Vrbický Martin, Macek Karel, Pochobradský Jaroslav, Svoboda Jan, Sedlák Miloš, Drabina Pavel
Institute of Organic Chemistry and Technology, Faculty of Chemical Technology, University of Pardubice, Studentská 573, 532 10 Pardubice, Czech Republic.
Beilstein J Org Chem. 2022 Apr 14;18:438-445. doi: 10.3762/bjoc.18.46. eCollection 2022.
The human drugs - the antibiotic linezolid () and the anticoagulant rivaroxaban () - belong among modern pharmaceutics, which contain an oxazolidine-2-one moiety bearing a stereogenic center. The chirality of these drugs is a fundamental attribute for their biological activity. Herein, one of the efficient asymmetric syntheses of these drugs was studied in detail. Highly enantioselective catalysts were tested in the key step of the synthetic procedure, i.e., the asymmetric Henry reaction, under different reaction conditions, using several starting aldehydes. The corresponding nitroaldols as chiral intermediates in the syntheses of these drugs were obtained in high yields and enantiomeric excesses of up to 91% ee.
人用药物——抗生素利奈唑胺()和抗凝剂利伐沙班()——属于现代药剂,其中含有带有手性中心的恶唑烷-2-酮部分。这些药物的手性是其生物活性的基本属性。在此,对这些药物的一种有效不对称合成方法进行了详细研究。在合成过程的关键步骤,即不对称亨利反应中,在不同反应条件下,使用几种起始醛,对高对映选择性催化剂进行了测试。在这些药物的合成中,相应的硝基醇作为手性中间体,以高产率和高达91%ee的对映体过量获得。