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Volumn 33, Issue 24, 1992, Pages 3523-3526

An efficient construction of 1,2-trans-β-glycosidic linkages capitalizing on glycopyranosyl N,N,N′,N′-tetramethylphosphroamidates as shelf-stable glycosyl donors

Author keywords

[No Author keywords available]

Indexed keywords

GLUCOSIDE;

EID: 0026780175     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)92679-0     Document Type: Article
Times cited : (46)

References (43)
  • 11
    • 0000467493 scopus 로고
    • A convenient 2-deoxy-.ALPHA.-D-glucopyranosylation reaction using dimethylphosphinothioate method.
    • (1990) Chemistry Letters , pp. 849
    • Yamanoi1    Inazu2
  • 29
    • 84919187174 scopus 로고    scopus 로고
    • 4, and then [[Truncated]]
  • 30
    • 84919187173 scopus 로고    scopus 로고
    • Glucosylation of the primary alcohol 9 in propionitrile or dichloromethane gave the corresponding glucoside with the α:β ratios of 3.97 and 10:90, respectively.
  • 37
    • 84988126671 scopus 로고
    • Nitriles as Solvents in Glycosylation Reactions: Highly Selective β-Glycoside Synthesis1
    • (1990) Synlett , pp. 694
    • Schmidt1    Behrendt2    Toepfer3
  • 40
    • 84919187172 scopus 로고    scopus 로고
    • No reaction occurred at 23 °C in the absence of TMSOTf.
  • 43
    • 84919187171 scopus 로고    scopus 로고
    • We are grateful to Misses H. Ishido and F. Taki for spectroscopic measurements. Partial financial support to this research from the Japan Research Foundation for Optically Active Compounds, Kato Memorial Bioscience Foundation, and the Ministry of Education, Science and Culture of Japan is gratefully acknowledged.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.