Sukbok Chang, Ph.D. - Publications

Affiliations: 
Chemistry Korea Advanced Institute of Science and Technology, Daejeon, South Korea 
Website:
http://sbchang.kaist.ac.kr

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Year Citation  Score
2021 Hong SY, Hwang Y, Lee M, Chang S. Mechanism-Guided Development of Transition-Metal-Catalyzed C-N Bond-Forming Reactions Using Dioxazolones as the Versatile Amidating Source. Accounts of Chemical Research. PMID 33979133 DOI: 10.1021/acs.accounts.1c00198  0.312
2021 Lee J, Jin S, Kim D, Hong SH, Chang S. Cobalt-Catalyzed Intermolecular C-H Amidation of Unactivated Alkanes. Journal of the American Chemical Society. PMID 33780628 DOI: 10.1021/jacs.1c01524  0.48
2020 Kim Y, Heo J, Kim D, Chang S, Seo S. Ring-opening functionalizations of unstrained cyclic amines enabled by difluorocarbene transfer. Nature Communications. 11: 4761. PMID 32958762 DOI: 10.1038/S41467-020-18557-8  0.332
2020 Zhang J, Chang S. cine-Silylative Ring-Opening of α-Methyl Azacycles Enabled by the Silylium-Induced C-N Bond Cleavage. Journal of the American Chemical Society. PMID 32627547 DOI: 10.1021/Jacs.0C05241  0.347
2020 Lee M, Jung H, Kim D, Park JW, Chang S. Modular Tuning of Electrophilic Reactivity of Iridium Nitrenoids for the Intermolecular Selective α-Amidation of β-Keto Esters. Journal of the American Chemical Society. PMID 32605371 DOI: 10.1021/Jacs.0C04344  0.313
2020 Lee J, Lee J, Jung H, Kim D, Park J, Chang S. A Versatile Cp*Co(III)(LX) Catalyst System for Selective Intramolecular C-H Amidation Reactions. Journal of the American Chemical Society. PMID 32551631 DOI: 10.1021/Jacs.0C04448  0.388
2020 Hwang Y, Jung H, Lee E, Kim D, Chang S. Quantitative Analysis on Two-Point Ligand Modulation of Iridium Catalysts for Chemodivergent C-H Amidation. Journal of the American Chemical Society. PMID 32307984 DOI: 10.1021/Jacs.0C02079  0.382
2020 Xie W, Heo J, Kim D, Chang S. Copper-Catalyzed Direct C-H Alkylation of Polyfluoroarenes by Using Hydrocarbons as an Alkylating Source. Journal of the American Chemical Society. PMID 32233362 DOI: 10.1021/Jacs.0C00169  0.383
2020 Jung H, Keum H, Kweon J, Chang S. Tuning Triplet Energy Transfer of Hydroxamates as the Nitrene Precursor for Intramolecular C()-H Amidation. Journal of the American Chemical Society. PMID 32129618 DOI: 10.1021/Jacs.0C00868  0.323
2020 Bordiga S, Chang S, Chen J, Crudden C, Dey A, Fornasiero P, Gunnoe TB, Jones CW, Linic S, Ma D, Maseras F, Ooi T, Cuenya BR, Sautet P, Scott SL, et al. Excellence versus Diversity? Not an Either/Or Choice Acs Catalysis. 10: 7310-7311. DOI: 10.1021/Acscatal.0C02590  0.574
2020 Kim E, Jeon HJ, Park S, Chang S. Double Hydroboration of Quinolines via Borane Catalysis: Diastereoselective One Pot Synthesis of 3‐Hydroxytetrahydroquinolines Advanced Synthesis & Catalysis. 362: 308-313. DOI: 10.1002/Adsc.201901050  0.546
2019 Jung H, Schrader M, Kim D, Baik MH, Park Y, Chang S. Harnessing Secondary Coordination Sphere Interactions Enables the Selective Amidation of Benzylic C-H Bonds. Journal of the American Chemical Society. PMID 31448912 DOI: 10.1021/Jacs.9B07795  0.381
2019 Jung HY, Chang S, Hong S. Strategic Approach to the Metamorphosis of γ-Lactones to NH γ-Lactams via Reductive Cleavage and C-H Amidation. Organic Letters. PMID 31418279 DOI: 10.1021/Acs.Orglett.9B02673  0.32
2019 Jeong J, Kim H, Hazra CK, Chang S, Baik MH. Disrotatory Ring-Opening of Furans Gives Stereocontrol. The Journal of Organic Chemistry. PMID 31408341 DOI: 10.1021/Acs.Joc.9B01627  0.777
2019 Kim J, Kim S, Kim D, Chang S. Ru-Catalyzed Deoxygenative Regioselective C8-H Arylation of Quinoline N-Oxides. The Journal of Organic Chemistry. PMID 31322347 DOI: 10.1021/Acs.Joc.9B01548  0.376
2019 Hong SY, Chang S. Stereodefined Access to Lactams via Olefin Difunctionlization: Iridium Nitrenoids as a Motif of LUMO-Controlled Dipoles. Journal of the American Chemical Society. PMID 31180662 DOI: 10.1021/Jacs.9B04317  0.331
2019 Wang H, Park Y, Bai Z, Chang S, He G, Chen G. Iridium-Catalyzed Enantioselective C(sp3)-H Amidation Controlled by Attractive Noncovalent Interactions. Journal of the American Chemical Society. PMID 30978019 DOI: 10.1021/Jacs.9B02811  0.409
2019 Chang S, Zhang J, Jung H, Kim DW, Park S. Sequential C-H Borylation and N-Demethylation of 1,1'-Biphenylamines: An Alternative Route to Polycyclic BN-Heteroarenes. Angewandte Chemie (International Ed. in English). PMID 30941843 DOI: 10.1002/Anie.201902499  0.552
