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198. ¡°Macaranga denticulata extract ameliorates renal fibrosis via anti-inflammatory and antioxidant effects in streptozotocin-induced diabetic rats¡± Sreevarsha, G.; Kundu, A.; Lee, J.-S.; Kim, J. R.; Ahn, M.-Y.; Puia, Z.; Kumar, V.; Kim, I. S.; Kwak, J. H.; Palit, P.*; Kim, H. S.* Int. J. Mol. Sci. 2024, submitted for publication.
197. ¡°Development of novel indole-quinoline hybridic molecules targeting bacterial proton motive force¡± Seo, J.; Kim, J.; Ko, N.; Moon, K.; Kim, I. S.*; Lee, W.* J. Appl. Microbiol. 2024, submitted for publication.
196. ¡°Manufacturing Process Development of Tegoprazan as a Potassium-Competitive Acid Blocker (P-CAB)¡± Kweon, J.-H.; Shin, H.; Lee, M. K.; Lee, S. A.; Singh, P.; Moon, K.; Kim, I. S.* Org. Process. Res. Dev. 2024, 28, in press.
195. ¡°Tandem Annulation and Dipolar Cycloaddition of Azomethine Imines in Catalytic C(sp2)-H Functionalization¡± Mishra, N. K.; Rakshit, A.; Moon, K.; Singh, P.; Kim, I. S.* Bull. Korean Chem. Soc. 2024, 45, 131-144 (invited for contribution on 24th Jang Sae-Hi award from Korean Chemical Society).
194. ¡°Sulfur-Directed ¥á-C(sp3)-H Amidation of Pyrrolidines with Dioxazolones Under Rhodium Catalysis¡± Singh, P.; Min, J.; Min, S. Moon, K.; Kim, H. S.; Kim, I. S.* Org. Lett. 2024, 26, 57-61.
193. ¡°Catalyst-Controlled C-H Allylation and Annulation of 2-Aryl Quinazolinones with 2-Methylidene Cyclic Carbonate ¡± Ko, N.; Min, S.; Moon, K.; Shin, H.; Kwon, N. Y.; Mishra, N. K.; Rakshit, A.; Singh, P.; Kim, I. S.* J. Org. Chem. 2023, 88, 13315-13326.
192. ¡°Design and Synthesis of 4th Generation EGFR Inhibitors Against Human Triple (Del19/T790M/C797S) Mutation¡± Jeon, J.; Jang, S. Y.; Kwak, E. J.; Lee, S. H.; Byun, J.-Y.; Kim, Y.-Y.; Ahn, Y. G.; Singh, P.; Moon, K.; Kim, I. S.* Eur. J. Med. Chem. 2023, 261, 115840.
191. ¡°Synthesis of 2-Formyl Carbazoles via Tandem Reaction of Indolyl Nitrones with 2-Methylidene Cyclic Carbonate¡± Min, S.; Kim, T.; Jeong, T.; Yang, J.; Oh, Y.; Moon, K.; Rakshit, A.; Kim, I. S.* Org. Lett. 2023, 25, 4298-4302.
190. ¡°Rh(III)-Catalyzed C8-Spiroannulation of 1-Aminonaphthalenes with Maleimides¡± Chung, E.; Kim, S.; Rakshit, A.; Singh, P.; Park, J.; Jeong, T.; Kim, I. S.* J. Org. Chem. 2023, 88, 11227-11239.
189. ¡°SPC-180002, a SIRT1/3 dual inhibitor, impairs mitochondrial function and redox homeostasis and represents an antitumor activity¡± Cho, Y.; Hwang, J. W.; Park, N.-J.; Moon, J.; Ali, K. H.; Seo, Y. H.; Kim, I. S.*; Kim, S.-N.*; Kim, Y. K.* Free Radic. Biol. Med. 2023, 208, 73-87.
188. ¡°Anticancer effects of the HDAC inhibitor, 3¥â,6¥â-dihydroxyurs-12-en-27-oic acid, in MCF-7 breast cancer cells via the inhibition of Akt/mTOR pathways¡± Lim, J. S.; Kyung, S. Y.; Jeon, Y.; Kim, I. S.; Kwak, J. H.; Kim, H. S.* Oncol. Rep. 2023, 49, 43.
187. ¡°Synthesis and Evaluation of ent-Conduramine C-1 Derivatives as ¥á-Glucosidase Inhibitors via CSI-Mediated Amination Reaction¡± Park, K.; Boggu, P. R.; Park, J. H.; Kang, J. E.; An, S. H.; Kim, H. S.; Kim, I. S.; Jung, Y. H.* Carbohydr. Res. 2023, 524, 108746.
186. ¡°Organic Redox Cascade Cyclization of 2-Alkynylquinones by Ascorbic Acid in Combination with Copper Catalyst and Its Application to Formal Synthesis of Liphagal¡± Jeong, T.; Okanishi, Y.; Yotsui, S.; Kim, I. S.*; Yoshimitsu, T.* New J. Chem. 2023, 47, 3425-3429.
185. ¡°Novel Specific Pyruvate Kinase M2 Inhibitor, Compound 3h, Induces Apoptosis and Autophagy through Suppressing Akt/mTOR Signaling Pathway in LNCaP Cells¡± Jiang, C.; Zhao, Z.; Jeong, T.; Kang, J. Y.; Park, J. H.; Kim, I. S.; Kim, H. S.* Cancers 2023, 15, 265.
184. ¡°Rhodium(III)-Catalyzed Conjugate Addition of ¥â-CF3-Enones with Quinoline N-Oxides¡± Ko, N.; Min, J.; Moon, J.; Ismail, N. F.; Moon, K.; Singh, P.; Mishra, N. K.; Lee, W.; Kim, I. S.* J. Org. Chem. 2023, 88, 602-612.
183. ¡°Cobalt(II)-Catalyzed C-H Alkylation of N-Heterocycles with 1,4-Dihydropyridines¡± Ghosh, P.; Kwon, N. Y.; Byun, Y.; Mishra, N. K.; Park, J. S.; Kim, I. S.* ACS Catal. 2022, 12, 15707-15714.
182. ¡°Methylene Thiazolidinediones as Alkylation Reagents in Catalytic C-H Functionalization: Rapid Access to Glitazones¡± Byun, Y.; Moon, K.; Park, J.; Ghosh, P.; Mishra, N. K.; Kim, I. S.* Org. Lett. 2022, 24, 8578-8583 (selected as a Cover Page of OL).
181. ¡°Tenovin-1 Ameliorates Renal Fibrosis in High-Fat-Diet-Induced Diabetic Nephropathy via Antioxidant and Anti-Inflammatory Pathways¡± Kundu, A.; Gali, S.; Sharma, S.; Park, J. H.; Kyeong, S. Y.; Kacew, S.; Kim, I. S.; Lee, K. Y.; Kim, H. S.* Antioxidants 2022, 11, 1812.
180. ¡°Ruthenium(II)-Catalyzed Tandem C-H Allylation and [3+2] Dipolar Cycloaddition to Construct Bridged Tetracycles¡± Moon, J.; Ko, N.; Jang, S.; Ghosh, P.; Kim, H. S.; Mishra, N. K.; Kim, I. S.* Org. Lett. 2022, 24, 8115-8119 (highlighted by Synfact 2023, 19, 0122).
179. ¡°C-H Amidation of 2-Aryl Azlactones Under Iridium(III) Catalysis: Access to Chiral Amino Acids¡± Park, M. S.; Chung, E.; Mishra, N. K.; Han, S. H.; Han, S.; Kim, S.; Kim, I. S.* Chem. Commun. 2022, 58, 13365-13368.
178. ¡°Molineria recurvata Ameliorates Streptozotocin-Induced Diabetic Nephropathy through Antioxidant and Anti-Inflammatory Pathways¡± Dey, P.; Kundu, A.; Lee, H. E.; Kar, B.; Vishal, V.; Dash, S.; Kim, I. S.; Bhakta, T.; Kim, H. S.* Molecules 2022, 27, 4985.
177. ¡°KOtBu-Promoted C3-Homocoupling of Quinoxalinones Through Single Electron Transfer from a sp2 Carbanion Intermediate¡± Kwon, N.; Mishra, N. K.; Park, J. S.; Woo, S. K.; Ghosh, P.; Kim, I. S.* Chem. Commun. 2022, 58, 7078-7081.
176. ¡°Total Synthesis of Eliglustat via Regioselective and Diastereoselective Amination of Chiral para-Methoxycinnamyl Benzyl Ether¡± Kong, Y.; Boggu, P. R.; Park, K. M.; Kim, Y. S.; An, S. H.; Kim, I. S.; Jung, Y. H.* Molecules 2022, 27, 2063.
175. ¡°Assembly of Hydroxycinnoline Core via Hydrazide-Assisted Rh(III)-Catalyzed C-H Functionalization and Annulation¡± Kim, S.; Park, H. K.; Kang, J. Y.; Mishra, N. K.; Kim, I. S.* Synthesis 2022, 54, 4461-4471 (invited as a special issue of SYNTHESIS, and highlighted by Synfact 2022, 18, 1315).
174. ¡°Total Synthesis of a-1-C-propyl-3,6-di-epi-nojirimycin and Polyhydroxyindolizidine Alkaloids via Regio- and Diastereoselective Amination of Anomeric Acetals¡± Kim, Y. S.; Boggu, P. R.; Kong, Y.; Park, K. M.; Kim, I. S.; Jung, Y. H.* Tetrahedron. 2022, 116, 132809.
173. ¡°Synthesis of Succinimide-Linked Indazol-3-ols Derived from Maleimides Under Rh(III) Catalysis¡± Kang, J. Y.; Kim, S.; Moon, J.; Chung, E.; Kim, J.; Kyung, S. Y.; Kim, H. S.; Mishra, N. K.; Park, J. S.; Kim, I. S.* ACS Omega 2022, 7, 14712-14722 (selected as a Cover Page of ACS Omega).
172. ¡°Reactivity of Triplet Diradical Intermediates in Aqueous Media for Transition-Metal-Free Csp2-H Alkylation¡± Ghosh, P.; Byun, Y.; Kwon, N. Y.; Kang, J. Y.; Mishra, N. K.; Park, J. S.; Kim, I. S.* Cell Rep. Phys. Sci. 2022, 3, 100819.
171. ¡°Novel Anti-Adipogenic Effect of CF3-Allylated Indole in 3T3-L1 Cells¡± Kim, H. J.; Im, D. U.; Chau, G. C.; Mishra, N. K.; Kim, I. S.*; Um, S. H.* Chem. Biol. Interact. 2022, 352, 109782.
170. ¡°Site-Selective and Metal-Free C-H Nitration of Biologically Relevant N-Heterocycles¡± Moon, J.; Ji, H. K.; Ko, N.; Oh, H.; Park, M. S.; Kim, S.; Ghosh, P.; Mishra, N. K.; Kim, I. S.* Arch. Pharm. Res. 2021, 44, 1012-1023.
169. ¡°Synthesis of Cinnolines via Rh(III)-Catalyzed Annulation of N-Aryl Heterocycles with Vinylene Carbonate¡± Kim, S.; Choi, S. B.; Kang, J. Y.; An, W.; Lee, S. H.; Oh, H.; Ghosh, P.; Mishra, N. K.; Kim, I. S.* Asian J. Org. Chem. 2021, 11, 3005-3014.
168. ¡°Synthesis of Spirosuccinimides via Annulative Cyclization Between N-Aryl Indazolols and Maleimides under Rhodium(III) Catalysis¡± Kang, J. Y.; An, W.; Kim, S.; Kwon, N. Y.; Jeong, T.; Ghosh, P.; Kim, H. S.; Mishra, N. K.; Kim, I. S.* Chem. Commun. 2021, 57, 10947-10950.
167. ¡°Synthesis of ¥ð-Extended Heterocycles via Rh(III)-Catalyzed Oxidative Annulation of 5-Aryl Pyrazinones with Alkynes¡± Oh, H.; Byun, H. W.; Moon, K.; Kim, S.; Ghosh, P.; An, W.; Kwak, J. H.; Park, J. S.; Mishra, N. K.; Kim, I. S.* J. Org. Chem. 2021, 86, 16349-16360 (selected as a Cover Page of JOC).
166. ¡°Transition-Metal-Free Alkylation and Acylation of Benzoxazinones with 1,4-Dihydropyridines¡± Byun, Y.; Moon, J.; An, W.; Mishra, N. K.; Kim, H. S.; Ghosh, P.; Kim, I. S.* J. Org. Chem. 2021, 86, 12247-12256.
