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Volumn , Issue 15, 2003, Pages 2415-2426

Synthesis of Quinolines and 2H-Dihydropyrroles by Nucleophilic Substitution at the Nitrogen Atom of Oxime Derivatives

Author keywords

2H dihydropyrroles; Nucleophilic substitution; Oxime derivatives; Quinolines; Tetrahydroquinolines

Indexed keywords

ACETIC ACID; DERIVATIVES; ISOMERIZATION; ISOMERS; KETONES; NITROGEN COMPOUNDS; SUBSTITUTION REACTIONS;

EID: 0242571912     PISSN: 00397881     EISSN: None     Source Type: Journal    
DOI: 10.1055/s-2003-42439     Document Type: Article
Times cited : (24)

References (45)
  • 7
    • 0242671044 scopus 로고    scopus 로고
    • note
    • In this manuscript syn-isomers mean the oximes having hydroxy or acyloxy and a nucleophilic moiety in the same side of oxime carbon-nitrogen double bond and anti-isomers mean the opposite.
  • 10
    • 84917889952 scopus 로고    scopus 로고
    • The Chemistry of the Carbon-Nitrogen Double Bond
    • Patai, S., Ed.; John Wiley & Sons Inc.: New York
    • McCarty, C. G. The Chemistry of the Carbon-Nitrogen Double Bond In The Chemistry of Functional Groups; Patai, S., Ed.; John Wiley & Sons Inc.: New York, 1996.
    • (1996) The Chemistry of Functional Groups
    • McCarty, C.G.1
  • 33
    • 0001189207 scopus 로고
    • Compound 9d was a single stereoisomer whose stereochemsitry was not determined. For the stereochemistry of α-keto ester oximes see: (a) Ernest, L. J. Phys. Chem. 1961, 65, 491. (b) Reinheckel, H.; Jovtsheff, A.; Spassov, S. Monatsh. Chem. 1965, 96, 1985.
    • (1961) J. Phys. Chem. , vol.65 , pp. 491
    • Ernest, L.1
  • 34
    • 0001189207 scopus 로고
    • Compound 9d was a single stereoisomer whose stereochemsitry was not determined. For the stereochemistry of α-keto ester oximes see: (a) Ernest, L. J. Phys. Chem. 1961, 65, 491. (b) Reinheckel, H.; Jovtsheff, A.; Spassov, S. Monatsh. Chem. 1965, 96, 1985.
    • (1965) Monatsh. Chem. , vol.96 , pp. 1985
    • Reinheckel, H.1    Jovtsheff, A.2    Spassov, S.3
  • 40
    • 0242671049 scopus 로고    scopus 로고
    • note
    • The spectral data were in good agreement with those of the authentic sample (commercially available from Tokyo Chemical Industry).
  • 42
    • 0242587260 scopus 로고    scopus 로고
    • note
    • The spectral data were in good agreement with those of the authentic sample.
  • 43
    • 0042327234 scopus 로고
    • For spectra data of 3,4-dihydroquinoline hydrobromide see: Cacchi, S.; Palmieri, G. Tetrahedron 1983, 39, 3373.
    • (1983) Tetrahedron , vol.39 , pp. 3373
    • Cacchi, S.1    Palmieri, G.2


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.