Yoonsu Park
Yoonsu Park
princeton.edu의 이메일 확인됨
Transition Metal-Catalyzed C–H Amination: Scope, Mechanism, and Applications
Y Park, Y Kim, S Chang
Chemical Reviews 117 (13), 9247-9301, 2017
Mechanistic Studies on the Rh(III)-Mediated Amido Transfer Process Leading to Robust C–H Amination with a New Type of Amidating Reagent
Y Park, KT Park, JG Kim, S Chang
Journal of the American Chemical Society 137 (13), 4534-4542, 2015
Mechanistic Studies of the Rhodium-Catalyzed Direct C–H Amination Reaction Using Azides as the Nitrogen Source
SH Park, J Kwak, K Shin, J Ryu, Y Park, S Chang
Journal of the American Chemical Society 136 (6), 2492-2502, 2014
Rh(III)-Catalyzed Traceless Coupling of Quinoline N-Oxides with Internal Diarylalkynes
U Sharma, Y Park, S Chang
The Journal of Organic Chemistry 79 (20), 9899-9906, 2014
Study of Sustainability and Scalability in the Cp*Rh(III)-Catalyzed Direct C–H Amidation with 1,4,2-Dioxazol-5-ones
Y Park, S Jee, JG Kim, S Chang
Organic Process Research & Development 19 (8), 1024, 2015
Selective formation of γ-lactams via C–H amidation enabled by tailored iridium catalysts
SY Hong*, Y Park*, Y Hwang, YB Kim, MH Baik, S Chang
Science 359 (6379), 1016-1021, 2018
Why is the Ir(III)-Mediated Amido Transfer Much Faster Than the Rh(III)-Mediated Reaction? A Combined Experimental and Computational Study
Y Park, J Heo, MH Baik, S Chang
Journal of the American Chemical Society 138 (42), 14020–14029, 2016
Regiodivergent access to five-and six-membered benzo-fused lactams: Ru-catalyzed olefin hydrocarbamoylation
B Li, Y Park, S Chang
Journal of the American Chemical Society 136 (3), 1125-1131, 2014
Iridium-catalysed arylation of C–H bonds enabled by oxidatively induced reductive elimination
K Shin, Y Park, MH Baik, S Chang
Nature chemistry 10 (2), 218, 2018
Mechanism‐Driven Approach to Develop a Mild and Versatile C‐H Amidation through Ir(III) Catalysis
Y Hwang*, Y Park*, S Chang
Chemistry A European Journal 23 (46), 11147-11152, 2017
Discovery of new benzothiazole-based inhibitors of breakpoint cluster region-Abelson kinase including the T315I mutant
S Hong, J Kim, SM Yun, H Lee, Y Park, SS Hong, S Hong
Journal of Medicinal Chemistry 56 (9), 3531-3545, 2013
Mechanism of Rh-Catalyzed Oxidative Cyclizations: Closed versus Open Shell Pathways
Y Park, S Ahn, D Kang, MH Baik
Accounts of Chemical Research 49 (6), 1263, 2016
Iridium-Catalyzed Enantioselective C(sp3)–H Amidation Controlled by Attractive Noncovalent Interactions
H Wang, Y Park, Z Bai, S Chang, G He, G Chen
Journal of the American Chemical Society 141 (17), 7194-7201, 2019
Asymmetric formation of γ-lactams via C–H amidation enabled by chiral hydrogen-bond-donor catalysts
Y Park, S Chang
Nature Catalysis 2, 219-227, 2019
Rhodium‐Catalyzed Direct Amination of Arene C–H Bonds Using Azides as the Nitrogen Source
SH Park, Y Park, S Chang
Organic Syntheses 91, 52-59, 2014
Quantifying Structural Effects of Amino Acid Ligands in Pd (II)-Catalyzed Enantioselective C–H Functionalization Reactions
Y Park, ZL Niemeyer, JQ Yu, MS Sigman
Organometallics 37 (2), 203-210, 2017
Delineating Physical Organic Parameters in Site-Selective C–H Functionalization of Indoles
Y Kim*, Y Park*, S Chang
ACS Central Science, 2018
Revisiting Arene C (sp2)− H Amidation by Intramolecular Transfer of Iridium Nitrenoids: Evidence for a Spirocyclization Pathway
Y Hwang*, Y Park*, YB Kim, D Kim, S Chang
Angewandte Chemie 130 (41), 13753-13757, 2018
Ni-Mediated Generation of “CN” Unit from Formamide and Its Catalysis in the Cyanation Reactions
L Yang, YT Liu, Y Park, SW Park, S Chang
ACS Catalysis 9 (4), 3360-3365, 2019
Harnessing Secondary Coordination Sphere Interactions That Enable the Selective Amidation of Benzylic C–H Bonds
H Jung, M Schrader, D Kim, MH Baik, Y Park, S Chang
Journal of the American Chemical Society 141 (38), 15356-15366, 2019
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