TY - JOUR
T1 - Chemical Constituents of Neolitsea parvigemma and Neolitsea konishii
AU - Chen, Keh Shaw
AU - Chang, Fang Rong
AU - Chia, Yi Chen
AU - Wu, Tian Shung
AU - Wu, Yang Chang
PY - 1998
Y1 - 1998
N2 - Twenty-four compounds including three flavonoids, kaempferol-3-O-rhamnoside (1), quercetin-3-O-rhamnoside (2), and taxifolin-3-O-rhamnoside (3); three ferulates, docosanylferulate (4), tetracosanylferulate (5), and hexacosanylferulate (6); two cyclohex-2-en-1-ones, blumenol A (7), and roseoside (8); two sesquiterpenes, zeylanidine (9), and zeylanicine (10); four triterpenes, lupeol (11), lupenone (12), taraxerol (13), and taraxerone (14); one steroid, β-sitosterol (15); one amide, N-trans-feruloylmethoxytyramine (16); eight alkaloids, roemerine (17), actinodaphnine (18), N-methylactinodaphnine (19), glaucine (20), and oxoglaucine (21), boldine (22), corydine (23) and methoxyannomontine (24) were isolated from Neolitsea parvigemma and N. konishii. These compounds were characterized and identified by physical and spectral evidence. Among them, compounds 1, 2, 3, 4, 5, 6, 7, 8, 13, 14, 16, 20, 21, 23, and 24, were isolated for the first time from this genus. This finding is useful as a basis for chemotaxonomy.
AB - Twenty-four compounds including three flavonoids, kaempferol-3-O-rhamnoside (1), quercetin-3-O-rhamnoside (2), and taxifolin-3-O-rhamnoside (3); three ferulates, docosanylferulate (4), tetracosanylferulate (5), and hexacosanylferulate (6); two cyclohex-2-en-1-ones, blumenol A (7), and roseoside (8); two sesquiterpenes, zeylanidine (9), and zeylanicine (10); four triterpenes, lupeol (11), lupenone (12), taraxerol (13), and taraxerone (14); one steroid, β-sitosterol (15); one amide, N-trans-feruloylmethoxytyramine (16); eight alkaloids, roemerine (17), actinodaphnine (18), N-methylactinodaphnine (19), glaucine (20), and oxoglaucine (21), boldine (22), corydine (23) and methoxyannomontine (24) were isolated from Neolitsea parvigemma and N. konishii. These compounds were characterized and identified by physical and spectral evidence. Among them, compounds 1, 2, 3, 4, 5, 6, 7, 8, 13, 14, 16, 20, 21, 23, and 24, were isolated for the first time from this genus. This finding is useful as a basis for chemotaxonomy.
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U2 - 10.1002/jccs.199800018
DO - 10.1002/jccs.199800018
M3 - Article
AN - SCOPUS:0001740259
SN - 0009-4536
VL - 45
SP - 103
EP - 110
JO - Journal of the Chinese Chemical Society
JF - Journal of the Chinese Chemical Society
IS - 1
ER -