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高明春

创建时间:  2021-09-22  孙湛蓉   浏览次数:   返回

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个人介绍

    高明春,博士,硕士生导师,上海市白玉兰人才计划获得者。2017年毕业于上海大学,获材料化学博士学位(导师:许斌 教授)。2018-2021年,美国加州大学戴维斯分校(UCD)化学系,进行博士后研究(导师:Jared T. Shaw教授)。2021年加入上海大学医学院。目前发表SCI学术论文20余篇,申请或授权多项国家发明专利。获批上海市科委扬帆计划、国家外国专家项目等



主要研究领域

       药物化学、有机合成方法学


代表性学术成果

论文

1. Gao, M.; Li, Y.; Gan, Y.; Xu, B.* Copper Nitrate-Mediated Regioselective [2+2+1] Cyclization of Alkynes with Alkenes: A Cascade Approach to Δ2-Isoxazolines. Angew. Chem. Int. Ed. 2015, 54, 8795-8799.

2. Gao, M.; Xu, B.* Copper Nitrate-Mediated Regio- and Stereoselective Difunctionalization of Alkynes: A Direct Approach to α-Chloro-β-nitroolefins. Org. Lett. 2016, 18, 4746- 4749.

3. Gao, M.; Zou, M.; Wang, J.; Tan, Q.; Liu, B.; Xu, B.* Palladium-Catalyzed Multicomponent Reaction of Alkynes, Carboxylic Acids, and Isocyanides: A Direct Approach to Captodative Olefins. Org. Lett. 2019, 21, 1593-1597.

4. Gao, M.; Gan, Y.; Xu, B.* From Alkenes to Isoxazolines via Copper-Mediated Alkene Cleavage and Dipolar Cycloaddition. Org. Lett. 2019, 21, 7435-7439.

5. Gao, M.; Zhou, K.; Xu, B.* Copper Nitrate-Mediated Selective Difunctionalization of Alkenes: A Rapid Access to β-Bromonitrates. Adv. Synth. Catal. 2019, 361, 2031-2036.

6. Gao, M.; Ruiz, J. M.; Jimenez, E.; Lo, A.; Laconsay, C. J.; Fettinger, J. C.; Tantillo, D. J.; Shaw, J. T.* Catalytic Generation of ortho-Quinone Dimethides via Donor/Donor Rhodium Carbenes. Chem. Sci. 2023, 14, 6443- 6448.

7. Zhou, L.; Huang, R.; Lu, S.; Liu, B.; Gao, M.*; Xu, B.* Direct Nitration of Vinylcycles with Copper Nitrate. Org. Lett. 2023, 25, 1415-1419.

8. Liu, J.; Zhou, K.; Sun, S.; Gao, M.*; Xu, B.* Copper Nitrate-Mediated Selective Bond Cleavage of Alkynes: Diverse Synthesis of Isoxazoles. Chin. J. Chem. 2023, 41, 3299-3304.

9. Huang, R.; Gao, M.; Yang, Z.; Han, W.; Wei, Z.; Li, Z.*; Xu, B.* 1,3-Difunctionalization of Donor-Acceptor Cyclopropanes Enabled by Copper Nitrate: A Direct Approach to γ-Halonitrates. Org. Lett. 2024, 26, 9659-9664.

10. Gao, M.; Lu, S.; Xu, B.* C–H Functionalization Enabled by Multiple Isocyanides. Chem. Soc. Rev. 2024, 53, 10147-10170.













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