165. ¡°Synthesis of (2H)-Indazoles and Dihydrocinnolinones through Annulation of Azobenzenes with Vinylene Carbonate under Rh(III) Catalysis¡± Park, M. S.; Moon, K.; Oh, H.; Lee, J. Y.; Ghosh, P.; Kang, J. Y.; Park, J. S.; Mishra, N. K.; Kim, I. S.* Org. Lett. 2021, 23, 5518-5522.
164. ¡°Catalyst-Free One-Pot Multi-Component Synthesis of 2-Substituted Quinazolin-4-carboxamides from 2-Aminophenyl-2-oxoacetamides, Aldehydes, and Ammonium Acetate¡± Shim, S.-H.; Park, H.; Mishra, N. K.; Kim, I. S.; Lee, J. K.; Lee, K.; Jalani, H. B.; Choi, Y.* ChemistrySelect 2021, 6, 5446-5450.
163. ¡°A Novel Synthetic Microtubule Inhibitor Exerts Antiproliferative Effects in Multidug Resistant Cancer Cells and Cancer Stem Cells¡± Park, M.; Hwang, J. W.; Cho, Y.; Kim, S.; Han, S. H.; Yu, J.; Ha, S.; Kim, W.-Y.; Kim, S.-N.; Kim, I. S.*; Kim, Y. K.* Sci. Rep. 2021, 11, 10822.
162. ¡°Site-Selective C8-Alkylation of Quinoline-N-Oxides with Maleimides Under Rh(III) Catalysis¡± An, W.; Lee, S. H.; Kim, D.; Oh, H.; Kim, S.; Byun, Y.; Kim, H. J.; Mishra, N. K.; Kim, I. S.* J. Org. Chem. 2021, 86, 7579-7587 (selected as a Cover Page of JOC).
161. ¡°Ruthenium(II)-Catalyzed C-H/N-H Carbonylative Cyclization of 2-Aryl Quinazolinones with Isocyanates as CO Surrogates¡± Choi, J. H.; Kim, H. D.; Kang, J. Y.; Jeong, T.; Ghosh, P.; Kim, I. S.* Bull. Korean Chem. Soc. 2021, 42, 542-547 (invited as a special issue "Chemical Synthesis and Reaction Development" of BKCS).
160. ¡°Identification of BR102910 as a Selective Fibroblast Activation Protein (FAP) Inhibitor¡± Jung, H. J.; Nam, E. H.; Park, J. Y.; Ghosh, P.; Kim, I. S.* Bioorg. Med. Chem. Let. 2021, 37, 127846.
159. ¡°Direct Integration of Phthalazinone and Succinimide Scaffolds via Rh(III)-Catalyzed C-H Functionalization¡± Cho, Y. S.; Kim, H. D.; Kim, E.; Han, S. H.; Han, S. B.; Kim, H. S.; Jeong, T.; Kim, I. S.* Asian J. Org. Chem. 2021, 10, 202-209 (selected as a Cover Page of AJOC).
158. ¡°C-H Methylation of Iminoamido Heterocycles with Sulfur Ylides¡± Ghosh, P.; Kwon, N. Y.; Kim, S.; Han, S.; Lee, S. H.; An, W.; Mishra, N. K.; Han, S. B.; Kim, I. S.* Angew. Chem. Int. Ed. 2021, 60, 191-196.
157. ¡°C2-Selective C-H Methylation of Heterocyclic N-oxides with Sulfonium Ylides¡± An, W.; Choi, S. B.; Kim, N.; Kwon, N. Y.; Ghosh, P.; Han, S. H.; Mishra, N. K.; Han, S.; Hong, S.; Kim, I. S.* Org. Lett. 2020, 22, 9004-9009.
156. ¡°Site-Selective C-H Amidation of 2-Aryl Quinazolinones Using Nitrene Surrogates¡± Kim, S.; Jeoung, D.; Kim, K.; Lee, S. B.; Lee, S. H.; Park, M. S.; Ghosh, P.; Mishra, N. K.; Hong, S.; Kim, I. S.* Eur. J. Org. Chem. 2020, 7134-7143 (selected as a Cover Page of EJOC).
155. ¡°Ratiometric Turn-On Fluorophore Displacement Ensembles for Ni-troaromatic Explosives Detection¡± Lee, J. Y.; Root, H. D.; Ali, R.; An, W.; Lynch, V. M.; Bahring, S.; Kim, I. S.*; Sessler, J. L.*; Park, J. S.* J. Am. Chem. Soc. 2020, 142, 19579-19587 (selected as a Cover Page of JACS).
154. ¡°Ru(II)-Catalyzed C-H Addition and Oxidative Cyclization of 2-Aryl Quinazolinones with Activated Aldehydes¡± Choi, J.; Kim, K.; Oh, H.; Han, S.; Mishra, N. K.; Kim, I. S.* Org. Biomol. Chem. 2020, 18, 9611-9622 (selected as a Cover Page of OBC).
153. ¡°Biological Evaluation of Oxindole Derivative as a Novel Anticancer Agent against Human Kidney Carcinoma Cells¡± Dey, P.; Kundu, A.; Son, J. Y.; Kim, K.-S.; Park, J. H.; Yoon, S.; Kim, I. S.*; Kim, H. S.* Biomolecules 2020, 10, 1260-1282.
152. ¡°Total Synthesis of (¡¾)-Liphagal via Organic-Redox-Driven Palladium-Catalyzed Hydroxybenzofuran Formation¡± Tao, E.; Inoue, M.; Jeong, T.; Kim, I. S.; Yoshimitsu, T.* J. Org. Chem. 2020, 85, 9064-9070.
151. ¡°Transition-Metal-Free and Site-Selective Selenylation of Heterocyclic N-Oxides in Anisole as a Green Solvent¡± Lee, S. H.; Kwon, N. Y.; Lee, J. Y.; An, W.; Jung, Y. H.; Mishra, N. K.; Ghosh, P.; Park, J. S.; Kim, I. S.* Eur. J. Org. Chem. 2020, 4886-4892 (selected as a Cover Page of EJOC).
150. ¡°Synthesis and Biological Evaluation of Quinoxaline Derivatives as Specific c-Met Kinase Inhibitors¡± Kim, S. C.; Boggu, P. R.: Yu, H. N.; Ki, S. Y.; Jung, J. M.; Kim, Y. S.; Park, K. M.; Ma, S. H.; Kim, I. S.; Jung, Y. H.* Bioorg. Med. Chem. Lett. 2020, 30, 127189.
149. ¡°EX-527 Prevents the Progression of High-fat Diet-induced Hepatic Steatosis and Fibrosis by Upregulating SIRT4 in Zucker Rats¡± Kundu, A.; Dey, P.; Park, J. H.; Kim, I. S.; Kwack, S, J.; Kim, H. S.* Cells 2020, 9, 1101.
148. ¡°Phthalazinone-Assisted C-H Amidation Using Dioxazolones Under Rh(III) Catalysis¡± Jeoung, D.; Kim, K.; Han, S. H.; Ghosh, P.; Lee, S. H.; Kim, S.; An, W.; Kim, H. S.; Mishra, N. K.; Kim, I. S.* J. Org. Chem. 2020, 85, 7014-7023 (selected as a Cover Page of JOC).
147. ¡°Deoxygenative Amination of Azine-N-oxides with Acyl Azides via [3+2] Cycloaddition¡± Kim, D.; Ghosh, P.; Kwon, N. Y.; Han, S. H.; Han, S.; Mishra, N. K.; Kim, S.; Kim, I. S.* J. Org. Chem. 2020, 85, 2476-2485.
146. ¡°Ru(II)-Catalyzed C-H Hydroxyalkylation and Mitsunobu Cyclization of N-Aryl Phthalazinones¡± Kim, K.; Han, S. H.; Jeoung, D.; Ghosh, P.; Kim, S.; Kim, S. J.; Ku, J.-M.; Mishra, N. K.; Kim, I. S.* J. Org. Chem. 2020, 85, 2520-2531.
145. ¡°Total Synthesis of Chromanol 293B and Cromakalim via Stereoselective Amination of Chiral Benzylic Ethers¡± Ma, S.-H.; Kim, Y. S.; Jung, J. M.; Boggu, P. R.; Kim, I. S.; Jung, Y. H.* Tetrahedron Lett. 2020, 61, 151431-151433.
144. ¡°Protective Effects of Dendropanax morbifera against Cisplatin-Induced Nephrotoxicity without Altering Chemotherapeutic Efficacy¡± Kim, J. S.; Kim, K. S.; Son, J. Y.; Kim, H. R.; Park, J. H.; Lee, S. H.; Lee, D. E.; Kim, I. S.; Lee, K. Y.; Lee, B. M.; Kwak, J. H.; Kim, H. S.* Antioxidants 2019, 8, 256-271.
143. ¡°Site-Selective C-H Alkylation of Diazine-N-Oxides Enabled by Phosphonium Ylides¡± Ghosh, P.; Kwon, N. Y.; Han, S.; Kim, S.; Han, S. H.; Mishra, N. K.; Jung, Y. H.; Chung, S. J.; Kim, I. S.* Org. Lett. 2019, 21, 6488-6493.
142. ¡°Estrogen Deficiency Potentiates Thioacetamide-Induced Hepatic Fibrosis in Sprague-Dawley Rats¡± Lee, Y. H.; Son, J. Y.; Kim, K. S.; Park, Y. J.; Kim, H. R.; Park, J. H.; Kim, K.-B.; Lee, K. Y.; Kang. K. W.; Kim, I. S.; Kacew, S.; Lee, B. M.; Kim, H. S.* Int. J. Mol. Sci. 2019, 20, 3709-3714.
141. ¡°Histamine Receptor Antagonists, Loratadine and Azelastine, Highly Sensitize P-gp-Overexpressing Antimitotic Drug-resistant KBV20C Cells Through Different Molecular Mechanisms¡± Kim, J. Y.; Kim, K. S.; Kim, I. S.; Yoon, S.* Anticancer Res. 2019, 39, 3767-3775.
140. ¡°Lewis Acid-Mediated Cross-Coupling Reaction of 7-Azaindoles and Aldehydes: Cytotoxic Evaluation of C3-Linked Bis-7-azaindoles¡± Lee, S.; Kim, K.; Jeon, Y.; Kundu, A.; Dey, P.; Kim, H. S.; Kim, I. S.* Tetrahedron Lett. 2019, 60, 150974-150978.
139. ¡°PKM2 Knockdown Induces Autophagic Cell Death Via AKT/mTOR Pathway in Human Prostate Cancer Cells¡± Dey, P.; Kundu, A.; Sachan, R.; Park, J. H.; Ahn, M. Y.; Yoon, K.; Lee, J.; Kim, N. D.; Kim, I. S.; Lee, B. M.; Kim, H. S.* Cell. Physiol. Biochem. 2019, 52, 1535-1552.
138. ¡°Allylic Acetals as Acrolein Oxonium Precursors in Tandem C-H Allylation and [3+2] Dipolar Cycloaddition¡± Lee, H.; Kang, D.; Han, S. H.; Chun, R.; Pandey, A. K.; Mishra, N. K.; Hong, S.; Kim, I. S.* Angew. Chem., Int. Ed. 2019, 58, 9470-9474.
137. ¡°Synthesis of (2H)-Indazoles from Azobenzenes Using Paraformaldehyde as One Carbon Synthon¡± Chun, R.; Kim, S.; Han, S. H.; Han, S.; Lee, S. H.; Mishra, N. K.; Jung, Y. H.; Kim, H. S.; Kim, I. S.* Adv. Synth. Catal. 2019, 361, 1617-1626.
136. ¡°Dendropanax morbifera Ameliorates Thioacetamide-Induced Hepatic Fibrosis via TGF-¥â1/Smads Pathways¡± Yang, H. Y.; Kim. K. S.; Lee, Y. H.; Park, J. H.; Kim, J.-H.; Lee, S.-Y.; Kim, Y.-M.; Kim, I. S.; Kacew, S.; Lee, B. M.; Kwak, J. H.; Yoon, K.; Kim, H. S.* Int. J. Biol. Sci. 2019, 15, 800-811.
135. ¡°Ruthenium(II)-Catalyzed Site-Selective Hydroxymethylation of Indolines with Paraformaldehyde¡± Lee S. H.; Jeong, T.; Kim, K.; Kwon, N. Y.; Pandey, A. K.; Kim, H. S.; Ku, J.-M.; Mishra, N, K.; Kim, I. S.* J. Org. Chem. 2019, 84, 2307-2315 (selected as a Cover Page of JOC).
