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Volumn 1, Issue 13, 1999, Pages 2149-2151

Convergent C-glycolipid synthesis via the Ramberg-Bäcklund reaction: Active antiproliferative glycolipids

Author keywords

[No Author keywords available]

Indexed keywords

ANTINEOPLASTIC AGENT; GLYCOLIPID;

EID: 0033619842     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol991211f     Document Type: Article
Times cited : (47)

References (25)
  • 3
    • 0002476212 scopus 로고    scopus 로고
    • Nucleophilic C-glycosyl donors for C-glycoside synthesis
    • (c) Beau, J.-M.; Gallagher, T. Nucleophilic C-Glycosyl Donors for C-Glycoside Synthesis. Top. Curr. Chem. 1997, 187, 1-54.
    • (1997) Top. Curr. Chem. , vol.187 , pp. 1-54
    • Beau, J.-M.1    Gallagher, T.2
  • 4
    • 0002212956 scopus 로고    scopus 로고
    • Synthesis of C-glycosides of biological interest
    • (d) Nicotra, F. Synthesis of C-Glycosides of Biological Interest. Top. in Curr. Chem. 1997, 187, 55-83.
    • (1997) Top. in Curr. Chem. , vol.187 , pp. 55-83
    • Nicotra, F.1
  • 17
    • 0002580741 scopus 로고    scopus 로고
    • Janoff, A. S., Ed.; Marcel Dekker: New York
    • Bittman, R.; Arthur, G. In Liposomes: Rational Design; Janoff, A. S., Ed.; Marcel Dekker: New York, 1999; pp 125-144.
    • (1999) Liposomes: Rational Design , pp. 125-144
    • Bittman, R.1    Arthur, G.2
  • 23
    • 0041630997 scopus 로고    scopus 로고
    • note
    • 2. The residue was purified by column chromatography on silica gel, with 10% EtOAc-PE as eluent, to afford 74 mg (60%) of alkene 22 (Z:E = 1:1).
  • 24
    • 0042632893 scopus 로고    scopus 로고
    • note
    • 3): δ 81.99, 80.64, 77.97, 73.44, 72.42, 68.56, 64.33, 58.26, 33.43, 32.69, 32.07, 31.69, 30.40, 30.25, 30.12, 28.44, 26.90, 23.46, 14.89.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.