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Configuration of functional trifluoromethylated dienoates, aryldienoates and trienoates
Author(s) -
Palmas P.,
Thibonnet J.,
Parrain J.L.,
Abarbri M.,
DavidQuillot F.,
Duchêne A.
Publication year - 2002
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/mrc.1040
Subject(s) - chemistry , coupling constant , computational chemistry , stereochemistry , particle physics , physics
The configuration of certain trifluoromethylated functional dienoates, aryldienoates and trienoates is presented by the measurement of their 13 C NMR and 19 F NMR chemical shifts, and their 3 J (C–F), 4 J (H–F) and through‐space 5 J (H–F) coupling constants. Copyright © 2002 John Wiley & Sons, Ltd.
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