134. ¡°Plumbagin from a Tropical Pitcher Plant (Nepenthes alata Blanco) Induces Apoptotic Cell Death via a p53-Dependent Pathway in MCF-7 Human Breast Cancer Cells¡± De, U.; Son, J. Y.; Jeon, Y.; Ha, S. Y.; Park, Y. J.; Yoon, S.; Ha, K.-T.; Choi, W. S.; Lee, B. M.; Kim, I. S.; Kwak, J. H.; Kim, H. S.* Food Chem. Toxicol. 2018, 123, 492-500.
133. ¡°Afrocyclamine A, a Triterpenoid Saponin, Induces Apoptosis and Autophagic Cell Death via the PI3k/Akt/mTOR Pathway in Human Prostate Cancer Cells¡± Sachan, R.; Kundu, A.; Jeon, Y.; Choi, W. S.; Yoon, K.; Kim, I. S.; Kwak, J. H.; Kim, H. S.* Phytomedicine 2018, 51, 139-150.
132. ¡°Recent Advances in N-Heterocycles Synthesis through Catalytic C-H Functionalization of Azobenzenes¡± Mishra, N. K.; Park, J.; Oh, H.; Han, S. H.; Kim, I. S.* Tetrahedron 2018, 74, 6769-6794.
131. ¡°One-pot Synthesis of 2-Naphthols Using Nitrones and MBH Adducts via Decarboxylative N-O Bond Cleavage¡± Han, S. H.; Pandey, A. K.; Lee, H.; Kim, S.; Kang, D.; Jung, Y. H.; Kim, H. S.; Hong, S.; Kim, I. S.* Org. Chem. Front. 2018, 5, 3210-3218 (selected as Cover Page of OCF).
130. ¡°A New Synthetic Histone Deacetylase Inhibitor, MHY2256, Induces Apoptosis and Autophagy Cell Death in Endometrial Cancer Cells via p53 Acetylation¡± De, U.; Son, J. Y.; Sachan, R.; Park, Y. J.; Kang, D.; Yoon, K.; Lee, B. M.; Kim, I. S.; Moon, H. R.; Kim, H. S.* Int. J. Mol. Sci. 2018, 19, 2743-2744.
129. ¡°Site-Selective C-H Nitration of N-Aryl-7-Azaindoles Under Palladium(II) Catalysis¡± Chun, R.; Kim, S.; Han, S. H.; Pandey, A. K.; Mishra, N. K.; Kim, I. S.* Tetrahedron Lett. 2018, 59, 3848-3852.
128. ¡°Direct Synthesis of 2-Acyl Acridines Using Aldimines and Anthranils: Evaluation of Cytotoxicity and Anti-inflammatory Activity¡± Kim, S.; Kundu, A.; Chun, R.; Han, S. H.; Pandey, A. K.; Yoo, S.; Park, J.; Kim, H.; Ku, J.-M.; Kim, I. S.* Asian J. Org. Chem. 2018, 7, 2069-2075 (selected as Cover Page of AJOC).
127. ¡°Reductive C2-Alkylation of Pyridine- and Quinoline-N-Oxides Using Wittig Reagents¡± Han, S.; Chakrasali, P; Park, J.; Oh, H.; Kim, S.; Kim, K.; Pandey, A. K.; Han, S. H.; Han, S. B.; Kim, I. S.* Angew. Chem., Int. Ed. 2018, 57, 12737-12740.
126. ¡°Reactivity of Morita-Baylis-Hillamn Adducts in C-H Functionalization of (Hetero)aryl Nitrones: Access to Bridged Cycles and Carbazoles¡± Pandey, A. K.; Kang, D.; Han, S. H.; Lee, H.; Mishra, N. K.; Kim, H. S.; Jung, Y. H.; Hong, S.; Kim, I. S.* Org. Lett. 2018, 20, 4632-4636.
125. ¡°Dual Role of Anthranils as Amination and Transient Directing Group Sources: Synthesis of 2-Acyl Acridines¡± Kim, S.; Han, S. H.; Mishra, N. K.; Chun, R.; Jung, Y. H.; Kim H. S.; Park, J. S.; Kim, I. S.* Org. Lett. 2018, 20, 4010-4014.
124. ¡°Disparate Downstream Reactions Mediated by an Ionically Controlled Supramolecular Tristate Switch¡± Park, J. S.; Park, J.; Yang, Y. J.; Tran, T. T.; Kim, I. S.*; Sessler, J. L.* J. Am. Chem. Soc. 2018, 140, 7598-7604 (selected as Cover Page of JACS).
123. ¡°Ru(II)-Catalyzed C-H Aminocarbonylation of N-(Hetero)aryl-7-azaindoles with Isocyanates¡± Jeong, T.; Lee, S. H.; Chun, R.; Han, S.; Han, S. H.; Jeon, Y. U.; Park, J.; Yoshimitsu, T.; Mishra, N. K.; Kim, I. S.* J. Org. Chem. 2018, 83, 4641-4649.
122. ¡°Synthesis of (2H)-Indazoles through Rh(III)-Catalyzed Annulation Reaction of Azobenzenes with Sulfoxonium Ylides¡± Oh, H.; Han, S.; Pandey, A. K.; Han, S. H.; Mishra, N. K.; Kim, S.; Chun, R.; Kim, H. S.; Park, J.; Kim, I. S.* J. Org. Chem. 2018, 83, 4070-4077.
121. ¡°Synthesis of TMPA derivatives through sequential Ir(III)-catalyzed C-H alkylation and their antidiabetic evaluation¡± Lee, S. H.; Kundu, A.; Han, S. H.; Mishra, N. K.; Kim, K. S.; Choi, M. H.; Pandey, A. K.; Park, J. S.; Kim, H. S.; Kim, I. S.* ACS Omega 2018, 3, 2661-2672.
120. ¡°Synthesis of 2-Benzazepines from Benzylamines and MBH Adducts Under Rhodium(III) Catalysis via C(sp2)-H Functionalization¡± Pandey, A. K.; Han, S. H.; Mishra, N. K.; Kang, D.; Lee, S. H.; Chun, R.; Hong, S.; Park, J. S.; Kim, I. S.* ACS Catal. 2018, 8, 742-746.
119. ¡°Total Synthesis and Anti-inflammatory Evaluation of Penchinone A and Its Structural Analogues¡± Oh, Y.; Jang, Y. J.; Jeon, M.; Kim, H. S.; Kwak, J. H.; Chung, K. H.; Pyo, S.; Jung, Y. H.; Kim, I. S.* J. Org. Chem. 2017, 82, 11566-11572.
118. ¡°Synthesis of Indenes that are Derived from Aldimines and Enones Under Rhodium(III) Catalysis¡± Han, S. H.; Kim, S.; Mishra, N. K.; Oh, H.; Choi, M. H.; Choi, D. S.; Lim, H. J.; Shin, D. Y.; Kim, I. S.* Asian J. Org. Chem. 2017, 6, 1823-1829.
117. ¡°Rhodium(III)-Catalyzed Diastereoselective Synthesis of 1-Aminoindanes via C-H Activation¡± Han, S. H.; Mishra, N. K.; Jeon, M.; Kim, S.; Kim, H. S.; Jung, S.-Y.; Jung, Y. H.; Ku, J.-M.; Kim, I. S.* Adv. Synth. Catal. 2017, 359, 3900-3904.
116. ¡°C(sp3)-H Amination of 8-Methylquinolines with Azodicarboxylates under Rh(III) Catalysis: Cytotoxic Evaluation of Quinolin-8-ylmethanamines¡± Jeong, T.; Mishra, N. K.; Dey, P.; Oh, H.; Han, S.; Lee, S. H.; Kim, H. S.; Park, J.; Kim, I. S.* Chem. Commun. 2017, 53, 11197-11200.
115. ¡°Synthesis and Anticancer Evaluation of 2,3-Disubstituted Indoles Derived from Azobenzenes and Internal Olefins¡± Oh, Y.; Han, S. H.; Mishra, N. K.; De, U.; Lee, J.; Kim, H. S.; Jung, Y. H.; Kim, I. S.* Eur. J. Org. Chem. 2017, 6265-6273 (selected as VIP paper and Cover Page of EJOC, and highlighted by Synfact 2018, 14, 0014).
114. ¡°Site-Selective Rh(III)-Catalyzed C-H Amination of 7-Azaindoles with Anthranils: Synthesis and Anticancer Evaluation¡± Jeon, M.; Park, J.; Dey, P.; Oh, Y.; Oh, H.; Han, S.; Um, S. H.; Kim, H. S.; Mishra, N. K.; Kim, I. S.* Adv. Synth. Catal. 2017, 359, 3471-3478 (selected as Cover Page of ASC).
113. ¡°Rh(III)-Catalyzed C-H Alkylation of Indolines with Enones through Conjugate Addition and Protonation Pathway¡± Oh, H.; Park, J.; Han, S. H.; Mishra, N. K.; Lee, S.; Oh, Y.; Jeon, M.; Seong, G.-J.; Chung, K. Y.; Kim, I. S.* Tetrahedron 2017, 73, 4739-4749 (highlighted by Synfact 2017, 13, 1015).
112. ¡°Synthesis and Anti-inflammatory Evaluation of 2-Aminobenzaldehydes via Ir(III)-Catalyzed C-H Amidation of Aldimines with Acyl Azides¡± Kim, S.; Chakrasali, P.; Suh, H. S.; Mishra, N. K.; Kim, T.; Han, S. H.; Kim, H. S.; Lee, B. M.; Han, S. B.; Kim, I. S.* J. Org. Chem. 2017, 82, 7555-7563.
111. ¡°One-pot Synthesis of Oxindoles through C-H Alkylation and Intramolecular Cyclization of Azobenzenes with Internal Olefins¡± Han, S. H.; Mishra, N. K.; Jo, H.; Oh, Y.; Jeon, M.; Kim, S.; Kim, W. J.; Lee, J. S.; Kim, H. S.; Kim, I. S.* Adv. Synth. Catal. 2017, 359, 2396-2401.
110. ¡°Synthesis and Cytotoxic Evaluation of N-Aroylureas through Rh(III)-Catalyzed C-H Functionalization of Indolines with Isocyanates¡± Jeong, T.; Lee, S. H.; Mishra, N. K.; De, U.; Park, J.; Dey, P.; Kwak, J. H.; Jung, Y. H.; Kim, H. S.; Kim, I. S.* Adv. Synth. Catal. 2017, 359, 2329-2336.
109. ¡°Total Synthesis of (-)-Codonopsinine via Regioselective and Diastereoselective Amination using Chlorosulfonyl Isocyanate¡± Choi, Y.; Kim, Y. C.; Park, S. J.; Jung, J. M.; Kim, Y. S.; Kim, I. S.; Jung, Y. H.* Tetrahedron 2017, 73, 4458-4463.
108. ¡°Synthesis and Anti-inflammatory Evaluation of N-Sulfonyl Anthranilic Acids via Ir(III)-Catalyzed C-H Amidation of Benzoic Acids¡± Han, S. H.; Suh, H. S.; Jo, H.; Oh, Y.; Mishra, N. K.; Han, S.; Kim, H. S.; Jung, Y. H.; Lee, B. M.; Kim, I. S.* Bioorg. Med. Chem. Lett. 2017, 27, 2129-2134.
107. ¡°Recent Advances in Catalytic C(sp2)-H Allylation Reactions¡± Mishra, N. K.; Sharma, S.; Park, J.; Han, S.; Kim, I. S.* ACS Catal. 2017, 7, 2821-2847.
106. ¡°Cp*Rh(III)-Catalyzed C(sp3)-H Alkylation of 8-Methylquinolines in Aqueous Media¡± Kim, S.; Han, S.; Park, J.; Sharma, S.; Mishra, N. K.; Oh, H.; Kwak, J. H.; Kim, I. S.* Chem. Commun. 2017, 53, 3006-3009 (selected as Cover Page of ChemComm).
105. ¡°Installation of ¥á-Ketocarboxylate Groups to C7-Position of Indolines via C-H Addition and Oxidation Approach Under Ruthenium Catalysis¡± Jo, H.; Park, J.; Mishra, N. K.; Jeon, M.; Sharma, S.; Oh, H.; Lee, S.-Y.; Jung, Y. H.; Kim, I. S.* Tetrahedron 2017, 73, 1725-1732..
104. ¡°Rhodium-Catalyzed [3+2] Annulation of Cyclic N-Acyl Ketimines with Activated Olefins: Anticancer Activity of Spiroisoindolinones¡± Sharma, S.; Oh, Y.; Mishra, N. K.; De, U.; Jo, H.; Sachan, R.; Kim, H. S.; Jung, Y. H.; Kim, I. S.* J. Org. Chem. 2017, 82, 3359-3367 (selected as Featured Article and Cover Page of JOC).
