at Peking University School of Pharmaceutical Sciences
中文版
​​​​the Jia Research Group
Independent research
109. Biomimetic synthesis of pallavicinin, neopallavicinin, pallambins A–D, pallaviambins A/B, and pallavicinolides B/CLijun Chen, Peng Chen, Xiwu Zhang, Yu Zhang, Yanxing Jia*Chem 2024https://doi.org/10.1016/j.chempr.2024.04.003.
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108. Gut symbionts alleviate MASH through a secondary bile acid biosynthetic pathwayQixing Nie, Xi Luo, Kai Wang, Yong Ding, Shumi Jia, Qixiang Zhao, Meng Li, Jinxin Zhang, Yingying Zhuo, Jun Lin, Chenghao Guo, Zhiwei Zhang, Huiying Liu, Guangyi Zeng, Jie You, Lulu Sun, Hua Lu, Ming Ma,  Yanxing Jia*, Ming-Hua Zheng*, Yanli Pang*, Jie Qiao*, Changtao Jiang*Cell 2024https://doi.org/10.1016/j.cell.2024.03.034.
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107. Total Synthesis of Pallamolides A−EYu Zhang, Lijun Chen, Yanxing Jia*Angew. Chem. Int. Ed. 2024e202319127.
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106. Bioinspired Total Syntheses of Grayanotoxins II/III, Kalmanol, and Rhodomollacetals A–C with Three Distinct SkeletonsHao Cheng, Tianhao Ma, Xiao Liu, Yanxing Jia*CCS Chem. 2024Just Published. DOI: 10.31635/ccschem.024.202303731.
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105. Bioinspired Total Synthesis of Bipolarolides A and BBo Li, Chuanzhen Tan, Tianhao Ma, Yanxing Jia*Angew. Chem. Int. Ed. 2024, e202319306.
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104. Design, syntheses and biological evaluation of natural product aiphanol derivatives and analogues: Discovery of potent anticancer agents, Licheng Yao, Wenqing Cai, Shanmei Chen, Aidan Wang, Xin Wang, Chuanke Zhao, Chengchao Shou*, Yanxing Jia*Bioorg. Med. Chem. Lett. 2023, 90, 129326.
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103. Total Synthesis of (+)-Aberrarone, Yang Wang, Yongjian Su, Yanxing Jia*J. Am. Chem. Soc. 2023, 145, 9459-9463.

          Organic Chemistry Portal (https://www.organic-chemistry.org/Highlights/2023/06November.shtm)D. F. Taber.

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102. Total Synthesis of (−)-Principinol C
  • Tianhao Ma
  • Hao Cheng
  • Mallesham Pitchakuntla
  • Weihao Ma
  • , Yanxing Jia*J. Am. Chem. Soc. 2022, 144, 20196-20200.
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    100. Bioinspired Total Synthesis of (+)-Euphorikanin AZhuang Chen, Kuan Zhao, Yanxing Jia*Angew. Chem. Int. Ed. 202261, e202200576.

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    99. Cascade Cyclization Reaction Initiated by Benzylic Carbocation of Indole: Scope and Mechanistic InsightsZhongrun Gao, Yuan Wang, Hang Song, Zhengren Xu*, Yanxing Jia*Chin. J. Org. Chem. 2021, 41, 3126-3133.
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    98. Protecting-Group-Free Total Synthesis of (–)-Pallambins A-DXiwu Zhang, Yuan Wang, Peng Chen, Xinxian Cai, Yanxing Jia*Chin. J. Chem. 2021, 39, 1983-1996.
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    97. “Total synthesis of Kopsine, Fruticosine, and structurally related polycyclic caged Kopsia indole alkaloids”, Bo Qin, Yuan Wang, Xin Wang*, Yanxing Jia*. Org. Chem. Front. 2021, 8(2), 3​69-383.
    96. “Synthesis of benzofuro[3,2-b]indolines via regioselective electrooxidative coupling of indoles and phenols”, Keyuan Li, Yuan Wang, Lijun Chen, Lei Li, Yanxing Jia*. Tetrahedron. Lett. 2021, 63(36), 152603.
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    95. “Total Synthesis of (−)-Glaucocalyxin A”, Jiuzhou Guo, Bo Li, Weihao Ma, Mallesham Pitchakuntla, Yanxing Jia*. Angew. Chem. Int. Ed. 2020, 59(35), 15195–15198. Angew. Chem. 2020, 132(35), 15307–15310.

    highlighted in synfacts, Synfacts 2020, 16(08), 0882.

    《有机化学》亮点介绍2020, 40(10), 3487-3489.

