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Knochel P. In: Trost B.M., Fleming I., and Schreiber S.L. (Eds). Comprehensive Organic Synthesis Vol. 1, Chapter 1.7 (1991), Pergamon Press, Oxford
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2Zn and RZnX species react sluggishly with aldehydes and not at all with ketones. See, for instance:
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2Zn and RZnX species react sluggishly with aldehydes and not at all with ketones. See, for instance:. Noyori R., and Kitamura M. Angew. Chem., Int. Ed. Engl. 30 (1991) 49-69
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57049158776
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See also Ref. 11c.
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See also Ref. 11c.
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42
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57049147491
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note
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The low transfer ability of the methyl group from triorganozincates has been shown in other addition reactions. For example, see Refs. 8d and 9b.
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43
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57049169826
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note
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The determination of the relative proportion of 2 and 3 by HPLC using UV detection is an estimate unless it has been proven that both diastereoisomers have the same UV response. The fact that the enantiomeric ratios of the free primary amines are equal to the corresponding 2:3 diastereomeric ratios determined by HPLC indicates that the latter technique is appropriate for estimating the diastereomeric ratios of this type of sulfinamides.
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44
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0033582571
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46
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0037189199
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3ZnLi and di-tert-butyl ketone, see:
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3ZnLi and di-tert-butyl ketone, see:. Maclin K.M., and Richey Jr. H.G. J. Org. Chem. 67 (2002) 4602-4604
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Maclin, K.M.1
Richey Jr., H.G.2
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47
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33750357957
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The reversal of diastereofacial selectivity in hydride reductions of N-(tert-butanesulfinyl)ketimines has been described. See:
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The reversal of diastereofacial selectivity in hydride reductions of N-(tert-butanesulfinyl)ketimines has been described. See:. Colyer J.T., Andersen N.G., Tedrow J.S., Soukup T.S., and Faul M.M. J. Org. Chem. 71 (2006) 6859-6862
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Aggarwal, V.K.6
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60
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57049140518
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note
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2O and dried under vacuum.
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63
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57049120606
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