讲师

龚宇昕

发布者:崔沁宇发布时间:2026-10-09浏览次数:24

姓名:龚宇昕

职称:讲师

联系方式:yuxin_gong@jsnu.edu.cn

个人简介

龚宇昕,理学博士。2025年于上海大学获得理学博士学位。主要研究方向为镍催化还原偶联和氧化还原偶联。近年来在Angew. Chem. Int. Ed., Acc.Chem.Res., Adv.Sci, Org. Lett等权威期刊发表多篇论文。

研究领域:

1.镍催化亲电试剂还原偶联

2.热条件下镍催化氧化还原偶联构建C(Sp2)-C(Sp3)和C(Sp3)-C(Sp3)

主讲课程:

药物分析、分析化学实验、仪器分析实验

教育背景:

2021年9月—2025年4月:上海大学,博士,导师:龚和贵教授;

2017年9月—2020年6月:上海大学,硕士,导师:龚和贵教授;

2013年9月—2017年6月:江苏师范大学本科生,导师:石枫教授;

近年来主要论文

[1]Yuxin Gong, Lei Su, Zhaodong Zhu, Yang Ye, and Hegui Gong*,“Nickel-Catalyzed Thermal Redox Functionalization of C(sp3)–H Bonds with Carbon Electrophiles”, Angew. Chem. Int. Ed. 2022, 61, e202201662.

[2]Yuxin Gong, Jie Hu, Canbin Qiu, and Hegui Gong*, “Insights into Recent Nickel-Catalyzed Reductive and Redox C−C Coupling of Electrophiles, C(sp3)−H Bonds and Alkenes”,Acc. Chem. Res.202457, 1149-1162.

[3] Yuxin Gong, Zhaodong Zhu, Qun Qian*, Weiqi Tong, and Hegui Gong*, “Zn- and Cu-Catalyzed Coupling of Tertiary Alkyl Bromides and Oxalates to Forge Challenging C–O, C–S, and C–N Bonds”, Org. Lett. 2021, 23, 1005−1010.

[4] Yu-Xin Gong, Qiong Wu, Hong-Hao Zhang, Qiu-Ning Zhu, Feng Shi*, “Enantioselective construction of a 2,2’-bisindolylmethane scaffold via catalytic asymmetric reactions of 2-indolylmethanols with 3-alkylindoles”, Org. Biomol. Chem., 2015, 13, 7993-8000.

[5] Deli Sun†, Yuxin Gong†, Yu Wu, Yunrong Chen* and Hegui Gong* “Bis(pinacolato)diboron-Enabled Ni-Catalyzed ReductiveArylation/Vinylation of Alkyl Electrophiles”, Adv. Sci. 2024, 2404301.

[6] Zhaodong Zhu† ,Yuxin Gong† Weiqi Tong, Weichao Xue* and Hegui Gong*, “Ni-Catalyzed Cross-Electrophile Coupling of Aryl Triflates with Thiocarbonates via C–O/C–O Bond Cleavage” Org. Lett.2021, 23, 6, 2158–2163

[7] Jiabao Wang†,Yuxin Gong†, Deli Sun and Hegui Gong Nickel-catalyzed reductive benzylation of tertiary alkyl halides with benzyl chlorides and chloroformates.Org. Chem. Front., 2021, 8, 2944-2948.

[8] 龚宇昕;龚和贵;雷川虎;童玮琦;钱群 半胱胺酸衍生物及其合成方法,中国发明专利,专利授权公告号:CN 112028800 B.

[9] Yan Gao, Yuxin Gong*, Fan Wu*, Hegui Gong*,Sterically Tolerant Nickel-Catalyzed Borylation of Aryl Triflates, Vinyl Triflates, and Vinyl Acetates.Org. Lett. 2026,28, 7141–7146.