首页> 美国政府科技报告 >Asymmetric Reduction of Alpha-Keto Esters with Potassium 9-O-(1,2:5,6-Di-O-Isopropylidene-Alpha-D-Glucofuranosyl)-9- Boratabicyclo(3.3.1)Nonane. Chiral Synthesis of Alpha-Hydroxy Esters with Optical Purity Approaching 100% ee
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Asymmetric Reduction of Alpha-Keto Esters with Potassium 9-O-(1,2:5,6-Di-O-Isopropylidene-Alpha-D-Glucofuranosyl)-9- Boratabicyclo(3.3.1)Nonane. Chiral Synthesis of Alpha-Hydroxy Esters with Optical Purity Approaching 100% ee

机译:用9-O-(1,2:5,6-二-O-异亚丙基-α-D-葡呋喃糖基)-9-硼代三环(3.3.1)壬烷不对称还原α-酮基酯。具有光学纯度接近100%ee的α-羟基酯的手性合成

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The asymmetric reduction of alpha-keto esters with potassium 9-O-(1,2:5,6-di-O-isopropylidene-alpha-D-glucofuranosyl)-9- boratabicyclo nonane (K 9-O-DIPGF-9-BBNH) to the corresponding alpha-hydroxy esters in optical purities approaching 100% ee has been achieved.

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