线性不对称损失时非正态分布过程均值优化

针对常见的两种非正态分布———梯形分布和三角分布，研究线性不对称质量损失时其过程均值的优化问题，建立了梯形分布在五种不同情况下线性不对称质量损失的数学模型，基于以上模型给出了线性不对称质量损失时梯形分布最优过程均值的确定方法；研究三角分布在四种不同情况下线性不对称质量损失的数学模型，并给出了线性不对称质量损失时三角分布最优过程均值的确定方法。最后，用实例验证本过程均值优化模型的有效性。实例表明，应用线性不对称损失函数，适当的改变过程均值，可以有效地降低产品的质量损失，通过调整工艺过程将获得最佳经济效益。     

Enantioconvergent Biocatalytic Redox Isomerization

Alcohol dehydrogenases can act as powerful catalysts in the preparation of optically pure γ‐hydroxy‐δ‐lactones by means of an enantioconvergent dynamic redox isomerization of readily available Achmatowicz‐type pyranones. Imitating the traditionally metal‐mediated “borrowing hydrogen” approach to shuffle hydrides across molecular architectures and interconvert functional groups, this chemoinspired and purely biocatalytic interpretation effectively expands the enzymatic toolbox and provides new opportunities in the assembly of multienzyme cascades and tailor‐made cellular factories.     

Synthesis of Stereochemically Flexible Cyclic Biphenylbisphosphinite Ligands: Control of the Dynamics and Selectivity

Novel l -tartaric acid based stereodynamic biphenylbisphosphinite ligands with anilino linkers were prepared as cyclic diamide compounds. The influence of the constitutional substitution pattern of the amino group at the aniline moiety on the diastereoselective formation of the ligand was investigated. While the meta-anilino bridged ligands showed a highly dynamic behavior and no discrimination between (R_ax) and (S_ax) configuration, l -tartaric acid substitution on ortho-anilino bridged ligands leads to diastereoselective self-alignment of the central biphenol axis, which controls the stereoselectivity of the ligand and catalyst. The experimental findings were corroborated by theoretical calculations. In the rhodium-catalyzed enantioselective hydrogenation of methyl 2-acetamidoacrylate (MAA), an enantiomeric ratio of 75 : 25 (R/S) was obtained for the ortho-substituted ligand.