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(a) Nakamura, M.; Liang, C.; Nakamura, E. Org. Lett. 2004, 6, 2015-2017.
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Recently transition metal-catalyzed Conia-ene type alkenylation reactions have been reported. (a) Au catalysis: Kennedy-Smith, J. J.; Staben, S. T.; Toste, F. D. J. Am. Chem. Soc. 2004, 126, 4526-4527.
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Recently transition metal-catalyzed Conia-ene type alkenylation reactions have been reported. (a) Au catalysis: Kennedy-Smith, J. J.; Staben, S. T.; Toste, F. D. J. Am. Chem. Soc. 2004, 126, 4526-4527.
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Au catalysis: Ochida, A.; Ito, H.; Sawamura, M. J. Am. Chem. Soc. 2006, 128, 16486-16487.
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(b) Au catalysis: Ochida, A.; Ito, H.; Sawamura, M. J. Am. Chem. Soc. 2006, 128, 16486-16487.
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Re catalysis: Kuninobu, Y.; Kawata, A.; Takai, K. Org. Lett. 2005, 7, 4823-4825.
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(c) Re catalysis: Kuninobu, Y.; Kawata, A.; Takai, K. Org. Lett. 2005, 7, 4823-4825.
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Ni/Yb catalysis: Gao, Q.; Zheng, B.-F.; Li, J.-H.; Yang, D. Org. Lett. 2005, 7, 2185-2188.
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(d) Ni/Yb catalysis: Gao, Q.; Zheng, B.-F.; Li, J.-H.; Yang, D. Org. Lett. 2005, 7, 2185-2188.
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39
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This auxiliary is used for a diastereoselective 1,4-addition reaction, a Guingant, A. Tetrahedron: Asymmetry 1991, 2, 415-418
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This auxiliary is used for a diastereoselective 1,4-addition reaction. (a) Guingant, A. Tetrahedron: Asymmetry 1991, 2, 415-418.
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Single crystal used for the X-ray structural analysis was analyzed by HPLC to provide the same retention time as the major enantiomer
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Single crystal used for the X-ray structural analysis was analyzed by HPLC to provide the same retention time as the major enantiomer.
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(S)-1-Methoxypentan-2-amine was prepared by methylation of L-(+)-isoleucinol with NaH/MeI according to Meyers et al.'s procedure: Meyers, A. I.; Williams, D. R.; Erickson, G. W.; White, S.; Druelinger, M. J. J. Am. Chem. Soc. 1981, 103, 3081-3087.
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(S)-1-Methoxypentan-2-amine was prepared by methylation of L-(+)-isoleucinol with NaH/MeI according to Meyers et al.'s procedure: Meyers, A. I.; Williams, D. R.; Erickson, G. W.; White, S.; Druelinger, M. J. J. Am. Chem. Soc. 1981, 103, 3081-3087.
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