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note
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3 (0.98M, 20.4 μL, 0.02 mmol) and t-BuLi (1.49M, 13.5 μL, 0.02 mmol) at -78°C. A white precipitate, obtained when the solution was warmed to room temperature, was directly used as an immobilized ALB catalyst.
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0141826804
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note
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2, acetone/hexane = 1/10) gave 7. The enantiomeric purity of 7 was determined by chiral HPLC analysis (Daicel CHIRALPAK AS, i-PrOH/hexane = 1/4, 1.0 mL/min, 254 nm).
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note
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2O (2 mL), 9 (46 μL, 0.45 mmol), and 10 (20 μL, 0.15 mmol). The enantiomeric purity of 11 was determined by chiral HPLC analysis (Daicel CHIRALPAK AS, i-PrOH/hexane = 1/4, 1.0 mL/min, 254 nm).
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Recently, we have demonstrated a new and general concept for constructing multicomponent asymmetric catalysts using a "catalyst analogue". In this method, after copolymerization of a catalyst analogue having olefinic moieties with a monomer (e.g., MMA), the resulting polymer was used to prepare an active catalyst by exchanging the connecting group in the catalyst analogue with a catalytically active group. Arai, T.; Sekiguti, T.; Otsuki, K.; Takizawa, S.; Sasai, H. Angew. Chem., Int. Ed. 2003, 42, 2144-2147.
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Arai, T.1
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Takizawa, S.4
Sasai, H.5
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