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[129]
Ahn, S.-H.; Lee, J.-K.; Kim, N. D.; Kim, S.-H.; Lee, S.; Jung, S.; Chay, K.-O.; Lee, T.-H.*
“DPIE [2-(1,2-diphenyl-1H-indol-3-yl)ethanamine] Augments Pro-Inflammatory Cytokine Production in IL-1β-Stimulated Primary Human Oral Cells”
Int. J. Mol. Sci. 2018, 19(7), 1835
DOI: 10.3390/ijms19071835
[128]
Yu, S. Shin, T.; Zhang, M.; Xia, Y.; Kim, H.; Lee, S.*
“Nickel/Briphos-Catalyzed Direct Transamidation of Unactivated Secondary Amides Using Trimethylsilyl Chloride”
Org. Lett. 2018, 20(23), 7563-7566.
DOI: 10.1021/acs.orglett.8b03304
[127]
Jayaraman, A.; Cho, E.; Kim, J.; Lee, S.*
“Decarboxylative Tribromination for the Selective Synthesis of Tribromomethyl Ketone and Tribromovinyl Derivatives”
Adv. Synth. Catal. 2018, 360 (20), 3978-3989.
DOI:10.1002/adsc.201800851
[126]
Son, Y.; Lee, S.; Kim, H.-S.; Eom, M. S.; Han, M. S. Lee, S.*
“Organosilane-Patterned Paper-based Colorimetric Sensors for High-Throughput Screening of Cross-Coupling reactions with Aryl Bromides”
Adv. Synth. Catal. 2018, 360 (20), 3916-3923.
Front Cover. Very Important Publication.
DOI: 10.1002/adsc.201800558
[125]
Park, J.; Song, K. H.; Lee, S. *
“Palladium-Catalyzed Decarboxylative Coupling Reactions of Propiolic Acid Derivatives and Arylsulfonyl Hydrazide”
Synthesis 2018, 50(16), 3197-3204.
DOI:10.1055/s-0036-1591596
[124]
Kim, M.; Yu, S.; Kim, J. G.; Lee, S.*
“Palladium-catalyzed carbonylation of thioacetates and aryl iodides for the synthesis of S-aryl thioesters”
Org. Chem. Front. 2018, 5(16), 2447-2452.
[123]
Yu, S.; Nam, K. C.; Lee, S.*
“Synthesis of Methylthiomethyl Esters by the Reaction of Carboxylic Acid with Dimethylsulfoxide”
Bull. Korean. Chem. Soc. 2018, 39 (7), 906-908
DOI:10.1002/bkcs.11498
[122]
Jang, J.; Byun, S.; Kim, B. M.; Lee, S.*
“Arylsilylation of aryl halides using the magnetically recyclable bimetallic Pd–Pt–Fe3O4 catalyst”
Chem. Commun. 2018, 54 (28), 3492-3495.
DOI:10.1039/c7cc09926f
[121]
Ko, B. H.; Yu, S.; Song, K. H.; Lee, S.*
“Continuous flow reaction system for the synthesis of 2,2,2-trichloroacetophenone derivatives and its application”
Tetrahedron Lett. 2018, 59 (11), 991-994.
DOI:10.1016/j.tetlet.2018.01.067
[120]
Cho, E.; Kim, M.; Jayaraman, A.; Kim, J.; Lee, S.*
“Synthesis of α,α-Dichloroketones through Sequential Reaction of Decarboxylative Coupling and Chlorination”
Eur. J. Org. Chem. 2018, 781-784
DOI:10.1002/ejoc.201701640
[119]
Pyo, A.; Yun, M.; Kim, H. S.; Kim, T.-Y.; Lee, J.-j.; Kim, J. Y.; Lee, S.; Kwon, S. Y.; Bom, H.-S.; Kim, H.-S.; Kim, D.-Y.; Min, J.-J.
“64Cu-Labeled Repebody Molecules for Imaging of Epidermal Growth Factor Receptor-Expressing Tumors”
J. Nucl. Med. 2018, 59(2), 340-346.
DOI:10.2967/jnumed.117.197020
[118]
Jayaraman, A.; Cho, E.; Irudayanathan, F. M.; Kim, J.; Lee, S.*
“Metal-Free Decarboxylative Trichlorination of Alkynyl Carboxylic Acids: Synthesis of Trichloromethyl ketones”
Adv. Synth. & Catal. 2018, 360(1), 130-141.
DOI:10.1002/adsc.201701116.
[117]
Jung, D.; Lee, S.* Na, K.*
“RuO2 supported NaY zeolite catalysts: Effect of preparation methods on catalytic performance during aerobic oxidation of benzyl alcohol”
Solid State Sciences 2017, 72, 150-155.
