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Tetrahedron Letters
Volumn 31, Issue 31, 1990, Pages 4421-4424
Synthesis of tigogenyl β-O-cellobioside heptaacetate and glycoside tetraacetate via Schmidt's trichloroacetimidate method; some new observatons.
Author keywords

[No Author keywords available]
Indexed keywords

TIGOGENYL BETA O CELLOBIOSIDE; UNCLASSIFIED DRUG;
EID: 0025375498     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)97637-8     Document Type: Article
Times cited : (113)
References (17)
  • 2
    • 84910784027 scopus 로고    scopus 로고
    • Malinow M.R., U.S. Patent 4,602,003, 1986
  • 8
    • 84910796831 scopus 로고    scopus 로고
    • 3: C, 43.06; H, 4.65; N, 1.79. Found: C, 43.02; H, 4.49; N, 1.81.
  • 9
    • 84910760461 scopus 로고    scopus 로고
    • 3, 300 MHz) δ 8.65 (s,1), 6.46 (d,1),5.59 (dd,1), 5.39(m, 2), 5.05 (t,1), 5.00 (dd, 1), 4.87 (dd,1), 4.49 (d,1), 4.20 (m, 3), 4.06 (m, 2), 3.92 (m,1), 2.15–1.95 (6s, 21). Both of these were one spot by tlc in several solvent systems.
  • 13
    • 0015456567 scopus 로고
    • These authors studied the reaction of tigogenin and α-bromo glucosyl tetraacetate under the influence of a variety of silver carboxylate salts.
    • (1972) Chem. Ber. , vol.105 , pp. 1097
    • Wulff1    Röhle2    Krüger3
  • 15
    • 84910811857 scopus 로고    scopus 로고
    • 1
  • 17
    • 84910772995 scopus 로고    scopus 로고
    • 20: C, 61.49; H, 7.60. Found: C, 61.14; H, 7.54.

* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.