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青年老师

郑洪星老师简介

作者: 发布时间:2018-12-17

 

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博士/讲师

TEL/

EMAIL/zhenghongxing@lcu.edu.cn


科研方向/有机化学



             讲授课程   《有机化学实验》

             教育经历

2009/9   -2013/6 聊城大学 化学专业,学士;

2013/9 -2018/6 中国科学技术大学 有机化学专业,博士。

             科研项目

聊城大学科研启动基金

             获奖情况

             论著一览

             相关成果

(1)   Zheng, H.-X.;   Xiao, Z.-F.; Yao, C.-Z.; Li, Q.-Q.; Ning, X.-S. Kang, Y.-B.*;   Tang, Y. Transition-Metal-Free   Self-Hydrogen-Transferring Allylic Isomerization. Org. Lett. 2015, 17, 6102-6105.

 (2) Zheng, H.-X.;   Shan, X.-H.; Qu, J.-P.; Kang, Y.-B.*   Transition-Metal-Free Hydrogenation of Aryl Halides: From Alcohol to   Aldehyde. Org.   Lett. 2017, 19, 5114-5117.

 (3) Zheng, H.-X.;   Yao, C.-Z.; Qu, J.-P.*; Kang, Y.-B.* nBu4NOTf-promoted   radical self-hydrogen transferring isomerization under transition-metal-free   conditions. Org. Chem. Front. 2018, 5, 1213-1216.

 (4) Zheng, H.-X.; Shan, X.-H.; Qu, J.-P.;   Kang, Y.-B.* Strategy   for Overcoming Full Reversibility of Intermolecular Radical Addition to   Aldehydes: Tandem C−H and C−O Bonds Cleaving Cyclization of   (Phenoxymethyl)arenes with Carbonyls to Benzofurans. Org. Lett. 2018, 20, 3310-3313.

 (5) Zheng, H.-X.; Qu, J.-P.; Kang,   Y.-B.* One-pot one-base conditions for two shots:   organocatalyzed tandem isomerization–olefination of allylic alcohols. Org.   Chem. Front. 2018, 5, 2349-2352.

(6) Liu,   J.; Zheng, H.-X.; Yao, C.-Z.; Sun,   B.-F.; Kang, Y.-B. * Pharmaceutical-Oriented Selective Synthesis   of Mononitriles and Dinitriles Directly from Methyl(hetero)arenes: Access to   Chiral Nitriles and Citalopram, J. Am.   Chem. Soc. 2016, 138, 3294-3297.

 (7) Ge,   J.-J.; Yao,   C.-Z.; Wang, M.-M.;   Zheng, H.-X.; Kang,   Y.-B. * Li, Y. Transition-Metal-Free Deacylative Cleavage of   Unstrained C(sp3)–C(sp2) Bonds: Cyanide-Free Access to Aryl and Aliphatic   Nitriles from Ketones and Aldehydes, Org. Lett. 2016, 18,   228-231.

 (8) Li,   Q.-Q.; Xiao, Z.-F.; Yao,   C.-Z.; Zheng, H.-X.; Kang,   Y.-B. * Direct Alkylation of   Amines with Alcohols Catalyzed by Base, Org. Lett. 2015,   17, 5328-5331.

 






 

 

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