103. ¡°Site-Selective Cp*Rh(III)-Catalyzed C-H Amination of Indolines with Anthranils¡± Mishra, N. K.; Jeon, M.; Oh, Y.; Jo, H.; Park, J.; Han, S.; Sharma, S.; Han, S. H.; Jung, Y. H.; Kim, I. S.* Org. Chem. Front. 2017, 4, 241-249.
102. ¡°Anticancer Effects of a New SIRT Inhibitor, MHY2256, against Human Breast Cancer MCF-7 Cells via Regulation of MDM2-p53 Binding¡± Park, E. Y.; Woo, Y.; Kim, S. J.; Kim, D. H.; Lee, E. K.; De, U.; Kim, K. S.; Lee, J.; Jung, J. H.; Ha, K.-T.; Choi, W. S.; Kim, I. S.; Lee, B. M.; Yoon, S.; Moon, H. R.; Kim, H. S.* Int. J. Biol. Sci. 2016, 12, 1555-1567.
101. ¡°Synthesis of Succinimide-Containing Chromones, Naphthoquinones, and Xanthones under Rh(III) Catalysis: Evaluation of Anticancer Activity¡± Han, S. H.; Kim, S.; De, U.; Mishra, N. K.; Park, J.; Sharma, S.; Kwak, J. H.; Han, S.; Kim, H. S.; Kim, I. S.* J. Org. Chem. 2016, 81, 12416-12425.
100. ¡°Divergent Total Synthesis of D-ribo-Phytosphingosine and L-ribo-Phytosphingosine from D-Ribose¡± Chun, J. S.; Hong, S. M.; Jeon, T. H.; Park, S. J.; Son, H. P.; Jung, J. M.; Choi, Y. J.; Kim, I. S.; Jung, Y. H.* Tetrahedron 2016, 72, 8550-8556.
99. ¡°Redox-Neutral Rh(III)-Catalyzed Olefination of Carboxamides with Trifluoromethyl Allylic Carbonate¡± Park, J.; Han, S.; Jeon, M.; Mishra, N. K.; Lee, S.-Y.; Lee, J. S.; Kwak, J. H.; Um, S. H.; Kim, I. S.* J. Org. Chem. 2016, 81, 11353-11359.
98. ¡°Rh(III)-Catalyzed C-H Functionalization of Indolines with Readily Accessible Amidating Reagent: Synthesis and Anticancer Evaluation¡± Jeon, M.; Mishra, N. K.; De, U.; Sharma, S.; Oh, Y.; Choi, M.; Jo, H.; Sachan, R.; Kim, H. S.; Kim, I. S.* J. Org. Chem. 2016, 81, 9878-9885.
97. ¡°Site-Selective C-H Amidation of Azobenzenes with Dioxazolones Under Rhodium Catalysis¡± Mishra, N. K.; Oh, Y.; Jeon, M.; Han, S.; Sharma, S.; Han, S. H.; Um, S. H.; Kim, I. S.* Eur. J. Org. Chem. 2016, 4976-4980.
96. ¡°Rhodium(III)-Catalyzed C(sp3)-H Alkylation of 8-Methylquinolines with Maleimides¡± Han, S.; Park, J.; Kim, S.; Lee, S. H.; Sharma, S.; Mishra, N. K.; Jung, Y. H.; Kim, I. S.* Org. Lett. 2016, 18, 4666-4669.
95. ¡°Rhodium-Catalyzed Vinylic C-H Functionalization of Enol Carbamates with Maleimides¡± Sharma, S.; Han, S. H.; Jo, H.; Han, S.; Mishra, N. K.; Choi, M.; Jeong, T.; Park, J.; Kim, I. S.* Eur. J. Org. Chem. 2016, 3611-3618.
94. ¡°Ruthenium(II)- or Rhodium(III)-Catalyzed Grignard-type Addition of Indolines and Indoles to Activated Carbonyl Compounds¡± Jo, H.; Park, J.; Choi, M.; Sharma, S.; Jeon, M.; Mishra, N. K.; Jeong, T.; Han, S.; Kim, I. S.* Adv. Synth. Catal. 2016, 358, 2714-2720 (highlighted as a Cover Page and selected as a Very Important Publication).
93. ¡°Synthesis of Phthalides through Tandem Rhodium-Catalyzed C-H Olefination and Annulation of Benzamides¡± Mishra, N. L.; Park, J.; Choi, M.; Sharma, S.; Jo, H.; Jeong, T.; Han, S.; Kim, S.; Kim, I. S.* Eur. J. Org. Chem. 2016, 3076-3083.
92. ¡°Trifluoromethylallylation of Heterocyclic C-H Bonds with Allylic Carbonates under Rhodium Catalysis¡± Choi, M.; Park, J.; Sharma, S.; Jo, H.; Han, S.; Jeon, M.; Mishra, N. K.; Han, S. H.; Lee, J. S.; Kim, I. S.* J. Org. Chem. 2016, 81, 4771-4778.
91. ¡°Cross-Coupling of Acrylamides and Maleimides Under Rhodium Catalysis: Controlled Olefin Migration¡± Sharma, S.; Han, S. H.; Oh, Y.; Mishra, N. K.; Lee, S. H.; Oh, J. S.; Kim, I. S.* Org. Lett. 2016, 18, 2568-2571.
90. ¡°Computer-Aided Identification of New Histone Deacetylase 6 Selective Inhibitor with Anti-Sepsis Activity¡± Yoo, J.; Kim, S.-J.; Son, D.; Seo, H.; Baek, S. Y.; Maeng, C.-Y.; Lee, C.; Kim, I. S.; Jung, Y. H.; Lee, S.-M.; Park, H.-J.* Eur. J. Med. Chem. 2016, 116, 126-135.
89. ¡°Mild and Site-Selective Allylation of Enol Carbamates with Allylic Carbonates under Rhodium Catalysis¡± Sharma, S.; Han, S. H.; Oh, Y.; Mishra, N. K.; Han, S.; Kwak, J. H.; Lee, S.-Y.; Jung, Y. H.; Kim, I. S.* J. Org. Chem. 2016, 81, 2243-2251.
88. ¡°Access to 3-Acyl-(2H)-indazoles via Rh(III)-Catalyzed C-H Addition and Cyclization of Azobenzenes with ¥á-Keto Aldehydes¡± Jeong, T.; Han, S. H.; Han, S.; Sharma, S.; Park, J.; Lee, J. S.; Kwak, J. H.; Jung, Y. H.; Kim, I. S.* Org. Lett. 2016, 18, 232-235.
87. ¡°Rhodium(III)-Catalyzed Heteroatom-Directed C-H Allylation with Allylic Phosphonates and Allylic Carbonates at Room Temperature¡± Jo, H.; Han, S.; Park, J.; Choi, M.; Han, S. H.; Jeong, T.; Lee, S.-Y.; Kwak, J. H.; Jung, Y. H.; Kim, I. S.* Tetrahedron 2016, 72, 571-578.
86. ¡°Discovery and SAR of N-(1-((substitutedpiperidin-4-yl)methyl)-3-methoxypiperidin-4-yl)-2-methoxybenzamide derivatives; 5-hydroxytryptamine receptor 4 agonist as a potent prokinetic agent¡± Park, J. S.; Im, W.; Choi, S.; Park, S. J.; Jung, J. M.; Baek, K. S.; Son, H. P.; Sharma, S.; Kim, I. S.; Jung, Y. H.* Eur. J. Med. Chem. 2016, 108, 75-88.
85. ¡°Transition-Metal-Catalyzed Oxidative and Decarboxylative Acylations through sp2 C-H Bond Activation¡± Sharma, S.; Mishra, N. K.; Shin, Y.; Kim, I. S.* Curr. Org. Chem. 2016, 20, 471-511.
84. ¡°Rh(III)-Catalyzed ortho-Alkylation of N-Benzyltriflamides with Diazo Compounds¡± Han, S. H.; Mishra, N. K.; Kim, I. S.* Bull. Korean Chem. Soc. 2015, 36, 2823-2828.
83. ¡°Direct C-H Alkylation and Indole Formation of Anilines with Diazo Compounds under Rhodium Catalysis¡± Mishra, N. K.; Choi, M.; Jo, H.; Oh, Y.; Sharma, S.; Han, S. H.; Jeong, T.; Han, S.; Lee, S.-Y.; Kim, I. S.* Chem. Commun. 2015, 51, 17229-17232.
82. ¡°Rhodium-Catalyzed C-H Alkylation of Indolines with Allylic Alcohols: Direct Access to ¥â-Aryl Carbonyl Compounds¡± Han, S. H.; Choi, M.; Jeong, T.; Sharma, S.; Mishra, N. K.; Park, J.; Oh, J. S.; Kim, W. J.; Lee, J. S.; Kim, I. S.* J. Org. Chem. 2015, 80, 11092-11099.
81. ¡°Effects of the CYP2D6*10 Allele on the Pharmacokinetics of Atomoxetine and Its Metabolites¡± Byeon, J.-Y.; Kim, Y.-H.; Na, H.-S.; Jang, J.-H.; Kim, S.-H.; Lee, Y.-J.; Bae, J.-W.; Kim, I. S.; Jang, C.-G.; Chung, M.-W.; Lee, S.-Y. Arch. Pharm. Res. 2015, 38, 2083-2091.
80. ¡°Synthesis of N-Sulfonylamidated and Amidated Azobenzenes under Rhodium Catalysis¡± Han, S.; Mishra, N. K.; Sharma, S.; Park, J.; Choi, M.; Lee, S.-Y.; Oh, J. S.; Jung, Y. H.; Kim, I. S.* J. Org. Chem. 2015, 80, 8026-8035.
79. ¡°Rh(III)-Catalyzed C-H Alkylation of 2-Arylbenzothiazoles with ¥á-Diazo Esters¡± Choi, M.; Park, J.; Mishra, N. K.; Lee, S.-Y.; Kim, J. H.; Jeong, K. M.; Lee, J.; Jung, Y. H.; Kim, I. S.* Tetrahedron Lett. 2015, 56, 4678-4682.
78. ¡°Rh(III)-Catalyzed C-H Amidation of Indoles with Isocyanates¡± Jeong, T.; Han, S.; Mishra, N. K.; Sharma, S.; Lee, S.-Y.; Oh, J. S.; Kwak, J. H.; Jung, Y. H.; Kim, I. S.* J. Org. Chem. 2015, 80, 7243-7250.
77. ¡°Rh(III)-Catalyzed Direct Coupling of Azobenzenes with ¥á-Diazo Esters: Facile Synthesis of Cinnolin-3(2H)-ones¡± Sharma, S.; Han, S. H.; Han, S.; Ji, W.; Oh, J.; Lee, S.-Y.; Oh, J. S.; Jung, Y. H.; Kim, I. S.* Org. Lett. 2015, 17, 2852-2855.
76. ¡°Divergent Synthesis of Aminocyclopentitol Analogs via Stereoselective Amination of Cyclic Polybenzyl Ether with Chlorosulfonyl Isocyanate¡± Jung, Y. H.; Kim, S. I.; Hong, Y. J.; Park, S. J.; Kang, K. T.; Kim, S. Y.; Park, J. S.; Kim, I. S. Synlett 2015, 26, 1089-1092.
75. ¡°Rh(III)-Catalyzed Selective C-H Cyanation of Indolines and Indoles with Easily Accessible Cyano Source¡± Mishra, N. K.; Jeong, T.; Sharma, S.; Shin, Y.; Han, S.; Park, J.; Oh, J. S.; Kwak, J. H.; Jung Y. H.; Kim, I. S.* Adv. Synth. Catal. 2015, 357, 1293-1298.
74. ¡°Rhodium-Catalyzed Mild and Selective C-H Allylation of Indolines and Indoles with 4-Vinyl-1,3-dioxolan-2-one: Facile Access to Indolic Scaffolds with an Allylic Alcohol Moiety¡± Sharma, S.; Shin, Y.; Mishra, N. K.; Park, J.; Han, S.; Jeong, T.; Oh, Y.; Lee, Y.; Choi, M.; Kim, I. S.* Tetrahedron 2015, 71, 2435-2441 (Selected as a Cover Page of Tetrahedron).
73. ¡°Total Synthesis of Carbocyclic Nucleoside (+)-Neplanocin A¡± Jung, Y. H.; Kim, S. I.; Hong, Y. J.; Park, S. J.; Kang, K. T.; Kim, S. Y.; Kim, I. S. Tetrahedron 2015, 71, 1068-1073.
