Jing Zhang

发表

Unprecedented FeCl(3)6 H(2)O-promoted skeleton rearrangement of 1-aryl-2,3,4,5-tetrahydro-1H-3-benzazepines: a new strategy for the synthesis of C1 quaternary tetrahydroisoquinolines.

A. Zhang, Jing Zhang, 2009, Chemistry.

Dopamine D 1 Receptor Ligands: Where AreWe Now and Where AreWe Going

Xuechu Zhen, A. Zhang, B. Xiong, 2009 .

Dopamine D1 receptor ligands: Where are we now and where are we going

Xuechu Zhen, A. Zhang, B. Xiong, 2009, Medicinal research reviews.

FeCl3·6H2O-promoted skeleton-rearrangement of 1-substituted-3-benzazepines: substrate extension and product utilization

Meining Wang, A. Zhang, Jing Zhang, 2011 .

Novel 2,4-Diarylaminopyrimidine Analogues (DAAPalogues) Showing Potent c-Met/ALK Multikinase Inhibitory Activities.

Yi Chen, M. Geng, Yin-chun Ji, 2014, ACS medicinal chemistry letters.

Synthesis of dihydrofuroaporphine derivatives: identification of a potent and selective serotonin 5-HT 1A receptor agonist.

Xuechu Zhen, Hai Zhang, Na Ye, 2010, Journal of medicinal chemistry.

Design of multivalent ligand targeting G-protein-coupled receptors.

Zhili Liu, A. Zhang, Jing Zhang, 2009, Current pharmaceutical design.

Structural manipulation on the catecholic fragment of dopamine D(1) receptor agonist 1-phenyl-N-methyl-benzazepines.

Xuechu Zhen, Lin Guo, A. Zhang, 2014, European journal of medicinal chemistry.

'Click' D(1) receptor agonists with a 5-HT(1A) receptor pharmacophore producing D(2) receptor activity.

Xuechu Zhen, Hai Zhang, A. Zhang, 2009, Bioorganic & medicinal chemistry.

Synthesis of 6-substituted 1-phenylbenzazepines and their dopamine D(1) receptor activities.

Xuechu Zhen, A. Zhang, Jing Zhang, 2008, Bioorganic & medicinal chemistry.