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Volumn 10, Issue 11, 2008, Pages 2227-2230

"Click" saccharide/β-lactam hybrids for lectin inhibition

Author keywords

[No Author keywords available]

Indexed keywords

BETA LACTAM; BIOMIMETIC MATERIAL; GLYCOPEPTIDE; LECTIN; VEGETABLE PROTEIN;

EID: 52649161380     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol8006259     Document Type: Article
Times cited : (42)

References (33)
  • 1
    • 0036430152 scopus 로고    scopus 로고
    • For reviews, see: a
    • For reviews, see: (a) Mehta, G.; Singh, V. Chem. Soc. Rev. 2002, 31, 324-334.
    • (2002) Chem. Soc. Rev , vol.31 , pp. 324-334
    • Mehta, G.1    Singh, V.2
  • 3
    • 38949125112 scopus 로고    scopus 로고
    • (c) Meunier, B. Chem. Rev. 2008, 104, 69-77.
    • (2008) Chem. Rev , vol.104 , pp. 69-77
    • Meunier, B.1
  • 8
    • 0346768307 scopus 로고    scopus 로고
    • For reviews, see: a, Wong, C.-H, Ed, Wiley-VCH: Weinheim
    • For reviews, see: (a) Carbohydrate-based Drug Discovery; Wong, C.-H., Ed.; Wiley-VCH: Weinheim, 2003.
    • (2003) Carbohydrate-based Drug Discovery
  • 13
    • 0000096835 scopus 로고    scopus 로고
    • This heterocycle is readily accessible by the copper-catalyzed azide-alkyne click cycloaddition reaction: (a) Kolb, H. C, Finn, M. G, Sharpless, K. B. Angew. Chem, Int. Ed. 2001, 40, 2004-2021
    • This heterocycle is readily accessible by the copper-catalyzed azide-alkyne "click" cycloaddition reaction: (a) Kolb, H. C.; Finn, M. G.; Sharpless, K. B. Angew. Chem., Int. Ed. 2001, 40, 2004-2021.
  • 14
    • 33947493431 scopus 로고    scopus 로고
    • For the use of glycosyl azides in click reactions, see: b
    • For the use of glycosyl azides in "click" reactions, see: (b) Dedola, S.; Nepogodiev, S. A.; Field, R. A. Org. Biomol. Chem. 2007, 5, 1006-1017.
    • (2007) Org. Biomol. Chem , vol.5 , pp. 1006-1017
    • Dedola, S.1    Nepogodiev, S.A.2    Field, R.A.3
  • 25
    • 59849121044 scopus 로고    scopus 로고
    • 3 in acetonitrile, followed by in situ treatment of the resulting intermediate N-nosylaziridine (I) with methyl α- aminoisobutirate 7 provided the N-peptidylazaserinate (II) in only 25% yield, along with several unidentified products. (Chemical Equation Presented)
    • 3 in acetonitrile, followed by "in situ" treatment of the resulting intermediate N-nosylaziridine (I) with methyl α- aminoisobutirate 7 provided the N-peptidylazaserinate (II) in only 25% yield, along with several unidentified products. (Chemical Equation Presented)
  • 28
    • 24944457136 scopus 로고    scopus 로고
    • For other glycosidic β-lactam hybrids, see: a
    • For other glycosidic β-lactam hybrids, see: (a) Kvaerno, L.; Werder, M.; Hauser, H.; Carreira, E. M. J. Med. Chem. 2005, 48, 6035-6053.
    • (2005) J. Med. Chem , vol.48 , pp. 6035-6053
    • Kvaerno, L.1    Werder, M.2    Hauser, H.3    Carreira, E.M.4


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.