YuTang

YuTang–Professor

Natura lProducts Synthesis

  

Phone: 0532-80932638

Email: tangyu@ouc.edu.cn

  

PhD:2005,Chinese Academy of Sciences, Shanghai, CN

PostDoc:2005, University of Minnesota, MN, USA

PostDoc:2006, University of Wisconsin-Madison, WI, USA

  

  

Research Area: The research in the group of Tang is focused on organic synthesis methodology and total synthesis of natural products, application of cycloaddition and cyclization strategy synthesis of natural products,and methodology research of stereo selectivity of ynamides and spiroketal. The group also extends efforts towards total synthesis of pre-drugs and drug molecules and investigation of their biological activities. The group cooperates with enterprises to investigate drug intermediates and pharmaceutical raw materials with potential market value.

  

SelectedPublications (2014-2016)

  1. Mechanistic insights into a catalyst-free method to construct quinazolinones through multiple oxidative cyclization”

    Zhen-zhen Wang, Yu Tang*Tetrahedron2016, 72, 1330-1336.

  2. Transition-Metal-Free Visible-Light driven Photoredox Oxidative Annulation of Arylamidines

    Zi-chao Shen, Pan Yang, Yu Tang*J. Org. Chem. 2016, 81, 309-317.

  3. Iron-catalyzed regioselective oxo- and hydroxy-phthalimidation of styrenes: a facile access to αhydroxyphthalimide ketones

    Ji-zong Zhang and Yu Tang* Adv. Synth. Catal.2016, 358, 752-764.

  4. A Highly Regio-and Stereoselective Synthesis of α-Fluorinated Imides via Fluorination of Chiral Enamides

    Yan-Shuang Xu, Yu Tang*, He-Jing Feng, Ji-Tian Liu, and Richard P. Hsung* Org. Lett. 2015,17, 572-575.

  5. IronCatalyzed Aerobic CH Functionalization of Pyrrolones

    Li-wei Liu, Zhen-zhen Wang, Hui-hui Zhang, Wan-shu Wang, Ji-zong Zhang and Yu Tang*Chem. Commun.2015, 51, 9531-9534.

  6. Tandem synthesis of pyrroloisoquinolines through 5-endo iodolactamization, oxidative functionalization and α-amidoalkylation reaction

    Yu Tang*, Ranran Han, Mingcan Lv, Yang Chen, Pan Yang Tetrahedron2015, 71, 4334-4343.

  7. Efficient Conversion of Carbohydrates to Ethoxymethylfurfural and LevulinicAcid Ethyl Ester under the Catalysis of Recyclable DMSO/Brønsted Acids

    Jitian Liu, Yu Tang*, Xu Fu Starch2015, 67, 765-771.

  8. Total Syntheses of Rhododaurichromanic Acid A and Hongoquercin A via an Oxa-[3 + 3] Annulation of Resorcinols

    Guo-Ying Luo, Hao Wu, Yu Tang*, Hui Li, Hyun-Suk Yeom, Ka Yang, and Richard P. Hsung* Synthesis2015, 47, 2713-2720.

  9. An Approachtoward Constructing the Trioxadispiroketal Core in the DEF-Ring of (+)-Spirastrellolide A

    Yi-Biao Wu, Yu Tang*, Guo-Ying Luo, Yang Chen, and Richard P. Hsung* Org. Lett.2014, 16, 4550-4553.

  10. Protecting-Group-Free Total Synthesis of Aplykurodinone1

    Yu Tang*, Ji-tian Liu, Ping Chen, Ming-can Lv, Zhen-zhen Wang, and Yi-kun Huang J. Org. Chem. 2014, 79, 11729-11734.