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Volumn 5, Issue 20, 2003, Pages 3627-3630

Synthesis of saponins using partially protected glycosyl donors

Author keywords

[No Author keywords available]

Indexed keywords

OLIGOSACCHARIDE; SAPONIN; SAPONIN DERIVATIVE;

EID: 0142011136     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol035353s     Document Type: Article
Times cited : (55)

References (32)
  • 1
    • 0027318961 scopus 로고
    • For reviews see: (a) Varki, A. Glycobiology 1993, 3, 97. (b) Lee, Y. C.; Lee, R. T. Acc. Chem. Res. 1995, 28, 321.
    • (1993) Glycobiology , vol.3 , pp. 97
    • Varki, A.1
  • 2
    • 0000358206 scopus 로고
    • For reviews see: (a) Varki, A. Glycobiology 1993, 3, 97. (b) Lee, Y. C.; Lee, R. T. Acc. Chem. Res. 1995, 28, 321.
    • (1995) Acc. Chem. Res. , vol.28 , pp. 321
    • Lee, Y.C.1    Lee, R.T.2
  • 3
  • 17
    • 5244279498 scopus 로고
    • For reviews, see: (a) Toshima, K.; Tasuta, K. Chem. Rev. 1993, 93, 1503. (b) Schmidt, R. R.; Kinzy, W. Adv. Carbohydr. Chem. Biochem. 1994, 50, 21. (c) Garegg, P. J. Adv. Carbohydr. Chem. Biochem. 1997, 52, 179.
    • (1993) Chem. Rev. , vol.93 , pp. 1503
    • Toshima, K.1    Tasuta, K.2
  • 18
    • 0028186224 scopus 로고
    • For reviews, see: (a) Toshima, K.; Tasuta, K. Chem. Rev. 1993, 93, 1503. (b) Schmidt, R. R.; Kinzy, W. Adv. Carbohydr. Chem. Biochem. 1994, 50, 21. (c) Garegg, P. J. Adv. Carbohydr. Chem. Biochem. 1997, 52, 179.
    • (1994) Adv. Carbohydr. Chem. Biochem. , vol.50 , pp. 21
    • Schmidt, R.R.1    Kinzy, W.2
  • 19
    • 37849189010 scopus 로고    scopus 로고
    • For reviews, see: (a) Toshima, K.; Tasuta, K. Chem. Rev. 1993, 93, 1503. (b) Schmidt, R. R.; Kinzy, W. Adv. Carbohydr. Chem. Biochem. 1994, 50, 21. (c) Garegg, P. J. Adv. Carbohydr. Chem. Biochem. 1997, 52, 179.
    • (1997) Adv. Carbohydr. Chem. Biochem. , vol.52 , pp. 179
    • Garegg, P.J.1
  • 28
    • 0142068766 scopus 로고    scopus 로고
    • note
    • 3N and concentrated to dryness. The residue was subjected to column chromatography on silica gel with petroleum ether/EtOAc (6/1-3/1) as the eluent to give the desired product.


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