[1] Li, J.-F.; Luan, Y.-X.; Ye, M.* Bimetallic anchoring catalysis for C–H and C–C activation. Sci. China Chem. 2021, 64, 1923 (review).
[2] Wang, Y.-X.; Ye, M.* Recent advances in Ni−Al bimetallic catalysis for unreactive bond transformation. Sci. China: Chem. 2018, 61, 1004 (review).
[3] Liu, Q.-S.; Wang, D.-Y.; Yang, Z.-J.; Luan, Y.-X.; Yang, J.-F.; Li, J.-F.; Pu, Y.-G.; Ye, M.* Ni−Al Bimetallic Catalyzed Enantioselective Cycloaddition of Cyclopropyl Carboxamide with Alkyne. J. Am. Chem. Soc. 2017, 139, 18150.
[4] Wang, Y.-X.; Qi, S.-L.; Luan, Y.-X.; Han, X.-W.; Wang, S.; Chen, H.; Ye, M.* Enantioselective Ni−Al Bimetallic Catalyzed exo-Selective C−H Cyclization of Imidazoles with Alkenes. J. Am. Chem. Soc. 2018, 140, 5360.
[5] Chen, H.; Wang, Y.-X.; Luan, Y.-X.; Ye, M.* Enantioselective Twofold C−H Annulation of Formamides and Alkynes without Built-in Chelating Groups. Angew. Chem., Int. Ed. 2020, 59, 9428.
[6] Zhang, T.; Luan, Y.-X.; Zheng, S.-J.; Peng, Q.*; Ye, M.* Chiral Aluminum-Controlled Ni-catalyzed Enantioselective Synthesis of Indenes via C-CN Bond Activation. Angew. Chem. Int. Ed. 2020, 59, 7439.
[7] Zhang, T.; Luan, Y.-X.; Lam, N. Y. S.; Li, J.-F.; Li, Y.; Ye, M.*; Yu, J.-Q.* A Directive Ni Catalyst Overrides Conventional Site-Selectivity in Pyridine C–H Alkenylation. Nat. Chem. 2021, 13, 1207.
[8] Li, J.-F.; Xu, W.-W.; Wang, R.-H.; Li, Y.; Yin, G.; Ye, M.* Construction 7-Membered Ring via Ni-Al Bimetal-Enabled C-H Cyclization for Synthesis of Tricyclic Imidazoles. Nat. Comm. 2021, 12, 3070.
[9] Rong-Hua Wang, Jiang-Fei Li, Yue Li, Shao-Long Qi, Tao Zhang, Yu-Xin Luan,* and Mengchun Ye* Selective C(sp3)−H Cleavage of Enamides for Synthesis of 2 Pyridones via Ligand-Enabled Ni−Al Bimetallic Catalysis. ACS Catal. 2021, 11, 858.
[10] Ge Yin, Yue Li, Rong-Hua Wang, Jiang-Fei Li, Xue-Tao Xu,* Yu-Xin Luan,* and Mengchun Ye* Ligand-Controlled Ni(0)−Al(III) Bimetal-Catalyzed C3−H Alkenylation of 2‑Pyridones by Reversing Conventional Selectivity. ACS Catal. 2021, 11, 4606.
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