2019 Huh S, Hong SY, Chang S. Synthetic Utility of N-Benzoyloxyamides as an Alternative Precursor of Acylnitrenoids for γ-Lactam Formation. Organic Letters. PMID 30920230 DOI: 10.1021/Acs.Orglett.9B00791  0.394
2019 Aspuru-Guzik A, Baik MH, Balasubramanian S, Banerjee R, Bart S, Borduas-Dedekind N, Chang S, Chen P, Corminboeuf C, Coudert FX, Cronin L, Crudden C, Cuk T, Doyle AG, Fan C, et al. Charting a course for chemistry. Nature Chemistry. 11: 286-294. PMID 30903035 DOI: 10.1038/S41557-019-0236-7  0.727
2019 Chang S, Jeong E, Heo J, Park S. Alkoxide-Promoted Selective Hydroboration of N-Heteroarenes: Pivotal Roles of in situ Generated BH3 in the Dearomatization Process. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 30882934 DOI: 10.1002/Chem.201901214  0.547
2019 Kim J, Shin K, Jin S, Kim D, Chang S. Oxidatively Induced Reductive Elimination: Exploring the Scope and Catalyst Systems with Ir, Rh, and Ru Complexes. Journal of the American Chemical Society. PMID 30762365 DOI: 10.1021/Jacs.9B00364  0.383
2019 Jeon C, Kim DW, Chang S, Kim JG, Seo M. Synthesis of Polypropylene via Catalytic Deoxygenation of Poly(methyl acrylate) Acs Macro Letters. 8: 1172-1178. DOI: 10.1021/Acsmacrolett.9B00522  0.729
2019 Yang L, Liu Y, Park Y, Park S, Chang S. Ni-Mediated Generation of “CN” Unit from Formamide and Its Catalysis in the Cyanation Reactions Acs Catalysis. 9: 3360-3365. DOI: 10.1021/Acscatal.8B05111  0.325
2019 Zhang J, Hazra CK, Park S, Chang S. Metal‐Free Carbocyclization of Homoallylic Silyl Ethers Leading to Cyclopropanes and Cyclobutanes Asian Journal of Organic Chemistry. 8: 1637-1640. DOI: 10.1002/Ajoc.201900270  0.783
2018 Kim H, Heo J, Kim J, Baik MH, Chang S. Copper-Mediated Amination of Aryl C-H Bonds with the Direct Use of Aqueous Ammonia via a Disproportionation Pathway. Journal of the American Chemical Society. PMID 30346156 DOI: 10.1021/Jacs.8B08826  0.59
2018 Zhang J, Park S, Chang S. Catalytic Access to Bridged Sila-N-Heterocycles from Piperidines via Cascade sp3 and sp2 C-Si Bond Formation. Journal of the American Chemical Society. PMID 30269485 DOI: 10.1021/Jacs.8B08733  0.555
2018 Hong SY, Son J, Kim D, Chang S. Ir(III)-Catalyzed Stereoselective Haloamidation of Alkynes Enabled by Ligand Participation. Journal of the American Chemical Society. PMID 30217108 DOI: 10.1021/Jacs.8B08134  0.333
2018 Chang S, Hwang Y, Park Y, Kim YB, Kim D. Revisiting Arene C(sp2)-H Amidation via Intramolecular Transfer of Iridium Nitrenoids: Evidence for a Spirocyclization Pathway. Angewandte Chemie (International Ed. in English). PMID 30151953 DOI: 10.1002/Anie.201808892  0.398
2018 Xie W, Park SW, Jung H, Kim D, Baik MH, Chang S. Conjugate Addition of Perfluoroarenes to α,β-Unsaturated Carbonyls Enabled by an Alkoxide-Hydrosilane System: Implication of a Radical Pathway. Journal of the American Chemical Society. PMID 29990423 DOI: 10.1021/Jacs.8B05744  0.335
2018 Kim Y, Park Y, Chang S. Delineating Physical Organic Parameters in Site-Selective C-H Functionalization of Indoles. Acs Central Science. 4: 768-775. PMID 29974073 DOI: 10.1021/Acscentsci.8B00264  0.323
2018 Zhang J, Park S, Chang S. Piers' borane-mediated hydrosilylation of epoxides and cyclic ethers. Chemical Communications (Cambridge, England). PMID 29901036 DOI: 10.1039/C8Cc03741H  0.526
2018 Hong SY, Park Y, Hwang Y, Kim YB, Baik MH, Chang S. Selective formation of γ-lactams via C-H amidation enabled by tailored iridium catalysts. Science (New York, N.Y.). 359: 1016-1021. PMID 29496875 DOI: 10.1126/Science.Aap7503  0.375
2018 Chang S, Kim E, Park S. Silylative Reductive Amination of a,b-Unsaturated Aldehydes: A Convenient Synthetic Route to b-Silylated Secondary Amines. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 29488264 DOI: 10.1002/Chem.201800958  0.555
2018 Chang S, Park J. Comparative reactivity and selectivity of group 9 Cp*M(III) catalysts in the C-H bond functionalization. Chemistry, An Asian Journal. PMID 29479837 DOI: 10.1002/Asia.201800204  0.348
2018 Shin K, Park Y, Baik MH, Chang S. Iridium-catalysed arylation of C-H bonds enabled by oxidatively induced reductive elimination. Nature Chemistry. 10: 218-224. PMID 29359741 DOI: 10.1038/Nchem.2900  0.382
