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Volumn 20, Issue 32, 1979, Pages 2965-2968

Preparation of N-carbomethoxyaminopyrroles

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EID: 1842706388     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/S0040-4039(00)70985-3     Document Type: Article
Times cited : (26)

References (12)
  • 5
    • 0004246823 scopus 로고
    • Dihydropyridazines are relatively unstable and are oxidized to pyridazines on exposure to air; see, Oxford University Press, Inc, Bristol
    • (1959) Heterocyclic Chemistry , pp. 113
    • Albert1
  • 6
    • 33646773355 scopus 로고
    • For details of the synthesis of 3b, see, In general, reactions of azoalkenes with β-dicarbonyl compounds (1 equiv) or enamines (1.1 equiv) are performed in THF solution.
    • (1978) J. Org. Chem. , vol.43 , pp. 3391
    • Schultz1    Hagmann2
  • 8
    • 84918343558 scopus 로고
    • N-aminopyrroles have been prepared by the reaction of semicarbazones of α-haloketones with β-diketones and base, Presumably, an azoalkene is an intermediate.
    • (1960) Ann. Chim. , vol.50 , pp. 1971
    • Spiro1    Madonia2
  • 10
    • 84918343557 scopus 로고    scopus 로고
    • Compounds 5a, 7a, 8, and 9a gave satisfactory elemental analyses.
  • 11
    • 84981871873 scopus 로고
    • Sterically-crowded pyrroles
    • Diketone 10 is prepared in modest yield by the reaction of 1-bromo phenylacetone with the pyrrolidine enamine of cyclopentanone. For the conversion of 1,4-diketones to N-dialkylaminopyrroles, see
    • (1968) Journal of Heterocyclic Chemistry , vol.5 , pp. 757
    • Broadbent1    Burnham2    Olsen3    Sheeley4
  • 12
    • 84918343556 scopus 로고    scopus 로고
    • This work was initiated in the Chemistry Department of Cornell University.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.