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Volumn 14, Issue 5, 2004, Pages 1169-1172

Synthesis and in vitro cytotoxicity of 5-substituted 2-cyanoimino-4- imidazodinone and 2-cyanoimino-4-pyrimidinone derivatives

Author keywords

Anticancer

Indexed keywords

4 PYRIMIDINONE DERIVATIVE; ANTINEOPLASTIC AGENT; HETEROCYCLIC COMPOUND; UNCLASSIFIED DRUG; [1 [6 (4 CHLOROPHENOXY)HEXYL] 5 OXO 4 PHENYL 3 (4 PYRIDYL)TETRAHYDRO 1H 2 IMIDAZOLYLIDEN]AMINOMETHANENITRILE;

EID: 1242294354     PISSN: 0960894X     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.bmcl.2003.12.073     Document Type: Article
Times cited : (16)

References (26)
  • 10
    • 0002805264 scopus 로고
    • Synthesis of 2-cyanoiminoimidazolidine:
    • Synthesis of 2-cyanoiminoimidazolidine: Baltzer C.M., McCarty C.G. J. Org. Chem. 38:1973;155.
    • (1973) J. Org. Chem. , vol.38 , pp. 155
    • Baltzer, C.M.1    McCarty, C.G.2
  • 16
    • 84980140427 scopus 로고
    • Synthesis of 2-cyanoimino-4-imidazolidinone:
    • Synthesis of 2-cyanoimino-4-imidazolidinone: Gante J., Mohr G. Chem. Ber. 108:1975;174.
    • (1975) Chem. Ber. , vol.108 , pp. 174
    • Gante, J.1    Mohr, G.2
  • 19
    • 0032514453 scopus 로고    scopus 로고
    • Synthetic applications of chloroacetyl chloride:
    • Synthetic applications of chloroacetyl chloride: Hughes R., Meyers A.I. Tetrahedron. 54:1998;9895.
    • (1998) Tetrahedron , vol.54 , pp. 9895
    • Hughes, R.1    Meyers, A.I.2
  • 26
    • 85030895573 scopus 로고    scopus 로고
    • note
    • 3) δ 8.71 (d, 2H, J=6.3 Hz), 7.34 (d, 2H, J=6.3 Hz), 7.19 (d, 2H, J=9.0 Hz), 6.80 (d, 2H, J=9.0 Hz), 4.60 (q, 1H, J=6.9 Hz), 3.93-3.88 (m, 4H), 1.80 (m, 4H), 1.55 (m, 4H), 1.46 (d, 3H, J=7.2 Hz); ESMS 426.1 (M+1), 448.1 (M+23).


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.