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Ang Li, Ph.D.
Professor
State Key Laboratory of Chemical Biology
Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences
345 Lingling Road
Shanghai 200032, China
Tel: 86–21–54925466
E-mail: ali@sioc.ac.cn
Research group website: http://angligroup.sioc.ac.cn

Research Area
Total synthesis and mechanistic characterization of natural products

Professional Experience
2010–
Professor, Shanghai Institute of Organic Chemistry, Chinese Academy of Sciences, China
2010
Postdoctoral fellow, Institute of Chemical and Engineering Sciences, Singapore
Advisor: Prof. K.C. Nicolaou

Education
2004–2009
Ph.D., The Scripps Research Institute, USA
Advisor: Prof. K.C. Nicolaou
2000–2004
B.Sc., Peking University, Beijing, China
Advisor: Prof. Zhen Yang

Honors and Awards
2022 China Youth Science and Technology Award
2022 Chinese Chemical Society–Royal Society of Chemistry Young Chemist Award
2020 XPLORER Prize
2020 Thieme–IUPAC Prize in Synthetic Organic Chemistry
2020 Chinese Chemical Letters Young Investigator Award
2019 Bayer Investigator Award at Shanghai Institute of Organic Chemistry
2019 Fellow, Royal Society of Chemistry
2019 Korea Advanced Institute of Science and Technology BK21 Lectureship Award
2017 Asian International Symposium Distinguished Lectureship Award, Chemical Society of Japan
2017 Tetrahedron Young Investigator Award for Organic Synthesis
2016 Chinese–American Chemistry and Chemical Biology Professors Association Distinguished Faculty Award
2016 ChemComm Emerging Investigator Lectureship
2015 WuXi PharmaTech Life Science and Chemistry Award
2015 Roche Chinese Young Investigator Award
2013 Chinese Chemical Society Wei-Shan Award for Natural Product Synthesis
2013 China Pharmaceutical Association–Servier Youth Medicinal Chemist Award
2013 Thieme Chemistry Journal Award
2012 Asian Core Program Lectureship Award
2007 Chinese Government Award for Outstanding Graduate Students Abroad
2007 Bristol–Myers Squibb Graduate Fellowship in Organic Synthesis

Professional Activities
2023–
Advisory Board Member, ChemistryEurope
2019–
Advisory Board, Organic Letters
2019–
Associate Editor, Synlett
2017–2018
Editorial Board Member, Organic and Biomolecular Chemistry
2017–2022
Editorial Board Member, Science China Chemistry
2017–2020
Advisory Board Member, Asian Journal of Organic Chemistry
2017–
Advisory Board Member, Tetrahedron/Tetrahedron Letters
2016–2019
Advisory Board Member, Organic Chemistry Frontiers
2016–
Editorial Board Member, Chinese Chemical Letters

Publications
1. Lu Ren, Zhaohong Lu, Dimin Wu, Mingchen Ma, Ang Li,* Total synthesis of paxdaphnine A and daphlongamine B via an aza-Prins cyclization strategy. J. Am. Chem. Soc. Manuscript accepted.
2. Shaonan Wang, Min Sun, Yajuan Su, Zhou Xu, Ang Li,* Weiwei He,* Deucravacitinib induces proteasomal degradation of YAP1 in human glioblastoma cells. Synlett DOI: 10.1055/a-2331-6463.
3. Shaonan Wang, Yali Wu, Mengyu Ba, Zhou Xu, Guoxing Gu, William G. Whittingham, Cong Liu, Ang Li,* Weiwei He,* Discovery of the lysosome-inhibiting function of acremolactone B. Synlett DOI: 10.1055/a-2325-3938.
4. Mengyu Ba, Fengqi He, Lu Ren, William G. Whittingham, Peng Yang, Ang Li,* Scalable total synthesis of acremolactone B, Angew. Chem. Int. Ed. 2024, 63, e202314800.
5. Yan Peng, Yumeng Zhang, Ruan Fang, Hao Jiang, Gongcai Lan, Zhou Xu, Yajie Liu, Zhaoyang Nie, Lu Ren, Fengcan Wang, Shou-De Zhang, Yuyong Ma, Peng Yang, Hong-Hua Ge, Wei-Dong Zhang, Cheng Luo,* Ang Li,* Weiwei He,* Target identification and mechanistic characterization of indole terpenoid mimics: proper spindle microtubule assembly is essential for Cdh1-mediated proteolysis of CENP-A, Adv. Sci. 2024, 2305593.
