Paper Publications

• [1]Shi-Jiang He, Jia-Wang Wang, Yan Li,Zhe-Yuan Xu, Xiao-Xu Wang.Xi Lu, Yao Fu .Nickel-Catalyzed Enantioconvergent Reductive Hydroalkylation of Olefins with α‑Heteroatom Phosphorus or Sulfur Alkyl Electrophiles.J. Am. Chem. Soc,2020,142214-221.
• [2]Xi Lu,Yan Wang, Ben Zhang, Jing-Jing Pi, Xiao-Xu Wang, Bin Xiao.Tian-Jun Gong, Yao Fu.Nickel-Catalyzed Defluorinative Reductive Cross-Coupling of gem-Difluoroalkenes with Unactivated Secondary and Tertiary Alkyl Halides.J. Am. Chem. Soc,2017,13912632-12637.
• [3]Xiao-Xu Wang, Yuan-Tai Xu,Zhi-Lin Zhang.Xi Lu, Yao Fu .NiH-catalysed proximal-selective hydroalkylation of unactivated alkenes and the ligand effects on regioselectivity.Nature Commun.,2022,131890.
• [4]Jia-Wang Wang, Yan Li,Wan Nie, Zhe Chang, Zi-An Yu, Yi-Fan Zhao.Xi Lu, Yao Fu .Catalytic asymmetric reductive hydroalkylation of enamides and enecarbamates to chiral aliphatic amines.Nature Commun.,2021,121313.
• [5]Xi Lu, Bin Xiao,Zhenqi Zhang, Tianjun Gong, Wei Su, Jun Yi.Yao Fu, Lei Liu.Practical carbon–carbon bond formation from olefins through nickel-catalyzed reductive olefin hydrocarbonation.Nature Commun.,2016,711129.
• [6]Xiao-Xu Wang, Lu Yu,Zhi-Lin Zhang, De-Guang Liu, Changlin Tian.Xi Lu, Yao Fu .NiH-Catalyzed Reductive Hydrocarbonation of Enol Esters and Ethers.CCS Chem.,2022,4605-615.
• [7]Xiao-Xu Wang,Shi-Jiang He.Xi Lu, Yao Fu .Nickel-catalyzed three-component olefin reductive dicarbofunctionalization to access alkylborates.Chem. Sci.,2020,117950-7956.
• [8]Xi Lu, Xiao-Xu Wang,Tian-Jun Gong, Jing-Jing Pi, Shi-Jiang He.Xi Lu,Xi Lu, Yao Fu .Nickel-catalyzed allylic defluorinative alkylation of trifluoromethyl alkenes with reductive decarboxylation of redox-active esters.Chem. Sci.,2019,10809-814.
• [9]Xiao-Xu Wang,Yan Li, Jia-Wang Wang.Xi Lu, Yao Fu .Recent advances in nickel-catalyzed reductive hydroalkylation and hydroarylation of electronically unbiased alkenes.Sci. China Chem.,2020,631586-1600.
• [10]Xiao-Xu Wang, Lei Li,Tian-Jun Gong, Bin Xiao.Xi Lu, Yao Fu .Vicinal Diboration of Alkyl Bromides via Tandem Catalysis.Org. Lett.,2019,214298-4302.