2018 Hazra CK, Jeong J, Kim H, Baik MH, Park S, Chang S. Reductive Carbocyclization of Homoallylic Alcohols to syn- Cyclobutanes via Boron-Catalyzed Dual Ring-Closing Pathway. Angewandte Chemie (International Ed. in English). PMID 29327487 DOI: 10.1002/Anie.201713285  0.784
2017 Kim H, Chang S. The Use of Ammonia as an Ultimate Amino Source in the Transition Metal-Catalyzed C-H Amination. Accounts of Chemical Research. 50: 482-486. PMID 28945419 DOI: 10.1021/Acs.Accounts.6B00489  0.561
2017 Chang S, Zhang J, Park S. In Situ Generated Piers' Borane-Catalyzed Selective C-O Bond Cleavage of Sugars with Hydrosilanes. Angewandte Chemie (International Ed. in English). PMID 28901040 DOI: 10.1002/Anie.201708109  0.539
2017 Bagal DB, Park SW, Song HJ, Chang S. Visible light sensitization of benzoyl azides: cascade cyclization toward oxindoles via a non-nitrene pathway. Chemical Communications (Cambridge, England). PMID 28736779 DOI: 10.1039/C7Cc04852A  0.774
2017 Chang S, Hwang Y, Park Y. Mechanism-Driven Approach to Develop a Mild and Versatile C-H Amidation via Ir(III) Catalysis. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 28556520 DOI: 10.1002/Chem.201702397  0.384
2017 Park J, Lee J, Chang S. Iterative C-H Functionalization Leading to Multiple Amidations of Anilides. Angewandte Chemie (International Ed. in English). PMID 28294489 DOI: 10.1002/Anie.201701138  0.326
2017 Kim H, Chang S. Intramolecular Amido Transfer Leading to Structurally Diverse Nitrogen-Containing Macrocycles. Angewandte Chemie (International Ed. in English). PMID 28185375 DOI: 10.1002/Anie.201700113  0.402
2017 Chang S, Park S. Catalytic Dearomatization of N-Heteroarenes with Silicon and Boron Compounds. Angewandte Chemie (International Ed. in English). PMID 28164423 DOI: 10.1002/Anie.201612140  0.528
2017 Hong SY, Jeong J, Chang S. [4+2] or [4+1] Annulation: Changing the Reaction Pathway of a Rhodium-Catalyzed Process by Tuning the Cp Ligand. Angewandte Chemie (International Ed. in English). PMID 28112471 DOI: 10.1002/Anie.201612559  0.334
2017 Park Y, Kim Y, Chang S. Transition Metal-Catalyzed C-H Amination: Scope, Mechanism, and Applications. Chemical Reviews. PMID 28051855 DOI: 10.1021/Acs.Chemrev.6B00644  0.378
2017 Gandhamsetty N, Park S, Chang S. Boron-Catalyzed Hydrogenative Reduction of Substituted Quinolines to Tetrahydroquinolines with Hydrosilanes Synlett. 28: 2396-2400. DOI: 10.1055/S-0036-1588442  0.575
2017 Chang S, Zhang J, Park S. In Situ Generated Piers' Borane‐Catalyzed Selective C‐O Bond Cleavage of Sugars with Hydrosilanes Angewandte Chemie. DOI: 10.1002/Ange.201708109  0.488
2017 Park S, Chang S. Katalytische Desaromatisierung von N-Heteroarenen mit Silicium- und Borverbindungen Angewandte Chemie. 129: 7828-7847. DOI: 10.1002/Ange.201612140  0.461
2017 Shin K, Joung S, Kim Y, Chang S. Selective Synthesis of Silacycles by Borane-Catalyzed Domino Hydrosilylation of Proximal Unsaturated Bonds: Tunable Approach to 1,n-Diols Advanced Synthesis & Catalysis. 359: 3428-3436. DOI: 10.1002/Adsc.201700698  0.405
2016 Jeong J, Park S, Chang S. Iridium-catalyzed selective 1,2-hydrosilylation of N-heterocycles. Chemical Science. 7: 5362-5370. PMID 30155189 DOI: 10.1039/C6Sc01037G  0.572
2016 Kim Y, Dateer RB, Chang S. Borane-Catalyzed Selective Hydrosilylation of Internal Ynamides Leading to β-Silyl (Z)-Enamides. Organic Letters. PMID 27936799 DOI: 10.1021/Acs.Orglett.6B03485  0.316
2016 Hazra CK, Gandhamsetty N, Park S, Chang S. Borane catalysed ring opening and closing cascades of furans leading to silicon functionalized synthetic intermediates. Nature Communications. 7: 13431. PMID 27892459 DOI: 10.1038/Ncomms13431  0.798
2016 Park Y, Heo J, Baik MH, Chang S. Why is the Ir(III)-Mediated Amido Transfer Much Faster Than the Rh(III)-Mediated Reaction? - A Combined Experimental and Computational Study. Journal of the American Chemical Society. PMID 27690406 DOI: 10.1021/Jacs.6B08211  0.39
2016 Xie W, Yoon JH, Chang S. (NHC)Cu-Catalyzed Mild C-H Amidation of (Hetero)Arenes with Deprotectable Carbamates: Scope and Mechanistic Studies. Journal of the American Chemical Society. PMID 27585065 DOI: 10.1021/Jacs.6B07486  0.387
2016 Chang SW, Kim HI, Kim GH, Park SJ, Kim IB. Increased Expression of Osteopontin in Retinal Degeneration Induced by Blue Light-Emitting Diode Exposure in Mice. Frontiers in Molecular Neuroscience. 9: 58. PMID 27504084 DOI: 10.3389/fnmol.2016.00058  0.391
