Nickel‐Catalyzed Asymmetric Hydrogenation of All‐Carbon Tetrasubstituted Alkenes Enabled by van der Waals Interactions
Abstract
Abstract The asymmetric hydrogenation of all‐carbon tetrasubstituted alkenes has long posed a significant challenge due to their pronounced steric hindrance. Conventional approaches typically rely on precious metal catalysts. Herein, we report the first nickel‐catalyzed asymmetric hydrogenation of all‐carbon tetrasubstituted electron‐deficient alkenes. The developed catalytic system exhibits a broad substrate scope, delivering excellent reactivity and enantioselectivity across 37 examples (up to 99% yield, >99% ee, and TON up to 500). Combined experimental and computational studies reveal that van der Waals interactions play a pivotal role in governing enantioselectivity. This strategy further enables concise asymmetric syntheses of pharmaceutically relevant compounds, including Valerate and Esfenvalerate.
Article Details
Authors (9)
Congcong Yin
Key Lab of Functional Polymers for Sustainability of Jiangsu, School of Energy and Environment
Zichang Wang
Yuli Liang
Hubei Key Laboratory of Novel Reactor and Green Chemical Technology School of Chemical Engineering & Pharmacy Wuhan Institute of Technology Wuhan 430205 China
Jiamu Deng
Hubei Key Laboratory of Natural Products Research and Development College of Biological and Pharmaceutical Sciences China Three Gorges University Yichang 443002 China
Yunxin Zheng
Qixing Liu
Department of Chemical and Biomolecular Engineering, National University of Singapore, 4 Engineering Drive 4, Singapore 117585, Singapore
Jie Zeng
School of Chemistry & Chemical Engineering
Xumu Zhang
Department of Chemistry and Shenzhen Grubbs Institute
Haifeng Zhou