加盟交大之后：
21. Mengqing Zhang, Jingjing Wu*. Bioinspired synthesis of cucurbalsaminones B and C. Angew Chem. Int. Ed. 2024, DOI: 10.1002/anie.202417318.
20. Zhaodong Zhu, Jingjing Wu*. Benzoyl cyanide, a general radical acylating reagent for photoredox-catalyzed benzylic site-selective acylation reactions. Sci. China Chem. 2024, DOI：10.1007/s11426-024-2309-5.
19. Xiaotong Li, Yuxuan Zhang, Zhaoguo Zhang*, Jingjing Wu*. Concise synthesis of (25S)-Δ4-dafachronic acid and desulfated boophiline enabled by photoinduced decarboxylative allylation and asymmetric hydrogenation. Org. Chem. Front., 2024,11, 3939-3945. DOI: 10.1039/d4QO00685b.
18. Ruoxi Li, Jingjing Wu*. Reductive Aldol Approach to Natural Products: Bioinspired Synthesis of abeo-11(12→13)-Oleanane Triterpenoids. Org. Lett. 2023, 25, 6278–6283. DOI: 10.1021/acs.orglett.3c02076.
17. Jingjing Wu, Chao Shu, Zhihang Li, Adam Noble, Varinder K. Aggarwal. Photoredox-Catalyzed Decarboxylative Bromination, Chlorination and Thiocyanation Using Inorganic Salts. Angew Chem. Int. Ed. 2023, e202309684. DOI: 10.1002/anie.202309684.
16. Zhi-hao Shang, Jun Pan, Zeyu Wang, Ze-xin Zhang, JingJing Wu*. Transition-Metal-Free Radical Borylation Reactions. Eur. J. Org. Chem. 2023, e202201379. DOI: 10.1002/ejoc.202201379.
15. Hui Wang, Jingjing Wu, Adam Noble and Varinder K. Aggarwal., Selective Coupling of 1,2-Bis-Boronic Esters at the more substituted site through Visible-Light Activation of Electron Donor-Acceptor Complexes. Angew. Chem. Int. Ed., 2022, 61, e202202061. DOI: 10.1002/anie.202202061.
Before Joining SJTU：
14. Jingjing Wu, Robin Bär, Lin Guo, Adam Noble and Varinder K. Aggarwal., Photoinduced Deoxygenative Borylations of Aliphatic Alcohols. Angew. Chem. Int. Ed., 2019, 58, 18830 –18834.
13. Jingjing Wu, Phillip S. Grant, Xiabing Li, Adam Noble and Varinder K. Aggarwal.,Catalyst-Free Deaminative Functionalizations of Primary Amines via Photoinduced Single-Electron Transfer. Angew. Chem. Int. Ed., 2019, 58, 5697-5701.
12. Jingjing Wu, Lin He, Adam Noble and Varinder K. Aggarwal*.,Photoinduced Deaminative Borylation of Alkylamines. J. Am. Chem. Soc., 2018, 140, 10700−10704.
11. Jiachen Deng†, Jingjing Wu†, Hailong Tian, Jiajing Bao, Yong Shi, Weisheng Tian* and Jinghan Gui*., Alkynes from furans: A general fragmentation method applied to the Synthesis of the Proposed Structure of Aglatomin B. Angew. Chem. Int. Ed., 2018, 57, 3617 –3621. († equal contribution)
10. JingJing Wu, Paula Lorenzo, Siying Zhong, Muhammad Ali, Craig P. Butts, Eddie L. Myers, Varinder K. Aggarwal.,Synergy of synthesis, computation and NMR reveals correct Baulamycin structures. Nature, 2017, 547, 436-440.
9. Jingjing Wu, Yong Shi*, Weisheng Tian*., Synthesis of the aglycon of Aspafiliosides E and F via a spiroketal-forming cascade. Tetrahedron. Lett., 2017, 58, 923-925.
8. Jingjing Wu, Yong Shi*, Weisheng Tian*., Synthesis of the aglycon of Aspafiliosides E and F based on cascade reactions. Chem. Commun., 2016, 52, 1942-1944.
7. Jingjing Wu, Ran Gao, Yong Shi*, Weisheng Tian*., Direct amination of EF spiroketal in steroidal sapogenins: an efficient synthetic strategy and method for related alkaloids. Tetrahedron. Lett. 2015, 56, 6639–6642.
6. Jingjing Wu, Yong Shi*, Weisheng Tian*., Facile synthesis of solasodine based on a mild halogenation ring opening reaction of spiroketals in steroidal spogenins. Tetrahedron. Lett. 2015, 56, 1215–1217.
5. LingLi Hou, Yong Shi, ZhiDan Zhang, JingJing Wu, QingXiong Yang, WeiSheng Tian., Divergent Synthesis of Solanidine and 22-epi-Solanidine. J. Org. Chem. 2017, 82, 7463−7469.
4. ZhiDan Zhang, Yong Shi*, JingJing Wu, JingRong Lin, and WeiSheng Tian*., Synthesis of Demissidine and Solanidine. Org. Lett. 2016, 18, 3038−3040.
3. Xiang Hao, Jingjing Wu, Hailong Tian, Yong Shi*, Jingrong Lin, and Weisheng Tian*., A Short Synthesis of Clionamine D. Chin. J. Chem. 2015, 33, 1235-1238.
2. Wangjun *, Jingjing Wu, Weisheng Tian*., BF3•Et2O Promoted Sulfuration of Steroidal Sapogenins. Chin. J. Chem. 2015, 33, 632-636.
1. Xiaofei Zhang, Jingjing Wu, Yong Shi*, Weisheng Tian*., Formal synthesis of osladin based on an activation relay process. Tetrahedron. Lett. 2014, 55 ,4639–4642.
