Advertisement

(+) - α-Hydrastine

Reference work entry

Open image in new window

Taxonomy: Physicochemical and Pharmacological Properties of Alkaloids – Isoquinoline Alkaloids

Biological sources: Fumaria capreolata, F. parviflora, F. schleicheri, F. vaillantii

C21H21NO6: 383.1369

Mp: 158–159°C (MeOH) [1]

[α]D+128° (CHCl3) [1]

UV: 296 [1]

IR: 1760, 1610, 1505, 1035, 940 [1]

1H NMR: 2.56(3H, s, NCH3), 3.86, 3.99(each 3H, s, 2 × OCH3), 3.99, 5.54(each 1H, d, J = 3.5), 5.81(2H, q), 6.38, 6.66(each 1H, s, p–H–Ar), 7.04, 7.30(each 1H, d, J = 8, p–H–Ar) [2]

Abs. conf.: 1S, 9S [3]

References

  1. 1.
    I.A. Israilov, M.S. Yunusov, S.Yu. Yunusov, Chem. Nat. Comp. 4, 167 (1968)Google Scholar
  2. 2.
    K.L. Seitanidi, M.R. Yagudaev, I.A. Israilov, M.S. Yunusov, Chem. Nat. Comp. 14, 395 (1978)Google Scholar
  3. 3.
    G.P. Moiseeva, I.A. Israilov, M.S. Yunusov, S.Yu. Yunusov, Chem. Nat. Comp. 14, 82 (1978)Google Scholar

Copyright information

© Springer Science+Business Media New York 2013

Personalised recommendations