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  4. Palladium-catalyzed arylative ring-opening reactions of norbornenols: entry to highly substituted cyclohexenes, quinolines, and tetrahydroquinolines
 
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research article

Palladium-catalyzed arylative ring-opening reactions of norbornenols: entry to highly substituted cyclohexenes, quinolines, and tetrahydroquinolines

Waibel, Michael
•
Cramer, Nicolai  
2010
Angewandte Chemie International Edition

Palladium-catalyzed stereoselective arylative ring-opening reaction of norbornenol derivs. was studied. In presence of aryl bromides, corresponding cyclohexene derivs. were obtained in good yields. Meanwhile, reaction with bromoanilines yielded quinolines and tetrahydroquinolines. The asym. version of this reaction was explored by using chiral ligand.

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Type
research article
DOI
10.1002/anie.201001752
Author(s)
Waibel, Michael
•
Cramer, Nicolai  
Date Issued

2010

Publisher

Wiley-VCH Verlag GmbH

Published in
Angewandte Chemie International Edition
Volume

49

Start page

4455

End page

4458

Subjects

substituted cyclohexene stereoselective prepn

•

quinoline stereoselective prepn

•

norbornenol aryl bromide arylative ring opening palladium

•

bromoanilne norbornenol arylative ring opening palladium

Note

CAPLUS AN 2010:758486(Journal)

Peer reviewed

REVIEWED

Written at

OTHER

EPFL units
LCSA  
Available on Infoscience
August 17, 2011
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/70133
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