Center for Catalytic Hydrocarbon functionalizations

AgSbF6-Controlled Diastereodivergence in Alkyne Hydroarylation: Facile Access to Z- and E-Alkenyl Arenes

Min, M.; Kim, D.; Hong, S. [Chem. Commun. 50, 8028-(2014)]

Biophysical characterization of sites of host adaptive mutation in the influenza A virus RNA polymerase PB2 RNA-binding domain

Lim, K.; Kim, M.; Lee, M.-K.; Ko, J.; Hong, S.; Choi, B.-S. [Int. J. Biochem. Cell Biol 53, 237-(2014)]

Development and Biological Evaluation of Potent and Selective c-KITD816V Inhibitors

Lee, S.; Lee, H.; Kim, J.; Lee, S.; Kim, S. J. ; Hong, S.-S.; Hong, S. [J. Med. Chem. 57, 6428-(2014)]

HS-438, a New Inhibitor of Imatinib-Resistant BCR-ABL T315I Mutation in Chronic Myeloid Leukemia

Yun, S.-M., Jung, K. H.; Kim S. J.; Fang, Z. H.; Son, M. K.; Yan, H. H.; Lee, H.; Kim, J.; Shin, S.; Hong, S.*; Hong, S.-S.* [Cancer Lett. 348, 50-(2014)]

Synthesis of Heterocyclic-Fused Benzopyrans via the Pd(II)-Catalyzed C–H Alkenylation/C–O Cyclization of Flavones and Coumarins

Kim, Y.; Moon, Y.; Kang, D.; Hong, S. [Org. Biomol. Chem 12, 3413-(2014)]

Selective and Potent Small-Molecule Inhibitors of Phosphatidylinositol 3-Kinases

Jeong, Y.; Kwon, D.; Hong, S. [Future Med. Chem. 6, 737-(2014)]

Structure-based de novo design and identification of D816V mutant-selective c-KIT inhibitors

Park, H.; Lee, S.; Lee, S.; Hong, S. [Org. Biomol. Chem. 12, 4644-(2014)]

One-Pot Dehydrogenative Aromatization and Ortho-Functionalization Sequence of N-Acetyl Enamides

Kim, J.; Moon, Y.; Lee, S. Hong, S. [Chem. Commun. 50, 3227-(2014)]