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35
H
35
O17 727.5374). UV–vis kmax 0.01% HCl–MeOH (nm) (loge):
2
(
84 (4.41), 311 (4.23), 534 (4.48); AlCl –MeOH: 289 (4.32), 311
3
4.31), 405 (3.80), 574 (4.57). For 1H and C NMR spectroscopic
13
1652–1659.
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C
35
H
35
O17 727.5374). UV–vis kmax 0.01% HCl–MeOH (nm) (loge):
2
(
84 (4.24), 312 (4.12), 531 (4.25); AlCl –MeOH: 290 (4.18), 313
3
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13
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topyranoside (4). HR ESI-MS m/z 743.5669 [M] (calc. for
C
35
H
35
O18 743.5323). UV–vis kmax 0.01% HCl–MeOH (nm) (loge):
7
9.
Mas, T., Susperregui, J., Berké, B., Chéze, C., Moreau, S., Nuhrich, A., Vercauteren, J.,
000. DNA triplex stabilization property of natural anthocyanins.
2
(
84 (4.32), 331 (4.18), 531 (4.40); AlCl –MeOH: 289 (4.12), 315
3
4.12), 355 (4.18), 567 (4.48). For 1H and C NMR spectroscopic
13
2
Phytochemistry 53, 679–687.
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Ming, T.L., 2000. cv. Queen of Dali. In: Ming, T.L. (Ed.), Monograph of the Genus
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ranoside (5). HR ESI-MS m/z 623.3951 [M] (calc. for C28
H
31
O
16
6
23.4412). UV–vis kmax 0.01% HCl–MeOH (nm) (loge): 283 (4.14),
35 (3.55), 381 (3.56), 531 (4.36); AlCl –MeOH: 287 (3.97), 312
38, 755–757.
3
3
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13
(
3.79), 403 (3.63), 572 (4.43). For 1H and C NMR spectroscopic
data, see Tables 1 and 2.
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Biochem. J. 25, 1687–1705.
A survey of anthocyanins. I.
Cyanidin 3-O-(2-O-b-xylopyranosyl-6-O-acetyl)-b-glucopyran-
+
oside (6). HR ESI-MS m/z 623.3868 [M] (calc. for C28
H
31
O
16
Saito, N., Yokoi, M., Yamaji, M., Honda, T., 1987. Cyanidin 3-p-coumaroylglucoside in
Camellia species and cultivars. Phytochemistry 26, 2761–2762.
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Camellia japonica ssp. rusticana (Honda) Kitamura and its occurrence in
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6
23.4412). UV–vis kmax 0.01% HCl–MeOH (nm) (loge): 283 (4.22),
36 (3.56), 382 (3.65), 531 (4.45); AlCl –MeOH: 286 (4.09), 313
3
3
13
(
3.89), 409 (3.71), 570 (4.52). For 1H and C NMR spectroscopic
82–88.
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Acknowledgments
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Silverstein, R.M., Webster, F.X. (Eds.), Spectrometric Identification of Organic
Compounds, sixth ed. John Wiley & Sons, Inc., New York, Chichester, Brisbane,
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tea (Benibana-cha), Camellia sinensis. Phytochemistry 56, 359–361.
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from berries of Fatsia japonica. Phytochemistry 31, 1446–1448.
Wang, L.-S., Hashimoto, F., Shiraishi, A., Aoki, N., Li, J.-J., Shimizu, K., Sakata, Y., 2001.
Phenetics in tree peony species from China by flower pigment cluster analysis. J.
Plant Res. 114, 213–221.
The authors are grateful to Prof. Li-Fang Xia of Kunming Insti-
tute of Botany at the Chinese Academy of Sciences, China, for
authenticating and certifying the typical phenotype of ‘Dalicha’
(C. reticulata), and thank Cong-Biao Xi of the Station of Forestry
of Chuxiong City, China, for helping to collect plant materials.
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