T. Yuan

发表

Synthesis and structure-activity relationship of 3-O-acylated (-)-epigallocatechins as 5α-reductase inhibitors.

Young-Sun Lin, R. Hiipakka, Chu-Bin Liao, 2010, European journal of medicinal chemistry.

Novel copper/PEG-400 catalyst systems for chemoselective S- and N-arylation of 2-mercaptobenzothiazole

Yu Yang, T. Yuan, Junmin Chen, 2014 .

Simple and efficient CuI/PEG-400 system for amination of aryl halides with aqueous ammonia

T. Yuan, Mingzhong Cai, Wenyan Hao, 2011 .

Efficient Copper-Catalyzed Double S-Arylation of Aryl Halides with Sodium Sulfide in Peg-400

Li Liu, T. Yuan, Junmin Chen, 2012 .

Efficient Copper(I)‐Catalyzed S‐Arylation of KSCN with Aryl Halides in PEG‐400

T. Yuan, Junmin Chen, Xiaokang Li, 2012 .

Highly Efficient and Practical Method for Synthesis of 2,2′-Azino-Bis(3-Ethyl-benzothiazoline-6-Sulfonic Acid) (ABTS) and Its Diammonium Salt

T. Yuan, Junmin Chen, Xiaomeng Zhou, 2014 .

Synthesis and biological evaluation of substituted 6-alkynyl-4-anilinoquinazoline derivatives as potent EGFR inhibitors.

Ying-Ta Wu, T. Yuan, L. Liu, 2007, Bioorganic & medicinal chemistry letters.

Discovery of pyrrole-indoline-2-ones as Aurora kinase inhibitors with a different inhibition profile.

Weilin Chi, Chu-Bin Liao, Yu-Hsiang Lin, 2010, Journal of medicinal chemistry.

Copper(I)-Catalyzed Nitrile-Addition/N-Arylation Ring-Closure Cascade: Synthesis of 5,11-Dihydro-6H-indolo[3,2-c]quinolin-6-ones as Potent Topoisomerase-I Inhibitors.

Chin‐Hung Lai, Yu-Hsiang Lin, S. Lin, 2021, Journal of medicinal chemistry.

Simple and efficient CuI/PEG-400 system for hydroxylation of aryl halides with potassium hydroxide

T. Yuan, Mingzhong Cai, Wenyan Hao, 2011 .

Discovery of pyrrole-indoline-2-ones as Aurora kinase inhibitors with a different inhibition profile.

Weilin Chi, Yu-Hsiang Lin, Chao-Cheng Chiang, 2010, Journal of medicinal chemistry.