Deng Zihang, Payne Jenna L, Vishe Mahesh, Jan Julius E L, Funk Cody M, Johnston Jeffrey N
Department of Chemistry and Vanderbilt Institute of Chemical Biology, Vanderbilt University, Nashville, Tennessee 37235, United States.
J Am Chem Soc. 2025 May 28;147(21):17584-17591. doi: 10.1021/jacs.5c05263. Epub 2025 May 14.
The development of highly enantioselective reactions often requires the adventitious discovery of a promising chiral catalyst and its resource-intensive optimization to high selectivity and generality. We report an approach less dependent on happenstance, whereby the performance of a single chiral ligand is enhanced not by modification of the architecturally complex chiral features but instead by an achiral counteranion. Critical to this strategy and its general application is the tactical development of -aryl trifluoromethyl sulfonamide Brønsted acid donors and their ability to unlock the full enantioselectivity potential of a single chiral Brønsted basic ligand for the enantioselective addition of azide to nitroalkene.
高对映选择性反应的发展通常需要偶然发现一种有前景的手性催化剂,并对其进行资源密集型优化以达到高选择性和通用性。我们报道了一种较少依赖偶然因素的方法,即通过非手性抗衡阴离子而非修饰结构复杂的手性特征来增强单一手性配体的性能。该策略及其普遍应用的关键在于策略性地开发芳基三氟甲基磺酰胺布朗斯特酸供体,以及它们释放单一手性布朗斯特碱配体在叠氮化物对硝基烯烃对映选择性加成反应中全部对映选择性潜力的能力。