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17 O NMR spectroscopy of 1‐(2‐hydroxyphenyl)‐3‐ naphthylpropane‐1,3‐diones. Influences of keto–enol tautomerism and substituents †
Author(s) -
Jios Jorge L.,
Duddeck Helmut
Publication year - 2000
Publication title -
magnetic resonance in chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.483
H-Index - 72
eISSN - 1097-458X
pISSN - 0749-1581
DOI - 10.1002/1097-458x(200007)38:7<512::aid-mrc664>3.0.co;2-z
Subject(s) - tautomer , chemistry , substituent , keto–enol tautomerism , enol , nuclear magnetic resonance spectroscopy , spectroscopy , computational chemistry , stereochemistry , medicinal chemistry , organic chemistry , catalysis , physics , quantum mechanics
The 17 O NMR data of 10 of the title compounds were assigned and interpreted in terms of keto–enol tautomerism, substituent effects and mesomeric structures. Copyright © 2000 John Wiley & Sons, Ltd.