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1
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0026715856
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We will use this name throughout the text. In most published articles the tautomeric form 4-hydroxyquinoline is used. For discussion of the keto-enol tautomerism see, A. Cruz, J. Elguero, P. Goya, and A. Martínez Tetrahedron 48 1992 6135 6150 and references cited therein
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(1992)
Tetrahedron
, vol.48
, pp. 6135-6150
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Cruz, A.1
Elguero, J.2
Goya, P.3
Martínez, A.4
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2
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0037401629
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A.L. Ruchelman, S.K. Singh, A. Ray, X.H. Wu, J.-M. Yang, T.-K. Li, A. Liu, L.F. Liu, and E.J. LaVoie Bioorg. Med. Chem. 11 2003 2061 2073
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Ruchelman, A.L.1
Singh, S.K.2
Ray, A.3
Wu, X.H.4
Yang, J.-M.5
Li, T.-K.6
Liu, A.7
Liu, L.F.8
Lavoie, E.J.9
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4
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0000443556
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A. Nishida, H. Sorimachi, M. Iwaida, M. Matsumizu, T. Kawate, and M. Nakagawa Synlett 1998 389 390
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(1998)
Synlett
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Nishida, A.1
Sorimachi, H.2
Iwaida, M.3
Matsumizu, M.4
Kawate, T.5
Nakagawa, M.6
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5
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0029014195
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C.A. Leach, T.H. Brown, R.J. Ife, D.J. Keeling, M.E. Parsons, C.J. Theobald, and K.J. Wiggald J. Med. Chem. 38 1995 2748
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Leach, C.A.1
Brown, T.H.2
Ife, R.J.3
Keeling, D.J.4
Parsons, M.E.5
Theobald, C.J.6
Wiggald, K.J.7
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6
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0028806997
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I.P. Andrews, R. Bannister, S.K. Etridge, N.J. Lewis, M.V. Mullane, and A.S. Wells Tetrahedron Lett. 36 1995 7743
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Andrews, I.P.1
Bannister, R.2
Etridge, S.K.3
Lewis, N.J.4
Mullane, M.V.5
Wells, A.S.6
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8
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0000767168
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B. Riegel, G.R. Lappin, B.H. Adelson, R.I. Jackson, C.J. Albisetti, R.M. Dodson, and R.H. Baker J. Am. Chem. Soc. 68 1946 1264
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Riegel, B.1
Lappin, G.R.2
Adelson, B.H.3
Jackson, R.I.4
Albisetti, C.J.5
Dodson, R.M.6
Baker, R.H.7
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13
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0031486562
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R. Atkins, G.F. Breen, L.P. Crawford, T.J. Grinter, M.A. Harris, J.F. Hayes, C.J. Moores, R.N. Saunders, A.C. Share, T.C. Walsgrove, and C. Wicks Org. Proc. Res. Dev. 1 1997 185 197
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Atkins, R.1
Breen, G.F.2
Crawford, L.P.3
Grinter, T.J.4
Harris, M.A.5
Hayes, J.F.6
Moores, C.J.7
Saunders, R.N.8
Share, A.C.9
Walsgrove, T.C.10
Wicks, C.11
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17
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11844256729
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note
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A highly non-polar by-product was observed on TLC when the catalyst:substrate ratio was 1:1. This side product was not characterized
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19
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84985641208
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We were not able to separate the isomers and the ratio of 3-methoxy-2-nitroacetophenone:3-methoxy-4-nitro-acetophenone (56:44) was determined by NMR spectrometry. We highly recommend the method published by Fürstner et al. for the preparation of pure 3-methoxy-2-nitroacetophenone A. Fürstner, D.N. Jumbam, and G. Seidel Chem. Ber. 127 1994 1125 1130
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(1994)
Chem. Ber.
, vol.127
, pp. 1125-1130
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Fürstner, A.1
Jumbam, D.N.2
Seidel, G.3
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