6. Qun Wang, Jinxin Wang, Dianping Yu , Qing Zhang, Hongmei Hu, Mengting Xu, Hongwei Zhang, Saisai Tian, Guangyong Zheng, Dong Lu, Jiajia Hu, Mengmeng Guo, Minchen Cai, Xiangxin Geng, Yanyan Zhang, Jianhua Xia, Xing Zhang, Ang Li, Sanhong Liu,* Weidong Zhang,* Benzosceptrin C induces lysosomal degradation of PD-L1 and promotes antitumor immunity by targeting DHHC3. Cell Rep. Med. 2024, 5, 101357.
7. Ruonan Wang, Hao Xu, Arpan Banerjee, Zhongwen Cui, Yuyong Ma, William G. Whittingham, Peng Yang,* Ang Li,* Mild approach to nucleoside analogues via photoredox/Cu-catalyzed decarboxylative C-N bond formation. Total synthesis of oxetanocin A, Org. Lett. 2024, 26, 2691–2696.
8. Wenhao Zhang, Ming Lu, Lu Ren, Xiang Zhang, Shaonan Liu, Mengyu Ba, Peng Yang, Ang Li,* Total synthesis of four classes of Daphniphyllum alkaloids, J. Am. Chem. Soc. 2023, 145, 26569–26579.
9. Fan Yang, Jie Zhang, Jiacheng Li, Wenbo Ye,* Ang Li,* Weiwei He,* Synthesis of a glucose conjugate of pristimerin and evaluation of its anticancer activity. Chin. Chem. Lett. 2023, 34, 107438.
10. Zhuo Wang, Yiren Xiao, Song Wu, Jianghua Chen, Ang Li, Evangelos C. Tatsis,* Deciphering and reprogramming the cyclization regioselectivity in bifurcation of indole alkaloid biosynthesis. Chem. Sci. 2022, 13, 12389–12395.
11. Shanxiang Liu, Jinxin Wang,* Yuyong Ma, Xin Cao, Wei-Dong Zhang,* Ang Li,* Construction of alkyl-substituted 7-norbornenones through Diels?Alder cycloaddition of electron-deficient olefins and a cyclopentadienone derivative generated in situ. Chin. Chem. Lett. 2022, 33, 2041–2043.
12. B.-C. Yan, M. Zhou, J. Li, X.-N. Li, S.-J. He, J.-P. Zuo, H.-D. Sun, A. Li,* P.-T. Puno,* (–)-Isoscopariusin A, a naturally occurring immunosuppressive meroditerpenoid: structure elucidation and scalable chemical synthesis. Angew. Chem. Int. Ed. 2021, 60, 12859–12867.
13. J. Li, Y. Ma, X. Zhang, X. Cao, H. Gong,* A. Li,* Expeditious and scalable preparation of a Li?Thiele reagent for amine-based bioconjugation. Chin. Chem. Lett. 2021, 32, 700–702.
14. P. Yang, J. Li, L. Sun, M. Yao, X. Zhang, W.-L. Xiao, J.-H. Wang, P. Tian,* H.-D. Sun,* P.-T. Puno,* A. Li,* Elucidation of the structure of pseudorubriflordilactone B by chemical synthesis. J. Am. Chem. Soc. 2020, 142, 13701–13708.
15. S. Zhou, K. Xia, X. Leng, A. Li,* Asymmetric total synthesis of arcutinidine, arcutinine, and arcutine. J. Am. Chem. Soc. 2019, 141, 13718–13723.
16. A. Aspuru-Guzik, M.-H. Baik, S. Balasubramanian, R. Banerjee, S. Bart, N. Borduas-Dedekind, S. Chang, P. Chen, C. Corminboeuf, F.-X. Coudert, L. Cronin, C. Crudden, T. Cu, A. G. Doyle, C. Fan, X. Feng, D. Freedman, S. Furukawa, S. Ghosh, F. Glorius, M. Jefries-EL, N. Katsonis, A. Li, S. S. Linse, S. Marchesan, N. Maulide, A. Milo, A. R. H. Narayan, P. Naumov, C. Nevado, T. Nyokong, R. Palacin, M. Reid, C. Robinson, G. Robinson, R. Sarpong, C. Schindler, G. S. Schlau-Cohen, T. W. Schmidt, R. Sessoli, Y. Shao-Horn, H. Sleiman, J. Sutherland, A. Taylor, A. Tezcan, M. Tortosa, A. Walsh, A. J. B. Watson, B. M. Weckhuysen, E. Weiss, D. Wilson, V. W.-W. Yam, X. Yang, J. Y. Ying, T. Yoon, S.-L. You, A. J. G. Zarbin, H. Zhang, Charting a course for chemistry. Nat. Chem. 2019, 11, 286–294.
