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41. |
Protecting‐Group‐Free Total Synthesis and Biological Investigation of Cabucine Oxindole A. S. Xie,+ C. Ning,+ Q. Yu,+ J. Hou, J. Xu,* Chin. J. Chem. 2021, 39, 137. (+ equal contribution) Invited manuscript for celebrating the 10th anniversary of the Department of Chemistry of SUSTech
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40. |
Total Synthesis of Daphniphyllum Alkaloids: From Bicycles to Diversified Caged Structures. L.-D. Guo,+ Y. Chen,+ J. Xu,* Acc. Chem. Res. 2020, 53, 2726–2737. (+ equal contribution)
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39. |
Asymmetric Total Synthesis of Yuzurimine-type Daphniphyllum Alkaloid (+)-Caldaphnidine J. L.-D. Guo, Y. Zhang,+ J. Hu,+ C. Ning, H. Fu, Y. Chen, J. Xu,* Nat. Commun. 2020, 11, 3538. (+ equal contribution)
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38. |
Enantioselective Total Synthesis of (−)-Caldaphnidine O via a Radical Cyclization Cascade. L.-D. Guo, J. Hu,+ Y. Zhang,+ W. Tu, Y. Zhang, F, Pu, J. Xu,* J. Am. Chem. Soc. 2019, 141, 13043−13048. (+ equal contribution)
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37. |
Total Synthesis of Dapholdhamine B and Dapholdhamine B Lactone. L.-D. Guo, J. Hou,+ W. Tu,+ Y. Zhang, Y. Zhang, L. Chen, J. Xu,* J. Am. Chem. Soc. 2019, 141, 11713−11720. (+ equal contribution)
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36. |
Synthesis of the Core Structure of Daphnimacropodines. Y. Chen, J. Hu, L.-D. Guo, P. Tian, T. Xu, J. Xu*, Org. Lett. 2019, 21, 4309−4312.
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35. |
Asymmetric Total Synthesis of (+)-Astellatol and (−)-Astellatene. N. Zhao, S. Xie, P. Tian, R. Tong, C. Ning,* J. Xu,* Org. Chem. Front. 2019, 6, 2014−2022.
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34. |
A Concise Total Synthesis of (–)-Himalensine A. Y. Chen, J. Hu, L.-D. Guo, W. Zhong, C. Ning, J. Xu,* Angew. Chem. Int. Ed. 2019, 58, 7390−7394.
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33. |
13-Step Total Synthesis of Atropurpuran. S. Xie,+ G. Chen,+ H. Yan,+ J. Hou, Y. He, T. Zhao, J. Xu,* J. Am. Chem. Soc. 2019, 141, 3435−3439. (+ equal contribution) Featured as Top 10 most read articles from JACS, Feb. 2019
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32. |
Innovation in Protecting-Group-Free Natural Product Synthesis. C. Hui, F. Chen,+ F. Pu,+ J. Xu,* Nature Reviews Chemistry 2019, 3, 85−107. (+ equal contribution)
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31. |
Gallic acid disruption of Aβ1–42 aggregation rescues cognitive decline of APP/PS1 double transgenic mouse. M. Yu, X. Chen, J. Liu, Q. Ma, Z. Zhuo, H. Chen, L. Zhou, S. Yang, L. Zheng, C. Ning, J. Xu, T. Gao, S.-T. Hou,* Neurobiol. Dis. 2019, 124, 67−80.
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30. |
Total Synthesis of Sesterterpenoids. Y. Chen, J. Zhao,* S.-P. Li, J. Xu,* Nat. Prod. Rep. 2019, 36, 263−288. (Invited manuscript)
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29. |
Efficient Synthesis of the AC Ring System of Daphnilactone B. Y. Zhang, L.-D. Guo,* J. Xu,* Chin. J. Org. Chem. 2019, 39, 1079−1084.
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28. |
Stereoselective Synthesis of the ABC Ring System of Aspterpenacids. S. Xie, P. Ren, J. Hou, C. Ning,* J. Xu,* J. Org. Chem. 2018, 83, 14152−14157.
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27. |
Total Synthesis of Astellatol: A Three-Decade Synthetic Puzzle. N. Zhao, S. Xie, H. Huang, J. Xu,* Synlett 2018, 15, 1933−1936. (Invited Synpacts)
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26. |
Total Synthesis of Astellatol. N. Zhao,+ S. Yin,+ S. Xie, H. Yan, P. Ren, G. Chen, F. Chen, J. Xu,* Angew. Chem. Int. Ed. 2018, 57, 3386−3390. (+ equal contribution) Highlighted in Synfacts, ChemViews Magazine, Organic Chemistry Portal and SUSTech News. |
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25. | Triptolide Derivatives as Potential Multifunctional Anti-Alzheimer Agents: Synthesis and Structure-Activity Relationship Studies. C. Ning, L. Mo, X. Chen, W. Tu, J. Wu,* S.-T. Hou,* J. Xu,* Bioorg. Med. Chem. Lett. 2018, 28, 689−693.
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24. |
Nine-Step Total Synthesis of (–)-Strychnofoline. Q. Yu, P. Guo, J. Jian, Y. Chen, J. Xu,* Chem. Comm. 2018, 54, 1125−1128.
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23. | Enantioselective Synthesis of (−)-Phaseic Acid. W. Tu, C. Ning, J. Xu,* Org. Chem. Front. 2018, 5, 29−31. (invited manuscript)
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22. | Metal Catalyzed Asymmetric Michael Addition in Natural Product Synthesis. S. Hui, F. Pu, J. Xu,* Chem. Eur. J. 2016, 23, 4023−4036.
