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Review on asymmetric reaction in aqueous media, see:
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Review on asymmetric reaction in aqueous media, see:. Manabe K., and Kobayashi S. Chem. Eur. J. 8 (2002) 4095-4101
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27744449807
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Typical examples of asymmetric reaction in aqueous media, see: (asymmetric transfer hydrogenation)
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Typical examples of asymmetric reaction in aqueous media, see:. Wang F., Liu H., Cun L., Zhu J., Deng J., and Jiang Y. J. Org. Chem. 70 (2005) 9424-9429 (asymmetric transfer hydrogenation)
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Itsuno, S.1
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22944492089
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For studies on polymer-supported chiral catalysts for asymmetric reaction in water, see:
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For studies on polymer-supported chiral catalysts for asymmetric reaction in water, see:. Ishida T., Akiyama R., and Kobayashi S. Adv. Synth. Catal. 347 (2005) 1189-1192
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For example, the standard ligand of aqueous biphase catalysis is 3,3′,3″-phosphinidynetris[benzenesulfonic acid], trisodium salt TPPTS.
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For example, the standard ligand of aqueous biphase catalysis is 3,3′,3″-phosphinidynetris[benzenesulfonic acid], trisodium salt TPPTS. Cornils B., and Kuntz E.G. J. Organomet. Chem. 502 (1995) 177-186
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27744449807
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Wang F., Liu H., Cui L., Zhu J., Deng J., and Jiang Y. J. Org. Chem. 70 (2005) 9424-9429
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Wang, F.1
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0345865488
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For examples of asymmetric transfer hydrogenation of ketones in organic solvent by using polymer-supported chiral catalyst, see:
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For examples of asymmetric transfer hydrogenation of ketones in organic solvent by using polymer-supported chiral catalyst, see:. Li X., Chen W., Hems W., King F., and Xiao J. Tetrahedron Lett. 45 (2004) 951-953
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42
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33645791568
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note
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2Ph), 6.4-7.1, 7.1-7.9 (br, Ar-H).
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43
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33645766416
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note
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2 (3.0 mg, 0.005 mmol) and polymer-supported chiral sulfonamide (0.012 mmol) were added in water (2 mL). After the mixture was degassed and stirred at 40 °C for 1 h under an argon atmosphere, sodium formate (340 mg, 5 mmol) was introduced. Ketone (1 mmol) was then added and the mixture was stirred at 40 °C for a certain period of time. After cooling to room temperature, the organic compounds were extracted with ether. The conversion and enantioselectivity were determined by GC and HPLC analysis, respectively.
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