个人简历

学习经历\r
1993-1997 理学学士，兰州大学化学系应用化学专业\r
1997-2002 理学博士，兰州大学化学系有机化学专业 （导师：涂永强 院士）\r
2002-2007 博士后，法国国家科学研究中心，天然产物化学研究所（导师：祝介平）\r
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任职\r
2007.8 副教授，北京大学，课题组长\r
2011.8 教授，北京大学

研究领域

"""""1.具有重要生物活性天然产物的全合成及仿生合成\r
2.药物合成及构效关系研究\r
3.有机合成新方法、新策略的研究\r
4.基于天然产物小分子探针的发现"

近期论文

Total Synthesis of (-)-Glaucocalyxin A, Jiuzhou Guo, Bo Li, Weihao Ma, Mallesham Pitchakuntla, Yanxing Jia, Angew. Chem. Int. Ed. 2020, 59, 1 – 5 \r
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Y. Wang, K. Liu, Z. Yu, Y. Jia. Type-II Pauson-Khand reaction of 1,8-enyne in the attempt of building 7/5 ring of (-)-caribenol A and DFT understanding. Tetrahedron Lett. 2019,\r
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Shibin Shi, Kuo Yuan, Yanxing Jia. Seven-step total synthesis of α-cyclopiazonic acid. Chin. Chem. Lett. 2019,\r
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Xiwu Zhang Xinxian Cai Bin Huang Lei Guo Zhongrun Gao Prof. Yanxing Jia. Enantioselective Total Syntheses of Pallambins A–D. Angew. Chem. Int. Ed. 2019, 58, 13380 –13384\r
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Weihao Ma, Zhi Huang, Yanxing Jia*. Improved synthesis of key intermediate of grayanotoxin III[J]. Chin. J. Org. Chem., 2019, 28(6): 402-407. \r
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H. Liu, L. Chen, K. Yuan, Y. Jia, A Ten‐Step Total Synthesis of Speradine C, Angew. Chem. Int. Ed. 2019, 58, 6362. \r
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L. Li, K. Yuan, Q. Jia, Y. Jia, Eight‐Step Total Synthesis of Phalarine by Bioinspired Oxidative Coupling of Indole and Phenol, Angew. Chem. Int. Ed. 2019, 58, 6074.\r
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Zhuang Chen, Mallesham Pitchakuntla and Yanxing Jia. Synthetic approaches to natural products containing 2,3-dihydrobenzofuran skeleton. Nat. Prod. Rep., 2019, 36, 666–690 \r
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Yuan Kuo, Jia Yanxing. Recent Progress in the Synthesis of 3,4-Fused Indole Alkaloids[J]. Chin. J. Org. Chem., 2018, 38(9): 2386-2399. \r
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Lei Li, Zhuang Chen, Xiwu Zhang, and Yanxing Jia. Divergent Strategy in Natural Product Total Synthesis. Chemical Reviews, 2018, 118 (7), pp 3752–3832 \r
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Lv, J.; Wang, B.; Yuan, K.; Wang, Y.; Jia, Y., Regioselective Direct C‑4 Functionalization of Indole: Total Syntheses of (−)-Agroclavine and (−)-Elymoclavine. Org. Lett. 2017,\r
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Ma, Y; Jia, Y. J. Synthetic study toward the total synthesis of fumigaclavines A–D. Chin. Pharm. Sci. 2017, 26, (7), 496–503. \r
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Liu, H.; Zhang, X.; Shan, D.; Pitchakuntla, M.; Ma, Y.; Jia, Y. Org. Lett. 2017, 19, 3323−3326. Link49. Liu, H.; Zhang, X.; Shan, D.; Pitchakuntla, M.; Ma, Y.; Jia, Y. Org. Lett. 2017, 19, 3323−3326.\r
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Shi, L.; Li, L.; Wang, J.; Huang, B.; Zeng, K.; Jin, H. Zhang, Q.; Jia, Y. Total synthesis of natural spiro-trisindole enantiomers similisines A, B and their stereoisomers. Tetrahedron Lett. 2017, 58(20), 1934-1938.\r
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Li, L.; Aibibula, P.; Jia, Q.; Jia, Y., Total Syntheses of Naucleamides A−C and E, Geissoschizine, Geissoschizol, (E)‑Isositsirikine, and 16-epi-(E)‑Isositsirikine. Org. 2017, 19, (10), 2642−2645.\r
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Liu, H.; Jia, Y., Ergot alkaloids: synthetic approaches to lysergic acid and clavine alkaloids. Nat. Prod. Rep. 2017, 34, 411-432.\r
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Huang, Z.; Lv, J.; Jia, Y., A Simple and Efficient Synthesis of Secondary Alkylamines from Nitroalkanes. ChemistrySelect 2016, 1, (18), 5892–5894. \r
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Tao, P.; Jia, Y., C–H bond activation in the total syntheses of natural products. Sci China Chem. 2016, 59, (9), 1109-1125.\r
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Tao, P.; Chen, Z.; Jia, Y., A concise gram-scale synthesis of ht-13-A via a rhodium-catalyzed intramolecular C–H activation reaction. Chem. Commun. 2016, 52, (75), 11300--1130\r
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Aibibula, P.; Huang, Z.; Jia, Y., Asymmetric total synthesis of 3-epi-naucleamide A. J. Chin. Pharm. Sci. 2016, 25, (1), 30-36.