17. X. Zhang, B. N. Kakde, R. Guo, S. Yadav, Y. Gu, A. Li,* Total synthesis of echitamine, akuammiline, rhazicine, and pseudoakuammigine. Angew. Chem. Int. Ed. 2019, 58, 6053–6058.
18. G. Lan, J. Zhang, W. Ye, F. Yang, A. Li,* W. He,* W.-D. Zhang,* Celastrol as a tool for the study of the biological events of metabolic diseases. Sci. China Chem. 2019, 62, 409–416.
19. Y. Chen, L. Liu, D. Wu, Y.-P. He,* A. Li,* A one-pot protocol for copper-mediated azide?alkyne cycloaddition using alkenyl triflate precursors. Chin. Chem. Lett. 2019, 30, 269–270.
20. S. R. Hare, A. Li, D. J. Tantillo,* Post-transition state bifurcations induce dynamical detours in Pummerer-like reactions. Chem. Sci. 2018, 9, 8937–8945.
21. W. Ye, A. Li,* A practical route to 3D molecular diversity. Nature 2018, 560, 314–316.
22. Z. Lu, X. Zhang, Z. Guo, Y. Chen, T. Mu, A. Li,* Total synthesis of aplysiasecosterol A. J. Am. Chem. Soc. 2018, 140, 9211–9218.
23. S. Zhou, R. Guo, P. Yang, A. Li,* Total synthesis of septedine and 7-deoxyseptedine. J. Am. Chem. Soc. 2018, 140, 9025–9029.
24. W. Zhang, M. Ding, J. Li, Z. Guo, M. Lu, Y. Chen, L. Liu, Y.-H. Shen, A. Li,* Total synthesis of hybridaphniphylline B. J. Am. Chem. Soc. 2018, 140, 4227–4231.
25. Y. Chen, W. Zhang, L. Ren, J. Li, A. Li,* Total syntheses of daphenylline, daphnipaxianine A, and himalenine D. Angew. Chem. Int. Ed. 2018, 57, 952–956.
26. J. Li, W. Zhang, F. Zhang, Y. Chen, A. Li,* Total synthesis of daphniyunnine C (longeracinphyllin A). J. Am. Chem. Soc. 2017, 139, 14893–14896.
27. Y. Li, J. Li, H. Ding,* A. Li,* Recent advances on the total synthesis of alkaloids in mainland China. Natl. Sci. Rev. 2017, 4, 397–425.
28. Q. Zhang, H. Li, L. Yu, Y. Sun, Y. Zhu, H. Zhu, L. Zhang, S.-M. Li, Y. Shen, C. Tian, A. Li, H.-w. Liu,* C. Zhang,* Characterization of the flavoenzyme XiaK as an N-hydroxylase and implications in indolosesquiterpene diversification. Chem. Sci. 2017, 8, 5067–5077.
29. Z. Zhang, J. Wang, J. Li, F. Yang, G. Liu, W. Tang, W. He, J.-J. Fu, Y.-H. Shen,* A. Li,* W.-D. Zhang,* Total synthesis and stereochemical assignment of delavatine A: Rh-catalyzed asymmetric hydrogenation of indene-type tetrasubstituted olefins and kinetic resolution through Pd-catalyzed triflamide-directed C?H olefination. J. Am. Chem. Soc. 2017, 139, 5558–5567.
30. W. Zhang, A. Li,* A radical step forward. Nature Chem. 2017, 9, 198–199.
31. H. Li, Q. Chen, Z. Lu, A. Li,* Total syntheses of aflavazole and 14-hydroxyaflavinine. J. Am. Chem. Soc. 2016, 138, 15555–15558.
32. Q.-Y. Zheng,* A. Li,* The bloom of natural product chemistry in China. Sci. China Chem. 2016, 59, 1059–1060.
33. J. Pei, S. Zhou, F. Yang, Y. Sun, A. Li,* W.-D. Zhang,* 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, 2715–2718.
34. P. Yang, M. Yao, J. Li, Y. Li, A. Li,* Total synthesis of rubriflordilactone B. Angew. Chem. Int. Ed. 2016, 55, 6964–6968.
