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2
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0343434371
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Resent reviews: a) Hirsh, A. Synthesis. 1995, 895.
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Hirsh, A.1
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4
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0000523401
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Prato. M.; Lucchini, V.; Maggini, M.; Stimpfl. E.; Scorrano, G.; Eiermann, M., Suzuki, T.; Wuld, F. J.Am.Chem.Soc. 1993, 115, 8479.
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Prato, M.1
Lucchini, V.2
Maggini, M.3
Stimpfl, E.4
Scorrano, G.5
Eiermann, M.6
Suzuki, T.7
Wuld, F.8
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5
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0002822176
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b) Banks, M.R.; Cadgan, J.I.C.; Gosney, I.; Hodgson, P.K.G.; Langridge-Smith, P.R.R.; Parkinson, J.A.; Rankin, D.W.H.; Taylor, A.T. J.Chem.Soc., Chem.Commun. 1995, 887.
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Banks, M.R.1
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Hodgson, P.K.G.4
Langridge-Smith, P.R.R.5
Parkinson, J.A.6
Rankin, D.W.H.7
Taylor, A.T.8
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9
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0001168866
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Ter Meer, H.U.8
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0028293771
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Muthu, S.1
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Vasudena Rao, P.R.4
Mathews, C.K.5
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12
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33751154715
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b) Matsubara, Y.; Tada, H.; Nagase, S.; Yoshida, Z. J.Org.Chem. 1995, 60, 5372
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Matsubara, Y.1
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84980175838
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Huisgen, R.; Stangl, H.; Strum, H.J.; Raab, R.; Bunge, K. Chem.Ber. 1972, 105, 1258.
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Huisgen, R.1
Stangl, H.2
Strum, H.J.3
Raab, R.4
Bunge, K.5
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14
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0343870147
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note
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3-C), 124.33 (2C), 128.54 (2C), 128.63, 128.94 (2C), 129.05, 129.15, 129.39, 129.49, 129.54, 129.59, 130.78 (2C), 131.05, 131.10, 134.34, 135.29, (2C), 140.15, 140.38, 140.43, 140.75 (2C), 141.07, 141.81, 142.17, 142.26, 142.37, 142.53, 142.59, 142.78, 142.96, 143.14, 143.20, 143.24, 143.29, 143.68, 144.46, 144.85, 144.92, 145.36, 145.43, 145.49, 145.60, 145.69, 145.79, 145.86, 145.89, 145.94, 145.99, 146.09, 146.30, 146.40, 146.47 (2C), 146.57, 146.84, 146.90, 147.24, 147.37, 147.45, 147.49, 148.42, 149.47, 149.55, 152.76, 155.32, 175.94 (C=N).
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15
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0343434369
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note
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3-C), 124.58, 128.86 (2C), 129.33, 129.83, 129.93, 131.41, 131.42 (2C), 131.89 (2C), 134.73, 134.86, 135.70, 136.63 (2C), 136.88, 140.49 (2C), 140.72, 141.09, 142.26, 142.30, 142.50, 142.57, 142.61 (2C), 142.76, 142.79, 142.82 (2C), 142.99, 143.25, 143.30, 143.32, 143.35, 143.74, 143,77, 144,60 (2C), 144.65, 144.80, 144.98, 145.36, 145.61 (2C), 145.72 (2C), 145.83, 145.93, 145.95, 146.10, 146.25, 146.39, 146.48, 146.50, 146.57, 146.60 (2C), 146.89, 146.94, 147.05, 147.55, 147.56, 147.70, 147.76 (2C), 148.00, 148.37, 149.05, 152.20, 155.30, 172.16 (C=N).
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16
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0342564339
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note
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2Ph)], the other protons signals cannot be distinguished from signals 3a.
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17
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0008275866
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1H-NMR spectra of 2 and 3a are closely similar to that of toluene (see Hansen, M.; Jakobsen, H.J. J.Magn.Reson. 1975, 20, 520). The values of coupling constants for 2 and 3 will be reported.
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(1975)
J.Magn.Reson.
, vol.20
, pp. 520
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Hansen, M.1
Jakobsen, H.J.2
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