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41
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See Ref. 14c.
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67
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33750463554
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note
-
15 for absolute configuration determination. Comparison of optical rotation data assigns the absolute configuration of our β-nitroamine adducts as (1S,2R).{A figure is presented}
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68
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33750446482
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Molecular Operating Environment 2004.03, MOE, Chemical Computing Group: Montreal, Quebec, Canada.
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70
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33750468802
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Similar models have been proposed for diastereoselective β-keto ester additions to nitroolefins, see:
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72
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73
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33750475009
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For conformational studies of cinchona alkaloid catalyzed reactions, see:
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