The aldol reactions of α-keto phosphonates and aldehydes were facilitated by an axially chiral biphenylprolinamide under mild conditions, affording the synthetically and pharmaceutically useful products in high yields and excellent enantioselectivities.
α-酮
膦酸酯和醛的 aldol 反应在温和条件下得到了一个轴性手性
联苯丙
氨酸的促进,合成了在合成和药物上有用的产物,产率高且不对称选择性优秀。