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  4. Synthesis of Indoles by Copper-Catalyzed Heteroannulation of o-Aminophenylboronic Acid Pinacol Esters with β-Keto Esters
 
research article

Synthesis of Indoles by Copper-Catalyzed Heteroannulation of o-Aminophenylboronic Acid Pinacol Esters with β-Keto Esters

Bunescu, Ala  
•
Wang, Qian  
•
Zhu, Jieping  
2012
Synthesis: Journal of Synthetic Organic Chemistry

Copper-catalyzed coupling of ortho-aminophenylboronic acid pinacol esters with β-ketoesters afforded, under mild base-free oxidative conditions, 2,3-disubstituted indoles featuring a key Chan-Lam type carbon-carbon bond forming reaction.

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Type
research article
DOI
10.1055/s-0032-1316813
Web of Science ID

WOS:000312003800012

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

2012

Publisher

Georg Thieme Verlag

Published in
Synthesis: Journal of Synthetic Organic Chemistry
Volume

44

Issue

24

Start page

3811

End page

3814

Subjects

Indole

•

Chan-Lam reaction

•

ortho-aminophenylboronic ester

•

β-ketoester

•

Copper

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LSPN  
Available on Infoscience
December 9, 2012
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/87336
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