Hong, J. E.; Jeon, H.; Kwak, J.-H.; Lee, S.*; Park, Y.* Electrochemical Aerobic Oxidation and Cyclization of 2‑Alkylbenzamides toward 3-Hydroxyisoindolinones. J. Org. Chem. 2025, 90, 8152
Hong, J. E.; Yoon, J.; Baek, W.; Kim, K.; Kwak, J.-H.*; Park, Y.* Electrochemical C(sp3)−H Lactonization of 2‑Alkylbenzoic Acids toward Phthalides. Org. Lett. 2023, 25, 298
Hong, J. E.; Jung, Y.; Min, D.; Jang, M.; Kim, S.; Park, J.; Park, Y.* Visible-Light-Induced Organophotocatalytic Difunctionallization: Open-Air Hydroxysulfurization of Aryl Alkenes with Aryl Thiols. J. Org. Chem. 2022, 87, 7378
Hwang, S. J.; Jung, Y.; Song, Y. S.; Park, S.; Park, Y.*; Lee. H.-J.* Enhanced anti‐angiogenic activity of novel melatonin‐like agents. J. Pineal. Res. 2021, 71, e12739
Jung, Y.; Hong, J. E.; Kwak, J.-H.; Park, Y.* Single-Step Approach toward Nitrones via Pyridinium Ylides: The DMAP-Catalyzed Reaction of Benzyl Halides with Nitrosoarenes. J. Org. Chem. 2021, 86, 6343
Yang, J.; Park, Y.; Yang, S.; Lee, G.; Ha, M. W.; Kim, M.-h.; Hong, S.; Park, H.-g.* Enantioselective Total Synthesis of Nitraria Alkaloids: (+)-Nitramine, (+)-Isonitramine, (-)-Isonitramine, and (-)-Sibirine via Asymmetric Phase-Transfer Catalytic α‑Allylations of α‑Carboxylactams. J. Org. Chem. 2021, 86, 4375
Jung, Y.; Hong, J. E.; Baek, S. T.; Hong, S.; Kwak, J.-H. and Park, Y.* 4-Dimethylaminopyridine-Catalyzed Metal-Free Aerobic Oxidation of Aryl α-Halo Esters to Aryl α-Keto Esters, ACS Omega, 2020, 5, 22951
Hong, J. E.; Jung, Y.; Park, Y.; Park, Y.* Highly Selective Synthesis of Hydrazoarenes from Nitroarenes via Polystyrene-Supported Au-Nanoparticle-Catalyzed Reduction: Application to Azoarenes, Aminoarenes, and 4,4′-Diaminobiaryls. ACS Omega, 2020, 5, 7576
Rampogu, S.; Parate, S.; Parameswaran, S. Park, C.; Baek, A.; Son, M.; Park, Y.; Park, S. J.*; Lee, K. W.* Natural compounds as potential Hsp90 inhibitors for breast cancer-Pharmacophore guided molecular modelling studies. Comput. Biol. Chem. 2019, 83, 107113
Choi, D. H.; Hong, J. E.; Jung, Y.; Park, H. I.; Baek, S. T.; Kim, S. J.; Lee, C. G.; Park, Y.; Park, S. J.; Park, Y.* Synthesis of gold nanoparticles supported at graphene derivatives using green reductants and evaluation of their catalytic activity in 4-nitrophenol reduction. Gold bull. 2019, 52, 165
Park, J. J.; Hwang, S. J.; Kang, Y. S.; Jung, J.; Park, S.; Hong, J. E.; Park, Y.*; Lee. H.-J.* Synthesis of arbutin–gold nanoparticle complexes and their enhanced performance for whitening. Arch. Pharm. Res. 2019, 42, 977
