Franchino Allegra, Jakubec Pavol, Dixon Darren J
Chemistry Research Laboratory, Department of Chemistry, University of Oxford, 12 Mansfield Road, Oxford, OX1 3TA, UK.
Org Biomol Chem. 2016 Jan 7;14(1):93-6. doi: 10.1039/c5ob02141c.
The highly enantio- and diastereoselective aldol reaction of isocyanoacetates catalysed by Ag2O and cinchona-derived amino phosphines applied to the synthesis of (-)- and (+)-chloramphenicol is described. The concise synthesis showcases the utility of this catalytic asymmetric methodology for the preparation of bioactive compounds possessing α-amino-β-hydroxy motifs.
描述了由Ag2O和金鸡纳衍生的氨基膦催化的异氰基乙酸酯的高度对映选择性和非对映选择性羟醛反应,该反应应用于(-)-和(+)-氯霉素的合成。简洁的合成展示了这种催化不对称方法在制备具有α-氨基-β-羟基基序的生物活性化合物方面的实用性。