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1
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35748950143
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For our recent papers on Pd-mediated reactions involving modified Baylis-Hillman adducts, see:
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For our recent papers on Pd-mediated reactions involving modified Baylis-Hillman adducts, see:. Gowrisankar S., Lee H.S., Lee K.Y., Lee J.-E., and Kim J.N. Tetrahedron Lett. 48 (2007) 8619-8622
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Gowrisankar, S.1
Lee, H.S.2
Lee, K.Y.3
Lee, J.-E.4
Kim, J.N.5
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4
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33745700297
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For the synthesis and synthetic applications of 6-oxacyclopropa[a]indene-1a-carboxylic acid derivatives, see:
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For the synthesis and synthetic applications of 6-oxacyclopropa[a]indene-1a-carboxylic acid derivatives, see:. Hedley S.J., Ventura D.L., Dominiak P.M., Nygren C.L., and Davies H.M.L. J. Org. Chem. 71 (2006) 5349-5356
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Hedley, S.J.1
Ventura, D.L.2
Dominiak, P.M.3
Nygren, C.L.4
Davies, H.M.L.5
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12
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34250726079
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Kanchiku S., Suematsu H., Matsumoto K., Uchida T., and Katsuki T. Angew. Chem., Int. Ed. 46 (2007) 3889-3891
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Kanchiku, S.1
Suematsu, H.2
Matsumoto, K.3
Uchida, T.4
Katsuki, T.5
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13
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33846246048
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For the synthesis of similar cyclopropane-fused ring compounds, see:
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For the synthesis of similar cyclopropane-fused ring compounds, see:. Nowak I., Cannon J.F., and Robins M.J. J. Org. Chem. 72 (2007) 532-537
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Nowak, I.1
Cannon, J.F.2
Robins, M.J.3
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0028835594
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Beddoes R.L., Lewis M.L., Quayle P., Johal S., Attwood M., and Hurst D. Tetrahedron Lett. 36 (1995) 471-474
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Beddoes, R.L.1
Lewis, M.L.2
Quayle, P.3
Johal, S.4
Attwood, M.5
Hurst, D.6
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20
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34248597739
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Witham C.A., Mauleon P., Shapiro N.D., Sherry B.D., and Toste F.D. J. Am. Chem. Soc. 129 (2007) 5838-5839
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Witham, C.A.1
Mauleon, P.2
Shapiro, N.D.3
Sherry, B.D.4
Toste, F.D.5
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34
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2942643950
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For the palladium migration and the following aryl coupling reactions, see:
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For the palladium migration and the following aryl coupling reactions, see:. Huang Q., Fazio A., Dai G., Campo M.A., and Larock R.C. J. Am. Chem. Soc. 126 (2004) 7460-7461
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Huang, Q.1
Fazio, A.2
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Larock, R.C.5
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35
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34249074441
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Campo M.A., Zhang H., Yao T., Ibdah A., McCulla R.D., Huang Q., Zhao J., Jenks W.S., and Larock R.C. J. Am. Chem. Soc. 129 (2007) 6298-6307
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Campo, M.A.1
Zhang, H.2
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Ibdah, A.4
McCulla, R.D.5
Huang, Q.6
Zhao, J.7
Jenks, W.S.8
Larock, R.C.9
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41
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0035910486
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The mechanism for the formation of compound 4a could be a β-carbon elimination from intermediate I, followed by decarboxylation. The formation of compound 8 could also be regarded similarly. Further studies on the mechanism are currently underway
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Sasaki K., Kondo Y., and Maruoka K. Angew. Chem., Int. Ed. 40 (2001) 411-414 The mechanism for the formation of compound 4a could be a β-carbon elimination from intermediate I, followed by decarboxylation. The formation of compound 8 could also be regarded similarly. Further studies on the mechanism are currently underway
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Sasaki, K.1
Kondo, Y.2
Maruoka, K.3
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42
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43049175274
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note
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4S: C, 68.39; H, 5.50; N, 3.32. Found: C, 68.27; H, 5.38; N, 3.26.
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44
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0000118679
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Legros J.-Y., Primault G., Toffano M., Riviere M.-A., and Fiaud J.-C. Org. Lett. 2 (2000) 433-436
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Legros, J.-Y.1
Primault, G.2
Toffano, M.3
Riviere, M.-A.4
Fiaud, J.-C.5
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