1.
W. Ye, A. Li,*
A practical route to 3D molecular diversity, Nature 2018, 560, 314–316.
2.
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.
3.
S. Zhou, R. Guo, P. Yang, A. Li,*
Total synthesis of septedine and 7-deoxyseptedine, J. Am. Chem. Soc. 2018, 140, 9025–9029.
4.
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.
5.
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.
6.
J. Li, W. Zhang, F. Zhang, Y. Chen, A. Li,*
Total synthesis of longeracinphyllin A, J. Am. Chem. Soc. 2017, 139, 14893‒14896.
7.
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.
8.
W. Zhang, A. Li,*
A radical step forward, Nature Chemistry 2017, 9, 198–199.
9.
H. Li, Q. Chen, Z. Lu, A. Li,*
Total syntheses of aflavazole and 14-hydroxyaflavinine, J. Am. Chem. Soc. 2016, 138, 15555–15558.
10.
P.
Yang, M. Yao, J. Li, Y. Li, A. Li,*
Total synthesis of rubriflordilactone B, Angew. Chem. Int. Ed. 2016, 55, 6964–6968.
11.
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.
12.
M. Yang, X. Yang, H. Sun, A. Li,* Total
Synthesis of Ileabethoxazole, Pseudopteroxazole, and seco-Pseudopteroxazole, Angew. Chem. Int. Ed. 2016, 55, 2851.
13.
Z. Lu, H. Li, M. Bian, A. Li,* Total
Synthesis of Epoxyeujindole A, J. Am.
Chem. Soc. 2015, 137,
13764–13767.
14.
S. Zhou, H. Chen, Y. Luo, W. Zhang, A. Li,* Asymmetric total synthesis of
mycoleptodiscin A, Angew. Chem. Int. Ed. 2015, 54, 6878–6882.
15. M. Yang, J. Li, A.
Li,* Total synthesis of clostrubin, Nature Communications 2015, 6, 6445.
16. 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, Nature Communications 2015, 6,
6096.
17. J. Li, P. Yang,
M. Yao, J. Deng, A. Li,* Total synthesis of rubriflordilactone A, J. Am. Chem. Soc. 2014, 136, 16477–16480.
18.
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.
19. 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.
20. 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.
21. 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.
22. Z. Lu, Y. Li, J.
Deng, A. Li,* Total synthesis of the Daphniphyllum alkaloid daphenylline, Nature Chemistry, 2013, 5, 679–684.
23. 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.
24. 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.