72. ¡°Direct and Site-Selective Palladium-Catalyzed C7-Acylation of Indolines with Aldehydes¡± Shin, Y.; Sharma, S.; Mishra, N. K.; Han, S.; Park, J.; Oh, H.; Ha, J.; Yoo, H.; Jung, Y. H.; Kim, I. S.* Adv. Synth. Catal. 2015, 357, 594-600.
71. ¡°Mild Rh(III)-Catalyzed C7-Allylation of Indolines with Allylic Carbonates¡± Park, J.; Mishra, N. K.; Sharma, S.; Han, S.; Shin, Y.; Jeong, T.; Oh, J. S.; Kwak, J. H.; Jung, Y. H.; Kim, I. S.* J. Org. Chem. 2015, 80, 1818-1827.
70. ¡°Decarboxylative Acylation of Indolines with ¥á-Keto Acids under Palladium Catalysis: A Facile Strategy for the Synthesis of 7-Substituted Indoles¡± Kim, M.; Mishra, N. K.; Park, J.; Han, S.; Shin, Y.; Sharma, S.; Lee, Y.; Lee, E.-K.; Kwak, J. H.; Kim, I. S.* Chem. Commun. 2014, 50, 14249-14252.
69. ¡°Ru(II)-Catalyzed Selective C-H Amination of Xanthones and Chromones with Sulfonyl Azides: Synthesis and Anticancer Evaluation¡± Shin, Y.; Han, S.; De, U.; Park, J.; Sharma, S.: Mishra, N. K.; Lee, E.-K.; Lee, Y.; Kim, H. S.; Kim, I. S.* J. Org. Chem. 2014, 79, 9262-9271.
68. ¡°Discovery of Novel 2-[2-(3-Hydroxy-pyridin-2-yl)-thiazol-4-yl]-acetamide Derivatives as HIF Prolyl 4-Hydroxylase Inhibitors; SAR, Synthesis and Modeling Evaluation¡± Hong, Y. R.; Kim, H. T.; Ro, S.; Cho, J. M.; Lee, S. H.; Kim, I. S.; Jung, Y. H. Bioorg. Med. Chem. Lett. 2014, 24, 3142-3145.
67. ¡°Direct Allylation of Aromatic and ¥á,¥â-Unsaturated Carboxamides under Ruthenium Catalysis¡± Kim, M.; Sharma, S.: Mishra, N. K.; Han, S.; Park, J.; Kim, M.; Shin, Y.; Kwak, J. H.; Han, S. H.; Kim, I. S.* Chem. Commun. 2014, 50, 11303-11306. (Selected as a Cover Page of ChemComm)
66. ¡°Antiviral Effect of Flavonol Glycosides Isolated from the Leaf of Zanthoxylum piperitum on Influenza Virus¡± Ha, S.-Y.; Youn, H.; Song, C.-S.; Kang, S. C.; Bae, J. J.; Kim, H. T.; Lee, K. M.; Eom, T. H.; Kim, I. S.; Kwak, J. H. J. Microbiol. 2014, 52, 340-344.
65. ¡°Rh(III)-Catalyzed Oxidative Coupling of 1,2-Disubstituted Hydrazines and Olefins: A New Strategy for 2,3-Dihydro-1H-Indazoles¡± Han, S.; Shin, Y.; Sharma, S.; Mishra, N. K.; Park, J.; Kim, M.; Kim, M.; Jang, J.; Kim, I. S.* Org. Lett. 2014, 16, 2494-2497.
64. ¡°Copper-Catalyzed Oxidative C-O Bond Formation of 2-Acyl Phenols and 1,3-Dicarbonyl Compounds with Ethers: Direct Access to Phenol Esters and Enol Esters¡± Park, J.; Han, S. H.; Sharma, S.; Han, S.; Shin, Y.; Mishra, N. K.; Kwak, J. H.; Lee, C. H.; Lee, J.; Kim, I. S.* J. Org. Chem. 2014, 79, 4735-4742.
63. ¡°Rh-Catalyzed Oxidative C2-Alkenylation of Indoles with Alkynes: Unexpected Cleavage of Directing Group¡± Sharma, S.; Han, S.; Shin, Y.; Mishra, N. K.; Oh, H.; Park, J.; Kwak, J. H.; Shin, B. S.; Jung, Y. H.; Kim, I. S.* Tetrahedron Lett. 2014, 55, 3014-3017.
62. ¡°Rh-Catalyzed Oxidative C-C Bond Formation and C-N Bond Cleavage: Direct Access to C2-Olefinated Free (NH)-Indoles and Pyrroles¡± Sharma, S.; Han, S.; Kim, M.; Mishra, N. K.; Park, J.; Shin, Y.; Ha, J.; Kwak, J. H.; Jung, Y. H.; Kim, I. S.* Org. Biomol. Chem. 2014, 12, 1703-1706.
61. ¡°Direct Access to Isoindolines through Tandem Rh(III)-Catalyzed Alkenylation and Cyclization of N-Benzyltriflamides¡± Mishra, N. K.; Park, J.; Sharma, S.; Han, S.; Kim, M.; Shin, Y.; Jang, J.; Kwak, J. H.; Jung, Y. H.; Kim, I. S.* Chem. Commun. 2014, 50, 2350-2352.
60. ¡°Pd-Catalyzed Oxidative Coupling of Arene C-H Bonds with Benzylic Ethers as Acyl Equivalents¡± Han, S.; Sharma, S.; Park, J.; Kim, M.; Shin, Y.; Mishra, N. K.; Bae, J. J.; Kwak, J. H.; Jung, Y. H.; Kim, I. S.* J. Org. Chem. 2014, 79, 275-284.
59. ¡°Pd(II)-Catalyzed Direct C-H Acylation of N-Boc Hydrazones with Aldehydes: One-Pot Synthesis of 1,2-Diacylbenzenes¡± Sharma, S.; Kim, A.; Park, J.; Kim, M.; Kwak, J. H.; Jung, Y. H.; Park, J. S.; Kim, I. S.* Org. Biomol. Chem. 2013, 11, 7869-7876.
58. ¡°Total Synthesis of (+)-Valienamine and (-)-1-epi-Valienamine via a Highly Diastereoselective Allylic Amination of Cyclic Polybenzyl Ether Using Chlorosulfonyl Isocyanate¡± Li, Q. R.; Kim, S. I.; Park, S. J.; Yang, H. R.; Baek, A. R.; Kim, I. S.; Jung, Y. H. Tetrahedron 2013, 69, 10384-10390.
57. ¡°[(4-Hydroxyl-benzo[4,5]thieno[3,2-c]pyridine-3-carbonyl)-amino]-acetic Acid Derivatives; HIF Prolyl 4-Hydroxylase Inhibitors as Oral Erythropoietin Secretagogues¡± Hong, Y. R.; Kim, H. T.; Lee, S.-C.; Ro, S.; Cho, J. M.; Kim, I. S.; Jung, Y. H. Bioorg. Med. Chem. Lett. 2013, 23, 5953-5957.
56. ¡°Synthesis and C2-Functionalization of Indoles with Allylic Acetates under Rhodium Catalysis¡± Kim, M.; Park, J.; Sharma, S.; Han, S.; Han, S. H.; Kwak, J. H.; Jung, Y. H.; Kim, I. S.* Org. Biomol. Chem. 2013, 11, 7427-7434.
55. ¡°Cu(II)-Catalyzed Oxidative Esterification of 2-Carbonyl Substituted Phenols from the Alcohol Oxidation Level¡± Sharma, S.; Park, J.; Kim, M.; Kwak, J. H.; Jung, Y. H.; Kim, I. S.* Tetrahedron 2013, 69, 9391-9397.
54. ¡°Palladium-Catalyzed Direct Acylation of Ketoximes and Aldoximes from the Alcohol Oxidation Level through C-H Bond Activation¡± Sharma, S.; Kim, M.; Park, J.; Kim, M.; Kwak, J. H.; Jung, Y. H.; Oh, J. S.; Lee, Y.; Kim, I. S.* Eur. J. Org. Chem. 2013, 6656-6665.
53. ¡°Pd-Catalyzed Oxidative Acylation of 2-Phenoxypyridines with Alcohols via C-H Bond Activation¡± Kim, M.; Sharma, S.; Park, J.; Kim, M.; Choi, Y.; Jeon, Y.; Kwak, J. H.; Kim, I. S.* Tetrahedron 2013, 69, 6552-6559.
52. ¡°Asymmetric Formal Synthesis of (-)-Swainsonine via a Highly Regioselective and Diastereoselective Allylic Amination Using Chlorosulfonyl Isocyanate¡± Li, Q. R.; Dong, G. R.; Park, S. J.; Hong, Y. R.; Kim, I. S.; Jung, Y. H. Eur. J. Org. Chem. 2013, 4427-4433.
51. ¡°Total Synthesis of D-Fagomine and 6-Deoxyfagomine¡± Min, I. S.; Kim, S. I.; Hong S.; Kim, I. S.; Jung, Y. H. Tetrahedron 2013, 69, 3901-3906.
50. ¡°Palladium-Catalyzed Decarboxylative Acylation of O-Phenylcarbamates with ¥á-Oxocarboxylic Acids at Room Temperature¡± Sharma, S.; Kim, A.; Park, E.; Park, J.; Kim, M.; Kwak, J. H.; Lee, S. H.; Jung, Y. H.; Kim, I. S.* Adv. Synth. Catal. 2013, 355, 667-672.
49. ¡°Direct Acylation of N-Benzyltriflamides from the Alcohol Oxidation Level via Palladium-Catalyzed C-H Bond Activation¡± Park, J.; Kim, A.; Sharma, S.; Kim, M.; Park, E.; Jeon, Y.; Lee, Y.; Kwak, J. H.; Jung, Y. H.; Kim, I. S.* Org. Biomol. Chem. 2013, 11, 2766-2771. (selected as a HOT article of OBC)
48. ¡°Palladium-Catalyzed Oxidative Acylation of N-Benzyltrilamides with Aldehydes via C-H Bond Activation¡± Sharma, S.; Park, J.; Park, E.; Kim, A.; Kim, M.; Kwak, J. H.; Jung, Y. H.; Kim, I. S.* Adv. Synth. Catal. 2013, 355, 332-336.
47. ¡°Pd(II)-Catalyzed Decarboxylative Acylation of Phenylacetamides with ¥á-Oxocarboxylic Acids via C-H Bond Activation¡± Park, J.; Kim, M.; Sharma, S.; Park, E.; Kim, A.; Lee, S. H.; Kwak, J. H.; Jung, Y. H.; Kim, I. S.* Chem. Commun. 2013, 49, 1654-1656.
46. ¡°Asymmetric Synthesis of (+)-trans-Aerangis Lactone¡± Kim, A.; Sharma, S.; Kwak, J. H.; Kim, I. S.* Bull. Korean Chem. Soc. 2013, 34, 75-78.
45. ¡°Asymmetric Total Synthesis of (+)-Indatraline via Diastrereoselective Amination of Chiral Ethers Using Chlorosulfonyl Isocyanate¡± Lee, S. H.; Park, S. J.; Kim, I. S.; Jung, Y. H. Tetrahedron 2013, 69, 1877-1880.
44. ¡°Palladium-Catalyzed Decarboxylative Acylation of O-Methyl Ketoximes with ¥á-Keto Acids¡± Kim, M.; Park, J.; Sharma, S.; Kim, A.; Park, E.; Kwak, J. H.; Jung, Y. H.; Kim, I. S.* Chem. Commun. 2013, 49, 925-927.
43. ¡°Self-Assembled Metalla-Rectangles Bearing Azodipyridyl Ligands: Synthesis, Characterization and Antitumor Activity¡± Vajpayee, V.; Lee, S.; Kim, S.-H.; Kang, S. C.; Cook, T. R.; Kim, H.; Kim, D. W.; Verma, S.; Lah, M. S.; Kim, I. S.; Wang, M.; Stang, P. J.; Chi, K.-W. Dalton Trans. 2013, 42, 466-475.
42. ¡°A Stereoselective Synthesis of ¥á-(-)-Conhydrine and Its Pyrrolidine Analogue¡± Dong, G. R.; Hong, S.; Kim, S. I.; Kim, I. S.*; Jung, Y. H. Eur. J. Org. Chem. 2012, 4200-4205.
