Lu Peng, Burgenson William R, Simmons Bryan J, Liu Shuang, Yeung Kap-Sun, Qiao Jennifer X, Yu Jin-Quan
Department of Chemistry, The Scripps Research Institute, 10550 N. Torrey Pines Road, La Jolla, California 92037, United States.
Research & Development, Bristol Myers Squibb, 10300 Campus Point Drive Suite 100, San Diego, California 92121, United States.
J Am Chem Soc. 2025 Jan 15;147(2):1427-1433. doi: 10.1021/jacs.4c15834. Epub 2024 Dec 31.
The development of catalytic methods for the synthesis of enantiopure saturated heterocycles has been a long-standing challenge in asymmetric catalysis. We describe the first highly enantioselective palladium-catalyzed βC(sp)-H arylation and olefination of lactams for the preparation of various chiral N-heterocycles bearing quaternary carbon centers. The presence of strongly electron-withdrawing groups on the chiral bifunctional MPAThio ligand is crucial to the reactivity of weakly coordinating lactams. The resulting enantioenriched lactams are readily converted to a family of chiral piperidines and imides that are highly desirable in drug discovery.
开发用于合成对映体纯饱和杂环的催化方法一直是不对称催化领域长期面临的挑战。我们描述了首例用于制备各种带有季碳中心的手性 N-杂环的、高度对映选择性的钯催化内酰胺的 βC(sp)-H 芳基化和烯基化反应。手性双功能 MPAThio 配体上强吸电子基团的存在对于弱配位内酰胺的反应活性至关重要。所得对映体富集的内酰胺可轻松转化为一系列在手性药物发现中非常有用的手性哌啶和酰亚胺。