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
This work is licensed under a Creative Commons Attribution 4.0 International License.