Narcissus and Daffodil

Table 6.3 Continued
Alkaloid* Formula MW Spectroscopic data References
55 cantabricine C18H23NO4 317 IR, MS, 1 H NMR,
13
C NMR
Bastida et al., 1995b
10 caranine C16H17NO3 271 UV, IR, MS,
1
H NMR
Evidente et al., 1986
CD
Kuriyama et al., 1967
53 crinamine C17H19NO4 301 UV, 1 H NMR Likhitwitayawuid et al.,
1993
IR, MS, CD Viladomat et al., 1994
13
C NMR
Viladomat et al., 1996
X-Ray
Roques et al., 1977
59 criwelline C18H21NO5 331 UV
Hauth and Stauffacher,
1964
MS
Duffield et al., 1965
1 13
H NMR, C NMR Razafimbello et al., 1996
CD
De Angelis and Wildman,
1969a
36 dubiusine C23H27NO8 445 UV, IR, MS,
1 13
H NMR, C NMR
Bastida et al., 1988a
69 galanthamine C17H21NO3 287 UV, IR, MS,
1
H NMR
Bastida et al., 1987b
13
C NMR
Abdallah et al., 1989
CD
De Angelis and Wildman,
1969a
X-Ray
Peeters et al., 1997
71 O-acetylgalanthamine
C19H23NO4 329 UV, MS, 1 H NMR,
13
C NMR
Kreh et al., 1995b
70 epigalanthamine C17H21NO3 287 UV, MS
IR, 1 H NMR
Kametani et al., 1969
Vlahov et al., 1989
CD
De Angelis and Wildman,
1969a
72 norgalanthamine C16H19NO3 273 UV
IR, MS, 1 H NMR,
13
C NMR
Laiho and Fales, 1964
Bastida et al., 1990c
CD
Li et al., 1987
X-Ray
Roques and Lapasset,
1976
73 epinorgalanthamine C16H19NO3 273 IR, MS, 1 H NMR,
13
C NMR
Bastida et al., 1993
74 N-formylnorgalanthamine
C17H19NO4 301 UV, IR, MS,
1 13
H NMR, C NMR
Bastida et al., 1987b
7 galanthine C18H23NO4 317 UV
MS, 1 H NMR,
13
C NMR
Kobayashi et al., 1977
Bastida et al., 1990a
8 goleptine C17H21NO4 303 IR Döpke, 1964
49 haemanthamine C17H19NO4 301 UV, IR, MS
1
H NMR
Bastida et al., 1987b
Pabuççuoglu et al., 1989
13
C NMR, CD Baudouin et al., 1994
X-Ray
Watson et al., 1984
50 11-O-acetylhaemanthamine
C19H21NO5 343 IR, MS, 1 H NMR,
13
C NMR, CD
Labraña et al., 1999