35. Y. Li, S. Zhu, J. Li, A. Li,* Asymmetric total syntheses of aspidodasycarpine, lonicerine, and the proposed structure of lanciferine. J. Am. Chem. Soc. 2016, 138, 3982–3985.
36. X. Yang, D. Wu, Z. Lu, H. Sun,* A. Li,* A mild preparation of alkynes from alkenyl triflates. Org. Biomol. Chem. 2016, 14, 5591–5594.
37. Y. Sun, Z. Meng, P. Chen, D. Zhang, M. Baunach, C. Hertweck, A. Li,* A concise total synthesis of sespenine, a structurally unusual indole terpenoid from Streptomyces. Org. Chem. Front. 2016, 3, 368–374.
38. M. Yang, X. Yang, H. Sun, A. Li,* Total synthesis of ileabethoxazole, pseudopteroxazole, and seco-pseudopteroxazole. Angew. Chem. Int. Ed. 2016, 55, 2851–2855.
39. Z. Lu, H. Li, M. Bian, A. Li,* Total synthesis of epoxyeujindole A. J. Am. Chem. Soc. 2015, 137, 13764–13767.
40. S. Zhou, H. Chen, Y. Luo, W. Zhang, A. Li,* Asymmetric total synthesis of mycoleptodiscin A. Angew. Chem. Int. Ed. 2015, 54, 6878–6882.
41. X. Xiong, D. Zhang, J. Li, Y. Sun, S. Zhou, M. Yang, H. Shao,* A. Li,* Synthesis of indole terpenoid mimics via a functionality-tolerated Eu(fod)3-catalyzed conjugate addition. Chem. Asian J. 2015, 10, 869–872.
42. M. Isobe,* A. Nishida,* Y.-M. Choo, N. A. Rahman,* P. Ploypradith, S. Ruchirawat,* G.-Q. Lin, A. Li,* Z.-J. Yao,* B.-J. Uang,* C.-C. Liao, P. Chiu,* B. M. Kim,* T. P. Loh,* The last and next decades of the Asian Core Program on Cutting-Edge Organic Chemistry in Asia. Chem. Asian J. 2015, 10, 790–804.
43. M. Wan, M. Yao, J. Gong, P. Yang, H. Liu,* A. Li,* Synthesis of the tetracyclic core of chlorospermines. Chin. Chem. Lett. 2015, 26, 272–276.
44. M. Yang, J. Li, A. Li,* Total synthesis of clostrubin. Nat. Commun. 2015, 6, 6445.
45. Z. Meng, H. Yu, L. Li, W. Tao, H. Chen, M. Wan, D. J. Edmonds, J. Zhong, A. Li,* Total synthesis and antiviral activity of indolosesquiterpenoids from the xiamycin and oridamycin families. Nat. Commun. 2015, 6, 6096.
46. H. Li, Y. Sun, Q. Zhang, Y. Zhu, S.-M. Li, A. Li, C. Zhang,* Elucidating the cyclization cascades in xiamycin biosynthesis by substrate synthesis and enzyme characterizations. Org. Lett. 2015, 17, 306–309.
47. J. Li, P. Yang, M. Yao, J. Deng, A. Li,* Total synthesis of rubriflordilactone A. J. Am. Chem. Soc. 2014, 136, 16477–16480.
48. Z. Lu, M. Yang, P. Chen, X. Xiong, A. Li,* Total synthesis of hapalindole-type natural products. Angew. Chem. Int. Ed. 2014, 53, 13840–13844.
49. S. Zhou, D. Zhang, Y. Sun, R. Li, W. Zhang, A. Li,* Intermolecular conjugate addition of pyrroloindoline and furoindoline radicals to α,β-unsaturated enones via photoredox catalysis. Adv. Synth. Catal. 2014, 356, 2867–2872
50. Y. Sun, P. Chen, D. Zhang, M. Baunach, C. Hertweck, A. Li,* Bioinspired total synthesis of sespenine. Angew. Chem. Int. Ed. 2014, 53, 9012–9016.
51. J. Deng, S. Zhou, W. Zhang, J. Li, R. Li, A. Li,* Total synthesis of taiwaniadducts B, C, and D. J. Am. Chem. Soc. 2014, 136, 8185–8188.
52. C. Wan, J. Deng, H. Liu,* M. Bian,* A. Li,* Recent advances of intermolecular Diels–Alder reaction in bio-inspired synthesis of natural products. Sci. China Chem. 2014, 57, 926–929.
