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Yolantinine

Reference work entry

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Taxonomy: Physicochemical and Pharmacological Properties of Alkaloids – Bisisoquinoline Alkaloids

Biological sources: Merendera jolantae

C38H44N2O5: 608.3250

IR: 3450, 1620, 1460, 890 [1]

MSm/z: 608(M+), 296, 192, 121 [1]

1H NMR: 1.00–4.00(18H, 8 × CH2, 2 × CH), 2.22, 2.33(each 3H, s, 2 × NCH3), 3.72, 3.74(each 3H, s, 2 × OCH3), 6.38–6.75(12H, H–Ar) [1]

13 C NMR: [ 1]

Table 1

=C

=CH–

N–CH–

N–CH2

N–CH3

OCH3

–CH2

155.1

129.3

62.7

47.8

42.1

56.1

36.4

149.2

129.3

62.0

47.4

41.7

55.9

36.4

146.0

124.4

       

31.3

146.0

119.3

       

31.0

144.6

118.3

       

25.4

144.4

116.6

       

24.5

134.1

115.7

         

132.8

115.7

         

130.0

115.7

         

129.7

113.6

         

128.7

112.6

         

124.4

111.2

         

References

  1. 1.
    A.M. Usmanov, M.K. Yusupov, Kh.A. Aslanov, Chem. Nat. Comp. 13, 360 (1977)Google Scholar

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© Springer Science+Business Media New York 2013

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