
PUBLICATIONS
2016 - current
- INDEPENDENT WORKS AT SNU -
Coming soon!
- POSTDOCTORAL WORKS AT MIT -
[10] Y. Kanda,† S. Y. Hong,† and A.T. Radosevich*, Selective C–H Fluoroalkylation of Azines Enabled by Tailored Phosphorus-Based Reagents, Chem, 2021, 7, 1420–1422. (†Equally contributed) – Invited Preview Article
- GRADUATED WORKS AT KAIST-
[8] S. Kim, D. Kim, S. Y. Hong* and S. Chang*, Tuning Orbital Symmetry of Iridium Nitrenoid Enables Catalytic Diastereoand Enantioselective Alkene Difunctionalizations, J. Am. Chem. Soc., 2021, 143, 10, 3993–4004. (*Co-corresponding authors)
• Highlighted in Organic Chemistry Portal.
[6] S. Y. Hong and S. Chang* Stereodefined Access to Lactams via Olefin Difunctionalization: Iridium Nitrenoids as a Motif of LUMO-Controlled Dipoles, J. Am. Chem. Soc., 2019, 141, 10399−10408.
• Highlighted in Synfacts 2019, 15, 1026.
[5] S. Huh,† S. Y. Hong,† and S. Chang* Synthetic Utility of N-Benzoyloxyamides as an Alternative Precursor of Acylnitrenoids for γ-Lactam Formation, Org. Lett., 2019, 21, 2808–2812. (†Equally contributed)
• Highlighted in Organic Chemistry Portal.
[4] S. Y. Hong, J. Son, D. Kim, and S. Chang*; Ir(III)-Catalyzed Stereoselective Haloamidation of Alkynes Enabled by Ligand Participation, J. Am. Chem. Soc., 2018, 140, 12359-12363.
• Highlighted in Synfacts 2018, 14, 1269.
[3] S. Y. Hong,† Y. Park,† Y. Hwang, Y. Kim, M.-H. Baik,* and S. Chang* Selective formation of γ-lactams via C–H amidation enabled by tailored iridium catalysts, Science, 2018, 359, 1016-1021. (†Equally contributed)
• Highlighted in Nature, March 2018 / Science Daily, March 2018/Phys.Org, March 2018 / Asian Scientist, March 2018/Synfacts 2018, 14, 0464
[2] S. Y. Hong, J. Jeong, and S. Chang*; [4+2] or [4+1] Annulation: Changing the Reaction Pathway of a Rhodium-Catalyzed Process by Tuning the Cp Ligand, Angew. Chem. Int. Ed., 2017, 56, 2408–2412.
[1] S. Y. Hong,† J. Kwak,† and S. Chang*; Rhodium-Catalyzed Selective C–H Functionalization of NNN Tridentate Chelating Compounds via a Rollover Pathway, Chem. Commun. 2016, 52, 3159-3162. (†Equally contributed)