Prior to FDU
1. Y. Sun, Y. Zhou, Y. Shi, J. del Pozo, S. Torker, and A. H. Hoveyda* Copper−Hydride-Catalyzed Enantioselective Processes with Allenyl Boronates. Mechanistic Nuances, Scope, and Utility in Target-Oriented Synthesis, J. Am. Chem. Soc. 2019, 141, 12087.
2. Y. Sun, P. Chen, D. Zhang, M. Baunach, C. Hertweck, and A. Li,* Bioinspired Total Synthesis of Sespenine, Angew. Chem. Int. Ed. 2014, 53, 9012.
3. Y. Sun, R. Li, W. Zhang, and A. Li,* Total Synthesis of Indotertine A and Drimentines A, F, and G, Angew. Chem. Int. Ed. 2013, 52, 9201.
4. Y. Sun, Z. Meng, P. Chen, D. Zhang, M. Baunach, C. Hertweck, and A. Li,* A concise total synthesis of sespenine, a structurally unusual indole terpenoid from Streptomyces, Org. Chem Front. 2016, 3, 368.
5. H. Li, Y. Sun, Q. Zhang, Y. Zhu, S. Li, A. Li, and C. Zhang,* Elucidating the Cyclization Cascades in Xiamycin Biosynthesis by Substrate Synthesis and Enzyme Characterizations, Org. Lett. 2015, 17, 306.
6. Q. Zhang, H. Li, L. Yu, Y. Sun, Y. Zhu, H. Zhu, L. Zhang, S. Li, Y. Shen, C. Tian, A. Li, H. Liu * and C. Zhang,* Characterization of the flavoenzyme Xia K as an N-hydroxylase and implications in indolosesquiterpene diversification, Chem. Sci. 2017, 8, 5067.
7. J. Pei, S. Zhou, F. Yang, Y. Sun, A. Li,* W. Zhang,* and W. He,* Identification and mechanistic studies of a cell cycle regulator JP18 from a library of synthetic indole terpenoid mimics, Chem. Asian J. 2016, 11, 2715.
8. X. Xiong, D. Zhang, J. Li, Y. Sun, S. Zhou, M. Yang, H. Shao,* and A. Li,* Synthesis of Indole Terpenoid Mimics via a Functionality-Tolerated Eu(fod)3-Catalyzed Conjugate Addition, Chem. Asian J. 2015, 10, 869.
9. S. Zhou, D. Zhang, Y. Sun, R. Li, W. Zhang, and A. Li,* Intermolecular Conjugate Addition of Pyrroloindoline and Furoindoline Radicals to α,β-Unsaturated Enones via Photoredox Catalysis, Adv. Synth. Catal. 2014, 2867.
10. M. Bian, Z. Wang, X. C. Xiong, Y. Sun, C. Matera, K. C. Nicolaou,* and A. Li,* Total Syntheses of Anominine and Tubingensin A, J. Am. Chem. Soc. 2012, 134, 8078.
