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Volumn 137, Issue 3, 2006, Pages 365-374

High-Yield Syntheses of Tetra-O-benzyl-α-D-glucopyranosyl bromide and Tetra-O-pivaloyl-α-D-glucopyranosyl bromide and their Advantage in the Koenigs-Knorr Reaction

Author keywords

Cholesteryl glycosides; Glycosidation; Koenigs Knorr reaction; Orthoester

Indexed keywords


EID: 33644780039     PISSN: 00269247     EISSN: None     Source Type: Journal    
DOI: 10.1007/s00706-005-0429-1     Document Type: Article
Times cited : (16)

References (44)
  • 4
    • 0006850084 scopus 로고
    • Glycosylation Methods in Oligosaccharide Synthesis
    • Ernst B, Leumann C (eds) Verlag Helvetica Chimica Acta
    • Barresi F, Hindsgaul O (1995) Glycosylation Methods in Oligosaccharide Synthesis. In: Ernst B, Leumann C (eds) Modern Synthetic Methods, ed 1, Verlag Helvetica Chimica Acta, p 283
    • (1995) Modern Synthetic Methods, Ed 1 , pp. 283
    • Barresi, F.1    Hindsgaul, O.2
  • 5
    • 33644765451 scopus 로고    scopus 로고
    • Carbohydrates
    • Harwood LM (ed) Academic Press
    • Osborn HMI (2003) Carbohydrates. In: Harwood LM (ed) Best Synthetic Methods, ed 1, Academic Press, p 69
    • (2003) Best Synthetic Methods, Ed 1 , pp. 69
    • Osborn, H.M.I.1
  • 17
    • 0003021993 scopus 로고
    • Acetobromoglucose
    • Horning EC (ed) John Wiley and Sons, Inc., New York
    • Redemann CE, Niemann C (1955) Acetobromoglucose. In: Horning EC (ed) Organic Syntheses Coll, vol. III John Wiley and Sons, Inc., New York, p 11
    • (1955) Organic Syntheses Coll , vol.3 , pp. 11
    • Redemann, C.E.1    Niemann, C.2
  • 22
    • 33644784362 scopus 로고    scopus 로고
    • note
    • This reagent is also commercially available at Sigma-Aldrich Company Ltd.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.