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Volumn 15, Issue 7, 2005, Pages 1821-1824

Asymmetric synthesis of novel tetrahydroquinoline derivatives with a sugar building block and their bioactivities

Author keywords

Asymmetric synthesis; Bioactivity; Building block; Carbohydrates; Tetrahydroquinoline

Indexed keywords

QUINOLINE DERIVATIVE; SUCROSE;

EID: 15044349585     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2005.02.024     Document Type: Article
Times cited : (22)

References (30)
  • 7
    • 0000730407 scopus 로고
    • B.M. Trost I. Fleming L.A. Paquette Pergamon Oxford
    • S.M. Weinreb B.M. Trost I. Fleming L.A. Paquette Comprehensive Organic Synthesis Vol. 5 1991 Pergamon Oxford 401
    • (1991) Comprehensive Organic Synthesis , vol.5 , pp. 401
    • Weinreb, S.M.1
  • 23
    • 85030811763 scopus 로고    scopus 로고
    • note
    • +
  • 24
    • 85030816617 scopus 로고    scopus 로고
    • note
    • 2 = 0.1448
  • 26
    • 85030808235 scopus 로고    scopus 로고
    • note
    • 2 = 0.1668.
  • 29
    • 85030816691 scopus 로고    scopus 로고
    • note
    • x, BIO-TEK INSTRUMENT, INC), respectively. OD values were achieved by subtracting the absorbance at 630 nm from the 570 nm absorbance
  • 30
    • 85030808645 scopus 로고    scopus 로고
    • note
    • 3 cells/well). The next day test substances were freshly dissolved in DMSO resulting in 10 mg/mL stock solutions. Stock solutions were diluted in culture medium and added (200 μL/well) at various concentrations to the wells, resulting in seven final concentrations between 1 and 100 μg/mL. 48 or 72 h later the MTT-test was performed


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.