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Volumn 65, Issue 9, 2005, Pages 2095-2105

Facile synthesis of 3-substituted and 1,3-disubstituted quinolin-2(1H)-ones from 2-nitrobenzaldehydes

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EID: 33646895174     PISSN: 03855414     EISSN: None     Source Type: Journal    
DOI: 10.3987/COM-05-10462     Document Type: Article
Times cited : (28)

References (42)
  • 7
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    • Katrizky A.R., and Rees C.W. (Eds), Pergamon Press, The Netherlands
    • Jones G. In: Katrizky A.R., and Rees C.W. (Eds). Comprehensive Heterocyclic Chemistry Vol. 2 (1984), Pergamon Press, The Netherlands 395-510
    • (1984) Comprehensive Heterocyclic Chemistry , vol.2 , pp. 395-510
    • Jones, G.1
  • 8
    • 0042989189 scopus 로고
    • Barton D., and Ollis W.D. (Eds), Pergamon Press, New York
    • Claret P.A. In: Barton D., and Ollis W.D. (Eds). Comprehensive Organic Chemistry Vol. 4 (1979), Pergamon Press, New York 157-166
    • (1979) Comprehensive Organic Chemistry , vol.4 , pp. 157-166
    • Claret, P.A.1
  • 20
    • 33646881520 scopus 로고
    • Chem. Abstr. 59 (1963) 565
    • (1963) Chem. Abstr. , vol.59 , pp. 565
  • 33
    • 33646880647 scopus 로고    scopus 로고
    • note
    • 2 and then reaction of the reduced product with acetyl chloride, but it gave 2-acetylaminobenzaldehyde (1a) with poorly reproducible and low yield.
  • 36
    • 33646871786 scopus 로고    scopus 로고
    • note
    • The overall yield of 2f from 2-nitrobenzaldehyde is 75% (Table 1, entry 6). If one assumes the yield of 1f as ca. 80%, the yield of the cyclization step becomes more than 90%.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.