Abstract
AbstractThe configuration of certain trifluoromethylated functional dienoates, aryldienoates and trienoates is presented by the measurement of their 13C NMR and 19F NMR chemical shifts, and their 3 J(C–F), 4J(H–F) and through‐space 5J(H–F) coupling constants. Copyright © 2002 John Wiley & Sons, Ltd.
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