41. ¡°Asymmetric Total Synthesis of (S)-Dapoxetine¡± Kim, S. J.; Jeon, T. H.; Min, I. S.; Kim, I. S.*; Jung, Y. H. Tetrahedron Lett. 2012, 53, 3680-3682.
40. ¡°Synthesis of Norlignans and In vitro Inhibitory Activity of Antigen-Induced Degranulation¡± Park, E.; Yang, Y. J.; Kim, A.; Kwak, J. H.; Jung, Y. H.; Kang, S. C.; Kim, I. S.* Bioorg. Med. Chem. Lett. 2012, 22, 3653-3655.
39. ¡°Coordination-Driven Self-Assembly of Ruthenium-Based Molecular-Rectangles: Synthesis, Characterization, Photophysical and Anticancer Potency Studies¡± Vajpayee, V.; Song, Y. H.; Jung, Y. J.; Kang, S. C.; Kim, H.; Kim, I. S.; Wang, M.; Cook, T. R.; Stang, P. J.; Chi, K.-W. Dalton Trans. 2012, 41, 3046-3052.
38. ¡°Tandem Rh(III)-Catalyzed Oxidative Acylation of Secondary Benzamides with Aldehydes and Intramolecular Cyclization: The Direct Synthesis of 3-Hydroxyisoindolin-1-ones¡± Sharma, S.; Park, E.; Park, J.; Kim, I. S.* Org. Lett. 2012, 14, 906-909.
37. ¡°Stereoselective Amination of Chiral Benzylic Ethers Using Chlorosulfonyl Isocyante: Total Synthesis of (+)-Sertraline¡± Lee, S. W.; Kim, I. S.; Li, Q. R.; Dong, G. R.; Jeong, L. S.; Jung, Y. H. J. Org. Chem. 2011, 76, 10011-10019 (highlighted by Synfact 2012, 8, 0233).
36. ¡°Self-Assembly of Cationic, Hetero- or Homonuclear Ruthenium(II) Macrocyclic Rectangles and Their Photophysical, Electrochemical, and Biological Studies¡± Vajpayee, V.; Song, Y. H.; Yang, Y. J.; Kang, S. C.; Cook, T. R.; Kim, D. W.; Lah, M. S.; Kim, I. S.; Wang, M.; Stang, P. J.; Chi, K.-W. Organometallics 2011, 30, 6482-6489.
35. ¡°Antioxidative Constituents from Friut of Sorbaria sorbifolia var. stellipila MAX.¡± Park, J. H.; Kwon, J. A.; Yang, Y. J.; Han, H.-S.; Han, M.-W.; Lee, Y.; Kim, I. S.; Lee, J.-I.; Kang, S. C. Korean J. Plant Res. 2011, 24, 337-342.
34. ¡°Recent Advances in the Total Synthesis of Indolizidine Iminosugars¡± Kim, I. S.*; Jung, Y. H. Heterocycles 2011, 83, 2489-2507.
33. ¡°A Catalytic Approach to the Synthesis of (+)-Fluvastatin Analogue¡± Kim, A.; Kim, I. S.* Bull. Korean Chem. Soc. 2011, 32, 3748-3751.
32. ¡°Rhodium-Catalyzed Oxidative ortho-Acylation of Benzamides with Aldehydes: Direct Functionalization of the sp2 C-H Bond¡± Park, J.; Park, E.; Kim, A.; Lee, Y.; Chi, K.-W.; Kwak, J. H.; Jung, Y. H.; Kim, I. S.* Org. Lett. 2011, 13, 4390-4393.
31. ¡°Coordination-Driven Self-Assembly and Anticancer Activity of Molecular Rectangles Containing Octahedral Ruthenium Metal Centers¡± Vajpayee, V.; Song, Y. H.; Yang, Y. J.; Kang, S. C.; Kim, H.; Kim, I. S.; Wang, M.; Stang, P. J.; Chi, K.-W. Organometallics 2011, 30, 3242-3245.
30. ¡°Pd-Catalyzed Decarboxylative Coupling of Propiolic Acids: One-Pot Synthesis of 1,4-Disubstituted 1,3-Diynes via Sonogashira-Homocoupling Sequence¡± Park, J.; Park, E.; Kim, A.; Park, S.-A.; Lee, Y.; Chi, K.-W.; Jung, Y. H.; Kim, I. S.* J. Org. Chem. 2011, 76, 2214-2219.
29. ¡°Hexanuclear Self-Assembled Arene-Ruthenium Nano-Prismatic Cages: Potential Anticancer Agents¡± Vajpayee, V.; Yang, Y. J.; Kang, S. C.; Kim, H.; Kim, I. S.; Wang, M.; Stang, P. J.; Chi, K.-W. Chem. Commun. 2011, 47, 5184-5186.
28. ¡°Novel Synthetic Method for Allylic Amination of Cyclic Allylic Ethers Using Chlorosulfonyl Isocyanate¡± Lee, S. W.; Kim, I. S.; Li, Q. R.; Dong, G. R.; Jung, Y. H. Tetrahedron Lett. 2011, 52, 1901-1904.
27. ¡°Screening and Compound Isolation from Natural Plants for Anti-Allergic Activity¡± Bak, J. P.; Kim, J. B.; Park, J. H.; Yang, Y. J.; Kim, I. S.*; Choung, E. S.; Kang, S. C. J. Korean Soc. Appl. Biol. Chem. 2011, 54, 367-375.
26. ¡°Total Synthesis of (+)-Roxaticin via C-C Bond Forming Transfer Hydrogenation: A Departure from Stoichiometric Chiral Reagents, Auxiliaries, and Premetalated Nucleophiles in Polyketide Construction¡± Han, S. B.; Hassan, A.; Kim, I. S.; Krische, M. J. J. Am. Chem. Soc. 2010, 132, 15559-15561.
25. ¡°A Facile Synthesis of Lentiginosine Analogues Based on a Highly Regio- and Diastereoselective Allylic Amination of Chlorosulfonyl Isocyanate¡± Kim, I. S.; Li, Q. R.; Dong, G. R.; Kim, Y. C.; Hong, Y. J.; Lee, M.; Chi, K.-W.; Oh, J. S.; Jung, Y. H. Eur. J. Org. Chem. 2010, 1569-1573.
24. ¡°Enantioselective Iridium-Catalyzed Carbonyl Allylation from the Alcohol Oxidation Level via Transfer Hydrogenation: Minimizing Pre-Activation for Synthetic Efficiency¡± Han, S. B.; Kim, I. S.; Krische, M. J. Chem. Commun. 2009, 7278-7287.
23. ¡°Enantioselective Carbonyl Reverse Prenylation from the Alcohol or Aldehyde Oxidation Level Employing 1,1-Dimethylallene as the Prenyl Donor¡± Han, S. B.; Kim, I. S.; Han, H.; Krische, M. J. J. Am. Chem. Soc. 2009, 131, 6916-6917.
22. ¡°1,n-Glycols as Synthetic Equivalents to Dialdehydes in Iridium-Catalyzed Enantioselective Carbonyl Allylation and Iterative Two-Directional Assembly of 1,3-Polyols¡± Lu, Y.; Kim, I. S.; Hassan, A.; Del Valle, D. J.; Krische, M. J. Angew. Chem. Int. Ed. 2009, 48, 5018-5021.
(highlighted as Hot Papers in Angew. Chem. Int. Ed. 2009)
(highlighted in Synfacts 2009, 9, 997)
21. ¡°anti-Diastereo- and Enantioselective Carbonyl Crotylation from the Alcohol or Aldehyde Oxidation Level Employing a Cyclometallated Iridium Catalyst: ¥á-Methyl Allyl Acetate as a Surrogate to Preformed Crotylmetal Reagents¡± Kim, I. S.; Han, S. B.; Krische, M. J. J. Am. Chem. Soc. 2009, 131, 2514-2520.
20. ¡°Catalytic Carbonyl Addition Through Transfer Hydrogenation: A Departure from Preformed Organometallic Reagents¡± Bower, J. F.; Kim, I. S.; Patman, R. L.; Krische, M. J. Angew. Chem. Int. Ed. 2009, 48, 34-46.
19. ¡°Formation of C-C Bonds via Catalytic Hydrogenation and Transfer Hydrogenation: Vinylation, Allylation, and Enolate Addition¡± Patman, R. L.; Bower, J. F.; Kim, I. S.; Krische, M. J. Aldrichim. Acta 2008, 41, 95-104.
18. ¡°Enantioselective Iridium-Catalyzed Carbonyl Allylation from the Alcohol or Aldehyde Oxidation Level via Transfer Hydrogenative Coupling of Allyl Acetate: Departure from Chirally Modified Allyl Metal Reagents in Carbonyl Addition¡± Kim, I. S.; Ngai, M.-Y.; Krische, M. J. J. Am. Chem. Soc. 2008, 130, 14891-14899.
17. ¡°Enantioselective Iridium-Catalyzed Carbonyl Allylation from the Alcohol or Aldehyde Oxidation Level Using Allyl Acetate as an Allyl Metal Surrogate¡± Kim, I. S.; Ngai, M.-Y.; Krische, M. J. J. Am. Chem. Soc. 2008, 130, 6340-6341.
(highlighted in Chemical & Engineering News 2008, 86, 10)
(highlighted in Synfacts 2008, 9, 957)
16. ¡°Iridium-Catalyzed Hydrocarboxylation of 1,1-Dimethylallene: Byproduct-Free Reverse Prenylatio n of Carboxylic Acids¡± Kim, I. S.; Krische, M. J. Org. Lett. 2008, 10, 513-515.
15. ¡°A Concise Synthesis of (+)-Polyoxamic Acid and (+)-5-O-Carbamoyl Polyoxamic Acid¡± Kim, I. S.; Li, Q. R.; Dong, G. R.; Woo, S. H.; Park, H.-j.; Zee, O. P.; Jung, Y. H. Synlett 2008, 2985-2988.
14. ¡°One-Pot Conversion of Trimethylsilyl Ethers into Urethanes Using Chlorosulfonyl Isocyanate: Application to the Synthesis of a Novel Neuromodulator Carisbamate¡± Dong, G. R.; Li, Q. R.; Woo, S. H.; Kim, I. S.; Jung, Y. H. Arch. Pharm. Res. 2008, 31, 1393-1398.
13. ¡°Palladium(II)-Catalyzed Isomerization of Olefins with Tributyltin Hydride¡± Kim, I. S.; Dong, G. R.; Jung, Y. H. J. Org. Chem. 2007, 72, 5424-5426.
12. ¡°Direct Etherification of Alkyl Halides by Sodium Hydride in the Presence of N,N-Dimethylformamide¡± Jin, C. H.; Lee, H. Y.; Lee, S. H.; Kim, I. S.; Jung, Y. H. Synlett 2007, 2695-2698.
11. ¡°An Efficient Stereoselective Synthesis of (+)-Deoxoprosophylline¡± Kim, I. S.; Ryu, C. B.; Li, Q. R.; Zee, O. P.; Jung, Y. H. Tetrahedron Lett. 2007, 48, 6258-6261.
10. ¡°An Efficient Synthesis of Aminocyclopentitols via the Stereoselective Amination of Polybenzyl Ethers Using Chlorosulfonyl Isocyanate¡± Kim, I. S.; Li, Q. R.; Lee, J. K.; Lee, S. H.; Lim, J. K.; Zee, O. P.; Jung, Y. H. Synlett 2007, 1711-1714.
9. ¡°Stereoselective Synthesis of D-1-Deoxynojirimycin and Its Stereoisomers¡± Kim, I. S.; Lee, H. Y.; Jung, Y. H. Heterocycles 2007, 71, 1787-1800.
8. ¡°Synthesis of (2R,5S)-Dihydroxymethyl-(3R,4R)-dihydroxypyrrolidine (DGDP) via Stereoselective Amination Using Chlorosulfonyl Isocyanate¡± Kim, I. S.; Kim, S. J.; Lee, J. K.; Li, Q. R.; Jung, Y. H. Carbohydr. Res. 2007, 342, 1502-1509.
7. ¡°Synthesis and Conformational Analysis of 3-Hydroxypipecolic Acid Analogs via CSI-mediated Stereoselective Amination¡± Kim, I. S.; Oh, J. S.; Zee, O. P.; Jung, Y. H. Tetrahedron 2007, 63, 2622-2633.
6. ¡°Synthesis of Psoralen Derivatives and Their Blocking Effect of hKv1.5 Channel¡± Eun, J. S.; Kim, K. S.; Kim, H. N.; Park, S. A.; Ma, T.-Z.; Lee, K. A.; Kim, D. K.; Kim, H. K.; Kim, I. S.; Jung, Y. H.; Zee, O. P.; Yoo, D. J.; Kwak, Y. G. Arch. Pharm. Res. 2007, 30, 155-160.
