Results 51 to 60 of about 89 (80)
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Hydroboration-oxidation of ricinoleic acid derivatives
Russian Journal of Organic Chemistry, 2008The regioselectivity in the hydroboration-oxidation of ricinoleic acid derivatives only slightly depends on the configuration of the optically active center: the fraction of the resulting 1,3-diol is larger by 6–10% than that of the 1,4-isomer.
R. R. Muslukhov +5 more
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Ricinoleic Acid in Common Vegetable Oils and Oil Seeds
Lipids, 2008AbstractAn original gas chromatography/mass spectrometry method for quantifying trace amounts of ricinoleic acid (12‐hydroxy‐cis‐9‐octadecenoic acid) is detailed. Data are presented on trace amounts of ricinoleic acid found in several common vegetable oils and oils extracted from common oil seeds: e.g., ca. 30 ppm in commercial olive oil was the lowest
Kouhei, Yamamoto +2 more
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Synthesis and Bioactivity of (R)-Ricinoleic Acid Derivatives: A Review
Current Medicinal Chemistry, 2016(R)-Ricinoleic acid (RA) [(12R,9Z)-hydroxyoctadecenoic acid], the main compound of castor seed oil, because of its unusual structure readily undergoes multi-directional chemical and biochemical transformations to produce derivatives with the retained carbon skeleton or with its degradation.
Sylwia, Pabiś, Józef, Kula
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Ricinoleic acid: Current view of an ancient oil
The American Journal of Digestive Diseases, 1975T S, Gaginella, S F, Phillips
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Production of conjugated linoleic acids through KOH-catalyzed dehydration of ricinoleic acid
Chemistry and Physics of Lipids, 2002Lin Yang, Yu Huang, Zhen-Yu Chen
exaly