[116]
Raja, G. C. E.; Ryu, J. Y.; Lee, J.; Lee, S.*
“Ruthenium-Catalyzed C-H Activation of Salicylaldehyde and Decarboxylative Coupling of Alkynoic Acids for the Selective Synthesis of Homoisoflavonoids and Flavones”
Org. Lett. 2017, 19(24), 6606-6609.
DOI:10.1021/acs.orglett.7b03325.
[115]
Raja, G. C. E.; Son, Y.; Kim, J.; Lee, S.*; Oh, J.
“One-pot synthesis of cinnamic anhydrides from cinnamic acids and 6-chloro-2,4-dimethoxy-sec-triazine (CDMT) at room temperature”
Synth. Commun. 2017, 47 (24), 2449-2455.
DOI:
[114]
Lee, J.-H.; Raja, G. C. E.; Kim, J.; Nam, K.-C.; Lee, S.*
“Aryl Chlorides as Coupling Partners in the Palladium-catalyzed Decarboxylative Coupling Reactions of Propiolic Acids”
Bull. Korean Chem. Soc. 2017, 38(11), 1368-1371
DOI:
[113]
Yu, S.; Cho, E.; Kim, J.; Lee, S.*
“Palladium-Catalyzed Decarboxylative Coupling of Alkynyl Carboxylic Acids and Alkenyl Tosylates for the Synthesis of Enynones”
J. Org. Chem. 2017, 82(20), 11150-
DOI:
[112]
Park, J.; Kim, J. D.; Raja, G. C. E.; Choi, H. C.; Lee, S.*
“Room temperature cyclization of arylpropiolic acid anhydride: Synthesis of naphtho[2,3-c]furan-1,3-dione derivatives”
Synth. Commun. 2017, 47 (21), 1973-1979.
DOI:
[111]
Lee, J.-H.; Raja, G. C. E.; Yu, S.; Lee, J.; Song, K. H.; Lee, S.*
“Palladium-Catalyzed Decarboxylative Coupling of Alkynyl Carboxylic Acids with Aryl Tosylates”
ACS Omega 2017, 2(9), 6259-6269,
DOI:
[110]
Bunescu, A.; Lee, S.; Li, Q.; Hartwig, J. F.
“Catalytic Hydroxylation of Polyethylenes”
ACS Central Sci. 2017, 3(8), 895-903.
DOI:
[109]
Kim, H.-S.; Kim, J. D.; Choi, H. C.; Lee, S.*
“UV-Irradiation-Mediated Palladium Nanoparticle Catalytic System: Heck and Decarboxylative coupling Reactions”
Mol. Catal. 2017, 441, 21-27
DOI:
[108]
Kim, H. J.; Choi, J.; Choe, J.; Song, K. H.; Lee, S.*
“Alternating magnetic field mediated micro reaction system for palladium-catalyzed coupling reactions”
RSC Adv. 2017, 7 (59), 37181-37184.
DOI:
[107]
Park, J.; Jung, D.; Kim, H.-S.; Na, K.; Lee, S.*
"Zeolite-based copper catalyst for decarboxylative coupling of alkynyl carboxylic acids with aryl iodides."
Catal. Commun. 2017, 99, 83-88.
DOI:
[106]
Ryu, J. Y.; Wi, E. H.; Pait, M.; Lee, S.; Stang, P. J.; Lee, J.
“Unique Ruthenium Bimetallic Supramolecular Cages From C4-Symmetric Tetrapyridyl Metalloligands”
Inorg. Chem. 2017, 56(9), 5471-5477.
DOI:
[105]
Kim, H.-S.; Eom, M. S.; Han, M. S.; Lee, S.*
“Paper-Based Colorimetric Sensor System for High-Throughput Screening of C-H Borylation”
Chem. Eur. J. 2017, 23(26), 6282-6285.
DOI:
[104]
Irudayanathan, F. M.; Lee, S.
“Selective Synthesis of (E)- and (Z)-Allyl Nitriles via Decarboxylative Reactions of Alkynyl Carboxylic Acids with Azobis(alkylcarbonitriles)”
Org. Lett. 2017, 19 (9), 2318-2321.
DOI:
[103]
Son, Y.; Kim, H.-S.; Lee, J.; Jang, J.; Lee, C.-F. Lee, S.*
“Nickel-catalyzed decarboxylative coupling of an alkynyl carboxylic acid with aryl iodides”
Tetrahedron Lett. 2017, 58(14),1413-1416.
DOI:
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