1. Q. Wu,1 S.-W. Li,1 H. Xu,1 H. Wang, P. Hu, H. Zhang, C. Luo, K.-X. Chen, B. Nay,* Y.-W. Guo*, X.-W. Li*. Complex Polypropionates from a South China Sea Photosynthetic Mollusk: Isolation and Biomimetic Synthesis Highlighting Novel Rearrangements. Angewandte Chemie International Edition. 2020, DOI: 10.1002/anie.202003643.
2. C.-L., Gao1, G.-G. Hou1, J. Liu1, T. Ru, Y.-Z. Xu, S.-Y. Zhao, H. Ye, L.-Y. Zhang, K.-X. Chen, Y.-W. Guo*, T. Pang*, X.-W. Li*. Synthesis and Target Identification of Benzoxepane Derivatives as Potential Anti-Neuroinflammatory Agents for Ischemic Stroke. Angewandte Chemie International Edition. 2020, 59, 2429-2439.
3. G. Li, H. Li, W. Tang, Y.-W. Guo*, X.-W. Li*. Klyflaccilides A and B, Diterpenoids with 6/5/8/3 Fused Tetracyclic Carbon Skeleton from the Hainan Soft Coral Klyxum flaccidum. Organic Letters. 2019, 21, 5660-5664.
4. Q. Wu, B. Nay, M. Yang, Y.-K. Ni, H. Wang, L.-G. Yao, X.-W. Li*. Marine sponges of the genus Stelletta as promising drug sources: Chemical and biological aspects. Acta Pharm. Sin. B. 2019. 9, 237-257.
5. M. Yang,1 X.-L. Li,1 J.-R. Wang, X. Lei, W. Tang, X.-W. Li*, H. Sun*, Y.-W. Guo*. Sarcomililate A, an Unusual Diterpenoid with Tricyclo[11.3.0.02,16]hexadecane Carbon Skeleton, and Its Potential Biogenetic Precursors from the Hainan Soft Coral Sarcophyton mililatensis. Journal of Organic Chemistry. 2019. 84, 2568-2576.
6. J. Liu,1 H. Li,1 K.-X. Chen, J.-P. Zuo, Y.-W. Guo*, W. Tang*, X.-W. Li*. Design and Synthesis of Marine Phidianidine Derivatives as Potential Immunosuppressive Agents. Journal of Medicinal Chemistry. 2018, 61, 11298-11308.
7. F. Ye, J. Li, Y. Wu, Z.-D. Zhu, E. Mollo, M. Gavagnin. Y.-C. Gu, W.-L. Zhu, X.-W. Li*, Y.-W. Guo*. Sarinfacetamides A and B, Nitrogenous Diterpenoids with Tricyclo[6.3.1.01,5]dodecane Scaffold from the South China Sea Soft Coral Sarcophyton infundibuliforme. Organic Letters. 2018, 20, 2637-2640.
8. D.-Y. Sun,1 G.-Y. Han,1 N.-N. Yang, L.-F. Lan, X.-W. Li*, Y.-W. Guo*. Racemic trinorsesquiterpenoids from the Beihai sponge Spongia officinalis: structure and biomimetic synthesis. Organic Chemistry Frontiers. 2018, 5, 1022-1027.
9. F. Ye, Z.-D. Zhu, J.-S. Chen, J. Li, Y.-C. Gu, W.-L. Zhu, X.-W. Li*, Y.-W. Guo*. Xishacorenes A-C, Diterpenes with Bicyclo[3.3.1]nonane Nucleus from the Xisha Soft Coral Sinularia polydactyla. Organic Letters. 2017, 19, 4183-4186.
10. D.-Y. Sun, G.-Y. Han, J.-X. Gong, B. Nay, X.-W. Li*, Y.-W. Guo*. Asymmetric Total Synthesis of Distaminolyne A and Revision of Its Absolute Configuration. Organic Letters. 2017, 19, 714-717.
11. X.-W. Li, B. Nay.* Transition metal-promoted biomimetic steps in total syntheses. Natural Product Reports. 2014, 31, 533-549.
12. X.-W. Li, A. Ear, B. Nay.* Hirsutellones and beyond: figuring out the biological and synthetic logics toward chemical complexity in fungal PKS-NRPS compounds. Natural Product Reports. 2013, 30, 765-782.
13. X.-W. Li, A. Ear, L. Roger, N. Riache, A. Deville, B. Nay.* Bio-inspired formal synthesis of hirsutellones A-C featuring an electrophilic cyclization triggered by remote Lewis acid-activation. Chemistry-A European Journal. 2013, 19, 16389-16393.
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