HONG RESEARCH GROUP
Seoul National University
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Seung Youn
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2016 - current
12. Chemoselective Primary Amination of Aryl Boronic Acids by PIII/PV=O Catalysis: Synthetic Capture of the Transient Nef Intermediate HNO
S. Y. Hong and A. T. Radosevich*
J. Am. Chem. Soc., 2022, 144, 8902–8907.
11. Enabling Reductive C–N Cross-Coupling of Nitroalkanes and Boronic Acids by Steric Design of P(III)/P(V)=O Catalysts
G. Li, Y. Kanda, S. Y. Hong and A. T. Radosevich*
J. Am. Chem. Soc., 2022, 144, 8242–8248.
10. Selective C–H fluoroalkylation of azines enabled by tailored phosphorus-based reagents
Y. Kanda,† S. Y. Hong† and A.T. Radosevich* (†Equally contributed)
Chem, 2021, 7, 1420–1422.
– Invited Preview Article
9. Mechanism-Guided Development of Transition-Metal Catalyzed C–N Bond-Forming Reactions Using Dioxazolones as the Versatile Amidating Source
S. Y. Hong, Y. Hwang, M. Lee and S. Chang*
Acc. Chem. Res., 2021, 54, 2683–2700.
8. Tuning Orbital Symmetry of Iridium Nitrenoid Enables Catalytic Diastereoand Enantioselective Alkene Difunctionalizations
S. Kim, D. Kim, S. Y. Hong* and S. Chang* (*Co-corresponding authors)
J. Am. Chem. Soc., 2021, 143, 3993–4004
• Highlighted in Organic Chemistry Portal
7. Catalytic Access to Carbocation Intermediates via Nitrenoid Transfer Leading to Allylic Lactams
S. Y. Hong, D. Kim and S. Chang*
Nat. Catal., 2021, 4, 79−88
• Highlighted in IBS
6. Stereodefined Access to Lactams via Olefin Difunctionalization: Iridium Nitrenoids as a Motif of LUMO-Controlled Dipoles
S. Y. Hong and S. Chang*
J. Am. Chem. Soc., 2019, 141, 10399−10408
• Highlighted in Synfacts 2019, 15, 1026
5. Synthetic Utility of N-Benzoyloxyamides as an Alternative Precursor of Acylnitrenoids for γ-Lactam Formation
S. Huh,† S. Y. Hong,† and S. Chang*
Org. Lett., 2019, 21, 2808–2812
4. Ir(III)-Catalyzed Stereoselective Haloamidation of Alkynes Enabled by Ligand Participation
S. Y. Hong, J. Son, D. Kim, and S. Chang*
J. Am. Chem. Soc., 2018, 140, 12359-12363
• Highlighted in Synfacts 2018, 14, 1269
3. Selective formation of γ-lactams via C–H amidation enabled by tailored iridium catalysts
S. Y. Hong,† Y. Park,† Y. Hwang, Y. Kim, M.-H. Baik,* and S. Chang*
Science, 2018, 359, 1016-1021
• Highlighted in Nature, March 2018 / Science Daily, March 2018 / Phys.Org, March 2018 / Asian Scientist, March 2018 / Synfacts 2018, 14, 0464
2. [4+2] or [4+1] Annulation: Changing the Reaction Pathway of a Rhodium-Catalyzed Process by Tuning the Cp Ligand
S. Y. Hong, J. Jeong, and S. Chang*
Angew. Chem. Int. Ed., 2017, 56, 2408–2412
1. Rhodium-Catalyzed Selective C–H Functionalization of NNN Tridentate Chelating Compounds via a Rollover Pathway
S. Y. Hong,† J. Kwak,† and S. Chang*
Chem. Commun., 2016, 52, 3159-3162