手性合成子 chiral synthon
手性合成反应 stereoselective synthesis
立体化学与手性合成 Stereochemistry and Chiral Synthesis
生物催化的手性合成 chiral synthesis with biocatalyst
不对称合成或手性合成 asymmetric or chiral synthesis
Enantiopure N-substituted phenyl α-alanines are important intermediates for the chiral synthesis, especially in the field of chiral pesticides.
手性N取代苯基α氨基丙酸是一类重要的手性合成中间体, 特别是在农药领域, 是很多手性农药的关键中间体。
参考来源 - 脂肪酶催化拆分N取代苯基α氨基丙酸的研究·2,447,543篇论文数据，部分数据来源于NoteExpress
在手性合成中利用了天然或合成的光学活性化合物。
Chiral synthesis can be achieved by taking advantage of natural or synthetic optically active compounds.
提到生物催化，我们通常会想到外消旋物的动力学拆分和手性合成。
When considering biocatalysis, terms like kinetic racemic resolution or chiral syntheses immediately come to mind.
生物催化因其高效和高度的立体选择性，成为手性合成最重要的方法之一。
Biocatalysis has become one of the most promising and effective methods in the asymmetric synthesis for its outstanding stereochemical specificity.
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