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1.Zhao Y, Gu Q, Morris-Natschke SL, Chen C-H, Lee K-H. Incorporation of Privileged Structures into Bevirimat Can Improve Activity against Wild-Type and Bevirimat-Resistant HIV-1. Journal of Medicinal Chemistry 2016, 59, 9262-9268.
2.Zhao Y, Su J, Goto M, Morris-Natschke SL, Li Y, Zhao Q-S, Yao Z-J, Lee K-H. Dual-Functional abeo-Taxane Derivatives Destabilizing Microtubule Equilibrium and Inhibiting NF-kappa B Activation. Journal of Medicinal Chemistry 2013, 56, 4749-4757.
3.Zhao Y, Liu Po-Yen, Hsieh Kan-Yen, Hsu Pei-Ling, Goto Masuo,. Morris-Natschke SL, Harn Horng-Jyh, Lee Kuo-Hsiung, Design, Synthesis and Structure-Activity Relationships of (±)-Isochaihulactone Derivatives, MedChemComm, 2017, 8, 2040-2049.
4.Luo P, Xia W-J, Morris-Natschke SL, Lee K-H, Zhao Y*, Gu Q, Xu J. Vitepyrroloids A-D, 2-cyanopyrrole-containing labdane diterponoids alkaloids from the leaves of Vitex trifolia. Journal of Natural Products, 2017, 80, 1679-1683.
5.Tan C-J, Zhao Y, Goto M, Hsieh K-Y, Yang X-M, Morris-Natschke SL, Liu L-N, Zhao B-Y, Lee K-H. Alkaloids from Oxytropis ochrocephala and antiproliferative activity of sophoridine derivatives against cancer cell lines Bioorganic Medicinal Chemistry Letters 2016, 26, 1495-1497 (Co-first author)
6.Zhao Y, Chen C-H, Goto M, Kuo-Hsiung Lee, Application of privileged structure into natural product-based drug discovery, 16th Meeting of Consortium for Globalization of Chinese Medicine, Guangzhou, 2017, August 18. (Co-corresponding author)
7.Liu L-N, Ran J-Q, Li L-J, Zhao Y, Goto M, Morris-Natschke SL, Lee K-H, Zhao B-Y, & Tan C-J Ochrocephalamine A, a new quinolizidine alkaloid from Oxytropis ochrocephala Bunge. Tetrahedron Letters 2016, 57(46):5047-5049.
8.Wada K, Ohkoshi E, Zhao Y, Goto M, Morris-Natschke SL, & Lee K-H Evaluation of Aconitum diterpenoid alkaloids as antiproliferative agents. Bioorganic & Medicinal Chemistry Letters 2015, 25, 1525-1531.
9. Yan M, Lu Y, Chen C-H, Zhao Y, Lee K-H, & Chen D-F Stelleralides D-J and Anti-HIV Daphnane Diterpenes from Stellera chamaejasme. Journal of Natural Products 2015, 78, 2712-2718.
10.Chen Y-F, Lin Y-C, Morris-Natschke SL, Wei C-F, Shen T-C, Lin H-Y, Hsu M-H, Chou L-C, Zhao Y, Kuo S-C, Lee K-H, & Huang L-J Synthesis and SAR studies of novel 6,7,8- substituted- substituted benzyloxyquinolin- 2(1H)-one derivatives for anticancer activity. British Journal of Pharmacology 2015, 172, 1195-1221.
11.Liu C-Y, Cheng Y-Y, Chang L-C, Huang L-J, Chou L-C, Huang C-H, Tsai M-T, Liao C-C, Hsu M-H, Lin H-Y, Wu T-S, Wen Y-F, Zhao Y, Kuo S-C, & Lee K-H Design and synthesis of new 2-arylnaphthyridin-4-ones as potent antitumor agents targeting tumorigenic cell lines. European Journal of Medicinal Chemistry 2015, 90, 775-787.
12.Zhao X-B, Goto M, Song Z-L, Morris-Natschke SL, Zhao Y, Wu D, Yang L, Li S-G, Liu Y-Q, Zhu G-X, Wu X-B, & Lee K-H Design and synthesis of new 7-(N-substituted-methyl)-camptothecin derivatives as potent cytotoxic agents. Bioorganic & Medicinal Chemistry Letters 2014, 24, 3850-3853.
13.Li R-J, Sun Y, Sun B, Wang X-N, Liu S-S, Zhou J-C, Ye J-P, Zhao Y, Liu L, Lee K-H, & Lou H-X Phytotoxic cis-clerodane diterpenoids from the Chinese liverwort Scapania stephanii. Phytochemistry 2014, 105, 85-91.