2016 Chang SH, Cho KC, Yu KN, Hong SH, Park S, Lee AY, Kim S, Lee S, Kang JW, Chae C, Park J, Kim KP, Cho MH. Alpha 1-antitrypsin activates lung cancer cell survival by acting on cap-dependent protein translation, vesicle-mediated transport, and metastasis. Oncotarget. PMID 27448969 DOI: 10.18632/Oncotarget.10695  0.477
2016 Park JB, Lee SH, Kim KJ, Lee GY, Yang JM, Kim DW, Lee SJ, Lee CH, Park EJ, Kim KH, Eun HC, Chang SE, Moon KC, Kim SH, Kim SJ, et al. Clinical Features and Awareness of Hand Eczema in Korea. Annals of Dermatology. 28: 335-343. PMID 27274632 DOI: 10.5021/ad.2016.28.3.335  0.427
2016 Ajitha MJ, Huang KW, Kwak J, Kim HJ, Chang S, Jung Y. A potential role of a substrate as a base for the deprotonation pathway in Rh-catalysed C-H amination of heteroarenes: DFT insights. Dalton Transactions (Cambridge, England : 2003). PMID 27071025 DOI: 10.1039/C6Dt00686H  0.378
2016 Gong C, Yao S, Gomes AR, Man EP, Lee HJ, Gong G, Chang S, Kim SB, Fujino K, Kim SW, Park SK, Lee JW, Lee MH, Khoo US, et al. BRCA1 positively regulates FOXO3 expression by restricting FOXO3 gene methylation and epigenetic silencing through targeting EZH2 in breast cancer. Oncogenesis. 5: e214. PMID 27043660 DOI: 10.1038/oncsis.2016.23  0.479
2016 Kim Y, Park J, Chang S. A Direct Access to 7-Aminoindoles via Iridium-Catalyzed Mild C-H Amidation of N-Pivaloylindoles with Organic Azides. Organic Letters. PMID 27023669 DOI: 10.1021/Acs.Orglett.6B00662  0.384
2016 Hyun MS, Park JP, Seo D, Chang SJ, Lee SJ, Lee SY, Kwak K, Park TJ. Enzymatic formation of carbohydrate rings catalyzed by single-walled carbon nanotubes. Bioprocess and Biosystems Engineering. PMID 26946491 DOI: 10.1007/s00449-016-1553-5  0.375
2016 Chang SC, Zhuang ZX, Lin MJ, Cheng CY, Lin TY, Jea YS, Huang SY. Effects of monochromatic light sources on sex hormone levels in serum and on semen quality of ganders. Animal Reproduction Science. PMID 26919910 DOI: 10.1016/j.anireprosci.2016.02.012  0.396
2016 Khachatryan V, Sirunyan AM, Tumasyan A, Adam W, Asilar E, Bergauer T, Brandstetter J, Brondolin E, Dragicevic M, Erö J, Friedl M, Frühwirth R, Ghete VM, Hartl C, Hörmann N, ... ... Chang S, et al. Measurement of differential cross sections for Higgs boson production in the diphoton decay channel in pp collisions at [Formula: see text]. The European Physical Journal. C, Particles and Fields. 76: 13. PMID 26855607 DOI: 10.1140/Epjc/S10052-015-3853-3  0.387
2016 Tsai CT, Hsieh CS, Chang SN, Chuang EY, Ueng KC, Tsai CF, Lin TH, Wu CK, Lee JK, Lin LY, Wang YC, Yu CC, Lai LP, Tseng CD, Hwang JJ, et al. Genome-wide screening identifies a KCNIP1 copy number variant as a genetic predictor for atrial fibrillation. Nature Communications. 7: 10190. PMID 26831368 DOI: 10.1038/ncomms10190  0.388
2016 Hong SY, Kwak J, Chang S. Rhodium-catalyzed selective CH functionalization of NNN tridentate chelating compounds via a rollover pathway. Chemical Communications (Cambridge, England). PMID 26805059 DOI: 10.1039/C5Cc09960A  0.395
2016 Kim EK, Choi JH, Song YB, Hahn JY, Chang SA, Park SJ, Lee SC, Choi SH, Choe YH, Park SW, Gwon HC. A protective role of early collateral blood flow in patients with ST-segment elevation myocardial infarction. American Heart Journal. 171: 56-63. PMID 26699601 DOI: 10.1016/j.ahj.2015.10.016  0.357
2016 Kim H, Park G, Park J, Chang S. A Facile Access to Primary Alkylamines and Anilines via Ir(III)-Catalyzed C-H Amidation Using Azidoformates Acs Catalysis. 6: 5922-5929. DOI: 10.1021/Acscatal.6B01869  0.584
2016 Kim H, Chang S. Transition-Metal-Mediated Direct C–H Amination of Hydrocarbons with Amine Reactants: The Most Desirable but Challenging C–N Bond-Formation Approach Acs Catalysis. 6: 2341-2351. DOI: 10.1021/Acscatal.6B00293  0.589
2016 Chang S, Gandhamsetty N, Jee S. Diastereoselective Construction of α-Silyltetrahydropyranols via Silyl-oxa-Prins Cyclization European Journal of Organic Chemistry. DOI: 10.1002/Ejoc.201601631  0.305
2015 Xie W, Chang S. [Cu(NHC)]-Catalyzed CH Allylation and Alkenylation of both Electron-Deficient and Electron-Rich (Hetero)arenes with Allyl Halides. Angewandte Chemie (International Ed. in English). PMID 26695120 DOI: 10.1002/Anie.201510180  0.398
