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53249107124
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Whereas ethyl(tri-n-butylstannyl)zinc (I) is generated by using equimolar amounts of reagents, other species, such as II, may be present. (Chemical Equation Presented)
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Whereas ethyl(tri-n-butylstannyl)zinc (I) is generated by using equimolar amounts of reagents, other species, such as II, may be present. (Chemical Equation Presented)
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44
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In contrast with our experience, at least one laboratory has reported transmetalation of trialkylstannyl hydrides with dialkylzinc leads to decomposed products: F. J. A. Des Tombe, G. J. M. Van Der Kerk, J. Organomet. Chem. 1972, 34, 247-252.
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In contrast with our experience, at least one laboratory has reported transmetalation of trialkylstannyl hydrides with dialkylzinc leads to decomposed products: F. J. A. Des Tombe, G. J. M. Van Der Kerk, J. Organomet. Chem. 1972, 34, 247-252.
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45
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53249085722
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2+) are capable of catalyzing the addition of uncomplexed stannylzinc to aldehydes. This assertion would explain why reagents generated from stannyllithium and stannylmagnesium halides were not useful for asymmetric additions.
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2+) are capable of catalyzing the addition of uncomplexed stannylzinc to aldehydes. This assertion would explain why reagents generated from stannyllithium and stannylmagnesium halides were not useful for asymmetric additions.
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46
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53249151518
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Erdik, E.1
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47
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53249107473
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The absolute configurations of all other adducts were assigned in analogy. Catalysts 3 and 7 furnished the same major stereoisomer in Table 2, entries 3, 5, 6, and 8.
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The absolute configurations of all other adducts were assigned in analogy. Catalysts 3 and 7 furnished the same major stereoisomer in Table 2, entries 3, 5, 6, and 8.
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