53. X. Xiong, Y. Li, Z. Lu, M. Wan, S. Wu, H. Shao,* A. Li*, Synthesis of the 6,6,5,7-tetracyclic core of daphnilongeranin B. Chem. Commun. 2014, 50, 5294–5297.
54. H. Yu, C. Wan, J. Han,* A. Li,* A protocol for α-bromination of β-substituted enones. Acta Chim. Sinica 2013, 71, 1488.
55. Y. Sun, R. Li, W. Zhang, A. Li,* Total synthesis of indotertine A and drimentines A, F, and G. Angew. Chem. Int. Ed. 2013, 52, 9201–9204.
56. Z. Lu, Y. Li, J. Deng, A. Li,* Total synthesis of the Daphniphyllum alkaloid daphenylline. Nat. Chem. 2013, 5, 679–684.
57. J. Deng, R. Li, Y. Luo, J. Li, S. Zhou, Y. Li, J. Hu, A. Li,* Divergent total synthesis of taiwaniaquinones A and F and taiwaniaquinols B and D. Org. Lett. 2013, 15, 2022–2025.
58. S. Li, J. Han,* A. Li,* Interrupted fisher indole synthesis and its applications to alkaloid synthesis. Acta Chim. Sinica 2013, 73, 295–298.
59. M. Bian, Z. Wang, X. Xiong, Y. Sun, C. Matera, K. C. Nicolaou,* A. Li,* Total syntheses of anominine and tubingensin A. J. Am. Chem. Soc. 2012, 134, 8078–8081.
60. J. Deng, B. Zhu, Z. Lu, H. Yu, A. Li,* Total synthesis of (–)-fusarisetin A and reassignment of the absolute configuration of its natural counterpart. J. Am. Chem. Soc. 2012, 134, 920–923.
61. C.-C. Tseng, H. Ding, A. Li, Y. Guan, D. Y.-K. Chen, A modular synthesis of salvileucalin B structural domains. Org. Lett. 2011, 13, 4410–4413.
62. K. C. Nicolaou, A. Li, D. J. Edmonds, G. S. Tria, S. P. Ellery, Total syntheses of platensimycin and related natural products. J. Am. Chem. Soc. 2009, 131, 16905–16918.
63. K. C. Nicolaou, A. Li, S. P. Ellery, D. J. Edmonds, Rhodium-catalyzed asymmetric enyne cycloisomerization of terminal alkynes and formal total synthesis of (–)-platensimycin. Angew. Chem. Int. Ed. 2009, 48, 6293–6295.
64. K. C. Nicolaou, A. F. Stepan, T. Lister, A. Li, A. Montero, G. S. Tria, C. I. Turner, Y. Tang, J. Wang, R. M. Denton, D. J. Edmonds, Design, synthesis and biological evaluation of platensimycin analogs with varying degrees of molecular complexity. J. Am. Chem. Soc. 2008, 13110–13119.
65. K. C. Nicolaou, A. Li, Total syntheses and structural revision of α- and β-diversonolic esters and total syntheses of diversonol and blennolide C. Angew. Chem. Int. Ed. 2008, 47, 6579–6582.
66. K. C. Nicolaou, Y. Tang, J. Wang, A. F. Stepan, A. Li, A. Montero, Total synthesis and antibacterial properties of carbaplatensimycin. J. Am. Chem. Soc. 2007, 129, 14850–14851.
67. K. C. Nicolaou, D. J. Edmonds, A. Li, G. S. Tria, Asymmetric total syntheses of platensimycin. Angew. Chem. Int. Ed. 2007, 46, 3942–3945.
68. K. C. Nicolaou, A. Li. D. J. Edmonds, Total synthesis of platensimycin. Angew. Chem. Int. Ed. 2006, 45, 7086–7090.
69. K. C. Nicolaou, R. M. Denton, A. Lenzen, D. J. Edmonds, A. Li, R. M. Milburn, S. T. Harrison, Stereocontrolled synthesis of model core systems of lomaiviticins A and B. Angew. Chem. Int. Ed. 2006, 45, 2076–2081.
70. B. Liang, J. Liu, Y.-X. Gao, K. Wongkhan, D.-X. Shu, Y. Lan, A. Li, A. S. Batsanov, J. A. H. Howard, T. B. Marder, J.-H. Chen, Z. Yang, Synthesis of thiourea-oxazolines, a new class of chiral S,N-heterobidentate ligands: application in Pd-catalyzed asymmetric bis(methoxycarbonylation) of terminal olefins. Organometallics 2007, 26, 4756–4762.
