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Volumn 58, Issue , 2002, Pages 359-369

Quinolone analogues 5. Synthesis of 1-methyl-pyridazino[3,4-b]quinoxalin-4(1H)-ones

Author keywords

[No Author keywords available]

Indexed keywords

1 METHYLPYRIDAZINO[3,4 B]QUINOXALIN 4(1H) ONE; 4 ACETYL 1,5 DIHYDRO 1 METHYLPYRIDAZINO[3,4 B]QUINOXALINE; 7 CHLORO 1 METHYLPYRIDAZINO[3,4 B]QUINOXALIN 4(1H) ONE; 7 CHLORO 1,4 DIHYDRO 1 METHYLPYRIDAZINO[3,4 B]QUINOXALINE 4,4 DICARBOXYLATE; 7 CHLORO 1,5 DIHYDRO 1 METHYLPYRIDAZINO[3,4 B]QUINOXALINE 4 CARBOXYLATE; ACETAL DERIVATIVE; ACETALDEHYDE; MALONIC ACID DERIVATIVE; QUINOLONE DERIVATIVE; QUINOXALINE DERIVATIVE; SELENIUM DERIVATIVE; UNCLASSIFIED DRUG;

EID: 0037159758     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/COM-02-S(M)30     Document Type: Article
Times cited : (14)

References (15)
  • 5
    • 0011776830 scopus 로고    scopus 로고
    • note
    • For example, the minimum inhibitory concentrations of compounds (3a, b) were between 1.0 and 2.0 ppm against Bacillus subtilis (bacteria) and Trichophyton mentagrophytes (fungi).
  • 6
    • 0011779254 scopus 로고    scopus 로고
    • The detailed screening data will be reported elsewhere
    • The detailed screening data will be reported elsewhere.
  • 9
    • 0011721166 scopus 로고    scopus 로고
    • note
    • 8) shown below.
  • 14
    • 0011731473 scopus 로고    scopus 로고
    • note
    • 13 were reported to predominate as the 1,4-dihydro form.
  • 15
    • 0011789334 scopus 로고    scopus 로고
    • note
    • The recovery was not so good.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.