25 Q. Zhao, C. Ren, L. Liu, J. Chen, Y. Shao, N. Sun, R. Sun, Y. Kong, X. Ding, X. Zhang, Y. Xu, B. Yang, Q. Yin,* X. Yang*;B. Jiang*, J Med Chemy, 2019, 62, 9281-9298.
24 Huang, R.; Zhu W.; Wu Y.; Chen, J. K.; Yu, J. H.; Jiang, B.*;Chen, H. L.*; Chen, W. Z.*,A novel mass spectrometry-cleavable, phosphate-based enrichableand multi-targeting protein cross-linkerChem. Sci., 2019, 10, 6443-6447.
23 Qiu, X.; Sun, N.; Kong, Y.; Li, Y.; Yang, X.*; Jiang, B.*, Chemoselective Synthesis of Lenalidomide-Based PROTAC Library Using Alkylation Reaction. Org Lett2019, 21 (10), 3838-3841.
22 Huang, R.; Li, Z. H.; Yu, J. H.; Chen, H. L.*; Jiang, B.*,H2O‑Regulated Chemoselectivity in Oxa- Versus Aza-Michael Reactions,Org. Lett., 2019, 21, 4159-4162.
22 Huang, R.; Li, Z. H.; Sheng, Y.; Yu, J. H.; Wu, Y.; Zhan, Y. X.; Chen, H. L.*; Jiang, B.*, N-Methyl- N-phenylvinylsulfonamides for Cysteine-Selective Conjugation,Org. Lett., 2018, 20, 6526-6529.
21 Huang, R.; Li, Z. H.; Ren, P. L.; Chen, W. Z.; Kuang, Y. Y.; Chen, J. K.; Zhan, Y. X.; Chen, H. L.*; Jiang, B.*,N‐Phenyl‐N‐aceto‐vinylsulfonamides as Efficient and Chemoselective Handles for N‐Terminal Modification of Peptides and Proteins,Eur. J. Org. Chem.2018, 829-836.
20 Li, Z. H.; Huang, R.; Xu, H. T.; Chen, J. K.; Zhan, Y. X.; Zhou, X. H.; Chen, H. L.*; Jiang, B.* Divinylsulfonamides as Specific Linkers for Stapling Disulfide Bonds in Peptides Org. Lett., 2017, 19, 4972–4975
19 Chen, H. L.*; Huang, R.; Li, Z. H.; Zhu, W.; Chen, J. K.; Zhan, Y. X.; Jiang, B.* Selective lysine modification of native peptides via aza-Michael addition, Org. Biomol. Chem.2017, 15, 7339 – 7345
18 Liu, X. Y.; Xu, H. T.; Zhan, Y. X.; Ma, P. X.*; Chen, H. L.*; Jiang, B.* Tris(2-carboxyethyl)phosphine promotes hydrolysis of imonoboronates Tetrahedron Lett., 2017, 58, 3101-3106
17 Wang, H.; Zhou, F.; Ren, G.R.; Zheng, Q. H.; Chen, H. L.; Gao, B.; Klivansky, L.; Liu, Y.; Wu, B.; Xiu, Q. F.; Lu, J. M.; Sharpless, K. B.; Wu, P. SuFEx-Based Polysulfonate Formation from Ethenesulfonyl Fluoride-Amine Adducts Angew Chem Int Ed Engl; 2017, 56, 11203 –11208.
16 Chen, H. L.*; Han, C. J.; Wu, J.; Liu, X. Y.; Zhan, Y. X.; Chen, J. K.; Chen, Y. K.; Gu, R. N.; Zhang, L.; Chen, S. S.; Jia, J.; Zhen, X. C.; Zheng, L. T.*; Jiang, B.* Accessible Method for the Development of Novel Sterol Analogues with Dipeptide-like Side Chains That Act as Neuroinflammation Inhibitors ACS Chem. Neurosci.2016, 7, 305-315.
15. Mao D., Dr. Liang Y., Liu Y., Zhou X., Ma J., Prof. Jiang B.*, Prof. Liu J.*, Prof. Ma D.*, Acid-Labile Acyclic Cucurbit[n]uril Molecular Containers for Controlled Release - Angewandte Chemie International Edition DOI: 10.1002/anie.201707164
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