Y. Gu

Heteroaryl and cycloalkyl sulfonamide hydroxamic acid inhibitors of matrix metalloproteinases.

F. C. Nelson, P. Chanda, J. Skotnicki, 2001, Bioorganic & medicinal chemistry letters.

Synthesis and SAR of bicyclic heteroaryl hydroxamic acid MMP and TACE inhibitors.

R. Black, J. Skotnicki, J. Levin, 2003, Bioorganic & medicinal chemistry letters.

Discovery of 4-amino-5-(3-bromophenyl)-7-(6-morpholino-pyridin-3-yl)pyrido[2,3-d]pyrimidine, an orally active, non-nucleoside adenosine kinase inhibitor..

M. Williams, S. Bhagwat, M. Jarvis, 2001, Journal of medicinal chemistry.

Design, synthesis and biological evaluation of bis-aryl ureas and amides based on 2-amino-3-purinylpyridine scaffold as DFG-out B-Raf kinase inhibitors.

T. Lu, Yadong Chen, Weifang Tang, 2015, European journal of medicinal chemistry.

Stereoselective synthesis of all four geometric isomers of internal 1,3-butadienes by the condensation reaction of aldehydes with the .gamma.-trimethylsilyl-substituted allylboranes

Kung K Wang, Kung K. Wang, Y. Gu, 1990 .

Stereoselective synthesis of terminal 1,3-butadienes by the condensation reaction of aldehydes and ketones with .gamma.-trimethylsilyl-substituted allylboranes

Kung K Wang, Kung K. Wang, Y. Gu, 1991 .