Laboratory of Biocatalysis and Biotransformation, Department of Drugs Technology and Biotechnology, Faculty of Chemistry, Warsaw University of Technology, Koszykowa 75, 00-662, Warsaw, Poland.
Chembiochem. 2024 Oct 16;25(20):e202400394. doi: 10.1002/cbic.202400394. Epub 2024 Aug 2.
The reported chemoenzymatic strategy involves the employment of vinyl 3-(dimethylamino)propanoate as an irreversible acyl donor in a chromatography-free lipase-catalyzed kinetic resolution (KR) of racemic sec-alcohols. This biotransformation is achieved in a sequential manner using CAL-B to affect the kinetic resolution, followed by a simple acidic extractive work-up furnishing both KR products with excellent enantioselectivity (E>200; up to 98 % ee). The elaborated method eliminates a single-use silica gel chromatographic separation and significantly reduces organic solvent consumption to foster a more environmentally friendly chemical industry.
所报道的化学酶法策略涉及使用乙烯基 3-(二甲基氨基)丙酸盐作为不可逆酰基供体,在无色谱的脂肪酶催化的外消旋仲醇动力学拆分(KR)中使用。这种生物转化是通过连续使用 CAL-B 来影响动力学拆分来实现的,然后通过简单的酸性萃取处理,同时获得具有出色对映选择性(E>200;最高 98%ee)的 KR 产物。该方法省去了单次使用的硅胶色谱分离,并显著减少了有机溶剂的消耗,以促进更环保的化学工业。