2015 Oh JK, Lim MK, Yun EH, Choi MH, Hong ST, Chang SH, Park SK, Cho SI, Kim DH, Yoo KY, Shin HR. Cohort Profile: Community-based prospective cohort from the National Cancer Center, Korea. International Journal of Epidemiology. PMID 26686839 DOI: 10.1093/ije/dyv302  0.368
2015 Shin SY, Shin SI, Kye SB, Hong J, Paeng JY, Chang SW, Yang SM. The Effects of Defect Type and Depth, and Measurement Direction on the Implant Stability Quotient Value. The Journal of Oral Implantology. 41: 652-656. PMID 26653132 DOI: 10.1563/AAID-JOI-D-13-0031  0.379
2015 Dateer RB, Chang S. Rh(III)-Catalyzed C-H Cyclization of Arylnitrones with Diazo Compounds: Access to N-Hydroxyindolines. Organic Letters. PMID 26651398 DOI: 10.1021/Acs.Orglett.5B03273  0.386
2015 Khachatryan V, Sirunyan AM, Tumasyan A, Adam W, Bergauer T, Dragicevic M, Erö J, Friedl M, Frühwirth R, Ghete VM, Hartl C, Hörmann N, Hrubec J, Jeitler M, Kiesenhofer W, ... Chang S, et al. Measurement of the differential cross section for top quark pair production in pp collisions at [Formula: see text]. The European Physical Journal. C, Particles and Fields. 75: 542. PMID 26640401 DOI: 10.1140/Epjc/S10052-015-3709-X  0.382
2015 Cameron C, Lee HY, Anderson C, Byars-Winston A, Baldwin CD, Chang S. The Role of Scientific Communication Skills in Trainees' Intention to Pursue Biomedical Research Careers: A Social Cognitive Analysis. Cbe Life Sciences Education. 14. PMID 26628562 DOI: 10.1187/cbe.14-09-0152  0.306
2015 Kang KS, Lee HU, Kim MI, Park SY, Chang SJ, Park JH, Huh YS, Lee J, Yang M, Lee YC, Park HG. In-vitro cytotoxicity assessment of carbon-nanodot-conjugated Fe-aminoclay (CD-FeAC) and its bio-imaging applications. Journal of Nanobiotechnology. 13: 88. PMID 26612177 DOI: 10.1186/S12951-015-0151-Z  0.363
2015 Kim KW, Park SH, Oh DH, Lee SH, Lim KS, Joo K, Chun YS, Chang SI, Min KM, Kim JC. Ribonuclease 5 coordinates signals for the regulation of intraocular pressure and inhibits neural apoptosis as a novel multi-functional anti-glaucomatous strategy. Biochimica Et Biophysica Acta. PMID 26581172 DOI: 10.1016/j.bbadis.2015.11.005  0.396
2015 Gandhamsetty N, Park S, Chang S. Selective Silylative Reduction of Pyridines Leading to Structurally Diverse Azacyclic Compounds with the Formation of sp3 C-Si Bonds. Journal of the American Chemical Society. PMID 26580152 DOI: 10.1021/Jacs.5B09209  0.531
2015 Khachatryan V, Sirunyan AM, Tumasyan A, Adam W, Bergauer T, Dragicevic M, Erö J, Friedl M, Frühwirth R, Ghete VM, Hartl C, Hörmann N, Hrubec J, Jeitler M, Kiesenhofer W, ... Chang S, et al. Measurements of the [Formula: see text][Formula: see text] production cross sections in the [Formula: see text] channel in proton-proton collisions at [Formula: see text] and [Formula: see text] and combined constraints on triple gauge couplings. The European Physical Journal. C, Particles and Fields. 75: 511. PMID 26549982 DOI: 10.1140/Epjc/S10052-015-3706-0  0.398
2015 Kim Y, Chang S. Borane-Catalyzed Reductive α-Silylation of Conjugated Esters and Amides Leaving Carbonyl Groups Intact. Angewandte Chemie (International Ed. in English). PMID 26549843 DOI: 10.1002/Anie.201508669  0.326
2015 Kim JH, Cho MJ, Hong JP, Bae JN, Cho SJ, Hahm BJ, Lee DW, Park JI, Lee JY, Jeon HJ, Chang SM. Gender Differences in Depressive Symptom Profile: Results from Nationwide General Population Surveys in Korea. Journal of Korean Medical Science. 30: 1659-66. PMID 26539012 DOI: 10.3346/jkms.2015.30.11.1659  0.385
2015 Kim HO, Yang YS, Ko HC, Kim GM, Cho SH, Seo YJ, Son SW, Lee JR, Lee JS, Chang SE, Che JW, Park CW. Maintenance Therapy of Facial Seborrheic Dermatitis with 0.1% Tacrolimus Ointment. Annals of Dermatology. 27: 523-30. PMID 26512166 DOI: 10.5021/ad.2015.27.5.523  0.379
2015 Hwang JW, Park SJ, Oh SY, Chang SA, Lee SC, Park SW, Kim DK. The Risk Factors That Predict Chronic Hypertension After Delivery in Women With a History of Hypertensive Disorders of Pregnancy. Medicine. 94: e1747. PMID 26496291 DOI: 10.1097/MD.0000000000001747  0.38
2015 Kim DW, Joung S, Kim JG, Chang S. Metal-Free Hydrosilylation Polymerization by Borane Catalyst. Angewandte Chemie (International Ed. in English). PMID 26474096 DOI: 10.1002/Anie.201507863  0.736
2015 Han YE, Lim A, Park SH, Chang S, Lee SH, Ho WK. Rac-mediated actin remodeling and myosin II are involved in KATP channel trafficking in pancreatic β-cells. Experimental & Molecular Medicine. 47: e190. PMID 26471000 DOI: 10.1038/emm.2015.72  0.381
