Conformation of the 1, 4, 7, 10-tetraoxocyclododeca-2, 3-dion was analysed by NMR and found out that the “gouch” from of a-diester carbonyls arrange the methylene groups as the “go«ch, gouch, anti” (g+ , gi, a) unitsin equilibrium of pseudorotermers so that o^ygens are in non corner positions of “sguare” conformation.
| Primary Language | English |
|---|---|
| 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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