메뉴 건너뛰기




Volumn 1, Issue 18, 2003, Pages 3147-3153

Efficient synthesis of glycosylated phenazine natural products and analogs with DISAL (methyl 3,5-dinitrosalicylate) glycosyl donors

Author keywords

[No Author keywords available]

Indexed keywords

BENZENE; CATALYST SELECTIVITY; ENZYME INHIBITION; GLUCOSE;

EID: 0141860915     PISSN: 14770520     EISSN: None     Source Type: Journal    
DOI: 10.1039/b306789k     Document Type: Article
Times cited : (14)

References (36)
  • 2
    • 0141623229 scopus 로고    scopus 로고
    • US Pat., 4316959, 1982
    • K. H. Michel, M. M. Hoehn, US Pat., 4316959, 1982 (Chem. Abstr. 1982, 96, 197888)
    • Michel, K.H.1    Hoehn, M.M.2
  • 3
    • 2042521196 scopus 로고
    • K. H. Michel, M. M. Hoehn, US Pat., 4316959, 1982 (Chem. Abstr. 1982, 96, 197888)
    • (1982) Chem. Abstr. , vol.96 , pp. 197888
  • 28
    • 0036026456 scopus 로고    scopus 로고
    • For a review of glycosylation protocols under neutral or mild basic conditions, see: K. J. Jensen, J. Chem. Soc., Perkin Trans. 1, 2002, 20, 2219-2233.
    • (2002) J. Chem. Soc., Perkin Trans. 1 , vol.20 , pp. 2219-2233
    • Jensen, K.J.1
  • 29
    • 0036603591 scopus 로고    scopus 로고
    • For a review of combinatorial synthesis of natural products, see: J. Nielsen, Curr. Opin. Chem. Biol., 2002, 6(3), 297-305.
    • (2002) Curr. Opin. Chem. Biol. , vol.6 , Issue.3 , pp. 297-305
    • Nielsen, J.1
  • 30
    • 0141623224 scopus 로고    scopus 로고
    • note
    • 3 or AcOH, rt, 24 h) leads to complete decomposition of the phenazine structure.
  • 34
    • 0141846594 scopus 로고    scopus 로고
    • note
    • The compounds were screened in growth inhibition studies by LEO Pharma A/S on a panel of Gram-positive skin flora (Micrococcus luteus, Propionibacterium acnes, Streptococcus pyogenes, Staphylococcus epidermidis, Staphylococcus aureus) and on two resistant Staphylococcus aureus strains: clinical isolates of fusidic acid resistant and rifampicin resistant MRSA.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.