Rampogu, S.; Park, C.; Ravinder, D.; Son, M.; Baek, A.; Zeb, A.; Bavi, R.; Kumar, R.; Lee, G.; Parate, S.; Pawar, S. C.; Park, Y.; Park, S. J.; Lee, K. W.* Pharmacotherapeutics and Molecular Mechanism of Phytochemicals in Alleviating Hormone-Responsive Breast Cancer. Oxidative Med. Cell. Longev. 2019, 2019, 5189490
Rampogu, S.; Baek, A.; Park, C.; Son, M.; Parate, S.; Parameswaran, S. Park, Y.; Shaik, B.; Kim, J. H.; Park, S. J.*; Lee, K. W.* Discovery of Small Molecules that Target Vascular Endothelial Growth Factor Receptor-2 Signalling Pathway Employing Molecular Modelling Studies. Cells, 2019, 8, 269
Rampogu, S.; Baek, A.; Son, M.; Zeb, A.; Park, C.; Kumar, R.; Lee, G.; Kim, D.; Choi, Y.; Cho, Y.; Park, Y.; Park, S. J.*; Lee, K. W.* Computational exploration for lead compounds that can reverse the nuclear morphology in progeria. BioMed. Res. Int. 2017, 2017, 5270940
Kwon, S. J.; Hwang, S. J.; Jung, Y.; Park, H.-g.; Kim, M.-h.; Park, Y.*; Lee, H.-J.* A synthetic nitraria alkaloid, isonitramine protects pancreatic β-cell and attenuates postprandial hyperglycemia. Metabolism, 2017, 70, 107
Seo, Y. S.; Ahn, E.-Y.; Park, J.; Kim, T. Y.; Hong, J. E.; Kim, K.; Park, Y.*; Park, Y.* Catalytic reduction of 4-nitrophenol with gold nanoparticles synthesized by caffeic acid. Nanoscale Res Lett. 2017, 12, 7
Hwang, S. J.; Park, H.-g.; Park, Y.*; Lee. H.-J.* An α-quaternary chiral lactam derivative, YH-304 as a novel broad-spectrum anticancer agent. Int. J. Oncol. 2016, 49, 2480
Park, Y.; Park, J.-H.; Park, S.; Lee, S. Y.; Cho, K. H.; Kim, D.-D.; Shin, W.-S.; Yoon, I.-S.; Cho, H.-J.*; Maeng, H.-J.* Enhanced cellular uptake and pharmacokinetic characteristics of Doxorubicin-Valine amide prodrug. Molecules, 2016, 21, 1272
Chae, Y.-J.; Cho, K. H.; Yoon, I.-S.; Noh, C.-K.; Lee, H.-J.; Park, Y.; Ji, E.; Seo, M.-D.*; Maeng, H.-J.* Vitamin D Receptor-Mediated Upregulation of CYP3A4 and MDR1 by Quercetin in Caco-2 cells. Planta. Med. 2016, 82, 121
Park, S.; Cha, S.-H.; Cho, I.; Park, S.; Park. Y.; Cho, S.; Park Y.* Antibacterial nanocarriers of resveratrol with gold and silver nanoparticles. Mat. Sci. Eng. C Mater. 2016, 58, 1160
Park, C.; Ha, M. W.; Kim, B.; Hong, S.; Kim D.; Park, Y.; Kim, M.-h.; Lee, J. K.; Lee, J.; Park, H.-g.* Enantioselective α-Alkylation of Benzylideneamino tert-Butyl Malonates by Phase-Transfer Catalysis. Adv. Synth. Catal. 2015, 357, 2841
Hwang, S. J.a; Jun, S. H.a; Park, Y.a; Cha, S.-H.; Yoon, M.; Cho, S.; Lee, H.-J.*; Park, Y.* Green synthesis of gold nanoparticles using chlorogenic acid and their enhanced performance for inflammation. Nanomedicine: NBM, 2015, 11, 1677. aThese authors contributed equally to this work
