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Volumn 8, Issue 22, 2010, Pages 5126-5132

Novel dialkoxytriazine-type glycosyl donors for cellulase-catalysed lactosylation

Author keywords

[No Author keywords available]

Indexed keywords

GLUCANASE; GLYCOSYL ACCEPTORS; GLYCOSYL DONORS; HYDROXY GROUPS; LABORATORY SCALE; TRANSGLYCOSYLATION; TRIAZINE DERIVATIVES; TRICHODERMA REESEI;

EID: 78049332874     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/c0ob00190b     Document Type: Article
Times cited : (30)

References (40)
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    • O. Blixt and N. Razi, in Glycoscience, 2nd edn, ed., B. O. F. Reid, K. Tatsuta, and, J. Thiem, Springer-Verlag, Berlin, Heiderberg, New York, 2008, Vol. 2, pp. 1361-1385
    • (2008) Glycoscience, 2nd Edn , vol.2 , pp. 1361-1385
    • Blixt, O.1    Razi, N.2
  • 8
    • 0001423011 scopus 로고    scopus 로고
    • ed. S. H. Khan and R. A. O'Neill, Harwood Academic Publishers
    • K. G. I. Nilsson, in Modern Methods in Carbohydrate Synthesis, ed., S. H. Khan, and, R. A. O'Neill, Harwood Academic Publishers, 1996, pp. 518-547
    • (1996) Modern Methods in Carbohydrate Synthesis , pp. 518-547
    • Nilsson, K.G.I.1
  • 9
    • 84961309849 scopus 로고    scopus 로고
    • ed. B. Ernst, G. W. Hart and P. Sinaÿ, Wiley-VCH, Weinheim
    • D. J. Vocadlo and S. G. Withers, in Carbohydrates in Chemistry and Biology, ed., B. Ernst, G. W. Hart, and, P. Sinaÿ, Wiley-VCH, Weinheim, 2000, Vol 2, pp. 723-844
    • (2000) Carbohydrates in Chemistry and Biology , vol.2 , pp. 723-844
    • Vocadlo, D.J.1    Withers, S.G.2
  • 10
    • 1442315217 scopus 로고    scopus 로고
    • B. O. Fraser-Reid, K. Tatsuta and J. Thiem, Springer-Verlag, Berlin, Heidelberg, New York
    • S. Shoda, in Glycoscience, ed., B. O. Fraser-Reid, K. Tatsuta, and, J. Thiem, Springer-Verlag, Berlin, Heidelberg, New York, 2001, Vol. II, pp. 1465-1496
    • (2001) Glycoscience , vol.2 , pp. 1465-1496
    • Shoda, S.1
  • 12
    • 64249123668 scopus 로고    scopus 로고
    • ed. B. O. Fraser-Reid, K. Tatsuta and J. Thiem Springer-Verlag, Berlin, Heidelberg, New York
    • J. Thiem, in Glycoscience, ed., B. O. Fraser-Reid, K. Tatsuta, and J. Thiem, Springer-Verlag, Berlin, Heidelberg, New York, 2008, Vol. II, pp. 1387-1409
    • (2008) Glycoscience , vol.2 , pp. 1387-1409
    • Thiem, J.1
  • 35
    • 78049321357 scopus 로고    scopus 로고
    • Use of other bases, 2,6-lutidine or triethylamine, resulted in a decrease of the yield
    • Use of other bases, 2,6-lutidine or triethylamine, resulted in a decrease of the yield.
  • 38
    • 78049330509 scopus 로고    scopus 로고
    • Phenyl thio-α-cellobioside 4 was found to be the best acceptor for an EGIII-catalysed lactosylation reaction using β-lactosyl fluoride as a glycosyl donor in comparison with α-glucoside, β-glucoside, and β-cellobioside, which will be reported elsewhere
    • Phenyl thio-α-cellobioside 4 was found to be the best acceptor for an EGIII-catalysed lactosylation reaction using β-lactosyl fluoride as a glycosyl donor in comparison with α-glucoside, β-glucoside, and β-cellobioside, which will be reported elsewhere.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.