华东师范大学化学与分子工程学院李艳忠

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李艳忠教授，现为华东师范大学博士生导师。2001年3月，获得日本北海道大学药学院博士学位；2001年4月-2004年5月，任日本北海道大学触媒化学研究中心研究员；2004年6月，受聘华东师范大学化学与分子工程学院教授、博士生导师。李艳忠教授主要研究方向：（1）惰性化学键的选择性活化及其后续转化反应研究（2）药物分子导向的有机合成方法学 （3）金属有机化学。受国际著名出版社WILEY-VCH 邀请，与他人合作撰写专著一部，书名为Titanium and Zirconium in Organic Synthesis。在国际高引用化学刊物如J. Am. Chem. Soc.； Org. Lett.； Chem. Commun.； Chem. Eur. J.； Adv. Synth. Catal. 发表论文60多篇。多篇论文被国际著名评述期刊Synfacts评述为重要进展。文章被同行专家学者引用达500多次。课题组还与国际著名企业如Sumitomo（住友化学）,Adeka（旭化成），Nippoh(日宝化学) 等合作研究。获国家自然科学基金委、教育部、企业合作课题多项，2014年以来，发表重要研究成果20余篇。


李艳忠
教授
化学与分子工程学院
联系电话： 021-54340106
办公时间： 周一-周六
传 真： 021-54340106
主页网址： faculty.ecnu.edu.cn/s/708/main.jspy
办公地点： 华东师范大学闵行校区化学楼517室
电子邮箱： yzli@chem.ecnu.edu.cn
通讯地址： 闵行区东川路500号华东师范大学闵行校区化学楼517室


