메뉴 건너뛰기




Volumn 12, Issue 19, 2002, Pages 2757-2760

Sordarin oxazepine derivatives as potent antifungal agents

Author keywords

[No Author keywords available]

Indexed keywords

ANTIFUNGAL AGENT; OXAZEPINE DERIVATIVE; SORDARIN DERIVATIVE;

EID: 0037037371     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0960-894X(02)00529-2     Document Type: Article
Times cited : (55)

References (25)
  • 5
    • 0035147012 scopus 로고    scopus 로고
    • For reviews, see (a) Odds F.C. Exp. Opin. Ther. Patents. 11:2001;283 (b) Ziegelbauer K., Spaltmann F. Drugs Future. 25:2000;63 (c) Gargolla-Viola D. Curr. Opin Anti-infective Invest. Drugs. 1:1999;297.
    • (2001) Exp. Opin. Ther. Patents , vol.11 , pp. 283
    • Odds, F.C.1
  • 6
    • 0034051031 scopus 로고    scopus 로고
    • For reviews, see (a) Odds F.C. Exp. Opin. Ther. Patents. 11:2001;283 (b) Ziegelbauer K., Spaltmann F. Drugs Future. 25:2000;63 (c) Gargolla-Viola D. Curr. Opin Anti-infective Invest. Drugs. 1:1999;297.
    • (2000) Drugs Future , vol.25 , pp. 63
    • Ziegelbauer, K.1    Spaltmann, F.2
  • 7
    • 0000585524 scopus 로고    scopus 로고
    • For reviews, see (a) Odds F.C. Exp. Opin. Ther. Patents. 11:2001;283 (b) Ziegelbauer K., Spaltmann F. Drugs Future. 25:2000;63 (c) Gargolla-Viola D. Curr. Opin Anti-infective Invest. Drugs. 1:1999;297.
    • (1999) Curr. Opin Anti-infective Invest. Drugs , vol.1 , pp. 297
    • Gargolla-Viola, D.1
  • 11
    • 0035147012 scopus 로고    scopus 로고
    • For reviews, see (a) Odds F.C. Exp. Opin. Ther. Patents. 11:2001;283 (b) Gargolla-Viola D. Curr. Opin. Anti-infective Invest. Drugs. 1:1999;297.
    • (2001) Exp. Opin. Ther. Patents , vol.11 , pp. 283
    • Odds, F.C.1
  • 18
    • 0005180942 scopus 로고    scopus 로고
    • note
    • This strain has been deposited with the ATCC for registration.
  • 19
    • 0005211707 scopus 로고    scopus 로고
    • note
    • 3CN (1.0 equiv), and the reaction was allowed to stir overnight at room temperature. Aqueous workup afforded the crude reductive amination product which was deprotected (TBAF in THF, then 1 N HCl in MeOH) according to standard procedures. The final targets 4a-n were purified to homogeneity by silica gel chromatography.
  • 21
    • 0019977893 scopus 로고
    • For other examples of syn-selective oxidation of triols, see (a) Jeong L.S., Shinazi R.F., Beach J.W., Kim H.O., Nampalli S. J. Med. Chem. 36:1993;181 (b) Stache U., Radscheit K., Haede W., Fritsch W. Liebigs Ann. Chem. 2:1982;342.
    • (1982) Liebigs Ann. Chem. , vol.2 , pp. 342
    • Stache, U.1    Radscheit, K.2    Haede, W.3    Fritsch, W.4
  • 22
    • 0005233490 scopus 로고    scopus 로고
    • note
    • -) 534.
  • 23
    • 0005151290 scopus 로고    scopus 로고
    • note
    • The fungal strains used in this study were obtained from the American Type Culture Collection. MICs were determined according to National Committee for Clinical Laboratory Standards (NCCLS); NCCLS Document M27-A; NCCLS: Villanova, PA, 1997.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.