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research article
Palladium-catalyzed arylative ring-opening reactions of norbornenols: entry to highly substituted cyclohexenes, quinolines, and tetrahydroquinolines
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.
Type
research article
Authors
Publication date
2010
Publisher
Published in
Volume
49
Start page
4455
End page
4458
Note
CAPLUS AN 2010:758486(Journal)
Peer reviewed
REVIEWED
EPFL units
Available on Infoscience
August 17, 2011
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