzylation of indole through eta(3)-benzyl palladium intermediate
Alternative Title经历η3-苄基钯中间体实现钯(0)催化的吲哚苄基化反应
Zhao ZL(赵正乐)1; Gu Q(顾庆)1; Wu XY(伍新燕)1; You SL(游书力)1
Source PublicationChin. J. Catal.
AbstractAn 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.
Subject Area金属有机化学
Indexed BySCI
WOS IDWOS:000348274200004
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Document Type期刊论文
Corresponding AuthorWu XY(伍新燕); You SL(游书力)
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
GB/T 7714
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.
APA 赵正乐,顾庆,伍新燕,&游书力.(2015).Pd(0)-catalyzed benzylation of indole through eta(3)-benzyl palladium intermediate.Chin. J. Catal.,36(1),15-18.
MLA 赵正乐,et al."Pd(0)-catalyzed benzylation of indole through eta(3)-benzyl palladium intermediate".Chin. J. Catal. 36.1(2015):15-18.
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