Publications

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  • 74. Ru(II)-Catalyzed Site-Selective Hydroxylation of Flavone and Chromone Derivatives: The Importance of the 5-Hydroxyl Motif for the Inhibition of Aurora Kinases 

    Kim, K.; Choe, H.; Jeong, Y.; Lee, J. H.; Hong, S.

    Org. Lett. 2015, 17, 2550.

  • 74. Asymmetric C–H functionalization of cyclopropanes using an isoleucine-NH2 bidentate

    directing group 

    Kim, J.; Sim, M.; Kim, N.; Hong, S.

    Chem. Sci. 2015, 6, 3611. (Highlighted in Literature Coverage in Synform: 2015, 10, A136-A139)

  • 72. Rh(III) and Ru(II)-Catalyzed Site-Selective C–H Alkynylation of Quinolones 

    Kang, D.; Hong, S.

    Org. Lett. 2015, 17, 1938.  

  • 71. Rh(I)-Catalyzed Site-Selective Decarbonylative Alkenylation and Arylation of Quinolones under Chelation Assistance

    Kwon, S.; Kang, D.; Hong, S.

    Eur. J. Org. Chem. 2015, 17, 3615. (Highlighted as a Front Cover)   

  • 70. Rh(III)-Catalyzed Direct C–H/C–H Cross-Coupling of Quinones with Arenes Assisted by Directing Group: Identification of Carbazole Quinones as GSKb Inhibitors

    Moon, Y.; Jeong, Y.; Kook, D.; Hong, S.

    Org. Biomol. Chem. 2015, 13, 3918.

  • 69. Efficient Synthesis of Frutinone A and Its Derivatives via Palladium-Catalyzed C-H Activation/Carbonylation

    Shin, Y.; Yoo, C.; Moon, Y.; Lee, Y.; Hong, S.

    Chem.-Asian J. 2015, 10, 878. 

    (Invited Article for 'The 10th Anniversary of the Asian Core Program (ACP)' themed collection)

  • 68. HS-543 Induces Apoptosis of Imatinib-Resistant Chronic Myeloid Cells with T315I Mutation

    Kim, S.-J.; Jung, K. H.; Yan, H. H., Son, M.-K.; Fang, Z.; Ryu, Y.-L.; Lee, H.; Kim, J.; Lee, S.; Hong, S.*; Hong, S.-S.*

    ONCOTARGET 2015, 6, 1507-1518. 

  • 67. Anticancer Activity of HS-527, a Novel Inhibitor Targeting PI3-Kinase in Human Pancreatic Cancer Cells

    Ryu, Y.-L.; Jung, K. H.; Son, M. K.; Yan, H. H.; Kim, S. J.; Shin, S.; Hong, S.*; Hong, S.-S.*

    Cancer Lett. 2014, 353, 68.

  • 66. HS-133, a Novel Fluorescent Phosphatidylinositol 3-Kinase Inhibitor as a Potential Imaging and Anticancer Agent for Targeted Therapy

    Lee, J.-H.; Jung, K. H.; Lee, H.; Yun, S.-M., Son, M.-K.; Ahn, S.-H.; Lee, S.; Kim, D.; Hong, S.*; Hong, S.-S.*

    ONCOTARGET 20145, 10180.

  • 65. Copper-Mediated Cross-Coupling Approach for the Synthesis of 3-Heteroaryl Quinolone and Related Analogues

    Shin, S.; Kim, Y.; Kim, K.; Hong, S.

    Org. Biomol. Chem. 2014, 12, 5719.