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Volumn 10, Issue 3, 2006, Pages 484-486

A concise, efficient and production-scale synthesis of a protected L-lyxonolactone derivative: An important aldonolactone core

Author keywords

[No Author keywords available]

Indexed keywords


EID: 33745738179     PISSN: 10836160     EISSN: None     Source Type: Journal    
DOI: 10.1021/op050222n     Document Type: Article
Times cited : (45)

References (19)
  • 5
    • 33745748666 scopus 로고    scopus 로고
    • Reaction on C: Oxidation, reduction and deoxygenation at the anomeric position
    • Fraser-Reid, B., Tatsuta, K., Thiem, J., Eds.; Springer: Heidelberg
    • Lundt, I. Reaction on C: Oxidation, Reduction and Deoxygenation at the Anomeric Position. In Glycoscience: Chemistry and Chemical Biology; Fraser-Reid, B., Tatsuta, K., Thiem, J., Eds.; Springer: Heidelberg, 2000.
    • (2000) Glycoscience: Chemistry and Chemical Biology
    • Lundt, I.1
  • 6
    • 0342771175 scopus 로고    scopus 로고
    • Iminosugars as powerful glycosidase inhibitors-synthetic approaches from aldonolactones
    • Stütz, A. E., Ed.; Wiley-VCH: Weinheim
    • (a) Lundt, I.; Madsen, R. Iminosugars as Powerful Glycosidase Inhibitors-Synthetic Approaches from Aldonolactones. In Iminosugars as Glycosidase Inhibitors-Norjirimycin and Beyond; Stütz, A. E., Ed.; Wiley-VCH: Weinheim, 1999; p 93.
    • (1999) Iminosugars as Glycosidase Inhibitors-Norjirimycin and Beyond , pp. 93
    • Lundt, I.1    Madsen, R.2
  • 17


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.