Prior Publications – Park Research Lab

Park Research Group

Prior Publications (~2019)

Graduate and Undergraduate Works

Graduate and Undergraduate Works

[20] Harnessing Secondary Coordination Sphere Interactions that Enable the Selective Amidation of Benzylic C−H Bonds

Jung, H.; Schrader, M.; Kim, D.; Baik, M.-H.*; Park, Y.*; Chang, S.*

J. Am. Chem. Soc. 2019, 141, 15356–15366. (*Co-corresponding authors).

[19] Asymmetric Formation of of γ-Lactams via C–H Amidation Enabled by Chiral Hydrogen-Bond-Donor Catalysts

Park, Y. & Chang, S.

Nature Catal. 2019, 2, 219.

Highlighted in News & Views of Nature Catalysis.

2020년 대한민국 국가연구개발 우수성과 100선 선정.

[18] Iridium-Catalyzed Enantioselective C(sp³)–H Amidation Controlled by Attractive Noncovalent Interactions

Wang, H.; Park, Y.; Bai, Z.; Chang, S.; He, G.; Chen, G.

J. Am. Chem. Soc. 2019,141, 7194–7201.

[17] Ni-Mediated Generation of "CN" Unit from Formamide and Its Catalysis in the Cyanation Reactions

Yang, L.; Liu, Y.-T.; Park, Y.; Park, S.-W., Chang, S.

ACS Catal. 2019, 9, 3360–3365.

[16] Revisiting Arene C(sp²)–H Amidation via Intramolecular Transfer of Iridium Nitrenoids: Evidence for a Spirocyclization Pathway

Hwang, Y.†; Park, Y.†; Kim, Y.B.; Kim, D.; Chang, S.

Angew. Chem. Int. Ed. 2018, 57, 13565–13569 (†Co-first authors).

[15] Selective Formation of γ-Lactams via C–H Amidation Enabled by Tailored Iridium Catalysts

Hong, S. Y.†; Park, Y.†; Hwang, Y.; Kim, Y.; Baik, M.-H.; Chang, S.

Science 2018, 359, 1016–1021 (†Co-first authors).

Highlighted in Nature, Synfacts, Organic Chemistry Portal, and Science Daily.

[14] Delineating Physical Organic Parameters in Site-Selective C–H Functionalization of Indoles

Kim, Y.†; Park, Y.†; Chang, S.

ACS Cent. Sci. 2018, 4, 768–775 (†Co-first authors).

[13] Quantifying Structural Effects of Amino Acid Ligands in Pd(II)-Catalyzed Enantioselective C–H Functionalization Reactions

Park, Y.; Niemeyer, Z. L.; Yu, J.-Q.; Sigman, M. S.

Organometallics 2018, 37, 203–210.

Featured as a Cover Art in Volume 37, Issue 2.

[12] Iridium-Catalysed Arylation of C–H Bonds Enabled by Oxidatively Induced Reductive Elimination

Shin, K.; Park, Y.; Baik, M.-H.; Chang, S.

Nat. Chem. 2018, 10, 218–224.

[11] Transition Metal-Catalyzed C–H Amination: Scope, Mechanism & Applications (Review Article)

Park, Y.; Kim, Y.; Chang, S.

Chem. Rev. 2017, 117, 9247–9301.

Special issue for C-H activation.

[10] Mechanism-Driven Approach to Develop a Mild and Versatile C–H Amidation through Ir(III) Catalysis

Hwang, Y.†; Park, Y.†; Chang, S.

Chem. Eur. J. 2017, 23, 11147–11152 (†Co-first author).

[9] Why is the Ir(III)-Mediated Amido Transfer So Much Faster than the Rh(III)-Mediated Reaction? A Combined Experimental and Computational Study

Park, Y.; Heo, J.; Baik, M.-H.; Chang, S.

J. Am. Chem. Soc. 2016, 138, 14020–14029.

[8] The Mechanism of Rh-Catalyzed Oxidative Cyclizations: Closed vs. Open Shell Pathways

Park, Y.; Ahn, S.; Kang, D.; Baik, M.-H.

Acc. Chem. Res. 2016, 49, 1263–1270.

[7] Study of Sustainability and Scalability in the Cp*Rh(III)-Catalyzed Direct C–H Amidation with 1,4,2-Dioxazol-5-ones

Park, Y.; Jee, S.; Kim, J. G.; Chang, S.

Org. Process Res. Dev. 2015, 19, 1024–1029.

Selected as ACS Editors’ Choice.

[6] Mechanistic Studies on the Rh(III)-Mediated Amido Transfer Process Leading to Robust C–H Amination with a New Type of Amidating Reagent

Park, Y.; Park, K. T.; Kim, J. G.; Chang, S.

J. Am. Chem. Soc. 2015, 137, 4534–4542.

[5] Rh(III)-Catalyzed Traceless Coupling of Quinoline N-Oxides with Internal Diarylalkynes

Sharma, U.; Park, Y.; Chang, S.

J. Org. Chem. 2014, 79, 9899–9906.

[4] Mechanistic Studies of the Rhodium-Catalyzed Direct C–H Amination Reaction Using Azides as the Nitrogen Source

Park, S. H.; Kwak, J.; Shin, K. Ryu, J.; Park, Y.; Chang, S.

J. Am. Chem. Soc. 2014, 136, 2492–2502.

[3] Regiodivergent Access to Five- and Six-Membered Benzo-Fused Lactams: Ru-Catalyzed Olefin Hydrocarbamoylation

Li, B.; Park, Y.; Chang, S.

J. Am. Chem. Soc. 2014, 136, 1125–1131.

[2] Rhodium-Catalyzed Direct Amination of Arene C–H Bonds Using Azides as the Nitrogen Source

Park, S. H.; Park, Y.; Chang, S.

Org. Synth. 2014, 91, 52–59.

[1] Discovery of New Benzothiazole-Based Inhibitors of Breakpoint Cluster Region-Abelson Kinase Including the T315I Mutant

Hong S.; Kim J.; Yun, S.-M.; Lee, H.; Park, Y.; Hong, S.-S.; Hong, S.

J. Med. Chem. 2013, 56, 3531–3545.

Home Research Yoonsu Team Publications Photos

© The Park Laboratory, 2023.

Address: Rm. 604, E6-6, KAIST, 291 Daehak-ro, Yuseong-gu, Daejeon 34141, Republic of Korea

© The Park Laboratory, 2023.

Address: Rm. 604, E6-6, KAIST, 291 Daehak-ro, Yuseong-gu, Daejeon 34141, Republic of Korea