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Volumn 60, Issue 11, 1997, Pages 1082-1087

Isolation, synthesis, and antiplatelet aggregation activity of resveratrol 3-O-β-D-glucopyranoside and related compounds

Author keywords

[No Author keywords available]

Indexed keywords

GLUCOPYRANOSIDE; RESVERATROL;

EID: 0030656388     PISSN: 01633864     EISSN: None     Source Type: Journal    
DOI: 10.1021/np970069t     Document Type: Article
Times cited : (175)

References (31)
  • 18
    • 15644377997 scopus 로고    scopus 로고
    • note
    • 29,30 which a priori appeared to be the most straightforward glucosidation procedure, led to recovery of starting material (48%), accompanied by a mixture of the tetra-O-acetyl-3-β-O-glucopyranosides of (E)-3,5-dihydroxy-4′-acetoxystilbene, (E)-4′-acetoxy-5-[(tert-butyldimethylsilyl)oxy]-3-hydroxystilbene, and (E)-3,4′-dihydroxy-5-[(tert-butyldimethylsilyl)oxy]stilbene. Acetylation of the mixture gave the tetra-O-acetyl-3-O-β-D-glucopyranoside of 4′,5-diacetoxy-3-hydroxystilbene, identical in all respect to an authentic sample.
  • 21
    • 15644376410 scopus 로고    scopus 로고
    • note
    • 15
  • 22
    • 15644370743 scopus 로고    scopus 로고
    • note
    • 28
  • 27
    • 0007023172 scopus 로고
    • Hostettmann, K., Ed.; Academic Press: New York
    • Bertz, A.; Cazenave, J. P. Methods in Plant Biochemistry; Hostettmann, K., Ed.; Academic Press: New York, 1991; Vol. 6, pp 235-260.
    • (1991) Methods in Plant Biochemistry , vol.6 , pp. 235-260
    • Bertz, A.1    Cazenave, J.P.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.