Journal of Chemistry / 2017 / Article / Tab 5 / Research Article
Volatile Composition and Enantioselective Analysis of Chiral Terpenoids of Nine Fruit and Vegetable Fibres Resulting from Juice Industry By-Products Table 5 Chiral markers, calculated LRI, and corresponding enantiomeric ratios for orange and tangerine fibres.
Chiral marker Configuration3 LRI Orange flesh Tangerine flesh Orange peel Tangerine peel Literature data [19 ] α -Pinene2 S 929 7.6–17.8 13.4 11.7 14.5 9.9–0.6 R 936 92.4–82.2 86.6 88.3 85.5 90.1–99.4 Camphene2 S 949 29.2 25.4 R 964 70.8 74.6 β -Pinene2 R 975 6.5–12.6 6.1 46.2 49.3 10.6–70.2 S 978 93.5–87.4 93.9 53.8 50.7 89.4–29.8 Limonene1 S 1056 0.6–0.8 0.6 0.5 0.6 0.0–1.1 R 1072 99.4–99.2 99.4 99.5 99.4 100–98.9 Linalool1 R 1175 9.7–20.4 16.4 8.1 11.3 2.2–17.9 S 1190 90.3–79.6 83.6 91.9 88.7 97.8–82.1 Terpinen-4-ol2 S 1319 42.9–51.1 28.9 55.7 57.8 65.3–71.5 R 1327 57.1–49.9 71.1 44.3 42.1 34.7–28.5 α -Terpineol1 R 1296 30.6–42.1 41.5 22.7 48.3 5.1–15.7 S 1309 69.4–57.9 58.5 77.3 51.7 94.9–84.3 Carvone2 R 1346 32.2–41.3 34.9 30.3 26.5 40.7 S 1352 67.8–58.7 65.1 69.7 73.5 59.3 α -Terpinyl acetate2 X 1378 21.0 73.5 Y 1381 79.2 26.5
and enantiomeric ratios calculated using diEt-CD column.2 LRI and enantiomeric ratios calculated using Pentyl-CD column. and were used to indicate that the absolute configuration of the enantiomers could not be determined.