实验室简介科学研究研究队伍开放交流人才培养仪器设备实验室动态通知公告友情链接

惠新平

2019-01-09 18:14:00
惠新平
惠新平
博士、教授、博士生导师
邮箱:
huixp@lzu.edu.cn
· EDUCATION AND EXPERIMENCE

2012-至今            兰州大学化学化工学院、功能有机分子化学国家重点实验室,教授

2002-2004           台湾国立中兴大学,博士后

1996-2001           兰州大学,理学博士

1992-1996           西北师范大学,理学学士

•荣誉奖励

2023                    国家级教学成果奖二等奖(第一完成人)

2021                    甘肃省高等教育教学成果特等奖(第一完成人)

2020                    甘肃省高等学校教学名师

2017                    兰州大学“师德标兵”

2010                    甘肃省自然科学一等奖

2010                    甘肃省科学技术进步奖二等奖

2009                    甘肃省第十六届高等学校青年教师成才奖

•研究兴趣

不对称催化及其相关有机合成方法学研究

•代表成果

1. Visible-Light-Mediated Formal Carbene Insertion Reaction: Enantioselective Synthesis of 1,4-Dicarbonyl Compounds Containing All-Carbon Quaternary Stereocenter. Hua Zhang, Zheyuan Wang, Zirui Wang, Yunpeng Chu, Shuncheng Wang, and Xin-Ping Hui*, ACS Catal. 2022, 12, 55102.

2. N-Heterocyclic Carbene-Catalyzed Atroposelective Synthesis of Pyrrolo[3,4-b] Pyridine Derivatives with Configurationally Stable C-N Axial Chirality. Yunpeng Chu, Meng Wu, Fang Hu, Panpan Zhou, Zhengqiang Cao, and Xin-Ping Hui*, Org. Lett. 2022, 24, 3884.

3. Enantioselective Synthesis of Functionalized Tetrahydropyridines Through Iridium-Catalyzed Formal [5+1] Annulation. Fang Hu, Yunpeng Chu, Zhengqiang Cao, Yucheng Li, and Xin-Ping Hui*, Org. Lett. 2022, 24, 6945.

4. N-Heterocyclic Carbene-Catalyzed Enantioselective Dearomatizing Annulation of Benzoxazoles with Enals. Yunpeng Chu, Fang Hu, Peng Feng, and Xin-Ping Hui*, Org. Chem. Front. 2022, 9, 1556.

5. Efficiently Enantioselective Synthesis of Pyrazolines and Isoxazolines Enabled by Iridium-Catalyzed Intramolecular Allylic Substitution Reaction. Fang Hu, Hua Zhang, Yun-Peng Chu, and Xin-Ping Hui*, Org. Chem. Front. 2022, 9, 2734.

6. Sequential Visible-Light and N-Heterocyclic Carbene Catalysis: Stereo- selective Synthesis of Tetrahydropyrano[2,3-b]indoles. Chengyuan Wang, Zheyuan Wang, Jin Yang, Shihui Shi, and Xinping Hui*. Org. Lett. 202022, 4440–4443.

7. Asymmetric N-Alkylation of Indoles with Isatins Catalyzed by N-Hetero-cyclic Carbene: Efficient Synthesis of Functionalized Cyclic N,O-Aminal indole Derivatives. Chengyuan Wang, Zhuopeng Li, Jiong Zhang, and Xinping Hui*. Org. Chem. Front20207, 1647-1652.

8. Efficiently Diastereoselective Synthesis of Functionalized Hydrocarbazoles by Base[1]Mediated Tandem Annulation of 1-(2-Amino-aryl)prop-2-en-1-ones and Sulfur Ylide. Chengyuan Wang, Jiong Zhang, Zheyuan Wang, and Xinping Hui*. Org. Chem. Front. 20207, 1469-1473.

9. Oxidative NHC Catalysis: Direct Activation of β sp3 Carbons of Saturated Acid Chlorides. Shiya Zhu, Hua Zhang, Qingwei Ma, Dou Liu and Xinping Hui *. Chem. Commun. 201955, 298–301.

10. Highly Enantioselective Synthesis of Functionalized Azepino[1,2-a]indoles via NHC-Catalyzed [3+4] Annulation. Shiya Zhu, Yuanzhen Zhang, Xinfa Chen, Jun Huang, Shihui Shi, and Xinping Hui*. Chem. Commun. 201955, 4363–4366.

11. Stereoselective Synthesis of Functionalized Tetrahydro-1H-1,2-diazepines by N-Heterocyclic Carbene-Catalyzed [3+4] Annulation. Shiya Zhu, Yuanzhen Zhang, Wei Wang, and Xinping Hui*. Org. Lett. 201719, 5380-5383.

12. Asymmetric Synthesis of Cyclopenta[3,4]pyrroloindolones via N-Heterocyclic Carbene- Catalyzed Michael/Aldol/Lactamization Cascade Reaction. Yujie Yang, Yuanyuan Ji, Liangliang Qi, Guanjun Wang, and Xinping Hui*.Org. Lett. 201719, 3271–3274.

13. Highly Stereoselective Synthesis of Functionalized Pyrrolo[3,2-c]-quinolines via N-Heterocyclic Carbene Catalyzed Cascade Sequence. Yujie Yang, Hairui Zhang, Shiya Zhu, Ping Zhu, and Xinping Hui*. Org. Lett. 201416, 5048–5051.

14 N-Heterocyclic Carbene-catalyzed Stereoselective Cascade Reaction: Synthesis of Functionalized Tetrahydroquinolines. Hairui Zhang, Zhenwen Dong, Yujie Yang, Pingluan Wang, and Xinping Hui*. Org. Lett. 201315, 4750–4753.

15. Synergistic Chiral Ion Pair Catalysts for Asymmetric Catalytic Synthesis of Quaternary αβ-Diamino Acids. Shihui Shi, Fuping Huang, Ping Zhu, Zhenwen Dong, and Xinping Hui*. Org. Lett. 201214, 2010-2013.

阅读:0

首页

栏目

联系