14.Li R-J, Zhao Y, Tokuda H, Yang X-M, Wang Y-H, Shi Q, Morris-Natschke SL, Lou H-X, & Lee K-H Total synthesis of plagiochin G and derivatives as potential cancer chemopreventive agents. Tetrahedron Letters 2014, 55, 6500-6503.
15.Shao L-D, Xu J, Gao X, He J, Zhao Y, Peng L-Y, Luo H-R, Xia C, & Zhao Q-S Synthesis and neurite outgrowth promoting activity of vibsanin B derivatives. Tetrahedron Letters 2014, 55, 3414-3417.
16.Deng X, Shen Y, Yang J, He J, Zhao Y, Peng L-Y, Leng Y, & Zhao Q-S Discovery and structure-activity relationships of ent-Kaurene diterpenoids as potent and selective 11 beta-HSD1 inhibitors: Potential impact in diabetes. European Journal of Medicinal Chemistry 2013, 65, 403-414.
17.Hour MJ, Lee KH, Chen TL, Lee KT, Zhao Y, & Lee HZ Molecular modelling, synthesis, cytotoxicity and anti-tumour mechanisms of 2-aryl-6-substituted quinazolinones as dual-targeted anti-cancer agents. British Journal of Pharmacology 2013, 169(7):1574-1586.
18.Deng X, Su J, Zhao Y, Peng L-Y, Li Y, Yao Z-J, & Zhao Q-S Development of novel conformation-constrained cytotoxic derivatives of cheliensisin A by embedment of small heterocycles. European Journal of Medicinal Chemistry 2011, 46, 4238-4244.
19.Zhao Y, Zhang H-B, Liu J-K, Su J, Li Y, Yao Z-J, Zhao Q-S, Fragmentations of 13-oxo-taxyunnansin A and their application to preparation of abeo-paclitaxel and abeo-docetaxel analogues, Tetrahedron Letters, 2011, 52, 139–142.
20.Zhao Y, Niu X-M, Qian L-P, Liu Z-Y, Zhao Q-S, Sun H-D, Synthesis and cytotoxicity of some new eriocalyxin B derivatives, European Journal of Medicinal Chemistry, 2007, 494–502. (IF: 3.90)
21.Zhao Y, Guo N, Lou L-G, Chong Y-W, Peng L-Y, Zhao Q-S, Synthesis, Cytotoxic Activity and SAR Analysis of the Derivatives of Taxchinin A and Brevifoliol, Bioorganic Medicinal Chemistry，2008，16，4860–4871.
22. Zhao Y, Wang F-S, Peng L-Y, Li X-L, Xu G, Luo X-X, Lu Y, Wu L, Zheng Q-T, Zhao Q-S, Taxoids from Taxus chinensis, Journal of Natural Products, 2006, 69, 1813–1815.
23. 5/7/6型紫杉烷二萜化合物，其药物组合物和其合成方法和用途，赵勤实，赵昱，丛玉文，专利号 ZL 200810058292.9
24. 5/7/6型紫杉烷二萜化合物，其药物组合物和其合成方法和用途，赵勤实，赵昱，丛玉文，专利号 ZL 200810058293.3
24. Bicyclic Compound And Pharmaceutical Composition Thereof for Treating Stroke And Use Thereof, Lee K-H, Zhao Y, Kuo C-Y, Hsu C-Y, Shyu W-C, Chen Y-C, Lin C-H, Lee W, Chiang C-W, Tsai C-H. US 10035791B2, JP6381605 B2, TWI641594B
25. Medicarpin, Its Derivatives, Manufacturing Method Thereof Lee, K-H, Wu, R-T, Yang, X-M, Zhao Y, Horng L-Y, Sung H-C,Hsu P-L, Cheng, C-H, Lee Y-L. EP3299373 A3， US 20180086772 A1，TW201813969A，CN107868091A
26. Medicinal Plants - Recent Advances in Research and Development. Chapter 1. Chinese Herbal Medicine-Derived Products for Prevention or Treatment of Diseases Affecting Quality of Life. Lee K-H, Morris-Natschke SL, Zhao Y, Musgrove K. Springer, 2016, pp 1-35
27.天然产物全合成荟萃——萜类，第一章紫杉醇全合成，赵昱，姚祝军，科学出版社，吴毓林，何子乐，2010，pp 1- 56.
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