5. ¡°Regioselective and Diastereoselective Amination of Polybenzyl Ethers Using Chlorosulfonyl Isocyanate: Total Syntheses of 1,4-Dideoxy-1,4-imino-D-arabinitol and (-)-Lentiginosine¡± Kim, I. S.; Zee, O. P.; Jung, Y. H. Org. Lett. 2006, 8, 4101-4104.
4. ¡°An Efficient Stereoselective Synthesis of (2S,3S)-3-Hydroxypipecolic Acid Using Chlorosulfonyl Isocyanate¡± Kim, I. S.: Ji, Y. J.: Jung, Y. H. Tetrahedron Lett. 2006, 47, 7289-7293.
3. ¡°A Concise Synthesis of (-)-Cytoxazone and (-)-4-epi-Cytoxazone Using Chlorosulfonyl Isocyanate¡± Kim, I. S.; Kim, J. D.; Ryu, C. B.; Zee, O. P.; Jung, Y. H. Tetrahedron 2006, 62, 9349-9358.
2. ¡°Regioselective and Diastereoselective Amination with Use of Chlorosulfonyl Isocyanate: A Short and Efficient Synthesis of (-)-Cytoxazone¡± Kim, J. D.; Kim, I. S.; Jin, C. H.; Zee, O. P.; Jung, Y. H. Org. Lett. 2005, 7, 4025-4028.
1. ¡°Diastereoselective Synthesis of Unsaturated 1,2-Amino Alcohols from ¥á-Hydroxy Allyl Ethers Using Chlorosulfonyl Isocyanate¡± Kim, J. D.; Kim, I. S.; Hua, J. C.; Zee, O. P.; Jung, Y. H. Tetrahedron Lett. 2005, 46, 1079-1082.
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43. <±¹³»Æ¯Çãµî·Ï> ¡°À̸®µã Ã˸Ÿ¦ ÀÌ¿ëÇÑ ¾Æ¹Ì³ëº¥Áî¾Ëµ¥È÷µåÀÇ Á¦Á¶¹æ¹ý, À̸¦ ÀÌ¿ëÇÑ È­ÇÕ¹° ¹× À̸¦ À¯È¿¼ººÐÀ¸·Î Æ÷ÇÔÇÏ´Â ¿°Áõ¼º ÁúȯÀÇ ¿¹¹æ ¶Ç´Â Ä¡·á¿ë ¾àÇÐÀû Á¶¼º¹°¡± ±èÀμö, ±èÇü½Ä, À̺´¹«, 2019³â 7¿ù 12ÀÏ, µî·Ï¹øÈ£: 10-2000201.
42. <±¹Á¦Æ¯Çãµî·Ï> ¡°Oxindoles derivatives, preparation method thereof and pharmaceutical compositions for the prevention or treatment of cancer containing the same as an active ingredient" ±èÀμö, ±èÇü½Ä, 2019³â 6¿ù 18ÀÏ, µî·Ï¹øÈ£: US 10,322,999 B2.
41. <±¹³»Æ¯Çãµî·Ï> ¡°½Å±Ô ½ºÆÄÀ̷ξÆÀ̼ÒÀε¹¸®³í À¯µµÃ¼, ÀÌÀÇ Á¦Á¶¹æ¹ý ¹× À̸¦ À¯È¿¼ººÐÀ¸·Î Æ÷ÇÔÇÏ´Â ¾Ï ¿¹¹æ ¹× Ä¡·á¿ë Á¶¼º¹°¡± ±èÀμö, ±èÇü½Ä, 2019³â 4¿ù 22ÀÏ, µî·Ï¹øÈ£: 10-1973244.
40. <±¹³»Æ¯Çãµî·Ï> ¡°Àε¹ À¯µµÃ¼¸¦ À¯È¿¼ººÐÀ¸·Î Æ÷ÇÔÇÏ´Â ´ç´¢º´ ¿¹¹æ ¶Ç´Â Ä¡·á¿ë ¾àÇÐÀû Á¶¼º¹°" ¾ö¼ºÈñ, ±èÀμö, ±èÇü½Ä, ¼­µ¿¼ö, ±èÈñÁ¤, 2019³â 4¿ù 22ÀÏ, µî·Ï¹øÈ£: 10-1973351.
39. <±¹³»Æ¯Çãµî·Ï> ¡°¾ÆÁ¶º¥Á¨°ú ÀÌÁß°áÇÕÀ» ÀÌ¿ëÇÑ 2,3-ÀÌÁßġȯ Àε¹ À¯µµÃ¼ÀÇ Á¦Á¶¹æ¹ý, À̸¦ ÀÌ¿ëÇÑ È­ÇÕ¹°, ¹× À̸¦ À¯È¿¼ººÐÀ¸·Î Æ÷ÇÔÇÏ´Â ¾Ï ¿¹¹æ ¶Ç´Â Ä¡·á¿ë ¾àÇÐÀû Á¶¼º¹°¡± ±èÀμö, ±èÇü½Ä, 2019³â 4¿ù 18ÀÏ, µî·Ï¹øÈ£: 10-1972223.
38. <±¹³»Æ¯ÇãÃâ¿ø> ¡°ÇǸðÀÚÀ̵åÀÇ Ç×¾ÏÁ¦ º´¿ë¿ä¹ý" À±¼ºÇÊ, ±èÇü½Ä, À̺´¹«, ±èÀμö, ±èÁö¿µ, 2019³â 4¿ù 12ÀÏ, Ãâ¿ø¹øÈ£: 10-2019-0042935.
37. <±¹³»Æ¯ÇãÃâ¿ø> ¡°ÇǸ®µòÀ» ÇÔÀ¯ÇÏ´Â À¯±â È­ÇÕ¹°ÀÇ ortho À§Ä¡¿¡ ¾ËųÀ» µµÀÔÇÏ´Â ¹æ¹ý" ÇѼöºÀ, Á¤¿µ½Ä, ±èÇýÁø, ±èÀμö, 2019³â 4¿ù 10ÀÏ, Ãâ¿ø¹øÈ£: 10-2019-0042046.
36. <±¹³»Æ¯Çãµî·Ï> ¡°¿Á½ÃÀε¹ À¯µµÃ¼, ÀÌÀÇ Á¦Á¶¹æ¹ý ¹× À̸¦ À¯È¿¼ººÐÀ¸·Î Æ÷ÇÔÇÏ´Â ¾Ï ¿¹¹æ ¶Ç´Â Ä¡·á¿ë Á¶¼º¹°¡± ±èÀμö, ±èÇü½Ä, 2019³â 3¿ù 6ÀÏ, µî·Ï¹øÈ£: 10-1957572.
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34. <±¹³»Æ¯ÇãÃâ¿ø> ¡°Àε¹ À¯µµÃ¼¸¦ À¯È¿¼ººÐÀ¸·Î Æ÷ÇÔÇÏ´Â ´ç´¢º´ ¿¹¹æ ¶Ç´Â Ä¡·á¿ë ¾àÇÐÀû Á¶¼º¹°" ¾ö¼ºÈñ, ±èÀμö, ±èÇü½Ä, ¼­µ¿¼ö, ±èÈñÁ¤, 2019³â 1¿ù 24ÀÏ, Ãâ¿ø¹øÈ£: 10-2019-0009010.
33. <±¹Á¦Æ¯ÇãÃâ¿ø> ¡°Oxindoles derivatives, preparation method thereof and pharmaceutical compositions for the prevention or treatment of cancer containing the same as an active ingredient" ±èÀμö, ±èÇü½Ä, 2018³â 11¿ù 29ÀÏ, Ãâ¿ø¹øÈ£: US 20180339965 A1.
32. <±¹³»Æ¯ÇãÃâ¿ø> ¡°½Å±Ô Àε¹ À¯µµÃ¼, ÀÌÀÇ Á¦Á¶¹æ¹ý, ¹× À̸¦ À¯È¿¼ººÐÀ¸·Î Æ÷ÇÔÇÏ´Â ´ç´¢º´ ¿¹¹æ ¶Ç´Â Ä¡·á¿ë ¾àÇÐÀû Á¶¼º¹°" ±èÀμö, ±èÇü½Ä, ¾ö¼ºÈñ, Â÷¿ÀÀÚ°¢, ÀÓµ¿¿í, 2018³â 11¿ù 7ÀÏ, Ãâ¿ø¹øÈ£: 10-2018-0136227.
31. <±¹³»Æ¯Çãµî·Ï> ¡°·Îµã Ã˸Ÿ¦ ÀÌ¿ëÇÑ ¾Æ¹ÌµåÈ­ Àε¹¸°ÀÇ Á¦Á¶¹æ¹ý, À̸¦ ÀÌ¿ëÇÑ È­ÇÕ¹° ¹× À̸¦ À¯È¿¼ººÐÀ¸·Î Æ÷ÇÔÇÏ´Â ¾Ï ¿¹¹æ ¶Ç´Â Ä¡·á¿ë ¾àÇÐÀû Á¶¼º¹°¡± ±èÀμö, ±èÇü½Ä, 2018³â 10¿ù 11ÀÏ, µî·Ï¹øÈ£: 10-1909386.
30. <±¹³»Æ¯ÇãÃâ¿ø> ¡°COX-2 ¾ïÁ¦Á¦¸¦ À¯È¿¼ººÐÀ¸·Î Æ÷ÇÔÇÏ´Â ¼Ò¿°ÁøÅë ¿¹¹æ ¶Ç´Â Ä¡·á¿ë Á¤Á¦ Á¶¼º¹°" ±èÀμö, ÀÌâ·¡, ÁöÇö±¸, 2018³â 9¿ù 20ÀÏ, Ãâ¿ø¹øÈ£: 10-2018-0113181.
29. <±¹³»Æ¯ÇãÃâ¿ø> ¡°½Å±Ô 2-¾Æ½Ç ¾ÆÅ©¸®µò À¯µµÃ¼, ÀÌÀÇ Á¦Á¶¹æ¹ý, ¹× À̸¦ À¯È¿¼ººÐÀ¸·Î Æ÷ÇÔÇÏ´Â ¾Ï ¿¹¹æ ¶Ç´Â Ä¡·á¿ë Á¶¼º¹°" ±èÀμö, ±èÇü½Ä, 2018³â 8¿ù 29ÀÏ, Ãâ¿ø¹øÈ£: 10-2018-0102326.
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26. <±¹³»Æ¯ÇãÃâ¿ø> ¡°1-¾Æ¹Ì³ëÀ뫆 ¹× ÀÌÀÇ Á¦Á¶¹æ¹ý¡± ±èÀμö, ±èÇü½Ä, ¾ö¼ºÈñ, 2018³â 1¿ù 4ÀÏ, Ãâ¿ø¹øÈ£: 10-2018-0001194.
25. <±¹³»Æ¯ÇãÃâ¿ø> ¡°Äû³î¸°-8-ÀϸÞź¾Æ¹Î, ÀÌÀÇ Á¦Á¶¹æ¹ý ¹× À̸¦ À¯È¿¼ººÐÀ¸·Î Æ÷ÇÔÇÏ´Â ¾Ï¿¹¹æ ¹× Ä¡·á¿ë Á¶¼º¹°¡± ±èÀμö, ±èÇü½Ä, 2017³â 11¿ù 17ÀÏ, Ãâ¿ø¹øÈ£: 10-2017-0154137.
24. <±¹³»Æ¯ÇãÃâ¿ø> ¡°ÆæÄ¡³í ¿¡ÀÌ ¹× ±× À¯µµÃ¼ÀÇ Á¦Á¶¹æ¹ý°ú À̸¦ À¯È¿¼ººÐÀ¸·Î Æ÷ÇÔÇÏ´Â Ç׿°Áõ Á¶¼º¹°¡± ±èÀμö, Á¤¿µÈÆ, Ç¥¼®´É, Á¤±ÔÇõ, ±èÇü½Ä, ¾ÈÀº°æ, °íÇýÁø, 2017³â 10¿ù 11ÀÏ, Ãâ¿ø¹øÈ£: 10-2017-0131446.
23. <±¹³»Æ¯Çãµî·Ï> ¡°ÇÔ¿°Áõ È°¼ºÀ» °®´Â Çö󺸳ëÀ̵å°è È­ÇÕ¹°À» À¯È¿¼ººÐÀ¸·Î ÇÏ´Â ¿°ÁõÁúȯ ¿¹¹æ ¶Ç´Â Ä¡·á¿ë ¾àÇÐÁ¶¼º¹° ¹× ÀÌÀÇ ÇÕ¼º¹æ¹ý¡± À̺´¹«, ±èÀμö, ±èÁöÀ±, 2017³â 7¿ù 25ÀÏ, µî·Ï¹øÈ£: 10-1763315.