2015 Gwon D, Hwang H, Kim HK, Marder SR, Chang S. Synthesis of 8-Aminoquinolines by Using Carbamate Reagents: Facile Installation and Deprotection of Practical Amidating Groups. Chemistry (Weinheim An Der Bergstrasse, Germany). PMID 26463666 DOI: 10.1002/Chem.201503511  0.37
2015 Seo JS, Min BS, Kwon YB, Lee SY, Cho JM, Park KH, Yang YJ, Maeng KE, Chang SJ, Kim DI. Characteristics of human cell line, F2N78, for the production of recombinant antibody in fed-batch and perfusion cultures. Journal of Bioscience and Bioengineering. PMID 26454770 DOI: 10.1016/j.jbiosc.2015.07.007  0.312
2015 Kim J, Park SW, Baik MH, Chang S. Complete Switch of Selectivity in the C-H Alkenylation and Hydroarylation Catalyzed by Iridium: The Role of Directing Groups. Journal of the American Chemical Society. PMID 26449465 DOI: 10.1021/Jacs.5B09824  0.54
2015 Kim HY, Lee SC, Park SJ, Choi JO, Chang SA, Kim SM, Choe YH, Oh JK, Park SW. A Rare Case of Iatrogenic Deep Neck Infection Secondary to Hypopharyngeal Injury Caused by the Transesophageal Echocardiography. Journal of Cardiovascular Ultrasound. 23: 181-185. PMID 26448827 DOI: 10.4250/jcu.2015.23.3.181  0.469
2015 Moon JR, Song J, Huh J, Kang IS, Park SW, Chang SA, Yang JH, Jun TG. Analysis of Cardiovascular Risk Factors in Adults with Congenital Heart Disease. Korean Circulation Journal. 45: 416-23. PMID 26413110 DOI: 10.4070/kcj.2015.45.5.416  0.355
2015 Kwon OB, Lee JH, Kim HJ, Lee S, Lee S, Jeong MJ, Kim SJ, Jo HJ, Ko B, Chang S, Park SK, Choi YB, Bailey CH, Kandel ER, Kim JH. Dopamine Regulation of Amygdala Inhibitory Circuits for Expression of Learned Fear. Neuron. PMID 26412489 DOI: 10.1016/j.neuron.2015.09.001  0.467
2015 Park J, Chang S. Comparative Catalytic Activity of Group 9 [Cp*M(III) ] Complexes: Cobalt-Catalyzed CH Amidation of Arenes with Dioxazolones as Amidating Reagents. Angewandte Chemie (International Ed. in English). PMID 26404541 DOI: 10.1002/Anie.201505820  0.369
2015 Ma SH, Jung W, Weiderpass E, Jang J, Hwang Y, Ahn C, Ko KP, Chang SH, Shin HR, Yoo KY, Park SK. Impact of alcohol drinking on gastric cancer development according to Helicobacter pylori infection status. British Journal of Cancer. PMID 26379079 DOI: 10.1038/bjc.2015.333  0.381
2015 Choi JH, Cho CW, Kim JH, Park SH, Chang S, Yu YB. Liquid Crystal Formulation and Optimization of Anti-Microbial Polyherbal Ointment. Journal of Nanoscience and Nanotechnology. 15: 5656-9. PMID 26369133 DOI: 10.1166/JNN.2015.10461  0.378
2015 Moon JR, Kang DR, Song J, Huh J, Kang IS, Chang SA, Park SW, Lee HJ. Clinical and Prognostic Value of Depressive Symptoms and N-Terminal Pro-B-Type Natriuretic Peptide in Patients With Eisenmenger Syndrome. Psychosomatic Medicine. 77: 816-22. PMID 26355727 DOI: 10.1097/PSY.0000000000000201  0.377
2015 Kim EK, Lee SC, Hwang JW, Chang SA, Park SJ, On YK, Park KM, Choe YH, Kim SM, Park SW, Oh JK. Differences in apical and non-apical types of hypertrophic cardiomyopathy: a prospective analysis of clinical, echocardiographic, and cardiac magnetic resonance findings and outcome from 350 patients. European Heart Journal Cardiovascular Imaging. PMID 26245912 DOI: 10.1093/ehjci/jev192  0.469
2015 Cho EJ, Son MK, Park SJ, Park SW, Chang SA, Lee SC, Kang IS. Aggravating factors associated with the severity of aortic regurgitation and clinical characteristics of patients with quadricuspid aortic valve. The Journal of Heart Valve Disease. 24: 148-55. PMID 26237781  0.366
2015 Khachatryan V, Sirunyan AM, Tumasyan A, Adam W, Bergauer T, Dragicevic M, Erö J, Friedl M, Frühwirth R, Ghete VM, Hartl C, Hörmann N, Hrubec J, Jeitler M, Kiesenhofer W, ... ... Chang S, et al. Constraints on the pMSSM, AMSB model and on other models from the search for long-lived charged particles in proton-proton collisions at [Formula: see text]. The European Physical Journal. C, Particles and Fields. 75: 325. PMID 26213486 DOI: 10.1140/Epjc/S10052-015-3533-3  0.371
2015 Kim SB, Lee DW, Chang SK, Ok KM. Pb3[C6(CH3)3(CO2)3H6]2[DMF]3: first layered Pb-Kemp's triacid complex. Chemical Communications (Cambridge, England). PMID 26208140 DOI: 10.1039/c5cc05360a  0.314
2015 Seo HY, Lee SP, Park JB, Lee JM, Park EA, Chang SA, Kim HK, Park SJ, Lee W, Kim YJ, Lee SC, Park SW, Sohn DW, Choe YH. Discrepancies in Left Ventricular Mass Calculation Based on Echocardiography and Cardiovascular Magnetic Resonance Measurements in Patients with Left Ventricular Hypertrophy. Journal of the American Society of Echocardiography : Official Publication of the American Society of Echocardiography. PMID 26194306 DOI: 10.1016/j.echo.2015.06.009  0.371
