| Autor: |
Herslöf, M., Gronowitz, S. |
| Zdroj: |
Journal of the American Oil Chemists' Society (JAOCS); Jun1985, Vol. 62 Issue 6, p1013-1015, 3p |
| Abstrakt: |
The enolate anions from isopropylidene protected monoacylglycerols have been successfully alkylated with alkyl iodides of various chain length. From these products the corresponding monoacylglycerols and triacylglycerols can be prepared. This is exemplified by the synthesis of 2-butyldodecanoyl-didodecanoyl glycerol, di-2-butyldodecanoyl-dodecanoyl glycerol and tri-2-butyldodecanoyl glycerol. [ABSTRACT FROM AUTHOR] |
| Databáze: |
Complementary Index |
| Externí odkaz: |
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