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2个国家一流专业建设点:化学、材料化学

2个教育部新工科建设项目专业:化学工程与工艺、材料化学

师资队伍

物理化学教研室

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黄建

发布日期:2024-09-10    作者:     来源:     

黄建,男,博士,讲师,2022年博士毕业于江西师范大学,以色列希伯来大学博士后,20248月入职井冈山大学。

邮箱:jian.huang@mail.huji.ac.il

主讲课程

主要承担留学生基础化学课程。

主要研究方向

1.有机绿色催化。

2.功能有机小分子的构建。

3.含硫和硒类多肽及蛋白质的修饰和检测。

5年代表性成果

1.J. Huang, W. Chen, J. Liang, Q. Yang, Z. Deng, Z. Song, Y. Peng.* Rhodium(III)-Catalyzed Annulation of 3-Arylquinazolinones with Alkynes via Double C−H Activation: An Efficient Route for Quinolino[2,1-b]quinazolinones. Org. Chem. Front. 2021, 8, 6837.

2.J. Huang,# W. Chen,# J. Liang, Q. Yang, Y. Fan, M.-W. Chen, Y. Peng.* α-Keto acids as Triggers and Partners for the Synthesis of Quinazolinones, Quinoxalinones, Benzooxazinones, and Benzothiazoles in Water. J. Org. Chem. 2021, 86, 14866.

3.J. Huang, Y. Fu, Z. Deng, W. Chen, Z. Song, Y. Peng.* Rhodium-Catalyzed Oxidative Annulation of 1H-indazoles with Alkynes for the Synthesis of Indazolo[3,2-a]isoquinolines via C-H Bond Functionalization. Org. Biomol. Chem. 2020, 18, 9863.

4.J.Liang, J. Huang, Q. Yang, Y. Fu, Q. Ding, Y. Peng.* Synthesis of Dihydroindazolo[2,3-f]phenanthridine-5(6H)-ones via Rh(III)-Catalyzed C-H Activation of 2-Aryl Indazoles and Annulation with Iodonium Ylides. Green Chem., 2022, 24, 8441.

5.X. Ye, J. Huang, Z. Deng, Y. Peng.* Palladium-Catalyzed Cross-Coupling of 4-(Tosyloxy)quinazolines with H-Phosphonates and Phosphine Oxides: An Efficient Access to 2-(Hetero)aryl-4-phosphorylated Quinazolines. Synthesis. 2022, 54, 788.

6.X. Ye, J. Huang, Z. Deng, J. Yuan, Y. Peng.* Palladium-Catalyzed Cross-Coupling Reactions of 4-Tosyloxyquinazolines with Indoles: An Efficient Approach to 4-(1H-Indol-1-yl)quinazolines. Synthesis. 2021, 53, 383.

7.Y. Zhang, J. Huang, Z. Deng, X. Mao, Y. Peng.* Rhodium(III)-Catalyzed C-H Amination of 2-Arylquinazolin-4(3H)-one with N-alkyl-O-benzoyl-hydroxylamines. Tetrahedron. 2018, 74, 2330.

8.M.-W. Chen, Z. Deng, Q. Yang, J. Huang, Y. Peng.* Enantioselective Synthesis of Trifluoromethylated Dihydroquinoxalinones via Palladium-Catalyzed Hydrogenation. Org. Chem. Front. 2019, 6, 746.