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Publications

 

49. Qingbo Zhang, Huixian Li, Lu Yu, Yu Sun, Yiguang Zhu, Hanning Zhu, Liping Zhang, ShuMing Li, Yuemao Shen, Changlin Tian, Ang Li, Hung-wen Liu,* and Changsheng Zhang,* Characterization of the flavoenzyme XiaK as an N-hydroxylase and implications in indolosesquiterpene diversification, Chem. Sci. 2017, 8, 5067–5077.

 

48. Yong Li, Jian Li, Hanfeng Ding,* and Ang Li,* Recent advances on the total synthesis of alkaloids in mainland China, National Science Review 2017, 4, 397–425. (Y.L. and J.L. contributed equally).

 

47. Zhongyin Zhang, Jinxin Wang, Jian Li, Fan Yang, Guodu Liu, Wenjun Tang, Weiwei He, Jian-Jun Fu, Yun-Heng Shen,* Ang Li,* and Wei-Dong 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, 55585567 (Z.Z., J.W. and J.L. contributed equally).

 

46. Wenhao Zhang and Ang Li,* A radical step forward, Nature Chemistry 2017, 9, 198–199.

 

45. Hailong Li, Qifeng Chen, Zhaohong Lu, and Ang Li,* Total Syntheses of Aflavazole and 14-Hydroxyaflavinine, J. Am. Chem. Soc. 2016, 138, 15555–15558. (H.L. and Q.C. contributed equally).

44. Q.-Y. Zheng* and A. Li,* The bloom of natural product chemistry in China, Sci. China Chem. 2016, 59, 1059–1060.

 

43. Jinpeng Pei, Shupeng Zhou, Fan Yang, Yu Sun, Ang Li,* Wei-Dong Zhang,* and Weiwei 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.

42. Peng Yang, Ming Yao, Jian Li, Yong Li, and Ang Li,* Total synthesis of rubriflordilactone B, Angew. Chem. Int. Ed. 2016, 55, 6964–6968 (P.Y. and M.Y. contributed equally).

41. Xiaowen Yang, Dimin Wu, Zhaohong Lu, Hongbin Sun, and Ang Li,* A mild preparation of alkynes from alkenyl triflates, Org. Biomol. Chem., 2016, 14, 5591–5594 (X.Y. and D.W. contributed equally).

40. Yong Li, Shugao Zhu, Jian Li, and Ang Li,* Asymmetric total syntheses of aspidodasycarpine, lonicerine, and the proposed structure of lanciferine, J. Am. Chem. Soc. 2016, 138, 3982–3985 (Y.L. and S.Z. contributed equally).

39. Yu Sun, Zhanchao Meng, Pengxi Chen, Deliang Zhang, Martin Baunach, Christian Hertweck, and Ang Li,* A concise total synthesis of sespenine, a structurally unusual indole terpenoid from Streptomyces, Org. Chem. Front. 2016, 3, 368–374 (Y.S. and Z.M. contributed equally).

38. Ming Yang, Xiaowen Yang, Hongbin Sun, and Ang Li,* Total synthesis of ileabethoxazole, pseudopteroxazole, and seco-pseudopteroxazole, Angew. Chem. Int. Ed. 2016, 55, 2851–2855.

37. Zhaohong Lu, Hailong Li, Ming Bian, and Ang Li,* Total synthesis of epoxyeujindole A, J. Am. Chem. Soc. 2015, 137, 1376413767 (Z.L. and H.L. contributed equally).

36. Shupeng Zhou, Hao Chen, Yijie Luo, Wenhao Zhang, and Ang Li,* Asymmetric total synthesis of mycoleptodiscin A, Angew. Chem. Int. Ed. 2015, 54, 68786882 (S.Z. and H.C. contributed equally).

35. Ming Yang, Jian Li, and Ang Li,* Total synthesis of clostrubin, Nature Communications 2015, 6, 6445, DOI: 10.1038/ncomms7445.

34. Ming Wan, Ming Yao, Junyu Gong, Peng Yang, Hua Liu,* and Ang Li,* Synthesis of the tetracyclic core of chlorospermines,
Chin. Chem. Lett.
2015, 26, 272–276 (M.W. and M.Y. contributed equally).

33. Huixian Li, Yu Sun, Qingbo Zhang, Yiguang Zhu, Shu-Ming Li, Ang Li, and Changsheng Zhang,*
Elucidating the cyclization cascades in xiamycin biosynthesis by substrate synthesis and enzyme characterizations, Org. Lett. 2015, 17, 306–309 (H.L. and Y.S. contributed equally).

32. Zhanchao Meng, Haixin Yu, Li Li, Wanyin Tao, Hao Chen, Ming Wan, Peng Yang, David J. Edmonds, Jin Zhong, and Ang Li,* Total synthesis and antiviral activity of indolosesquiterpenoids from the xiamycin and oridamycin families, Nature Communications 2015, 6, 6096, DOI: 10.1038/ncomms7096.

31. Xiaochun Xiong, Deliang Zhang, Jian Li, Yu Sun, Shupeng Zhou, Ming Yang, Huawu Shao,* and Ang Li,* Synthesis of indole terpenoid mimics via a functionality-tolerated Eu(fod)3-catalyzed conjugate addition, Chem. Asian J. 2015, 10, 869–872 (X.X. and D.Z. contributed equally).

30. 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,* and 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.

 

29. Jian Li, Peng Yang, Ming Yao, Jun Deng, and Ang Li,* Total synthesis of rubriflordilactone A, J. Am. Chem. Soc. 2014, 136, 1647716480 (J.L. and P.Y. contributed equally).

