Yunho Jin

D- and L-2',3'-didehydro-2',3'-dideoxy-3'-fluoro-carbocyclic nucleosides: synthesis, anti-HIV activity and mechanism of resistance.

R. Schinazi, C. K. Chu, K. Rapp, 2007, Journal of medicinal chemistry.

Synthesis, antiviral activity, and mechanism of drug resistance of D- and L-2',3'-didehydro-2',3'-dideoxy-2'-fluorocarbocyclic nucleosides.

R. Schinazi, C. K. Chu, M. Bennett, 2005, Journal of medicinal chemistry.

Discovery of EGFR selective 4,6-disubstituted pyrimidines from a combinatorial kinase-directed heterocycle library.

N. Gray, W. Hur, F. Gao, 2006, Journal of the American Chemical Society.

Optimization of an Enzymatic Antibody-Drug Conjugation Approach Based on Coenzyme A Analogs.

Ansgar Brock, Julie Vance, A. Brock, 2017, Bioconjugate chemistry.

Syntheses of 1,3-dioxolanyl and carbocyclic nucleosides as potential antiviral agnets [sic]

Yunho Jin, 2004 .

Design and synthesis of novel selective anaplastic lymphoma kinase inhibitors.

Sungjoon Kim, Nanxin Li, Christian C. Lee, 2016, Bioorganic & medicinal chemistry letters.

Synthesis, structure-activity relationships, and in vivo efficacy of the novel potent and selective anaplastic lymphoma kinase (ALK) inhibitor 5-chloro-N2-(2-isopropoxy-5-methyl-4-(piperidin-4-yl)phenyl)-N4-(2-(isopropylsulfonyl)phenyl)pyrimidine-2,4-diamine (LDK378) currently in phase 1 and phase 2

Sungjoon Kim, Nanxin Li, M. Warmuth, 2013, Journal of medicinal chemistry.

Tuning a Protein‐Labeling Reaction to Achieve Highly Site Selective Lysine Conjugation

Susan E. Cellitti, G. Spraggon, A. Brock, 2018, Chembiochem : a European journal of chemical biology.

Syk inhibitors with high potency in presence of blood.

Jianwei Che, E. Vangrevelinghe, Christian C. Lee, 2014, Bioorganic & medicinal chemistry letters.