1974
DOI: 10.1002/mrc.1270060108
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Phosphates d'énols: XI—Etude des constantes de couplage 3J(POCH) et 4J(POCCH)

Abstract: Abstract-NMR studies on E and 2 enolic phosphates with no substituent on carbon 1 provided evidence for the existence of planar and gauche conformations. When no bulky substituents are present in the cisoid position of the phosphates two planar and twogauche forms are possible. The most stable conformation is the planar form having the phosphate group trans to the double bond. With a bulky substituent in the cisold position of the phosphates the planar form with the group cis to the double bond could not be ob… Show more

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Cited by 4 publications
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