2015 Khachatryan V, Sirunyan AM, Tumasyan A, Adam W, Bergauer T, Dragicevic M, Erö J, Friedl M, Frühwirth R, Ghete VM, Hartl C, Hörmann N, Hrubec J, Jeitler M, Kiesenhofer W, ... ... Chang S, et al. Distributions of topological observables in inclusive three- and four-jet events in pp collisions at [Formula: see text][Formula: see text]. The European Physical Journal. C, Particles and Fields. 75: 302. PMID 26190937 DOI: 10.1140/Epjc/S10052-015-3491-9  0.375
2015 Khachatryan V, Sirunyan AM, Tumasyan A, Adam W, Bergauer T, Dragicevic M, Erö J, Friedl M, Frühwirth R, Ghete VM, Hartl C, Hörmann N, Hrubec J, Jeitler M, Kiesenhofer W, ... ... Chang S, et al. Evidence for Collective Multiparticle Correlations in p-Pb Collisions. Physical Review Letters. 115: 012301. PMID 26182092 DOI: 10.1103/Physrevlett.115.012301  0.368
2015 Park S, Hatim Sulaiman A, Srisurapanont M, Chang SM, Liu CY, Bautista D, Ge L, Choon Chua H, Pyo Hong J. The association of suicide risk with negative life events and social support according to gender in Asian patients with major depressive disorder. Psychiatry Research. 228: 277-82. PMID 26160206 DOI: 10.1016/j.psychres.2015.06.032  0.363
2015 Gandhamsetty N, Jeong J, Park J, Park S, Chang S. Boron-Catalyzed Silylative Reduction of Nitriles in Accessing Primary Amines and Imines. The Journal of Organic Chemistry. PMID 26152758 DOI: 10.1021/Acs.Joc.5B00941  0.562
2015 Cho S, Shin A, Park SK, Shin HR, Chang SH, Yoo KY. Alcohol Drinking, Cigarette Smoking and Risk of Colorectal Cancer in the Korean Multi-center Cancer Cohort. Journal of Cancer Prevention. 20: 147-52. PMID 26151048 DOI: 10.15430/JCP.2015.20.2.147  0.371
2015 Le OT, Cho OY, Tran MH, Kim JA, Chang S, Jou I, Lee SY. Phosphorylation of phosphatidylinositol 4-phosphate 5-kinase γ by Akt regulates its interaction with talin and focal adhesion dynamics. Biochimica Et Biophysica Acta. PMID 26149501 DOI: 10.1016/j.bbamcr.2015.07.001  0.318
2015 Khachatryan V, Sirunyan AM, Tumasyan A, Adam W, Bergauer T, Dragicevic M, Erö J, Friedl M, Frühwirth R, Ghete VM, Hartl C, Hörmann N, Hrubec J, Jeitler M, Kiesenhofer W, ... ... Chang S, et al. Constraints on parton distribution functions and extraction of the strong coupling constant from the inclusive jet cross section in pp collisions at [Formula: see text][Formula: see text]. The European Physical Journal. C, Particles and Fields. 75: 288. PMID 26146483 DOI: 10.1140/Epjc/S10052-015-3499-1  0.391
2015 Yu KN, Chang SH, Park SJ, Lim J, Lee J, Yoon TJ, Kim JS, Cho MH. Titanium Dioxide Nanoparticles Induce Endoplasmic Reticulum Stress-Mediated Autophagic Cell Death via Mitochondria-Associated Endoplasmic Reticulum Membrane Disruption in Normal Lung Cells. Plos One. 10: e0131208. PMID 26121477 DOI: 10.1371/journal.pone.0131208  0.372
2015 Hong EH, Song JH, Shim A, Lee BR, Kwon BE, Song HH, Kim YJ, Chang SY, Jeong HG, Kim JG, Seo SU, Kim H, Kwon Y, Ko HJ. Coadministration of Hedera helix L. Extract Enabled Mice to Overcome Insufficient Protection against Influenza A/PR/8 Virus Infection under Suboptimal Treatment with Oseltamivir. Plos One. 10: e0131089. PMID 26098681 DOI: 10.1371/journal.pone.0131089  0.404
2015 Khachatryan V, Sirunyan AM, Tumasyan A, Adam W, Bergauer T, Dragicevic M, Erö J, Friedl M, Frühwirth R, Ghete VM, Hartl C, Hörmann N, Hrubec J, Jeitler M, Kiesenhofer W, ... ... Chang S, et al. Search for a standard model Higgs boson produced in association with a top-quark pair and decaying to bottom quarks using a matrix element method. The European Physical Journal. C, Particles and Fields. 75: 251. PMID 26097407 DOI: 10.1140/Epjc/S10052-015-3454-1  0.384
2015 Lee M, Chang SA, Cho EJ, Park SJ, Choi JO, Lee SC, Oh JK, Park SW. Erratum to: Role of strain values using automated function imaging on transthoracic echocardiography for the assessment of acute chest pain in emergency department. The International Journal of Cardiovascular Imaging. PMID 26084428 DOI: 10.1007/s10554-015-0692-0  0.36
2015 Shin K, Park SW, Chang S. Cp*Ir(III)-Catalyzed Mild and Broad C-H Arylation of Arenes and Alkenes with Aryldiazonium Salts Leading to the External Oxidant-Free Approach. Journal of the American Chemical Society. 137: 8584-92. PMID 26075945 DOI: 10.1021/Jacs.5B04043  0.394