28. Zhaohong Lu, Ming Yang, Pengxi Chen, Xiaochun Xiong, and Ang Li,* Total synthesis of hapalindole-type natural products, Angew. Chem. Int. Ed. 2014, 53, 1384013844 (Z.L. and M.Y. contributed equally).

27. Shupeng Zhou, Deliang Zhang, Yu Sun, Ruofan Li, Wenhao Zhang, and Ang Li,* Intermolecular conjugate addition of pyrroloindoline and furoindoline radicals to α,β-unsaturated enones via photoredox catalysis, Adv. Synth. Catal. 2014, 2867–2872 (S.Z. and D.Z. contributed equally).

26. Yu Sun, Pengxi Chen, Deliang Zhang, Martin Baunach, Christian Hertweck, and Ang Li,* Bioinspired total synthesis of sespenine, Angew. Chem. Int. Ed. 2014, 53, 90129016 (Y.S. and P.C. contributed equally).

sespenine

25. Jun Deng, Shupeng Zhou, Wenhao Zhang, Jian Li, Ruofan Li, and Ang Li,* Total synthesis of taiwaniadducts B, C, and D, J. Am. Chem. Soc. 2014, 136, 8185–8188. (J.D. and S.Z. contributed equally).

24. Chunyun Wan, Jun Deng, Hua Liu,* Ming Bian,* and Ang Li,* Recent advances of intermolecular DielsAlder reaction in bio-inspired synthesis of natural products, Sci China Chem. 2014, 57, 926929 (C.W. and J.D. contributed equally).

23. Xiaochun Xiong, Yong Li, Zhaoyong Lu, Ming Wan, Jun Deng, Shuhang Wu, Huawu Shao,* and Ang Li,* Synthesis of the 6,6,5,7-tetracyclic core of daphnilongeranin B, Chem. Commun. 2014, 50, 52945297 (X.X. and Y.L. contributed equally). This article is part of themed collection: 2014 Emerging Investigators.

22. Haixin Yu, Chunyun Wan, Jing Han,* and Ang Li,* A protocol for α-bromination of β-substituted enones, Acta Chim. Sinica 2013, 71, 14881491 (H.Y and C.W. contributed equally).

21. Yu Sun, Ruofan Li, Wenhao Zhang, and Ang Li,* Total synthesis of indotertine A and drimentines A, F, and G, Angew. Chem. Int. Ed. 2013, 52, 92019204 (Y.S. and R.L. contributed equally).

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20. Zhaoyong Lu, Yong Li, Jun Deng, and Ang Li,* Total synthesis of the Daphniphyllum alkaloid daphenylline, Nature Chemistry 2013, 5, 679–684 (Z.L. and Y.L. contributed equally).

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19. Jun Deng, Ruofan Li, Yijie Luo, Jian Li, Shupeng Zhou, Yongjian Li, Jingyu Hu, and Ang Li,* Divergent total synthesis of taiwaniaquinones A and F and taiwaniaquinols B and D, Org. Lett. 2013, 15, 2022–2025 (J.D. and R.L. contributed equally).


18. Sen Li, Jing Han,* and A. Li,* Interrupted Fisher indole synthesis and its applications to alkaloid synthesis (highlight), Acta Chim. Sinica 2013, 71, 295–298.

17. Ming Bian, Zhen Wang, Xiaochun Xiong, Yu Sun, Carlo Matera, K. C. Nicolaou,* and Ang Li,* Total syntheses of anominine and tubingensin A, J. Am. Chem. Soc. 2012, 134, 8078–8081. [M.B. and Z.W. contributed equally; JACS Most Read Articles in 12 months (08/2011–07/2012)].


16. Jun Deng, Bo Zhu, Zhaoyong Lu, Haixin Yu, and Ang Li,* Total synthesis of (–)-fusarisetin A and reassignment of the absolute configuration of its natural counterpart, J. Am. Chem. Soc. 2012, 134, 920–923. [J.D. and B.Z. contributed equally; JACS Most Read Articles in 12 months (05/2011–04/2012)].


15. C.-C. Tseng, H. Ding, A. Li, Y. Guan, D. Y.-K. Chen, A Modular Synthesis of Salvileucalin B Structural Domains, Org. Lett. 2011, 1, 4410–4413.

14. 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.

13. 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.

12. 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.

11. 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.

10. K. C. Nicolaou, Y. Tang, J. Wang, A. F. Stepan, A. Li, A. Montero, Total Synthesis and Antibacterial Propoties of Carbaplatensimycin, J. Am. Chem. Soc. 2007, 129, 14850–14851.

9.  K. C. Nicolaou, D. J. Edmonds, A. Li, G. S. Tria, Asymmetric Total Syntheses of Platensimycin, Angew. Chem. Int. Ed. 2007, 46, 3942–3945.

8.  K. C. Nicolaou, A. Li. D. J. Edmonds, Total Synthesis of Platensimycin, Angew. Chem. Int. Ed. 2006, 45, 7086–7090. This work was highlighted by Nature 2006, 443, 726, Chemical and Engineering News 2006, 84(41), 12, and Chemistry World 2006, 3(11), 21.

7.  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.

6.  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.

5.  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.

4. 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, Journal of Solid State Chemistry 2003, 171, 434–438.

3. 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, Journal of Solid State Chemistry 2003, 171, 439–443.

2. 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), Journal of the Chinese Rare Earth Society (Chinese Edition) 2002, 20, 170–172.

1. 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), Journal of the Chinese Rare Earth Society (Chinese Edition) 2001, 19, 471–473.





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