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Volumn , Issue 24, 2002, Pages 4131-4136

Synthesis of quinolinylphosphane oxides and -phosphonates from N-arylimines derived from phosphane oxides and phosphonates

Author keywords

Enamines; Phosphane oxides; Phosphonates; Quinolines

Indexed keywords

(2 ETHYL 6 METHYLQUINOLIN 3 YL)DIPHENYLPHOSPHANE OXIDE; (2 METHYL 7 TRIFLUOROMETHYLQUINOLIN 3 YL)DIPHENYLPHOSPHANE OXIDE; (2,6 DIMETHYLQUINOLIN 3 YL)DIPHENYLPHOSPHANE OXIDE; (6 CHLORO 2 METHYLQUINOLIN 3 YL)DIPHENYLPHOSPHANE OXIDE; (6 METHOXY 2 METHYLQUINOLIN 3 YL)DIPHENYLPHOSPHANE OXIDE; (6 METHOXYQUINOLIN 3 YL)DIPHENYLPHOSPHANE OXIDE; (6,7 DIMETHOXY 2 METHYLQUINOLIN 3 YL)PHOSPHONIC ACID; 2 [(3,4 DIMETHYLPHENYL)AMINO] 1 PROPENYLDIPHENYLPHOSPHANE OXIDE; DIETHYL(2 METHYLQUINOLIN 3 YL)PHOSPHONATE; DIETHYL(2,6 DIMETHYLQUINOLIN 3 YL)PHOSPHONATE; DIETHYL(4,6 DIMETHOXY 2 METHYLQUINOLIN 3 YL)PHOSPHONATE; DIETHYL(QUINOLIN 3 YL)PHOSPHONATE; DIPHENYL(2,6,7 TRIMETHYLQUINOLIN 3 YL)PHOSPHANE OXIDE; DIPHENYL[2 [(3 TRIFLUOROMETHYLPHENYL)IMINO]PROPYL]PHOSPHANE OXIDE; IMINE; N,N DIMETHYLFORMAMIDE; OXIDE; PHOSPHONIC ACID DERIVATIVE; QUINOLINE; UNCLASSIFIED DRUG; [2 [(2 CHLOROPHENYL)IMINO]PROPYL]DIPHENYLPHOSPHANE OXIDE; [2 [(3,4 DIMETHYLPHENYL)IMINO]PROPYL]DIPHENYLPHOSPHANE OXIDE;

EID: 0036919610     PISSN: 1434193X     EISSN: None     Source Type: Journal    
DOI: 10.1002/1099-0690(200212)2002:24<4131::AID-EJOC4131>3.0.CO;2-W     Document Type: Article
Times cited : (35)

References (44)
  • 1
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    • [1a] C. D. Johnson, in Rodd's Chemistry of Carbon Compounds, 2nd Ed. (Ed.: M. Sainsbury), Elsevier, Amsterdam, 1998, vol. 4 (part F), pp. 129-161.
    • (1998) Rodd's Chemistry of Carbon Compounds, 2nd Ed. , vol.4 , Issue.PART F , pp. 129-161
    • Johnson, C.D.1
  • 4
    • 0012212037 scopus 로고    scopus 로고
    • (Eds.: A. R. Katritzky, C. W. Rees, E. F. V. Scriven), Pergamon Press, Amsterdam
    • [1d] Comprehensive Heterocyclic Chemistry II (Eds.: A. R. Katritzky, C. W. Rees, E. F. V. Scriven), Pergamon Press, Amsterdam, 1996, vol. 5, pp. 1-300.
    • (1996) Comprehensive Heterocyclic Chemistry II , vol.5 , pp. 1-300
  • 11
    • 0034752697 scopus 로고    scopus 로고
    • For recent reviews see: [3a] J. P. Michael, Nat. Prod. Rep. 2001, 18, 543-559.
    • (2001) Nat. Prod. Rep. , vol.18 , pp. 543-559
    • Michael, J.P.1
  • 13
    • 0000993737 scopus 로고    scopus 로고
    • (Ed.: M. Sainsbury), Elsevier, Amsterdam
    • [3c] J. P. Michael, in Rodd's Chemistry of Carbon Compounds, 2nd ed. (Ed.: M. Sainsbury), Elsevier, Amsterdam, 1998, vol. 4 (part F), pp. 423-482.
    • (1998) Rodd's Chemistry of Carbon Compounds, 2nd Ed. , vol.4 , Issue.PART F , pp. 423-482
    • Michael, J.P.1
  • 40
    • 0012208816 scopus 로고    scopus 로고
    • note
    • Obtained as the imino derivative in the case of 1b, 1c, 1d and as mixture of β-imino (major) and β-enamino (minor) phosphane oxides for 1a, 1e, 1f.
  • 42
    • 0012176268 scopus 로고    scopus 로고
    • note
    • A mixture of β-imino (85%) and β-enamino (15%) phosphane oxide was used without separation.
  • 44
    • 0012199745 scopus 로고    scopus 로고
    • note
    • The regioselective ring junction in 5d and 5e was determined by analysis of their NMR patterns of the aromatic protons and by NOE experiments.


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.