Narcissus and Daffodil

Table 6.3 Continued
Alkaloid* Formula MW Spectroscopic data References
32 O-methyllycorenine C19H25NO4 331 IR, MS, 1 H NMR,
13
C NMR
X-Ray
1 lycorine C16H17NO4 287 UV, IR, MS,
1 13
H NMR, C NMR
13
C NMR
CD
X-Ray
61 3-epimacronine C18H19NO5 329 IR, MS, 13 C NMR
1
H NMR
CD
X-Ray
40 maritidine C17H21NO3 287 UV
IR
MS, 1 H NMR
1 13
H NMR, C NMR
CD
Codina et al., 1993
Labraña et al., 1999
Likhitwitayawuid et al.,
1993
Spohn et al., 1994
Wagner et al., 1996
Gopalakrishna et al., 1976
Viladomat et al., 1990
Kihara et al., 1987
Wagner et al., 1996
X-Ray
Linden et al., 1998
Hung et al., 1981
Tomioka et al., 1977
Ghosal et al., 1985a
Youssef and Frahm, 1998
De Angelis and Wildman,
1969b
Zabel et al., 1979
41 8-O-demethylmaritidine
C16H19NO3 273 IR, MS
1
H NMR
Kihara et al., 1987
Pabuççuoglu et al., 1989
13
C NMR
Bastida et al., 1994
42 9-O-demethylmaritidine
C16H19NO3 273 IR, MS, 1 H NMR Bastida et al., 1988c
43 O-methylmaritidine C18H23NO3 301 UV, IR, MS,
1 13
H NMR, C NMR
Suau et al., 1990a
CD
Ma et al., 1986
47 6α-hydroxy-3-Omethylepimaritidine
C18H23NO4 317 UV, IR, MS,
1
H NMR, CD
Ma et al., 1986
48 6β-hydroxy-3-Omethylepimaritidine
C18H23NO4 317 UV, IR, MS,
1
H NMR, CD
Ma et al., 1986
27 masonine C17H17NO4 299 UV, IR, MS,
1 13
H NMR, C NMR
Kreh and Matusch, 1995
CD
Jeffs et al., 1985
28 normasonine C16H15NO4 285 UV, IR, MS,
1 13
H NMR, C NMR
Kreh and Matusch, 1995
82 mesembrenone C17H21NO3 287 IR, MS, 1 H NMR
13
C NMR
Bastida et al., 1989
Jeffs et al., 1974
63 narciclasine C14H13NO7 307 UV, IR
MS, 1 H NMR,
13
C NMR
Piozzi et al., 1968
Evidente, 1991
X-Ray
Bi et al., 1998
54 narcidine C17H21NO4 303 UV, IR, MS,
1
H NMR
Tojo, 1991
56 narcimarkine C21H27NO5 373 IR, MS Döpke and Sewerin,
1981
64 narciprimine C14H9NO5 271 UV, IR, 1 H NMR
MS
Piozzi et al., 1968
Spenglers and Trimiño,
1989