研究方向
一、药物分子导向的有机合成方法学
二、金属有机化学


学术成果
[17] Transition-metal-free Ring Expansion Reactions of Indene-1,3-dione: Synthesis of Functionalized Benzoannulated Seven-Membered Ring Compounds，Qiyi Yao, Lingkai Kong, Mengdan Wang, Yang Yuan, Ruizhuo Sun,Yanzhong Li* Org. Lett.,  DOI: 10.1021/acs.orglett.8b00206
[16] Base-Promoted Tandem Reaction towards Conjugated Dienone or Chromone Derivatives with a Cyano Group: Insertion of Alkynes into C–C σ-Bonds of 3-Oxopropanenitriles, Qiyi Yao, Lingkai Kong, Fangfang Zhang, Xianghua Tao and Yanzhong Li*，Adv. Synth. Catal. 2017, 359, 3079–3084.
[15] Insertion of Isolated Alkynes into Carbon–Carbon s-Bonds of Unstrained Cyclic b-Ketoesters via Transition-Metal-Free Tandem Reactions: Synthesis of Medium-Sized Ring Compounds，Yuanyuan Zhou, Xianghua Tao, Qiyi Yao, Yulei Zhao, and Yanzhong Li*，Chem. Eur. J., 2016, 22, 17936 – 17939
[14] Base-Promoted Tandem Reaction Involving Insertion into Carbon–Carbon s-Bonds: Synthesis of Xanthone and Chromone Derivatives，Xingcan Cheng, Yuanyuan Zhou, Fangfang Zhang, Kai Zhu, Yuanyuan Liu, and Yanzhong Li*，Chem. Eur. J., 2016, 22, 1 – 6
[13] Base-mediated insertion reaction of alkynes into carbon–carbon σ-bonds of ethanones: synthesis of hydroxydienone and chromone derivatives，Fangfang Zhang, Qiyi Yao, Yang Yuan, Murong Xu, Lingkai Kong and Yanzhong Li*，Org. Biomol. Chem., 2017, 15, 2497-2500.
[12] Selective synthesis of pyrrolo[1,2-a]azepines or 4,6-dicarbonyl indoles via tandem reactions of alkynones with pyrrole derivatives, Yulei Zhao, Yang Yuan, Murong Xu, Zhong Zheng, Runhua Zhang and Yanzhong Li*, Org. Biomol. Chem., 2017, 15, 6328-6332.
[11] Tertiary amine self-catalyzed intramolecular Csp3–H functionalization with in situ generated allenes for the formation of 3-alkenyl indolines，Yulei Zhao, Murong Xu, Zhong Zheng, Yang Yuan and Yanzhong Li*，Chem. Commun..2017, 53, 3721-3724.
[10] Copper-Catalyzed Oxidative Dearomatization/Spirocyclization of Indole-2-Carboxamides: Synthesis of 2‑Spiro-pseudoindoxyls, Lingkai Kong, Mengdan Wang, Fangfang Zhang, Murong Xu, and Yanzhong Li*, Org. Lett., 2016, 18, 6124-6127.
[9] Metal/Benzoyl Peroxide (BPO)-Controlled Chemoselective Cycloisomerization of (o‑Alkynyl)phenyl Enaminones: Synthesis of α‑Naphthylamines and Indeno[1,2‑c]pyrrolones, Fangfang Zhang, Zhengchen Qin, Lingkai Kong, Yulei Zhao, Yuanyuan Liu, and Yanzhong Li*, Org. Lett.,2016, 18, 5150-5153.  
[8] Synthesis of polycyclic benzoindolo[3,2,1-de]acridines via sequential allenylation/Diels-Alder cyclization/hydrogen migration reaction, Yulei Zhao, Yang Yuan, Xiaoyu Wang and Yanzhong Li*, J. Org. Chem., 2017, 82，11198–11205.
[7] Synthesis of 1-Alkyl-3-(2-oxo-2-aryl/alkyl-ethyl)indolin-2-ones through Gold/Brønsted Acid Relay Actions: Observation of Selective C=C Bond Cleavage of Enaminones, Yulei Zhao, Yang Yuan, Lingkai Kong, Fangfang Zhang and Yanzhong Li*, Synthesis, 2017, 49, 3609-3618.  
[6] Pd-Catalyzed C-H/N-H Arylation: One-Pot Synthesis of Indolo[1,2-f]phenanthridines, Lingkai Kong, Qiyi Yao, Mengdan Wang, Ruizhuo Sun and Yanzhong Li *, ChemSelect, 2018, 3, 456–460.   
[5] Insertion of Isolated Alkynes into Carbon–Carbon s-Bonds of Unstrained Cyclic b-Ketoesters via Transition-Metal-Free Tandem Reactions: Synthesis of Medium-Sized Ring Compounds, Yuanyuan Zhou, Xianghua Tao, Qiyi Yao, Yulei Zhao, and Yanzhong Li*，Chem. Eur. J., 2016, 22, 17936–17939.
[4] Base-Promoted Tandem Reaction Involving Insertion into Carbon– Carbon s-Bonds: Synthesis of Xanthone and Chromone Derivatives, X. Cheng, Y. Zhou, F. Zhang, K. Zhu, Y. Liu and Y. Li*, Chem. Eur. J., 2016, 22, 12655–12659.
[3] Gold-catalyzed chemo- and diastereoselective C(sp2)–H functionalization of enaminones for the synthesis of pyrrolo[3,4-c]-quinolin-1-one derivatives，Y. Zhao, Q. Duan, Y. Zhou, Q. Yao and Y. Li*，Org. Biomol. Chem., 2016, 14, 2177-2181.
[2] Copper-Catalyzed Synthesis of Substituted Quinolines via C-N Coupling/Condensation from ortho-Acylanilines and Alkenyl Iodides，L. Kong, Y. Zhou, H. Huang, Y. Yang, Y. Liu, Y. Li*, J. Org. Chem., 2015, 80, 1275.
[1] LDA-Promoted Synthesis of 3‑Amino Furans by Selective Lithiation of Enaminones，L. Kong, Y. Shao, Y. Li, Y. Liu, and Y. Li*, J. Org. Chem.,2015, 80, 12641-12645.