13688
当前位置: 首页   >  组员介绍   >  施江陵
施江陵 博士后     进组时间: 2021-08

20218-          至今:四川大学,博士后(合作导师:夏莹研究员)

20169-20217月:北京大学,理学博士(导师:王剑波教授)

20137-20169月:北京大学,访问学者(导师:施章杰教授)

20129-20156月:四川师范大学,理学硕士 (导师:汪必琴教授)

个人邮箱:jlingshi@scu.edu.cn

1. Bin Li+, Jiang-Ling Shi+, and Ying Xia. "Diversified Synthesis of All-Carbon Quaternary gem-Difluorinated Cyclopropanes via Copper-Catalyzed Cross-Coupling" Org. Lett. 2023, 15, 2674–2679 (+equal contribution).

2. Jiang-Ling Shi+, Zi-Xuan Wang+, Ze-Yu He, and Jian-Bo Wang. “Visible Light-Promoted Ring-Opening Alkenylation of Cyclic Hemiacetals through β-Scission of Alkoxy Radicals”. Chin. J. Chem. 2023, 41, 259-264 (+equal contribution, Article).

3. Jiang-Ling Shi, Yuan-Kai Wang, Zi-Xuan Wang, Bo-Wen Dou, and Jian-Bo Wang. “Ring-opening iodination and bromination of unstrained cycloalkanols through ß-scission of alkoxy radicals”. Chem. Commun. 2020, 56, 5002-5005.

4. Jiang-Ling Shi, Qin-Yu Luo, Wei-Zhi Yu, Bo Wang, Zhang-Jie Shi and Jian-Bo Wang. “Fe(II)-catalyzed oxidative alkenylation of benzylic C-H bond with diazo compounds”. Chem. Commun. 2019, 55, 4047-4050.

5. Jiang-Ling Shi, Zi-Xuan Wang, Rui Zhang, Yuan-Kai Wang, and Jian-Bo Wang. “Visible light-promoted ring-opening alkynylation, alkenylation and allylation of cyclic hemiacetals through ß-scission of alkoxy radicals”. Chem. -Eur. J. 2019, 25, 8992-8995. (Hot paper)

6. Jiang-Ling Shi+, Ding Wang+, Xi-Sha Zhang+, Xiao-Lei Li, Yu-Qin Chen, Yu-Xue Li, and Zhang-Jie Shi. “Oxidative coupling of sp2 and sp3 C–H bonds to construct dihydrobenzofurans”. Nature Commun. 2017, 8, 238-244. (+equal contribution, Article)

7. Jiang-Ling Shi, Ji-Cheng Zhang, Bi-Qin Wang, Ping Hu, Ke-Qing Zhao, and Zhang-Jie Shi. “Fe-promoted chlorobenzylation of terminal alkynes through benzylic C(sp3)-H bond functionalization”. Org. Lett. 2016, 18, 1238-1241.

8. Ji-Cheng Zhang+, Jiang-Ling Shi+, Bi-Qin Wang, Ping Hu, Ke-Qing Zhao, and Zhang-Jie Shi. “Direct oxidative arylation of aryl C-H bonds with aryl boronic acids via Pd catalysis directed by the N, N-dimethylaminomethyl group”. Chem. Asian J. 2015, 10, 840-843. (+equal contribution)