Engineering Research Center of Organosilicon Compounds & Materials, Ministry of Education, College of Chemistry and Molecular Sciences, Wuhan University, Wuhan 430072, China.
State Key Laboratory of Elemento-organic Chemistry, Nankai University, Tianjin 300071, China.
Org Lett. 2020 Jun 19;22(12):4852-4857. doi: 10.1021/acs.orglett.0c01687. Epub 2020 Jun 6.
A stereodivergent preparation of α-quaternary serine/cysteine derivatives incorporating two adjacent stereogenic centers has been developed through Cu/Ir-catalyzed asymmetric allylation of 2-oxazoline-4-carboxylates and 2-thiazoline-4-carboxylates. Tuning the electronic effect is the key to enhancing the reactivity of 2-oxazoline-4-carboxylates and suppressing the undesired β-elimination. The salient feature of this protocol is that all four stereoisomers of α-quaternary serine and cysteine derivatives could be achieved from the identical starting materials through pairwise combination of two distinct chiral catalysts.
通过铜/铱催化的 2-恶唑啉-4-羧酸酯和 2-噻唑啉-4-羧酸酯的不对称烯丙基化反应,开发了一种包含两个相邻手性中心的α-季碳型丝氨酸/半胱氨酸衍生物的立体发散性制备方法。调整电子效应是提高 2-恶唑啉-4-羧酸酯反应性和抑制不必要的β-消除的关键。该方法的显著特点是,通过两种不同手性催化剂的两两组合,从相同的起始原料中可以得到α-季碳型丝氨酸和半胱氨酸衍生物的所有四个立体异构体。