71. Z. Xiong, N. Wang, M. Dai, A. Li, J. Chen, Z. Yang, Synthesis of novel palladacycles and their application in Heck and Suzuki reactions under aerobic conditions. Org. Lett. 2004, 6, 3337–3340.
72. Y. Zhang, A. Li, Z. Yan, G. Xu, C. Liao, C. Yan, (ZrO2)0.85(REO1.5)0.15 (RE = Sc, Y) solid solutions prepared via three Pechini-type gel routes: 1. gel formation and calcination behaviors. J. Solid State Chem. 2003, 171, 434–438.
73. Y. Zhang, A. Li, Z. Yan, G. Xu, C. Liao, C. Yan, (ZrO2)0.85(REO1.5)0.15 (RE=Sc, Y) solid solutions prepared via three Pechini-type gel routes: 2. sintering and electrical properties. J. Solid State Chem. 2003, 171, 439–443.
74. Y. Zhang, A. Li, Z. Yan, C. Liao, C. Yan, Calcination time effects on the particle size, specific surface area and morphology of rare earth oxides (III). J. Chin. Rare Earth Soc. (Chinese Edition) 2002, 20, 170–172.
75. Y. Zhang, Z. Yan, A. Li, X, Jiang, L. Gu, C. Liao, C. Yan, Effects of precipitation conditions on specific surface area and morphology of rare earth oxides (II). J. Chin. Rare Earth Soc. (Chinese Edition) 2001, 19, 471–473.

Selected Presentations
1. Institute of Chemical Research of Catalonia School, Tarragona, Spain, September 14, 2023.
2. The 3rd Alpine Winter Conference on Medicinal and Synthetic Chemistry (Virtual Event), January 28, 2022.
3. Basel Chemical Society Lecture (Virtual Event), Basel, Switzerland, May 27, 2021.
4. Boehringer Ingelheim Lecture (Virtual Event), The Scripps Research Institute, USA, October 30, 2020.
5. Bristol–Myers Squibb Lecture in Organic Synthesis, Yale University, USA, May 16, 2019.
6. The 2nd KAIST BK21 Symposium, Korea Advanced Institute of Science and Technology, Korea, February 18, 2019.
7. The 15th International Symposium for Chinese Organic Chemists, Taipei, October 26–29, 2018.
8. The 33rd Annual W.S. Johnson Symposium in Organic Chemistry, Stanford University, USA, October 12, 2018.
9. Merck Symposium in Organic Chemistry, Boston College, USA, October 5, 2018.
10. The 24th Conference on Isoprenoids, Bialystok, Poland, September 9–12, 2018.
11. Gordon Research Conference on Stereochemistry, Salve Regina College, Rhode Island, USA, July 22–27, 2018.
12. Organic Syntheses Symposium, Massachusetts Institute of Technology, USA, May 10, 2018.
13. The 53rd Swiss Chemical Society Conference on Stereochemistry (Bürgenstock Conference), Brunnen, Switzerland, April 29–May 3, 2018.
14. Gordon Research Conference on Natural Products & Bioactive Compounds, Proctor Academy, New Hampshire, USA, July 30–Aug 4, 2017.
15. The 25th International Symposium: Synthesis in Organic Chemistry, University of Oxford, UK, July 17–20, 2017.
16. The 18th Tetrahedron Symposium, Budapest, Hungary, June 27–30, 2017.
17. Organic/Green Chemistry Joint Symposium, The 97th Annual Meeting of The Chemical Society of Japan, Keio University, Japan, March 18, 2017.
18. Bristol-Myers Squibb Lecture, University of California, Irvine, USA, February 22, 2017.
19. The 26th Symposium on Optically Active Compounds, Tokyo, Japan, November 25, 2016.
20. The 15th Tateshina Conference on Organic Chemistry, Chino, Japan, November 6–8, 2015.
21. The 5th Pharmaron Symposium, Beijing, September 12, 2015.
22. The 2nd International Symposium on Natural Product Synthesis and Process Methods for Drug Manufacture, Nanjing, September 21–24, 2014.
23. New Horizons in Natural Products Chemistry, Syngenta Lecture, University of Nottingham, UK, November 7, 2012.



Copyright @ 2013 The Ang Li Group, Shanghai Institute of Organic Chemistry, CAS