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Volumn 5, Issue 23, 2003, Pages 4257-4259

A Mild and Efficient One-Step Synthesis of Quinolines

Author keywords

[No Author keywords available]

Indexed keywords

QUINOLINE DERIVATIVE; TIN CHLORIDE; ZINC CHLORIDE;

EID: 0344927986     PISSN: 15237060     EISSN: None     Source Type: Journal    
DOI: 10.1021/ol035333q     Document Type: Article
Times cited : (270)

References (14)
  • 4
    • 0042730088 scopus 로고    scopus 로고
    • A subset of recent work in this area includes: (a) Du, W.; Curran, D. P. Org. Lett. 2003, 5, 1765-1768. (b) Lindsay, D. M.; Dohle, W.; Jensen, A. E.; Kopp, F.; Knochel, P. Org. Lett. 2002, 4, 1819-1822. (c) Matsugi, M.; Tabusa, F.; Minamikawa, J. Tetrahedron Lett. 2000, 41, 8523-8525. (d) Dormer, P. G.; Eng, K. K.; Farr, R. N.; Humphrey, G. R.; McWilliams, J. C.; Reider, P. J.; Sager, J. W.; Volante, R. P. J. Org. Chem. 2003, 68, 467-477.
    • (2003) Org. Lett. , vol.5 , pp. 1765-1768
    • Du, W.1    Curran, D.P.2
  • 5
    • 0001651959 scopus 로고    scopus 로고
    • A subset of recent work in this area includes: (a) Du, W.; Curran, D. P. Org. Lett. 2003, 5, 1765-1768. (b) Lindsay, D. M.; Dohle, W.; Jensen, A. E.; Kopp, F.; Knochel, P. Org. Lett. 2002, 4, 1819-1822. (c) Matsugi, M.; Tabusa, F.; Minamikawa, J. Tetrahedron Lett. 2000, 41, 8523-8525. (d) Dormer, P. G.; Eng, K. K.; Farr, R. N.; Humphrey, G. R.; McWilliams, J. C.; Reider, P. J.; Sager, J. W.; Volante, R. P. J. Org. Chem. 2003, 68, 467-477.
    • (2002) Org. Lett. , vol.4 , pp. 1819-1822
    • Lindsay, D.M.1    Dohle, W.2    Jensen, A.E.3    Kopp, F.4    Knochel, P.5
  • 6
    • 0034727305 scopus 로고    scopus 로고
    • A subset of recent work in this area includes: (a) Du, W.; Curran, D. P. Org. Lett. 2003, 5, 1765-1768. (b) Lindsay, D. M.; Dohle, W.; Jensen, A. E.; Kopp, F.; Knochel, P. Org. Lett. 2002, 4, 1819-1822. (c) Matsugi, M.; Tabusa, F.; Minamikawa, J. Tetrahedron Lett. 2000, 41, 8523-8525. (d) Dormer, P. G.; Eng, K. K.; Farr, R. N.; Humphrey, G. R.; McWilliams, J. C.; Reider, P. J.; Sager, J. W.; Volante, R. P. J. Org. Chem. 2003, 68, 467-477.
    • (2000) Tetrahedron Lett. , vol.41 , pp. 8523-8525
    • Matsugi, M.1    Tabusa, F.2    Minamikawa, J.3
  • 7
    • 0037462413 scopus 로고    scopus 로고
    • A subset of recent work in this area includes: (a) Du, W.; Curran, D. P. Org. Lett. 2003, 5, 1765-1768. (b) Lindsay, D. M.; Dohle, W.; Jensen, A. E.; Kopp, F.; Knochel, P. Org. Lett. 2002, 4, 1819-1822. (c) Matsugi, M.; Tabusa, F.; Minamikawa, J. Tetrahedron Lett. 2000, 41, 8523-8525. (d) Dormer, P. G.; Eng, K. K.; Farr, R. N.; Humphrey, G. R.; McWilliams, J. C.; Reider, P. J.; Sager, J. W.; Volante, R. P. J. Org. Chem. 2003, 68, 467-477.
    • (2003) J. Org. Chem. , vol.68 , pp. 467-477
    • Dormer, P.G.1    Eng, K.K.2    Farr, R.N.3    Humphrey, G.R.4    McWilliams, J.C.5    Reider, P.J.6    Sager, J.W.7    Volante, R.P.8
  • 14
    • 0344848407 scopus 로고    scopus 로고
    • note
    • 4, and filtered through Celite. Following reduction of the solvent in vacuo, the material remaining was subjected to chromatography on silica (20% ethyl acetate in hexane). The desired quinoline (7) was obtained in 94% yield as an orange oil.


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