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  • 86. Discovery of Low Micromolar Dual Inhibitors for Wild Type and L1196M Mutant of Anaplastic Lymphoma Kinase through the Structure-Based Virtual Screening 

    Shin, S.; Mah, S.; Hong, S.*; Park, H.* 

    J. Chem. Inf. Model. 2016, 56, 802.

  • 85. Unraveling Innate Substrate Control in Site-Selective Palladium-Catalyzed C−H Heterocycle Functionalization 

    Choi, H.; Min, M; Peng, Q.; Kang, D.; Paton, R. S.Hong, S.

    Chem. Sci. 2016, 7, 3900.  

  • 84. Rhodium-Catalyzed Direct C−H Phosphorylation of (Hetero)arenes Suitable for Late-Stage Functionalization

    Min, M.; Kang, D.; Jung, S.; Hong, S. 

    Adv. Synth. Catal., 2016, 358, 1296. (Selected as a VIP Paper by the Editorial Office.)

  • 83. Palladium-Catalyzed Divergent Arylation with Triazolopyridines: One-Pot Synthesis of 6-Aryl-2-α-styrylpyridines 

    Moon, Y.; Kwon, S.; Kang, D.; Im, H.; Hong, S. 

    Adv. Synth. Catal., 2016358, 958. (Selected as a VIP Paper by the Editorial Office & Highlighted as a Cover)

  • 82. Computational Design and Discovery of Nanomolar Inhibitors of IκB Kinase b 

    Park, H.; Shin, Y.; Choe, H.; Hong, S.

    J. Am. Chem. Soc. 2015137, 337.

  • 81. Regioselective palladium(II)-catalyzed aerobic oxidative Heck-type C3 alkenylation of sulfocoumarins

    Kim, N.; Min, M.; Hong, S. 

    Org. Chem. Front., 2015, 2, 1621. (Invited Article for 'Emerging Investigator' themed collection)

  • 80. Identification of β-lapachone analogs as novel MALT1 inhibitors to treat an aggressive subtype of diffuse large B-cell lymphoma 

    Lim, S. M.; Jeong, Y.; Lee, S.; Im, H.; Tae, H. S.; Kim, B. G.; Park, H. D.; Park, J.Hong, S.

    J. Med. Chem. 2015, 58, 8491.

  • 79. Discovery of Wrightiadione as a Novel Template for the TrkA Kinase Inhibitors 

    Jeong, Y.; Lim, S. M.; Hong, S.

    Bioorg. Med. Chem. Lett. 201525, 5186.

  • 78. Catalyst Controlled Divergent C4/C8-Site Selective C–H Arylation of Isoquinolones
    Lee, S.; Mah, S.; Hong, S.
    Org. Lett. 201517, 3864.
    Highlighted in Organic Chemistry Portal

  • 77. Structure-based de novo design and synthesis of aminothiazole-based p38 MAP kinase inhibitors 

    Park, H.; Lee, S.; Hong, S.

    Bioorg. Med. Chem. Lett. 201525, 3784.