Hong, S.; Shin, Y.; Jung, M.; Ha, M. W.; Park, Y.; Lee, Y.-J.; Shin, J.; Oh, K. B.; Lee, S. K.; Park, H.-g.* Efficient synthesis and biological activity of Psammaplin A and its analogues as antitumor agents. Eur. J. Med. Chem. 2015, 96, 218
Ha, M. W.; Lee, M.; Choi, S.; Kim, S.; Hong, S.; Park, Y.; Kim, M.-h.; Kim, T.-S.; Lee, J.; Lee, J. K.; Park, H.-g.* Construction of Chiral alpha-Amino Quaternary Stereogenic Centers via Phase-Transfer Catalyzed Enantioselective alpha-Alkylation of alpha-Amidomalonates. J. Org. Chem. 2015, 80, 3270
Hwang, S. J.; Kim, Y.-W.; Park, Y.; Lee, H.-J.*; Kim, K.-W.* Anti-inflammatory effects of chlorogenic acid in lipopolysaccharide-stimulated RAW 264.7 cells. Inflamm. Res. 2014, 63, 81
Jun, S. H.; Kim, H.-S.; Koo, Y. K.; Park, Y.; Kim, J.; Cho, S.; Park, Y.* Root Extracts of Polygala Tenuifolia for the Green Synthesis of Gold Nanoparticles. J. Nanosci. Nanotechnol. 2014, 14, 1
Jung, J.; Park, S.; Hong, S; Ha. M. W.; Park. H.-g.; Park, Y.; Lee, H.-J.*; Park, Y.* Synthesis of gold nanoparticles with glycosides: synthetic trends based on the structures of glycones and aglycones. Carbohydr. Res. 2014, 386, 57
Lee, H.; Hwang, S. J.; Jung, J.; Hong, S.; Lee, M.; Park, H.-g.; Lee, H.-J.*; Park, Y.* Asymmetric synthesis and evaluation of α-quaternary chiral lactam derivatives as novel anticancer agent. Arch. Pharm. Res. 2014, 37, 1264
Hong, S.; Kim, M.; Jung, M.; Ha, M. W.; Lee, M.; Park, Y.; Kim, M.-h.; Kim, T.-S.; Lee, J.; Park, H.-g.* Enantioselective Synthesis of α-Halo-α-alkylmalonates via Phase-Transfer Catalytic α-Alkylation. Org. Biomol. Chem. 2014, 12, 1510
Hong, S.; Jung, M.; Park, Y.; Ha, M. W.; Park, C.; Lee, M.; Park, H.-g.* Efficient Enantioselective Total Synthesis of (-)-Horsfiline. Chem. Eur. J. 2013, 19, 9599
Ha, M. W.; Hong, S.; Park, C.; Park, Y.; Lee, J.; Kim, M.-h.; Lee, J.; Park, H.-g.* Enantioselective phase-transfer catalytic α-alkylation of 2-methylbenzyl tert-butyl malonates. Org. Biomol. Chem. 2013, 11, 4030
Ha, M. W.; Lee, H.; Yi, H. Y.; Park, Y.; Kim, S.; Hong, S.; Lee, M.; Kim, M.-h.; Kim, T.-S.; Park, H.-g.* Enantioselective Phase-Transfer Catalytic α-Benzylation and α-Allylation of α-tert-Butoxycarbonyllactones. Adv. Synth. Catal. 2013, 355, 637
Lee, M.; Lee, Y.-J.; Park, E.; Park, Y.; Ha, M. W.; Hong, S.; Lee, Y.-J.; Kim, T.-S.; Kim, M.-h.; Park, H.-g.* Highly enantioselective synthesis of 5-phenyl-2-alkylprolines using phase-transfer catalytic alkylation. Org. Biomol. Chem. 2013, 11, 2039
Park, Y.; Hong, S.; Lee, M.; Jung, H.; Cho, W.-J.; Kim, E.-J.; Son, H.-Y.; Lee, M.-O.; Park, H.-g.* N-Methylthioureas as New Agonists of Retinoic Acid Receptor-Related Orphan Receptor. Arch. Pharm. Res. 2012, 35, 1393
