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Core-Shell Composite as the Racemization Catalyst in the Dynamic Kinetic Resolution of Secondary Alcohols

机译:核 - 壳复合物作为次生醇的动态动态分辨率的外消旋催化剂

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Beta-Silicalite-1 core-shell microcomposites with controllable shell thickness were synthesized and used as racemization catalysts in the one-pot dynamic kinetic resolution (DKR) of secondary alcohols by using lipase-catalyzed transesterification. The inert Silicalite-1 shell covered the external acidic sites of the Beta zeolite core, suppressing dehydration and non-enantioselective transesterification of the alcohol. The alcohols could penetrate the Silicalite-1 shell to access the acidic sites at the core Beta for racemization, however, the enzymatically formed (R)-esters were excluded owing to their larger size. As a result, the high ee of the (R)-ester products was conserved and dehydration side products were minimized. Owing to the shape selective nature of the composite racemization catalyst, small and readily available acyl donors could be used in the enzyme-catalyzed transesterification to obtain the esters with high enantiopurity. The DKR of 1-phenylethanol with isopropenyl acetate using an optimized core-shell catalyst, CS-60, gave 92% selectivity to ester formation and the desired (R)-1-phenylethyl acetate was formed with 94% ee.
机译:通过使用脂肪酶催化的酯酯化,合成具有可控壳厚度的β-硅钛-1具有可控壳厚度的核心 - 壳体微型复合材料,并用作二级醇的一次性动态动力学分辨率(DKR)中的外消旋催化剂。惰性硅沸石-1壳覆盖了β沸石核的外酸性位点,抑制醇的脱水和非对辅助酯切选。醇可以渗透硅沸石-1壳,以进入核心β的酸性位点进行外消旋化,然而,由于其尺寸更大,酶形成的(R) - 术语被排除在外。结果,(R)-eSter产物的高EE被保守,并且脱水侧产物被最小化。由于复合外消旋化催化剂的形状选择性,可以在酶催化的酯交换中使用小而易于获得的酰基供体,以获得具有高映储备的酯。使用优化的核 - 壳催化剂CS-60具有异丙苯基乙酸二苯基乙醇的DKR,得到92%对酯形成的选择性,并且用94%EE形成所需的(R)-1-苯基乙酯。

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