22. <±¹³»Æ¯ÇãÃâ¿ø> ¡°¾ÆÁ¶º¥Á¨°ú ÀÌÁß°áÇÕÀ» ÀÌ¿ëÇÑ 2,3-ÀÌÁßġȯ Àε¹ À¯µµÃ¼ÀÇ Á¦Á¶¹æ¹ý, À̸¦ ÀÌ¿ëÇÑ È­ÇÕ¹°, ¹× À̸¦ À¯È¿¼ººÐÀ¸·Î Æ÷ÇÔÇÏ´Â ¾Ï ¿¹¹æ ¶Ç´Â Ä¡·á¿ë ¾àÇÐÀû Á¶¼º¹°¡± ±èÀμö, ±èÇü½Ä, 2017³â 8¿ù 1ÀÏ, Ãâ¿ø¹øÈ£: 10-2017-0097610.
21. <±¹³»Æ¯ÇãÃâ¿ø> ¡°À̸®µã Ã˸Ÿ¦ ÀÌ¿ëÇÑ ¾Æ¹Ì³ëº¥Áî¾Ëµ¥È÷µåÀÇ Á¦Á¶¹æ¹ý, À̸¦ ÀÌ¿ëÇÑ È­ÇÕ¹° ¹× À̸¦ À¯È¿¼ººÐÀ¸·Î Æ÷ÇÔÇÏ´Â ¿°Áõ¼º ÁúȯÀÇ ¿¹¹æ ¶Ç´Â Ä¡·á¿ë ¾àÇÐÀû Á¶¼º¹°¡± ±èÀμö, ±èÇü½Ä, À̺´¹«, 2017³â 7¿ù 28ÀÏ, Ãâ¿ø¹øÈ£: 10-2017-0096491.
20. <±¹³»Æ¯ÇãÃâ¿ø> ¡°¿Á½ÃÀε¹ À¯µµÃ¼, ÀÌÀÇ Á¦Á¶¹æ¹ý ¹× À̸¦ À¯È¿¼ººÐÀ¸·Î Æ÷ÇÔÇÏ´Â ¾Ï ¿¹¹æ ¶Ç´Â Ä¡·á¿ë Á¶¼º¹°¡± ±èÀμö, ±èÇü½Ä, 2017³â 5¿ù 26ÀÏ, Ãâ¿ø¹øÈ£: 10-2017-0065385.
19. <±¹³»Æ¯Çãµî·Ï> ¡°·Îµã Ã˸ÅÇÏ C-H ¾Æ¸¶À̵åÈ­ ¹ÝÀÀ¿¡ ÀÇÇØ Á¦Á¶µÈ ½Å±ÔÇÑ Àε¹-2-Ä«º¹»ç¸¶À̵å À¯µµÃ¼ ¹× ÀÌÀÇ Á¦Á¶¹æ¹ý¡± ±èÀμö, 2017³â 5¿ù 25ÀÏ, µî·Ï¹øÈ£: 10-1742377.
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16. <±¹³»Æ¯ÇãÃâ¿ø> ¡°N-¾Æ·ÎÀÏ¿ì·¹¾Æ À¯µµÃ¼, ÀÌÀÇ Á¦Á¶¹æ¹ý ¹× À̸¦ À¯È¿¼ººÐÀ¸·Î Æ÷ÇÔÇÏ´Â ¾Ï ¿¹¹æ ¹× Ä¡·á¿ë Á¶¼º¹°¡± ±èÀμö, ±èÇü½Ä, 2017³â 4¿ù 17ÀÏ, Ãâ¿ø¹øÈ£: 10-2017-0049253.
15. <±¹³»Æ¯ÇãÃâ¿ø> ¡°¾ÈÆ®¶ó´Ò»ê À¯µµÃ¼ÀÇ Á¦Á¶¹æ¹ý°ú ±× ¾ÈÆ®¶ó´Ò»ê À¯µµÃ¼ÀÇ ÇÔ¿µÁõ ¿ëµµ¡± ±èÀμö, À̺´¹«, Á¤¿µÈÆ, Á¤±ÔÇõ, ±èÇü½Ä, È«¼ºÇö, 2017³â 4¿ù 6ÀÏ, Ãâ¿ø¹øÈ£: 10-2017-0044736.
14. <±¹³»Æ¯ÇãÃâ¿ø> ¡°½Å±Ô ½ºÆÄÀ̷ξÆÀ̼ÒÀε¹¸®³í À¯µµÃ¼, ÀÌÀÇ Á¦Á¶¹æ¹ý ¹× À̸¦ À¯È¿¼ººÐÀ¸·Î Æ÷ÇÔÇÏ´Â ¾Ï ¿¹¹æ ¹× Ä¡·á¿ë Á¶¼º¹°¡± ±èÀμö, ±èÇü½Ä, 2016³â 12¿ù 13ÀÏ, Ãâ¿ø¹øÈ£: 10-2016-0169438.
13. <±¹³»Æ¯ÇãÃâ¿ø> ¡°·Îµã Ã˸Ÿ¦ ÀÌ¿ëÇÑ ¾Æ¹ÌµåÈ­ Àε¹¸°ÀÇ Á¦Á¶¹æ¹ý, À̸¦ ÀÌ¿ëÇÑ È­ÇÔ¹° ¹× À̸¦ À¯È¿¼ººÐÀ¸·Î Æ÷ÇÔÇÏ´Â ¾Ï ¿¹¹æ ¹× Ä¡·á¿ë ¾àÇÐÀû Á¶¼º¹°¡± ±èÀμö, ±èÇü½Ä, 2016³â 9¿ù 26ÀÏ, Ãâ¿ø¹øÈ£: 10-2016-0123108.
12. <±¹³»Æ¯ÇãÃâ¿ø> ¡°¸ñ½ÃÇ÷ϻç½Å ¿°»ê¿°À» Æ÷ÇÔÇÏ´Â µ¿¹° ÁÖ»ç¿ë Ç×»ýÁ¦ Á¶¼º¹° ¹× ÀÌÀÇ Á¦Á¶¹æ¹ý¡± ±èÀμö, ¹Ú¼®¿ë, ÁöÇö±¸, 2016³â 9¿ù 12ÀÏ, Ãâ¿ø¹øÈ£: 10-2016-0117255.
11. <±¹³»Æ¯ÇãÃâ¿ø> ¡°Åڹ̻縣źÀ» Æ÷ÇÔÇÏ´Â °íü ºÐ»êü ¹× ÀÌÀÇ Á¦Á¶¹æ¹ý¡± ±èÀμö, ÀÌâ·¡, 2016³â 9¿ù 12ÀÏ, Ãâ¿ø¹øÈ£: 10-2016-0117255.
10. <±¹³»Æ¯ÇãÃâ¿ø> ¡°ÇÔ¿°Áõ È°¼ºÀ» °®´Â Çö󺸳ëÀ̵å°è È­ÇÕ¹°À» À¯È¿¼ººÐÀ¸·Î ÇÏ´Â ¿°ÁõÁúȯ ¿¹¹æ ¶Ç´Â Ä¡·á¿ë ¾àÇÐÁ¶¼º¹° ¹× ÀÌÀÇ ÇÕ¼º¹æ¹ý¡± À̺´¹«, ±èÀμö, ±èÁöÀ±, 2016³â 3¿ù 22ÀÏ, Ãâ¿ø¹øÈ£: 10-2016-0033946.
9. <±¹³»Æ¯Çãµî·Ï> ¡°½Ç·Îµµ½ÅÀÇ ¿ëÃâ ƯÀ̼ºÀÌ Çâ»óµÈ ¾àÁ¦ÇÐÀû Á¦Á¦¡± ±èÀμö, Á¤±¤µ·, ÁöÇö±¸, 2015³â 12¿ù 11ÀÏ, µî·Ï¹øÈ£: 10-1578627.
8. <±¹³»Æ¯ÇãÃâ¿ø> ¡°·Îµã Ã˸Ÿ¦ ÀÌ¿ëÇÑ ½Ã³î¸®³í À¯µµÃ¼ÀÇ ½Å±Ô Á¦Á¶¹æ¹ý¡± ±èÀμö, ÀÌÇÊÈ£, 2015³â 11¿ù 27ÀÏ, Ãâ¿ø¹øÈ£: 10-2015-0167209.
7. <±¹³»Æ¯ÇãÃâ¿ø> ¡°·Îµã Ã˸ÅÇÏ C-H ¾Æ¸¶À̵åÈ­ ¹ÝÀÀ¿¡ ÀÇÇØ Á¦Á¶µÈ ½Å±ÔÇÑ Àε¹-2-Ä«º¹»ç¸¶À̵å À¯µµÃ¼ ¹× ÀÌÀÇ Á¦Á¶¹æ¹ý¡± ±èÀμö, 2015³â 6¿ù 8ÀÏ, Ãâ¿ø¹øÈ£: 10-2015-0080822.
6. <±¹³»Æ¯ÇãÃâ¿ø> ¡°½Ç·Îµµ½ÅÀÇ ¿ëÃâ ƯÀ̼ºÀÌ Çâ»óµÈ ¾àÁ¦ÇÐÀû Á¦Á¦¡± ±èÀμö, Á¤±¤µ·, ÁöÇö±¸, 2014³â 12¿ù 22ÀÏ, Ãâ¿ø¹øÈ£: 10-2014-0185875.
5. <±¹³»Æ¯ÇãÃâ¿ø> ¡°·Îµã Ã˸Ÿ¦ ÀÌ¿ëÇÑ À̼ÒÀε¹¸° À¯µµÃ¼ÀÇ ÇÕ¼º¹æ¹ý¡± ±èÀμö, ¹Ú¾ðÁ¤, 2012³â 1¿ù 31ÀÏ, Ãâ¿ø¹øÈ£: 10-2012-0009903.
4. <±¹³»Æ¯Çãµî·Ï> ¡°(1S,2S,3S,4S)-5-¾Æ¹Ì³ë»çÀÌŬ·ÎÆæź-1,2,3,4-Å×Æ®¶ó¿ÃÀ» Æ÷ÇÔÇÏ´Â Ç׺ñ¸¸ Á¶¼º¹°¡± Á¤¿µÈÆ, Áö¿ÁÇ¥, ¿ÀÁ¼·, ¾ÈÀº°æ, ÀÌÁ¤¾Æ, ±èÀμö, ÀÌ°æÀÏ, 2011³â 10¿ù 12ÀÏ, µî·Ï¹øÈ£: 10-1074954.
3. <±¹Á¦Æ¯ÇãÃâ¿ø> ¡°Anti-Obesity Compositon Containing (1S,2S,3S,4S)-5-Aminocyclopentane-1,2,3,4-Tetraol¡± Á¤¿µÈÆ, Áö¿ÁÇ¥, ¿ÀÁ¼·, ¾ÈÀº°æ, ÀÌÁ¤¾Æ, ±èÀμö, ÀÌ°æÀÏ, 2011³â 8¿ù 4ÀÏ, Ãâ¿ø¹øÈ£: WO2011/093664 A2.
2. <±¹³»Æ¯ÇãÃâ¿ø> ¡°ÀüÀÌ±Ý¼Ó Ã˸Ÿ¦ ÀÌ¿ëÇÑ º¥Áî¾Æ¸¶À̵å°è È­ÇÕ¹°ÀÇ Ä«º¸´ÒÈ­ ¹æ¹ý¡± ±èÀμö, ¹ÚÁöÇý, ¹Ú±âÈ£, 2011³â 4¿ù 25ÀÏ, Ãâ¿ø¹øÈ£: 10-2011-0038321.
1. <±¹³»Æ¯ÇãÃâ¿ø> ¡°(+) Ç÷ç¹Ù½ºÅ¸Æ¾ÀÇ »õ·Î¿î Á¦Á¶¹æ¹ý¡± ±èÀμö, ±è¾ÖÁø, 2011³â 2¿ù 25ÀÏ, Ãâ¿ø¹øÈ£: 10-2011-0016922.
1. ¡°C(sp2)-H Functionalization of Indolines at the C7-Position¡± Mishra, N. K.; Kim, I. S.* In "Transition-Metal-Catalyzed C-H Functionalization of Heterocycles", Edited by Punniyamurthy, T.; Kumar. A., John Wiley & Sons, 251-317, 2023. ISBN 9781119774136.