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  4. The tautomeric persistence of electronically and sterically biased 2-quinolinones
 
research article

The tautomeric persistence of electronically and sterically biased 2-quinolinones

Volle, Jean-Noel
•
Mavers, Ursula
•
Schlosser, Manfred  
2008
European Journal Of Organic Chemistry

One dozen of tailormade model 3-fluoro-2(1H)-quinolinones were synthesized, in order to be investigated by UV-, IR- and NMR spectroscopic techniques. All of these compounds were found to exist predominantly, if not exclusively, in the lactam (carboxamide, 1,2-dihydro-2-oxoquinoline) form. No tautomeric lactim (iminol, azaphenol) structure was detected. ((C) Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008).

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Type
research article
DOI
10.1002/ejoc.200800123
Web of Science ID

WOS:000256233400010

Author(s)
Volle, Jean-Noel
Mavers, Ursula
Schlosser, Manfred  
Date Issued

2008

Published in
European Journal Of Organic Chemistry
Start page

2430

End page

2438

Subjects

acidity constants

•

amide-hydroxyimine tautomerism

•

3-fluoro-2(1H)-quinolinones

•

keto-enol tautomerism

•

Knorr-Effenberger cyclizations

•

Nuclear-Magnetic-Resonance

•

Keto-Enol-Tautomerism

•

Heteroaromatic Hydroxy-Compounds

•

Multiwavelength Spectrophotometric Determination

•

Acid Dissociation-Constants

•

Gas-Phase

•

Prototropic Tautomerism

•

Heterocyclic-Compounds

•

Equilibrium-Constants

•

Ionization Constants

Editorial or Peer reviewed

REVIEWED

Written at

EPFL

EPFL units
LSCO  
Available on Infoscience
November 30, 2010
Use this identifier to reference this record
https://infoscience.epfl.ch/handle/20.500.14299/61348
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