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Conformation of 1,4, 7,10-tetraoxacyclododeca-2,3-dion by nmr.

Year 1980, Volume: 26 , 0 - 0, 01.01.1980
https://doi.org/10.1501/Commub_0000000167
https://izlik.org/JA25SM85YF

Abstract

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.

References

  • Communications Faculty of Sciences University of Ankara Series B Chemistry and Chemical Engineering

Year 1980, Volume: 26 , 0 - 0, 01.01.1980
https://doi.org/10.1501/Commub_0000000167
https://izlik.org/JA25SM85YF

Abstract

References

  • Communications Faculty of Sciences University of Ankara Series B Chemistry and Chemical Engineering
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Details

Primary Language English
Subjects Chemical Engineering
Journal Section Research Article
Authors

Çakıl Erk This is me

Publication Date January 1, 1980
DOI https://doi.org/10.1501/Commub_0000000167
IZ https://izlik.org/JA25SM85YF
Published in Issue Year 1980 Volume: 26

Cite

Vancouver 1.Erk Ç. Conformation of 1,4, 7,10-tetraoxacyclododeca-2,3-dion by nmr. Commun. Fac. Sci. Univ. Ank. Ser. B [Internet]. 1980 Jan. 1;26. Available from: https://izlik.org/JA25SM85YF

Communications Faculty of Sciences University of Ankara Series B Chemistry and Chemical Engineering

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