学校: | 三峡大学 |
专业: | - |
年级: | 2022 |
招生人数: | 3 |
招生状态: | 正在招生中 |
研究方向
有机合成化学,药物化学与糖化学:高效糖苷化方法的开发及其在药物与天然产物合成中的应用;中药与天然产物活性分子的合成、结构修饰与优化。
https://syxy.ctgu.edu.cn/info/1055/5396.htm
联系方式:
yaohui@ctgu.edu.cn; 1820623598@qq.com.
科研论文
1. Qiuyuan Wang,‡ Mengnan Lai,‡ Huajun Luo, Keke Ren, Jingrui Wang, Nianyu Huang,* Zhangshuang Deng, Kun Zou,* and Hui Yao*, Stereoselective O-Glycosylation of Glycals with Arylboronic Acids Using Air as the Oxygen Source, Org. Lett., 2022, 24, 1587–1592. (通讯作者,IF: 6.01,中科院1区)
2. Zhiqiang Lu,* Yanzhi Li, Yi Ru, Shujian Yang, Chu Hao, Mengke Zuo, Rongkai Jiao, Weilong Wu, Yan Zhou, Hui Yao,* Nianyu Huang,* Yuqin Fu*, Coordination Effect Enabled Palladium-Catalyzed Regioselective O-Alkylation of 2-Pyridones, Chem. Commun., 2022, 58, 1215–1218. (通讯作者,IF: 6.22, 中科院2区).
3. Yuexin Liu,# Yang Jiao,# Huajun Luo, Nianyu Huang*, Mengnan Lai, Kun Zou*, Hui Yao*, Catalyst-Controlled Regiodivergent Synthesis of 1- and 3-Thiosugars with High Stereoselectivity and Chemoselectivity, ACS Catal. 2021, 11, 5287–5293. (通讯作者,IF: 13.08,中科院1区)
4. Wei-Lin Leng,# Hui Yao,# Jing-Xi He,# and Xue-Wei Liu*, Venturing beyond Donor-Controlled Glycosylation: New Perspectives toward Anomeric Selectivity, Acc. Chem. Res., 2018, 51, 628–639. (并列一作,IF: 22.38,中科院1区)
5. Hui Yao, Shasha Zhang, Wei-Lin Leng, Min-Li Leow, Shaohua Xiang, Jingxi He, Hongze Liao, Kim Le Mai Hoang, Xue-Wei Liu*, Catalyst-Controlled Stereoselective O-Glycosylation: Pd(0) vs Pd(II), ACS Catal., 2017, 7, 5456–5460. (IF: 13.08,中科院1区)
6. Mengnan Lai, Karwan Abdulmajed Othman, Hui Yao*, Qiuyuan Wang, Yongkui Feng, Nianyu Huang,* Mingguo Liu, Kun Zou,* Open-Air Stereoselective Construction of C-Aryl Glycosides, Org. Lett., 2020, 22, 1144–1148.(通讯作者,IF: 6.01,中科院1区)
7. Ying Wang,# Hui Yao#,*, Min Hua, Yang Jiao, Haibo He, Ming-Guo Liu, Nianyu Huang,* Kun Zou*, Direct N-Glycosylation of Amides/Amines with Glycal Donors, J. Org. Chem. 2020, 85, 7485-7493. (并列一作, 通讯作者,IF: 4.35,中科院2区)
8. Tao Xiong, Rui Xie, Cai Huang, Xin Lan, Nianyu Huang* and Hui Yao*, Recent advances in the synthesis of thiosugars using glycal donors, J. Carbohydr. Chem. 2022, 40, 401-439. (通讯作者,IF: 1.667,中科院4区)
9. Hui Yao,# Ronny Willam,# Siming Wang, Tai Guo, Xue-Wei Liu, One-Pot Cascade Transformation of Glycal into Structurally Diverse Drug-Like Scaffolds, Chem. Asian J. 2019, 14, 4024-4030. (IF: 4.57,中科院2区)
10. Hui Yao,# Minh Duy Vu,# Xue-Wei Liu*, Recent advances in reagent-controlled stereoselective/stereospecific glycosylation, Carbohydr. Res., 2019, 473, 72–81. (IF: 2.10,中科院3区)
11. Yu Ji, Hui Yao, Yi Liu, Nianyu Huang*, Mingguo Liu*, Synthesis and Cytotoxic Activity of C-Vinyl-rhamnopyranoside Derivatives, Chinese J. Org. Chem., 2020, 40, 2051-2061. (IF: 1.65,中科院3区)
12. Yang Jiao, Jiading Zhang, Shuzhang Wang, Hui Yao, Mingguo Liu,* Niangyu Huang,* Synthesis and Cytotoxic Activity of C-Vinyl-Rhamnopyranosides Derivatives, Chinese J. Struc. Chem. 2021, 40, 1238-1245. (IF: 0.893,中科院3区)
13. Hongze Liao, Jimei Ma, Hui Yao, Xue-Wei Liu*, Recent progress of C-glycosylation methods in the total synthesis of natural products and pharmaceuticals, Org. Biomol. Chem., 2018, 16, 1791–1806. (IF: 3.88,中科院3区)
14. Nianyu Huang, Hongze Liao, Hui Yao, Tianpeng Xie, Shasha Zhang, Kun Zou, and Xue-Wei Liu*, Diastereoselective Synthesis of C-Vinyl Glycosides via Gold(I)-Catalyzed Tandem 1,3-Acyloxy Migration/Ferrier Rearrangement, Org. Lett., 2018, 20, 16–19. (IF: 6.01,中科院1区)
15. Wei-Lin Leng, Hongze Liao, Hui Yao, Zi-En Ang, Shaohua Xiang, Xue-Wei Liu*, Palladium-Catalyzed Decarboxylative Allylation/Wittig Reaction: Substrate-Controlled Synthesis of C-Vinyl Glycosides, Org. Lett., 2017, 19, 416-419. (IF: 6.01,中科院1区)
16. Hongze Liao, Wei-Lin Leng, Kim Le Mai Hoang, Hui Yao, Jingxi He, Amanda Ying Hui Voo, Xue-Wei Liu*, Asymmetric syntheses of 8-oxabicyclo[3,2,1]octane and 11-oxatricyclo[5.3.1.0]undecane from glycals, Chem. Sci., 2017, 8, 6656-6661. (IF: 9.83,中科院1区)
17. Ming Lang,# Hui Yao,# Pengfei Fu, Wei Cai, Yuqiang Wang, Pei Yu*, An unexpected replacement of a methyl with an amino in the tetramethylpyrazine system. Res. Chem. Intermed. 2015, 41,5621–5626. (IF: 2.91,并列一作,中科院3区)