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Volumn , Issue 10, 2010, Pages 1678-1686

One-pot friedlnder quinoline synthesis: Scope and limitations

Author keywords

Aldehydes; Condensation; Heterocycles; Ketones; Quinolines

Indexed keywords

AMINO-COMPOUNDS; CATALYTIC AMOUNTS; HETEROCYCLES; IN-SITU; ONE POT;

EID: 77952059997     PISSN: 00397881     EISSN: 1437210X     Source Type: Journal    
DOI: 10.1055/s-0029-1218701     Document Type: Article
Times cited : (34)

References (30)
  • 25
    • 0002801544 scopus 로고
    • 2N group is -0.205, suggesting that it has an electron-donating effect. See
    • 2N group is -0.205, suggesting that it has an electron-donating effect. See:, Hammett L P., J. Am. Chem. Soc. 1937 59 96
    • (1937) J. Am. Chem. Soc. , vol.59 , pp. 96
    • Hammett, L.P.1
  • 26
    • 5244267486 scopus 로고    scopus 로고
    • Longer condensation times have also been reported for the reaction of the intermediate 1-aminonaphthalene-2-carboxaldehyde with 1,3-diacetylbenzene (31 h) and 2,6-diacetylpyridine (17 h) under essentially the same reaction conditions (KOH in refluxing EtOH); see
    • Longer condensation times have also been reported for the reaction of the intermediate 1-aminonaphthalene-2-carboxaldehyde with 1,3-diacetylbenzene (31 h) and 2,6-diacetylpyridine (17 h) under essentially the same reaction conditions (KOH in refluxing EtOH); see:, Riesgo E C., Jin X, Thummel R P., J. Org. Chem. 1996 61 3017
    • (1996) J. Org. Chem. , vol.61 , pp. 3017
    • Riesgo, E.C.1    Jin, X.2    Thummel, R.P.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.