ABSTRACT
The conformation of some pentaoxacyclopentadecanediones «ere investigated by 'H-'3C NMR and conformations were found as regular anti, gouch, anti (a, g+ ,a) units. However the role of a side group was observed that the rate of interconvertion was strongly influenced so that the polyoxa-lactone ring could excist as diastereomere of in equilibrium.
Primary Language | English |
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Subjects | Chemical Engineering |
Journal Section | Research Article |
Authors | |
Publication Date | January 1, 1980 |
Published in Issue | Year 1980 Volume: 26 |
Communications Faculty of Sciences University of Ankara Series B Chemistry and Chemical Engineering
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