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36048942764
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See the Supporting Information for full details.
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36048952156
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10a by using modified reaction conditions: [2a] = 1 M, 0.5 mol% Rh.
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10a by using modified reaction conditions: [2a] = 1 M, 0.5 mol% Rh.
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46
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36049027824
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The procedure was said to take place in 12 h; however, the reaction conditions were not optimized. On the other hand, in the course of the TOF measurements, the hydrosilylation reaction from phenylacetylene (2a) by using Id took place within 5 min (see the Supporting Information). Moreover, we carried out the coupling reaction from the resulting crude mixture and the reaction was complete after 30 min.
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The procedure was said to take place in 12 h; however, the reaction conditions were not optimized. On the other hand, in the course of the TOF measurements, the hydrosilylation reaction from phenylacetylene (2a) by using Id took place within 5 min (see the Supporting Information). Moreover, we carried out the coupling reaction from the resulting crude mixture and the reaction was complete after 30 min.
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47
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36048960867
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See the Supporting Information for measurements of the TOF values and the kinetic profiles
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See the Supporting Information for measurements of the TOF values and the kinetic profiles.
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48
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36049007884
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See the Supporting Information
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See the Supporting Information.
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After 2 h at 60°C, the hydrosilylation step gave a mixture of isomers (EIZ 37:63 with less than 5% of the α-regioisomer).
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After 2 h at 60°C, the hydrosilylation step gave a mixture of isomers (EIZ 37:63 with less than 5% of the α-regioisomer).
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