Isolation and absolute structures of enantiomeric 1,2-bis(4-hydroxy-3- methoxyphenyl)-1,3-propanediol 1-O-glucosides from the bark of Hovenia trichocarpa

Journal of Natural Products

Volumn 61, Issue 9, 1998, Pages 1137-1139

  Yoshikawa, Kazuko ^a   Mimura, Noriko ^a   Arihara, Shigenobu ^a  

^a TOKUSHIMA BUNRI UNIVERSITY   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

1,2 BIS(4 HYDROXY 3 METHOXYPHENYL) 1,3 PROPANEDIOL 1 O GLUCOSIDE; GLUCOSIDE; HOVETRICHOSIDE A; HOVETRICHOSIDE B; PLANT EXTRACT; UNCLASSIFIED DRUG;

ARTICLE; CARBON NUCLEAR MAGNETIC RESONANCE; DRUG ISOLATION; DRUG STRUCTURE; ENANTIOMER; HERBAL MEDICINE; JAPAN; NONHUMAN; REVERSED PHASE HIGH PERFORMANCE LIQUID CHROMATOGRAPHY; TREE;

GLUCOSIDES; HYDROLYSIS; MAGNETIC RESONANCE SPECTROSCOPY; MASS SPECTROMETRY; SPECTROPHOTOMETRY, ULTRAVIOLET; SPECTROSCOPY, FOURIER TRANSFORM INFRARED; STEREOISOMERISM; TREES;

HOVENIA; HOVENIA TRICHOCARPA;

EID: 0031694648     PISSN: 01633864     EISSN: None     Source Type: Journal    
DOI: 10.1021/np980003d     Document Type: Article

References (10)

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9. 5), erythro isomer: δ 74.9 (C-1), 64.7 (C-2), 57.0 (C-2), 5.73 (1H, d, J = 5.5 Hz), threo isomer: δ 78.0 (C-1), 66.0 (C-2), 56.3 (C-2), 5.61 (1H, d, J = 8.0 Hz).
10. Seo, S.; Tomita, Y.; Tori, K.; Yoshimura, Y. J. Am. Chem. Soc. 1978, 100, 3331-3339.