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For recent reviews of Cu-catalyzed AAA reactions, see: a) A. Alexakis, C. Malan, L. Lea, K. Tissot-Croset, D. Polet, C. Falciola, Chimia 2006, 60, 124;
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38
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34250891551
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The enantioselectivity and the geometry of the olefin were followed during the addition of the organomagnesium reagent to the cis-2 substrate, and no isomerization was observed during the course of the reaction
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The enantioselectivity and the geometry of the olefin were followed during the addition of the organomagnesium reagent to the cis-2 substrate, and no isomerization was observed during the course of the reaction.
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39
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33645450637
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40
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0036162329
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3) for 91% ee, R. W. Hoffmann et al., Synthesis 2002, 207).
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3) for 91% ee, R. W. Hoffmann et al., Synthesis 2002, 207).
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41
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34250799907
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The ligand L5, which was found to be best for the previous substrate, afforded ee values < 40 % in this case.
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The ligand L5, which was found to be best for the previous substrate, afforded ee values < 40 % in this case.
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42
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4544235332
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a) A. O. Larsen, W. Leu, C. N. Oberhuber, J. E. Campbell, A. H. Hoveyda, J. Am. Chem. Soc. 2004, 126, 11130;
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34250839657
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K. Tissot-Croset, PhD Thesis Dissertation, No. 3634, 2005, Geneva (Switzerland).
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E. Negishi, D. R. Swanson, C. J. Rousset, J. Org. Chem. 1990, 55, 5406.
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48
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34250860306
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Chiral homoallylic chlorides also underwent transformations with retention of ee value, either through Grignard reaction or through prior formation of the iodide, although they were less reactive.
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Chiral homoallylic chlorides also underwent transformations with retention of ee value, either through Grignard reaction or through prior formation of the iodide, although they were less reactive.
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