Abstract
The hydrophobation of rosmarinic acid with saturated aliphatic primary alcohols of various chain lengths (methanol to eicosanol) was achieved via an acid-catalyzed esterification in the presence of a highly acidic sulfonic resin. The resulting alkyl rosmarinates were isolated, characterized and their global free radical scavenging activity was determined by the 2,2-diphenyl-1-picrylhy- drazyl method in the stationary state. Only the dodecyl ester showed a stronger activity than rosmarinic acid. © 2010 AOCS.
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Lecomte, J., Giraldo, L. J. L., Laguerre, M., Baréa, B., & Villeneuve, P. (2010). Synthesis, characterization and free radical scavenging properties of rosmarinic acid fatty esters. JAOCS, Journal of the American Oil Chemists’ Society, 87(6), 615–620. https://doi.org/10.1007/s11746-010-1543-8
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