Educational and Professional Background:
2017.9-2020.10, Ph. D. in Organic Chemistry, Advisor Prof. Yong-Gui Zhou, Dalian Institute of Chemical Physics.
2014.9-2017.6, MS. in Organic Chemistry, Dalian University of Technology.
2011.9-2015.7, B.S. in Chemistry Engineering and Technology, Changzhou Institute of Technology . |
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Awards:
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Representative Publications: |
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8. Zi-Biao Zhao, Xiang Li, Mu-Wang Chen, Bo Wu and Yong-Gui Zhou.* Enantioselective Synthesis of Tetrahydroquinolines via One-pot Cascade Biomimetic Reduction. Chin. J. Chem. 2020, 38, 1691-1695. |
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7. Zi-Biao Zhao, Xiang Li, Mu-Wang Chen, Zongbao K. Zhao* and Yong-Gui Zhou.* Biomimetic Asymmetric Reduction of Benzoxazinones and Quinoxalinones Using Ureas as Transfer Catalysts. Chem. Commun. 2020, 56, 7309-7312. |
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6. Xiang Li, Zi-Biao Zhao, Mu-Wang Chen, Bo Wu, Chang-Bin Yu* and Yong-Gui Zhou.* Palladium-catalyzed Asymmetric Hydrogenation of 2-Aryl Cyclic Ketones for the Synthesis of trans Cycloalkanols through Dynamic Kinetic Resolution under Acidic Conditions. Chem. Commun. 2020, 56, 5815-5818. |
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5. Zi-Biao Zhao, Xiang Li, Bo Wu and Yong-Gui Zhou.* Biomimetic Asymmetric Reduction of Quinazolinones with Chiral and Regenerable NAD(P)H Models. Chin. J. Chem. 2020, 38, 714-718. |
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4. Jie Wang, Zi-Biao Zhao, Yanan Zhao, Gen Luo, Zhou-Hao Zhu, Yi Luo* and Yong-Gui Zhou.* Chiral and Regenerable NAD(P)H Models Enabled Biomimetic Asymmetric Reduction: Design, Synthesis, Scope, and Mechanistic Studies. J. Org. Chem. 2020, 85, 2355-2368. |
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3. Zi-Biao Zhao, Lei Shi,* Yaming Li, Fan-Jie Meng and Yong-Gui Zhou.* Facile Synthesis of Chiral ε-Sultams via an Organocatalytic Aza-Friedel-Crafts Reaction. Org. Biomol. Chem. 2019, 17, 6364-6368. |
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2. Guang-Shou Feng, Zi-Biao Zhao, Lei Shi* and Yong-Gui Zhou.* Iridium-catalyzed Asymmetric Hydrogenation of Quinazolinones. Org. Chem. Front. 2019, 6, 2250-2253. |
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1. Zi-Biao Zhao, Lei Shi,* Fan-Jie Meng, Yaming Li and Yong-Gui Zhou.* Synthesis of Chiral Seven-membered Cyclic Sulfonamides through Palladium-catalyzed Arylation of Cyclic Imines. Org. Chem. Front. 2019, 6, 2019, 6, 1572-1576. |
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