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Spectroscopy / Proton NMR / Keto-enol tautomerism / Ketone / Solvent effects / Chemical shift / Nuclear magnetic resonance spectroscopy / Carbonyl / Enol / Chemistry / Nuclear magnetic resonance / Functional groups


MAGNETIC RESONANCE IN CHEMISTRY Magn. Reson. Chem. 2003; 41: 26–36 Published online in Wiley InterScience (www.interscience.wiley.com). DOI: [removed]mrc[removed]
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Document Date: 2012-01-10 04:05:11


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Rochester / Monroe / Liverpool / Oxford / Silbersteifen / Pittsburgh / Santiago / London / /

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Pergamon Press / John Wiley & Sons Ltd. / GE / INTRODUCTION / GlaxoSmithKline / SCS / Serena Software / Eqn / Baboul AG / Eastman Kodak / /

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Germany / /

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Facility

University of Liverpool / /

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chloroform solution / methoxy / minimum energy / proton chemical shifts / free energy difference / chemical shift / proton chemical shift / chemical shift calculations / chemical shift tensors / observed chemical shifts / chemical grounds / non-symmetric / energy difference / chemical shift value / energy / routine gives proton chemical shifts / polarizable systems / hydroxy / carbonyl substituent chemical shifts / chemical effects / chemical shifts / chemical shielding tensor / conformer energy difference / pharmaceutical investigations / symmetrical energy profile / energy profile / low-field chemical shift / aromatic carbonyl / chemical shift data / carbonyl / aromatic and aliphatic systems / /

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MestRe-C. Universidad / University of Liverpool / Chemistry Department / Medicinal Research Centre / /

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Reid M. J. Chem / M. H. Abraham / J. Chem / Williamson / Raymond J. Abraham / /

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Schlegel HB / MP / chair / MP / Asakura T. J. Magn / D. J. / /

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C / /

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D C / New York / Pennsylvania / /

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spectroscopy / /

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www.interscience.wiley.com / /

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