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Jørgensen, M.1
Hadwiger, P.2
Madsen, R.3
Stütz, A.E.4
Wrodnigg, T.M.5
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9
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0002202416
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Dragutan, V.; Dragutan, I.; Balaban, A. T. Platinum Metals Rev. 2000, 44, 58-66, 112-118, 168-172.
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Dragutan, V.1
Dragutan, I.2
Balaban, A.T.3
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16
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0033603294
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Ackermann L., Fürstner A., Weskamp T., Kohl F.J., Herrmann W.A. Tetrahedron Lett. 40:1999;4787-4790.
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Ackermann, L.1
Fürstner, A.2
Weskamp, T.3
Kohl, F.J.4
Herrmann, W.A.5
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17
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0011931581
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Kinderman S.S., Doodeman R., van Beijma J.W., Russcher J.C., Tjen K.C.M.F., Kooistra T.M., Mohaselzadeh H., van Maarseveen J.H., Hiemstra H., Schoemaker H.E., Rutjes F.P.J.T. Adv. Synth. Catal. 344:2002;736-748.
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Kinderman, S.S.1
Doodeman, R.2
Van Beijma, J.W.3
Russcher, J.C.4
Tjen, K.C.M.F.5
Kooistra, T.M.6
Mohaselzadeh, H.7
Van Maarseveen, J.H.8
Hiemstra, H.9
Schoemaker, H.E.10
Rutjes, F.P.J.T.11
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21
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0011989390
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note
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This work is taken from the MSc work of E. L. Ngidi and the postdoctoral fellowship of Dr. E. M. Coyanis.
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22
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0011963815
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2H- and 4H-1-Benzopyrans
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Ellis, G. P., Ed.; John Wiley & Sons: New York
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Schweizer, E. E.; Meeder-Nycz, D. 2H- and 4H-1-Benzopyrans. In The Chemistry of Heterocyclic Compounds; 31; Chromenes, Chromanones and Chromones; Ellis, G. P., Ed.; John Wiley & Sons: New York, 1977; pp. 11-139.
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(1977)
The Chemistry of Heterocyclic Compounds; 31; Chromenes, Chromanones and Chromones
, pp. 11-139
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Schweizer, E.E.1
Meeder-Nycz, D.2
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24
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0011984590
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a 6.42-6.46 (1H, m, H-2).
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a 6.42-6.46 (1H, m, H-2).
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27
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0037060942
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Demyttenaere J., Van Syngel K., Markusse A.P., Vervisch S., Debenedetti S., De Kimpe N. Tetrahedron. 58:2002;2163-2166.
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(2002)
Tetrahedron
, vol.58
, pp. 2163-2166
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Demyttenaere, J.1
Van Syngel, K.2
Markusse, A.P.3
Vervisch, S.4
Debenedetti, S.5
De Kimpe, N.6
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29
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0011969325
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2CH); 5.82 (1H, br s, OH); 6.59 (1H, d, J=7.3, H-7); 7.12-7.20 (2H, m, 2×Ar-H); 7.63 (1H, d, J=7.9, Ar-H); 7.86 (1H, d, J=9.2, H-4).
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2CH); 5.82 (1H, br s, OH); 6.59 (1H, d, J=7.3, H-7); 7.12-7.20 (2H, m, 2×Ar-H); 7.63 (1H, d, J=7.9, Ar-H); 7.86 (1H, d, J=9.2, H-4).
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32
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0011969326
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1H NMR spectrum at δ 5.98 (1H, dt, J=9.9 and 4.1) and 6.91 (1H, br d, J=9.9).
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1H NMR spectrum at δ 5.98 (1H, dt, J=9.9 and 4.1) and 6.91 (1H, br d, J=9.9).
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36
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0011964918
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2CH); 5.17 (1H, br s, CHOH); 6.23 (1H, d, J=2.0, -CH=C); 6.77 (1H, d, J=7.9, 6-H); 7.23 (1H, d, J=7.6 Hz, 7-H); 7.31-7.38 (3H, m, Ar-H); 7.47-7.52 (2H, m, Ar-H).
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2CH); 5.17 (1H, br s, CHOH); 6.23 (1H, d, J=2.0, -CH=C); 6.77 (1H, d, J=7.9, 6-H); 7.23 (1H, d, J=7.6 Hz, 7-H); 7.31-7.38 (3H, m, Ar-H); 7.47-7.52 (2H, m, Ar-H).
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