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21. | Concise Synthesis of Astellatol Core Skeleton. N. Zhao, S. Xie, G. Chen. J. Xu,* Chem. Eur. J. 2016, 22, 12634−12636.
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20. | Palladium-Catalyzed sp3 C–H Oxidation Using Oxime as Directing Group—Applications in Total Synthesis. C. Hui, J. Xu,* Tetrahedron Lett. 2016, 57, 2692−2696. (invited manuscript)
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Before SUSTech: 19. Synthetic strategies toward the decalin motif of maklamicin and related spirotetronates, M. H. Lacoske, J. Xu, N. Mansour, C. Gao, E. A. Theodorakis*, Org. Chem. Front. 2015, 2, 388. (invited manuscript) 18. Synthesis of mulinane diterpenoids, K. P. Reber, J. Xu, C. A. Guerrero*, J. Org. Chem. 2015, 80, 2397. 17. Proximity enabled protein crosslinking (PEPC) via genetically en-coding haloalkane unnatural amino acids, Z. Xiang, V. Lacey, H. Ren, J. Xu, D. Burban, P. Jennings, L. Wang*, Angew. Chem. Int. Ed. 2014, 53, 2190. 16. Fusarisetins: structure-function studies on a novel class of cell migration inhibitors, E. J.E. Caro-Diaz, A. Aung, J. Xu, S. Varghese, E. A. Theodorakis*, Org. Chem. Front. 2014, 1, 135-139. (invited manuscript) 15. Neurotrophic natural products: chemistry and biology, J. Xu, M. H. Lacoske and E. A. Theodorakis*, Angew. Chem. Int. Ed. 2014, 53, 956. (invited manuscript) 14. A-ring oxygenation modulates the chemistry and bioactivity of caged Garcinia Xanthones, K. M. Elbel, G. Guizzunti, M. Theodoraki, J. Xu, A. Batova, M. Dakanali and E. A. Theodorakis*, Org. Biomol. Chem. 2013, 11, 3341. 13. Illicium sesquiterpenes: divergent synthetic strategy and neurotrophic activity studies, L. Trzoss, J. Xu*, M. H. Lacoske, W. C. Mobley and E. A. Theodorakis*, Chem. Eur. J. 2013, 19, 6398. 12. Synthesis of the tetracyclic core of Illicium sesquiterpenes using an organocatalyzed asymmetric Robinson annulation, L. Trzoss, J. Xu, M. H. Lacoske, and E. A. Theodorakis*, Beilstein J. Org. Chem. 2013, 9, 1135. (invited manuscript) 11. Fusarisetin A: Scalable total synthesis and related studies, J. Xu, E. J. E. Caro-Diaz, M. H. Lacoske, C.-I. Hung, C. Jamora* and E. A. Theodorakis*, Chem. Sci. 2012, 3, 3378. 10. Nature-inspired total synthesis of (–)-fusarisetin A, J. Xu, E. J. E. Caro-Diaz, L. Trzoss, and E. A. Theodorakis*, J. Am. Chem. Soc. 2012, 134, 5072. 9. Formal synthesis of (–)-englerin A and discovery of truncated englerin analogues with cytotoxicity against leukemia cells, J. Xu, E. J. E. Caro-Diaz, A. Batova and E. A. Theodorakis*, Chem. Asian J. 2012, 7, 1052. 8. Enantioselective synthesis of (–)-jiadifenin, a potent neurotrophic modulator, L. Trzoss, J. Xu*, M. H. Lacoske, W. C. Mobley, E. A. Theodorakis*, Org. Lett. 2011, 13, 4554. 7. Enantioselective total synthesis of (–)-jiadifenolide, J. Xu, L. Trzoss, W. K. Chang and E. A. Theodorakis*, Angew. Chem. Int. Ed. 2011, 50, 3672. 6. Synthesis of (–)-callicarpenal, a potent arthropod-repellent, T. T. Ling, J. Xu, R. Smith, A. Ali, C. L. Cantrell and E. A. Theodorakis*, Tetrahedron 2011, 67, 3023. 5. Enantioselective formal synthesis of (–)-englerin A via a Rh-catalyzed [4+3] cycloaddition reaction, J. Xu, E. J. E. Caro-Diaz and E. A. Theodorakis*, Org. Lett. 2010, 12, 3708. 4. Serotonin derivatives as a new class of non-ATP competitive receptor tyrosine kinase inhibitors, A. Büttner, T. Cottin, J. Xu, L. Tzagkaroulaki, A. Giannis*, Bioorg. Med. Chem. 2010, 18, 3387. 3. Development and biological evaluation of a novel Aurora A kinase inhibitor, T. Sardon, T. Cottin, J. Xu, A. Giannis*, I. Vernos*, ChemBioChem 2009, 10, 464. 2. Synthesis of 5-amino-2-(N,N-dibenzylamino)-3-hydroxy-1,6-diphenylhexane, R.-H. Zhang*, P. Zhao, J. Xu, Z.-L. Zhu, Chin. J. Med. Chem. 2004, 14, 357. 1. Synthesis process of cyclohexyl methyl dichlorosilane, R.-H. Zhang*, J. Xu, Y.-J. Li, Z.-L. Zhu, Y.-M. Ni, Chin. J. Syn. Chem. 2003, 11, 421. |
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