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Aldehydes 1a,d-f,h were prepared from the corresponding enantiopure α-amino alcohols under conditions known to prevent racemization; see: Ocejo, M.; Vicario, J. L.; Badia, D.; Carrillo, L.; Reyes, E. Synlett 2005, 2110-2112. Aldehydes 1b,c,g were prepared from racemic α-amino alcohols by the same method.
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27
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33749521180
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note
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Silane 2b was prepared by the same procedure as 2a.
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28
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37049088928
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0346488967
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30
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33749506139
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note
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3.
-
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31
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33749533718
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note
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The ratio of 3b:diene was approximately 4:1.
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-
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32
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33749518642
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note
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iPrOH 99:1, 1 mL/min).
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33
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33749516578
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note
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The crystals were prepared from rac-3b; see Supporting Information.
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35
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33751158182
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Keck, G. E.; Savin, K. A.; Cressman, E. N. K.; Abbott, D. E. J. Org. Chem. 1994, 59, 7889-7896.
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