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  4. Pd-Catalyzed Dehydrogenative Aryl−Aryl Bond Formation via Double C(sp2)−H Bond Activation: Efficient Synthesis of [3,4]-Fused Oxindoles
 
research article

Pd-Catalyzed Dehydrogenative Aryl−Aryl Bond Formation via Double C(sp2)−H Bond Activation: Efficient Synthesis of [3,4]-Fused Oxindoles

Bunescu, Ala  
•
Piou, Tiffany
•
Wang, Qian  
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2015
Organic Letters

A Pd(0)-catalyzed double cyclization of easily available o-bromoanilides leading to strained [3,4]-fused oxindoles was developed. The reaction proceeded through a highly ordered sequence involving key carbopalladation, 1,4-Pd migration, and C(sp2)−H functionalization steps.

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Type
research article
DOI
10.1021/ol503442n
Web of Science ID

WOS:000348331800042

Author(s)
Bunescu, Ala  
Piou, Tiffany
Wang, Qian  
Zhu, Jieping  
Date Issued

2015

Published in
Organic Letters
Volume

17

Issue

2

Start page

334

End page

337

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LSPN  
Available on Infoscience
January 17, 2015
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/110359
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