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    94. “Seven-step total synthesis of α-cyclopiazonic acid”, Shibin Shi, Kuo Yuan, Yanxing Jia*. Chin. Chem. Lett. 2020, 31(2), 401403.
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    93. “A concise total synthesis of secoisolariciresinol”, Jiuzhou Guo, Yanxing Jia*. J. Chin. Pharm. Sci. 2019, 28(10), 699703.
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    92. “Improved synthesis of key intermediate of grayanotoxin III”, Weihao Ma, Zhi Huang, Yanxing Jia*. J. Chin. Pharm. Sci. 2019, 28(6), 402407.
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    91. “Type-II Pauson-Khand Reaction of 1,8-enyne in the Attempt of Building 7/5 Ring of (-)-Caribenol A and DFT Understanding”, Yang Wang, Kang Liu, Zhi-Xiang Yu*, Yanxing Jia*. Tetrahedron Lett. 2019, 60(36), 151001 .
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    90. “Natural product incarvillateine aggravates epileptic seizures by inhibiting GABAA currents”, Xiling Bian*, Yu Zhang, Bin Huang, Xintong Wang, Gongxin Wang, Yuhao Zhu, Yan Liu, Jianhui Liang, Yanxing Jia*, Kewei Wang*. Eur. J. Pharmaco. 2019, 858, 172496.
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    89. Enantioselective Total Syntheses of Pallambins A-D”, Xiwu Zhang, Xinxian Cai, Bin Huang, Lei Guo, Zhongrun Gao, Yanxing Jia*. Angew. Chem. Int. Ed. 2019, 58(38), 13380–13384. Angew. Chem. 2019, 131(38), 13514–13518.
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    88. “A Ten-Step Total Synthesis of Speradine C”, Haichao Liu, Lijun Chen, Kuo Yuan, Yanxing Jia*. Angew. Chem. Int. Ed. 2019, 58(19), 6362–6365. Angew. Chem. 2019, 131(19), 6428–6431.

    highlighted in synfacts, Synfacts 2019, 15(7), 0714.

         《有机化学》亮点介绍2019, 39(8), 2344.

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    87. “Eight-Step Total Synthesis of Phalarine by Bioinspired Oxidative Coupling of Indole and Phenol”, Lei Li, Kuo Yuan, Qianlan Jia, Yanxing Jia*. Angew. Chem. Int. Ed. 2019, 58(18), 60746078. Angew. Chem. 2019, 131(18), 6135–6139.

    highlighted in synfacts, Synfacts 2019, 15(7), 0712.

    x-mol化学资讯平台亮点介绍.

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    86. “Synthetic approaches to natural products containing a 2,3-dihydrobenzofuran skeleton”, Zhuang Chen, Mallesham Pitchakuntla, Yanxing Jia*. Nat. Prod. Rep. 2019, 36(4), 666690.
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    85. “Recent Progress in the Synthesis of 3,4-Fused Indole Alkaloids 3,4-桥环吲哚类生物碱的合成进展, Kuo Yuan, Yanxing Jia*. Chin. J. Org. Chem. 2018, 38(9), 2386-2399. 《有机化学》,2018, 38(9), 2386-2399.
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    84. “Divergent Strategy in Natural Product Total Synthesis”, Lei Li, Zhuang Chen, Xiwu Zhang, Yanxing Jia*. Chem. Rev. 2018, 118(7), 37523832.
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    83. “Synthetic Study toward the Total Synthesis of Fumigaclavines A–D”, Yongfan Ma, Yanxing Jia*. J. Chin. Pharm. Sci. 2017, 26(7), 496503.
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    82. “Regioselective Direct C-4 Functionalization of Indole: Total Syntheses of (–)-Agroclavine and (–)-Elymoclavine”, Jianbo Lv, Bin Wang, Kuo Yuan, Yuan Wang, Yanxing Jia*. Org. Lett. 2017, 19(13), 3664 3667.
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    81.“Total Syntheses of Festuclavine, Pyroclavine, Costaclavine, epi-Costaclavine, Pibocin A, 9-Deacetoxyfumigaclavine C, Fumigaclavine  G, and Dihydrosetoclavine”, Haichao Liu, Xiwu Zhang, Dong Shan, Mallesham Pitchakuntla, Yongfan Ma, Yanxing Jia*. Org. Lett. 2017, 19(12), 33233326.
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    80. “Total Syntheses of Naucleamides A−C and E, Geissoschizine, Geissoschizol, (E)-Isositsirikine, and 16-epi-(E)-Isositsirikine”, Lei Li, Paruke Aibibula, Qianlan Jia, Yanxing Jia*.