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For recent advances in the field of catalytic asymmetric Michael (conjugate) addition reactions, see: Feringa, B. L.; de Vries, A. H. M. in Advances in Catalytic Processes; JAI Press: Greenwich, 1995; Vol. 1, pp 151-192; Kanai, M.; Nakagawa, Y.; Tomioka, K. J. Synth. Org. Chem. Jpn. 1997, 54, 474; Shibasaki, M.; Sasai, H.; Arai, T. Angew. Chem., Int. Ed. Engl. 1997, 36, 1236; Krause, N. ibid. 1998, 37, 283; Shibasaki, M.; Iida, T. Yamada, Y. M. A. J. Synth. Org. Chem. Jpn. 1998, 56, 344; Leonard, J.; DÌez-Barra, E.; Merino, S. Eur. J. Org. Chem. 1998, 2051.
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For recent advances in the field of catalytic asymmetric Michael (conjugate) addition reactions, see: Feringa, B. L.; de Vries, A. H. M. in Advances in Catalytic Processes; JAI Press: Greenwich, 1995; Vol. 1, pp 151-192; Kanai, M.; Nakagawa, Y.; Tomioka, K. J. Synth. Org. Chem. Jpn. 1997, 54, 474; Shibasaki, M.; Sasai, H.; Arai, T. Angew. Chem., Int. Ed. Engl. 1997, 36, 1236; Krause, N. ibid. 1998, 37, 283; Shibasaki, M.; Iida, T. Yamada, Y. M. A. J. Synth. Org. Chem. Jpn. 1998, 56, 344; Leonard, J.; DÌez-Barra, E.; Merino, S. Eur. J. Org. Chem. 1998, 2051.
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For recent advances in the field of catalytic asymmetric Michael (conjugate) addition reactions, see: Feringa, B. L.; de Vries, A. H. M. in Advances in Catalytic Processes; JAI Press: Greenwich, 1995; Vol. 1, pp 151-192; Kanai, M.; Nakagawa, Y.; Tomioka, K. J. Synth. Org. Chem. Jpn. 1997, 54, 474; Shibasaki, M.; Sasai, H.; Arai, T. Angew. Chem., Int. Ed. Engl. 1997, 36, 1236; Krause, N. ibid. 1998, 37, 283; Shibasaki, M.; Iida, T. Yamada, Y. M. A. J. Synth. Org. Chem. Jpn. 1998, 56, 344; Leonard, J.; DÌez-Barra, E.; Merino, S. Eur. J. Org. Chem. 1998, 2051.
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For recent advances in the field of catalytic asymmetric Michael (conjugate) addition reactions, see: Feringa, B. L.; de Vries, A. H. M. in Advances in Catalytic Processes; JAI Press: Greenwich, 1995; Vol. 1, pp 151-192; Kanai, M.; Nakagawa, Y.; Tomioka, K. J. Synth. Org. Chem. Jpn. 1997, 54, 474; Shibasaki, M.; Sasai, H.; Arai, T. Angew. Chem., Int. Ed. Engl. 1997, 36, 1236; Krause, N. ibid. 1998, 37, 283; Shibasaki, M.; Iida, T. Yamada, Y. M. A. J. Synth. Org. Chem. Jpn. 1998, 56, 344; Leonard, J.; DÌez-Barra, E.; Merino, S. Eur. J. Org. Chem. 1998, 2051.
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g) Kotsuki, H.; Teraguchi, M.; Shimomoto, N.; Ochi, M. ibid. 1996, 37, 3727.
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25
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0344616436
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note
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3 were used, respectively.
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-
-
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26
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0344184881
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note
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7+H, 357.1913; found, 357.1905.
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-
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27
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0345478698
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-
note
-
An excess amount of 4 did not improve the product yield.
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-
-
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28
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0344184879
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For similar findings, see: ref. 8h
-
For similar findings, see: ref. 8h.
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-
-
-
29
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0344616435
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note
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The use of 2-methylcydohexanone as a donor molecule was also fruitless due to the formation of a complex mixture.
-
-
-
-
30
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0345047231
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2O is reported to be 6.40. See ref. 4
-
2O is reported to be 6.40. See ref. 4.
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