The synthesis of deuterium labelled, maturated, iscsneric fatty acids was required for a series of triplelabelled feeding experiments. The preparation of the cis and trans isamers of methyl 8-octadecenoate-17,18-d2, methyl 8-octadecmoate-13,13,14,14-dq, methyl 13-octadecenoate-17,18-d2 and methyl 13
Cis and Trans isomers of 4-hydroxy-8-sphingenine in plant cerebrosides
β Scribed by W.R. Morrison
- Publisher
- Elsevier Science
- Year
- 1973
- Tongue
- English
- Weight
- 144 KB
- Volume
- 11
- Category
- Article
- ISSN
- 0009-3084
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β¦ Synopsis
lhare cerebroside was isolated from hay and concentrate (extracted oilseed used for cattle feed), and the composition of the long-chain bases determined. The principal base was the cis isomer of 4-hydroxy-8-sphingenine (t 18:18c) which has not been reported before. The other trihydroxy bases were t 18 : 18t and t 18 : 0.
Allylic and non-allylic dihydroxy bases were found in concentrate cerebroside and identified as dl 8 : 14, dl 8 : 24, x, dl 8:0 and dl 8 : I x (x = 8?). Cis and trans isomers of mid-chain double bonds (position x) were tentatively identified, and the dihydroxy bases are probably identical to those recently found in wheat flour cerebroside [2J.
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