舒兴中，兰州大学“萃英学者”特聘教授，博士生导师。于2010年毕业于兰州大学并取得博士学位，师从梁永民教授；之后在威斯康辛大学麦迪逊分校从事博士后研究，师从Weiping Tang教授；并于2012年进入加州大学伯克利分校和劳伦斯伯克利国家实验室从事博士后研究，师从F. Dean Toste教授和Paul Alivisatos教授；于2015年起在兰州大学化学化工学院、功能有机分子化学国家重点实验室从事教学科研工作。研究兴趣为有机合成方法学。目前主要的研究方向包括：（1）还原偶联反应；（2）不对称催化；（3）有机硅化学。迄今为止，已在Chem. Soc. Rev.、 J. Am. Chem. Soc.、 Angew. Chem. Int. Ed. 、 Chem. Sci.等国际著名刊物上发表论文四十余篇，他引1000余次，H因子20。主持国家自然科学基金项目两项。获Thieme Chemistry Journals Award 2020、第六届中国青少年科技创新奖、中国科学院奖学金和宝钢教育奖学金等奖项。

[1] Rong-De He, Chun-Ling Li, Qiu-Quan Pan, Peng Guo, Xue-Yuan Liu, and Xing-Zhong Shu*. Reductive Coupling between C−N and C−O Electrophiles. J. Am. Chem. Soc. 2019, 141, 12481−12486.

[2] Jicheng Duan, Yun-Fei Du, Xiaobo Pang and Xing-Zhong Shu*. Ni-catalyzed cross-electrophile coupling between vinyl/aryl and alkyl sulfonates: synthesis of cycloalkenes and modification of peptides. Chem. Sci. 2019, 10, 8706–8712.

[3] Zhi-Xiong Tian, Jin-Bao Qiao, Guang-Li Xu, Xiaobo Pang, Liangliang Qi, Wei-Yuan Ma,Zhen-Zhen Zhao, Jicheng Duan, Yun-Fei Du, Peifeng Su, Xue-Yuan Liu, and Xing-Zhong Shu*. Highly Enantioselective Cross-Electrophile Aryl-Alkenylation of Unactivated Alkenes. J. Am. Chem. Soc. 2019, 141, 7637−7643.

[4] Xue-Gong Jia, Peng Guo, Jicheng Duan and Xing-Zhong Shu*. Dual nickel and Lewis acid catalysis for cross-electrophile coupling: the allylation of aryl halides with allylic alcohols. Chem. Sci. 2018, 9, 640-645.

[5] Xiao-Biao Yan, Chun-Ling Li, Wen-Jie Jin, Peng Guo and Xing-Zhong Shu*. Reductive coupling of benzyl oxalates with highly functionalized alkyl bromides by nickel catalysis. Chem. Sci. 2018, 9, 4529-4534.

[6] Xing-Zhong Shu, Son C. Nguyen, Ying He, Fadekemi Oba, Qiao Zhang, Christian Canlas, Gabor A. Somorjai*, A. Paul Alivisatos*, F. Dean Toste*. Silica-Supported Cationic Gold(I) Complexes as Heterogeneous Catalysts for Regio- and Enantioselective Lactonization Reactions. J. Am. Chem. Soc., 2015, 137, 7083.

[7] Xing-zhong Shu, Miao Zhang, Ying He, Heinz, Frei*, F. Dean Toste*. Dual Visible Light Photoredox and Gold-catalyzed Arylative Ring Expansion. J. Am. Chem. Soc. 2014, 136, 5844.

[8] Xing-zhong Shu, Casi M. Schienebeck, Wangze Song, Ilia A. Guzei, and Weiping Tang*. Transfer of Chirality in Rhodium-Catalyzed Intramolecular (5+2) Cycloaddition of 3-Acyloxy-1,4-enyne (ACE) and Alkyne: Enantioselective Synthesis of Bicyclo[5.3.0]decatrienes. Angew. Chem. Int. Ed. 2013, 52, 13601. 

[9] Xing-Zhong Shu, Dongxu Shu, Casi M. Schienebeck and Weiping Tang*. Rhodium-catalyzed Acyloxy Migration of Propargylic Esters in Cycloadditions, Inspiration from the Recent "Gold Rush". Chem. Soc. Rev. 2012, 41, 7698. 

[10] Xing-Zhong Shu, Xiaoxun Li, Dongxu Shu, Suyu Huang, Casi Mae Schienebeck, Xin Zhou, Patrick J. Robichaux, Weiping Tang. Rhodium-Catalyzed Intra- and Intermolecular 5+2 Cycloaddition of 3-Acyloxy-1,4-enyne and Alkyne with Concomitant 1,2-Acyloxy Migration. J. Am. Chem. Soc., 2012, 134, 5211. 

[11] Xing-Zhong Shu, Suyu Huang, Dongxu Shu, Ilia A. Guzei, Weiping Tang*. Interception of a Rautenstrauch Intermediate by Alkynes for 5+2 Cycloaddition: Rhodium-Catalyzed Cycloisomerization of 3-Acyloxy-4-ene-1,9-diynes to Bicyclo 5.3.0 decatrienes. Angew. Chem. Int. Ed. 2011, 50, 8153.