Narcissus and Daffodil

Table 6.3 Continued
Alkaloid* Formula MW Spectroscopic data References
75 narcisine C18H21NO4 315 UV, IR, MS,
1 13
H NMR, C NMR
16 narcissidine C18H23NO5 333 UV
IR, X-Ray
MS
1
H NMR
X-Ray
Abdallah, 1993
Fales and Wildman, 1958
Clardy et al., 1970
Kinstle et al., 1966
Kihara et al., 1995
Immirzi and Fuganti,
1971
17 nartazine C 20H 23NO 6 373 IR Boit and Döpke, 1956
76 narwedine C 17H 19NO 3 285 UV
IR, MS, 1 H NMR
80 O-methylnorbelladine
C 16H 19NO 3 273 IR, MS, 1 H NMR,
13 C NMR
62 obesine C16H17NO4 287 MS, 1 H NMR,
13
C NMR
33 oduline C17H19NO4 301 UV, IR, MS,
1 13
H NMR, C NMR
34 6-O-methyloduline C18H21NO4 315 UV, IR, MS,
1 13
H NMR, C NMR
35 2α-hydroxy-6-Omethyloduline
C 18H 21NO 5 331 IR, MS, 1 H NMR,
13 C NMR
81 pallidiflorine C34H40N2O7 588 IR, MS, 1 H NMR,
13
C NMR
68 pancracine C16H17NO4 287 UV, MS,
1 13
H, C NMR, CD
44 papyramine C18H23NO4 317 UV
IR, MS, 1 H NMR,
13
C NMR
45 6-epipapyramine C18H23NO4 317 UV
IR, MS, 1 H NMR,
13
C NMR
46 O-methyl-6epipapyramine
C 19 H 25 NO 4 331 UV, IR, MS,
1 H NMR, 13 C NMR
11 pluviine C 17 H 21 NO 3 287 UV
IR
13 9-O-demethylpluviine
14 1-O-acetyl-9-Odemethylpluviine
15 1,9-O-diacetyl-9-Odemethylpluviine
C 16 H 19 NO 3 273 UV, MS, 1 H NMR,
13 C NMR
C 18H 21NO 4 315 UV, MS, 1 H NMR,
13 C NMR
C 20H 23NO 5 357 UV, MS, 1 H NMR,
13 C NMR
12 norpluviine C 16H 19NO 3 273 UV
IR
Kametani et al., 1969
Li et al., 1987
Machocho et al., 1999
Viladomat et al., 1992
Kreh and Matusch, 1995
Kreh and Matusch, 1995
Almanza et al., 1996
Codina et al., 1990
Ali et al., 1984
Suau et al., 1990a
Bastida et al., 1990a
Suau et al., 1990a
Bastida et al., 1990a
Suau et al., 1990a
Kirby and Tiwari, 1966
Boit et al., 1957a
Kreh et al., 1995b
Kreh et al., 1995b
Kreh et al., 1995b
Kirby and Tiwari, 1966
Sandberg and Michel,
1968
2 poetaminine C 18H 19NO 5 329 UV, IR Döpke and Dalmer,
1965b