메뉴 건너뛰기




Volumn 35, Issue 21, 1996, Pages 2510-2512

Orthogonal glycosylation strategy for rapid assembly of oligosaccharides on a polymer support

Author keywords

Glycoproteins; Glycosylations; Oligosaccharides; Solid phase syntheses

Indexed keywords


EID: 0030445494     PISSN: 05700833     EISSN: None     Source Type: Journal    
DOI: 10.1002/anie.199625101     Document Type: Article
Times cited : (128)

References (28)
  • 4
    • 0028886622 scopus 로고
    • S. P. Douglas, D. Whitfield, J. J. Krepinsky, J. Am. Chem. Soc. 1991, 113, 5095-5097; ibid. 1995, 117, 2116-2117.
    • (1995) J. Am. Chem. Soc. , vol.117 , pp. 2116-2117
  • 11
    • 0027467776 scopus 로고
    • For the use of an SE group in an SE glycoside as a hydrophobic aglycon in chemoenzymatic synthesis of ganglioside, see Y. Ito, J. C. Paulson, J. Am. Chem. Soc. 1993, 115, 1603-1604. A more hydrophobic aglycon similar to SE was reported recently: P. Stangier, M. M. Palcic, D. R. Bundle, Carbohydr. Res. 1995, 267, 153-159.
    • (1993) J. Am. Chem. Soc. , vol.115 , pp. 1603-1604
    • Ito, Y.1    Paulson, J.C.2
  • 12
    • 0028881538 scopus 로고
    • For the use of an SE group in an SE glycoside as a hydrophobic aglycon in chemoenzymatic synthesis of ganglioside, see Y. Ito, J. C. Paulson, J. Am. Chem. Soc. 1993, 115, 1603-1604. A more hydrophobic aglycon similar to SE was reported recently: P. Stangier, M. M. Palcic, D. R. Bundle, Carbohydr. Res. 1995, 267, 153-159.
    • (1995) Carbohydr. Res. , vol.267 , pp. 153-159
    • Stangier, P.1    Palcic, M.M.2    Bundle, D.R.3
  • 14
    • 85033009546 scopus 로고    scopus 로고
    • note
    • All PEG-supported products were isolated by precipitation from tert-butyl methyl ether as described [3], Yields were calculated based on mass balances and do not necessarily reflect the purity.
  • 15
    • 0001325832 scopus 로고
    • Y. Ito, T. Ogawa, Angew. Chem. 1994, 106, 1843-1845; Angew. Chem. Int. Ed. Engl. 1994, 33, 1765-1767.
    • (1994) Angew. Chem. , vol.106 , pp. 1843-1845
    • Ito, Y.1    Ogawa, T.2
  • 16
    • 26844498306 scopus 로고
    • Y. Ito, T. Ogawa, Angew. Chem. 1994, 106, 1843-1845; Angew. Chem. Int. Ed. Engl. 1994, 33, 1765-1767.
    • (1994) Angew. Chem. Int. Ed. Engl. , vol.33 , pp. 1765-1767
  • 18
    • 85033033320 scopus 로고    scopus 로고
    • 1H NMR spectrometer
    • 1H NMR spectrometer.
  • 19
    • 85033007378 scopus 로고    scopus 로고
    • note
    • 2; 2. NaOMe/ MeOH).
  • 21
    • 85033017144 scopus 로고    scopus 로고
    • note
    • 2).
  • 22
    • 85033020484 scopus 로고    scopus 로고
    • note
    • 2O/MeOH (1/1).
  • 25
    • 85033026793 scopus 로고    scopus 로고
    • note
    • 2 (α:β = 1.2:1).
  • 27
    • 46549104605 scopus 로고
    • K. Jansson, S. Ahlfors, T. Freid, J. Kihlberg, G. Magnusson, J. Org. Chem. 1988, 53, 5629-5647; T. Fukuyama, A. A. Laird, L. M. Hotchkiss, Tetrahedron Lett. 1985, 26, 6291-6292.
    • (1985) Tetrahedron Lett. , vol.26 , pp. 6291-6292
    • Fukuyama, T.1    Laird, A.A.2    Hotchkiss, L.M.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.