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Volumn 76, Issue 3, 2003, Pages 485-500

Synthesis and biological activities of lipid A analogs possessing β-glycosidic linkage at 1-position

Author keywords

[No Author keywords available]

Indexed keywords

ESCHERICHIA COLI; SYNTHESIS (CHEMICAL);

EID: 0037252208     PISSN: 00092673     EISSN: None     Source Type: Journal    
DOI: 10.1246/bcsj.76.485     Document Type: Article
Times cited : (13)

References (43)
  • 6
    • 0004041866 scopus 로고    scopus 로고
    • ed by H. Brade, S. M. Opal, S. N. Vogel, and D. C. Morrison, Marcel Dekker, New York·Basel
    • "Endotoxin in Health and Disease," ed by H. Brade, S. M. Opal, S. N. Vogel, and D. C. Morrison, Marcel Dekker, New York·Basel (1999).
    • (1999) Endotoxin in Health and Disease
  • 34
    • 0034718355 scopus 로고    scopus 로고
    • An unsubstituted benzyl group used for protection of the hydroxy function on the 3-hydroxyacyl residue is prone to air-oxidation and gradually transformed into the corresponding benzoyl group. We recently found the 4-(trifluoromethyl)benzyl group at this position is resistant to oxidation but readily removable by conventional hydrogenolysis, a) Y. Sakai, M. Oikawa, H. Yoshizaki, T. Ogawa, Y. Suda, K. Fukase, and S. Kusumoto, Tetrahedron Lett., 41, 6843 (2000).
    • (2000) Tetrahedron Lett. , vol.41 , pp. 6843
    • Sakai, Y.1    Oikawa, M.2    Yoshizaki, H.3    Ogawa, T.4    Suda, Y.5    Fukase, K.6    Kusumoto, S.7


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.