Jee, J.-P.; Nam, S.-H.; Park, Y.; Lee, H.-J.; Park, Y.; Maeng, H.-J.; Kim, C.-K.* Simplified Analysis of Lipoprotein Lipase Activity: Evaluation of Lipasemic Activity of Low Molecular Weight Heparin in Rats. Arch. Pharm. Res. 2012, 35, 1107
Hong, S.; Lee, M.; Jung, M.; Park, Y.; Kim, M.-h.; Park, H.-g.* Efficient Synthetic Method of Psammaplin A. Tetrahedron Lett. 2012, 53, 4209
Park, Y.; Lee, Y. J.; Hong, S.; Lee, M.; Park, H.-g.* Highly Enantioselective Synthesis of (+)-Isonitramine. Org. Lett. 2012, 14, 852
Jee, J.-P.; Jin, S.-E.; Ban, E.; Lee, H.-J.; Park, Y.; Park, Y.; Maeng, H.-J.; Kim, H. T.; Kim, C.-K.* Isolation and Identification of Steroidogenic Peptides from Calf Spleen. Arch. Pharm. Res. 2012, 35, 653
Lee, M.; Zhang, L.; Park, Y.; Park, H.-g.* Chiral 2-aminobenzimidazole bifunctional organocatalysts: effect of di-CF3 and TFA on catalytic mechanisms. Tetrahedron, 2012, 68, 1452
Choi, J.-Y.; Jin, S.-E.; Park, Y.; Lee, H.-J.; Park, Y.; Maeng, H.-J.; Kim, C.-K.* Development of Coated Nifedipine Dry Elixir as a Long Acting Oral Delivery with Bioavailability Enhancement. Arch. Pharm. Res. 2011, 34, 1711
Park, Y.; Lee, Y. J.; Jeong, B.-S.; Park, H.-g.*; Jew, S.-s.* Highly Enantioselective Phase-Transfer Catalytic Alkylation of tert-Butoxycarbonyllactams: Construction of β-Quaternary Chiral Pyrrolidine and Piperidine System. Adv. Synth. Catal. 2011, 353, 3313
Hong, S.; Lee, J.; Kim, M.; Park, Y.; Park, C.; Kim, M.-h.; Jew, S.-s.; Park, H.-g.* Highly Enantioselective Synthesis of α,α-Dialkylmalonates by Phase-Transfer Catalytic Desymmetrization. J. Am. Chem. Soc. 2011, 133, 4924
Lee, Y.-J.; Park, Y.; Kim, M.-h.; Jew, S.-s.; Park, H.-g.* An Enantioselective Synthesis of (+)-Polyoxamic Acid via Phase-Transfer Catalytic Conjugate Addition and Asymmetric Dihydroxylation. J. Org. Chem. 2011, 76, 740
Park, Y.; Jung, H.; Jew, S.-s.*; Park, H.-g.* Cinchona-derived Ammonium Salts-catalyzed aza Diels-Alder Reaction of Danishefsky’s Diene with N-Benzylideneaniline. Tetrahedron, 2011, 67, 1166
Kim, M.-h.; Park, Y.; Jeong, B.-S.; Park, H.-g.*; Jew, S.-s.* Synthesis of (-)-Paroxetine via Enantioselective Phase-Transfer Catalytic Monoalkylation of Malonamide Ester. Org. Lett. 2010, 12, 2826
Park, Y.; Kang, S.; Lee, Y. J.; Kim, T.-S.; Jeong, B.-S.; Park, H.-g.*; Jew, S.-s.* Highly Enantioselective Synthesis of (S)-α-Alkyl-α,β-diaminopropionic Acids via Asymmetric Phase-Transfer Catalytic Alkylation of 2-Phenyl-2-imidazoline-4-carboxylic Acid tert-Butyl Esters. Org. Lett. 2009, 11, 3738