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Volumn 27, Issue 4, 1990, Pages 1135-1142

Transaminations of enaminones:A Synthesis of tricyclic, N‐aryl, 1,2,3‐triazole‐fused pyridones

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EID: 84986467876     PISSN: 0022152X     EISSN: 19435193     Source Type: Journal    
DOI: 10.1002/jhet.5570270462     Document Type: Article
Times cited : (12)

References (21)
  • 6
    • 84986506891 scopus 로고
    • a, U. S. Patent Appl. 137,306, Dec. 23
    • (1987)
    • Friary, R.1
  • 7
    • 84986459421 scopus 로고
    • b J. Heterocyclic Chem.
    • (1989)
  • 9
    • 84986490859 scopus 로고
    • b, Enamines, M. Dekker, New York
    • (1969) , pp. 384-396
    • Kuehne, M.G.1
  • 10
    • 84986485774 scopus 로고    scopus 로고
    • H(2′) and (6′) were magnetically equivalent in 8.4 and 8.5. In each compound the two protons resonated as a single doublet.
  • 11
    • 84986485775 scopus 로고    scopus 로고
    • The perhaps unlikely regioisomer 20 might have arisen indirectly from 4.1. Conceivably, formation of 20 would have begun with attack of enamine on 0(5) of 4.1. Rearrangement of the resulting acid chloride‐enamine followed by transamination and ring‐closure would have produced 20.
  • 18
    • 84986490849 scopus 로고
    • Studies on 1,2,3-triazoles. Part XI. A new entry to the benzopyrano[2,3-D]-1,2,3-triazole system. Cyclization of 1-benzyl-5-chloro-4-(2-hydroxybenzoyl)-1H-1,2,3-triazoles
    • (1985) Journal of Heterocyclic Chemistry , vol.22 , pp. 77-80
    • Buckle, D.R.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.