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Volumn 47, Issue 32, 2006, Pages 5633-5636

A new ruthenium-catalyzed approach for quinoxalines from o-phenylenediamines and vicinal-diols

Author keywords

Cyclization; o Phenylenediamines; Quinoxalines; Ruthenium catalyst; Vicinal diols

Indexed keywords

DIAMINE DERIVATIVE; POTASSIUM HYDROXIDE; QUINOXALINE; RUTHENIUM;

EID: 33745617379     PISSN: 00404039     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.tetlet.2006.06.038     Document Type: Article
Times cited : (98)

References (36)
  • 9
    • 0003151465 scopus 로고
    • For a review for Friedläender quinoline synthesis, see:
    • For a review for Friedläender quinoline synthesis, see:. Cheng C.-C., and Yan S.-J. Org. React. 28 (1982) 37
    • (1982) Org. React. , vol.28 , pp. 37
    • Cheng, C.-C.1    Yan, S.-J.2
  • 10
    • 2342627915 scopus 로고    scopus 로고
    • For a detailed mechanism for Friedläender quinoline synthesis, see:
    • For a detailed mechanism for Friedläender quinoline synthesis, see:. Muchowski J.M., and Maddox M.L. Can. J. Chem. 82 (2004) 461
    • (2004) Can. J. Chem. , vol.82 , pp. 461
    • Muchowski, J.M.1    Maddox, M.L.2
  • 16
    • 0002946125 scopus 로고    scopus 로고
    • For our recent report on ruthenium-catalyzed synthesis of indoles:
    • For our recent report on ruthenium-catalyzed synthesis of indoles:. Cho C.S., Lim H.K., Shim S.C., Kim T.J., and Choi H.-J. Chem. Commun. (1998) 995
    • (1998) Chem. Commun. , pp. 995
    • Cho, C.S.1    Lim, H.K.2    Shim, S.C.3    Kim, T.J.4    Choi, H.-J.5
  • 20
    • 0033582781 scopus 로고    scopus 로고
    • For our recent report on ruthenium-catalyzed synthesis of quinolines:
    • For our recent report on ruthenium-catalyzed synthesis of quinolines:. Cho C.S., Oh B.H., and Shim S.C. Tetrahedron Lett. 40 (1999) 1499
    • (1999) Tetrahedron Lett. , vol.40 , pp. 1499
    • Cho, C.S.1    Oh, B.H.2    Shim, S.C.3
  • 25
    • 0001565788 scopus 로고
    • For ruthenium-catalyzed synthesis of N-heterocycles using alcohols:
    • For ruthenium-catalyzed synthesis of N-heterocycles using alcohols:. Tsuji Y., Huh K.-T., and Watanabe Y. Tetrahedron Lett. 27 (1986) 377
    • (1986) Tetrahedron Lett. , vol.27 , pp. 377
    • Tsuji, Y.1    Huh, K.-T.2    Watanabe, Y.3
  • 28
    • 33745628483 scopus 로고    scopus 로고
    • note
    • We confirmed in a separate experiment (run 3 of Table 1) that 2-hydroxyacetophenone is formed as an intermediate in 4% yield with complete conversion of 2a (99%) by GLC analysis.
  • 29
    • 4243378570 scopus 로고
    • For recent reviews on transition metal-catalyzed transfer hydrogenation, see:
    • For recent reviews on transition metal-catalyzed transfer hydrogenation, see:. Zassinovich G., Mestroni G., and Gladiali S. Chem. Rev. 92 (1992) 1051
    • (1992) Chem. Rev. , vol.92 , pp. 1051
    • Zassinovich, G.1    Mestroni, G.2    Gladiali, S.3


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.