2015 Aad G, Abbott B, Abdallah J, Abdinov O, Aben R, Abolins M, AbouZeid OS, Abramowicz H, Abreu H, Abreu R, Abulaiti Y, Acharya BS, Adamczyk L, Adams DL, Adelman J, ... Chang S, et al. Combined Measurement of the Higgs Boson Mass in pp Collisions at sqrt[s]=7 and 8 TeV with the ATLAS and CMS Experiments. Physical Review Letters. 114: 191803. PMID 26024162 DOI: 10.1103/Physrevlett.114.191803  0.69
2015 Gandhamsetty N, Park J, Jeong J, Park SW, Park S, Chang S. Chemoselective Silylative Reduction of Conjugated Nitriles under Metal-Free Catalytic Conditions: β-Silyl Amines and Enamines. Angewandte Chemie (International Ed. in English). 54: 6832-6. PMID 25907098 DOI: 10.1002/Anie.201502366  0.56
2015 Dateer RB, Chang S. Selective Cyclization of Arylnitrones to Indolines under External Oxidant-Free Conditions: Dual Role of Rh(III) Catalyst in the C-H Activation and Oxygen Atom Transfer. Journal of the American Chemical Society. 137: 4908-11. PMID 25846477 DOI: 10.1021/Jacs.5B01065  0.366
2015 Shin K, Kim H, Chang S. Transition-metal-catalyzed C-N bond forming reactions using organic azides as the nitrogen source: a journey for the mild and versatile C-H amination. Accounts of Chemical Research. 48: 1040-52. PMID 25821998 DOI: 10.1021/Acs.Accounts.5B00020  0.623
2015 Jeong J, Lee D, Chang S. Copper-catalyzed oxygen atom transfer of N-oxides leading to a facile deoxygenation procedure applicable to both heterocyclic and amine N-oxides. Chemical Communications (Cambridge, England). 51: 7035-8. PMID 25805702 DOI: 10.1039/C5Cc01739D  0.328
2015 Park Y, Park KT, Kim JG, Chang S. Mechanistic studies on the Rh(III)-mediated amido transfer process leading to robust C-H amination with a new type of amidating reagent. Journal of the American Chemical Society. 137: 4534-42. PMID 25789561 DOI: 10.1021/Jacs.5B01324  0.773
2015 Lee D, Chang S. Direct C-H amidation of benzoic acids to introduce meta- and para-amino groups by tandem decarboxylation. Chemistry (Weinheim An Der Bergstrasse, Germany). 21: 5364-8. PMID 25688935 DOI: 10.1002/Chem.201500331  0.375
2015 Hung PY, Ho BC, Lee SY, Chang SY, Kao CL, Lee SS, Lee CN. Houttuynia cordata targets the beginning stage of herpes simplex virus infection. Plos One. 10: e0115475. PMID 25643242 DOI: 10.1371/Journal.Pone.0115475  0.329
2015 Pawar AB, Chang S. Cobalt-catalyzed C-H cyanation of (hetero)arenes and 6-arylpurines with N-cyanosuccinimide as a new cyanating agent. Organic Letters. 17: 660-3. PMID 25602639 DOI: 10.1021/Ol503680D  0.391
2015 Patel P, Chang S. Cobalt(III)-Catalyzed C–H Amidation of Arenes using Acetoxycarbamates as Convenient Amino Sources under Mild Conditions Acs Catalysis. 5: 853-858. DOI: 10.1021/Cs501860B  0.378
2015 Kim H, Chang S. Iridium-Catalyzed Direct C–H Amination with Alkylamines: Facile Oxidative Insertion of Amino Group into Iridacycle Acs Catalysis. 5: 6665-6669. DOI: 10.1021/Acscatal.5B02165  0.58
2015 Park Y, Jee S, Kim JG, Chang S. Study of Sustainability and Scalability in the Cp∗Rh(III)-Catalyzed Direct C-H Amidation with 1,4,2-Dioxazol-5-ones Organic Process Research and Development. 19: 1024-1029. DOI: 10.1021/Acs.Oprd.5B00164  0.761
2015 Gwon D, Park S, Chang S. Dual role of carboxylic acid additive: mechanistic studies and implication for the asymmetric C–H amidation Tetrahedron. 71: 4504-4511. DOI: 10.1016/J.Tet.2015.02.065  0.532
2014 Jung SK, Lee KH, Jeon JW, Lee JW, Kwon BO, Kim YJ, Bae JS, Kim DI, Lee SY, Chang SJ. Physicochemical characterization of Remsima. Mabs. 6: 1163-77. PMID 25517302 DOI: 10.4161/mabs.32221  0.32
2014 Gandhamsetty N, Joung S, Park SW, Park S, Chang S. Boron-catalyzed silylative reduction of quinolines: selective sp3 C-Si bond formation. Journal of the American Chemical Society. 136: 16780-3. PMID 25412033 DOI: 10.1021/Ja510674U  0.539
2014 Kim H, Park J, Kim JG, Chang S. Synthesis of phosphoramidates: a facile approach based on the C-N bond formation via Ir-catalyzed direct C-H amidation. Organic Letters. 16: 5466-9. PMID 25289690 DOI: 10.1021/Ol502722J  0.788
2014 Sharma U, Park Y, Chang S. Rh(III)-catalyzed traceless coupling of quinoline N-oxides with internal diarylalkynes. The Journal of Organic Chemistry. 79: 9899-906. PMID 25263712 DOI: 10.1021/Jo501995C  0.539
2014 Chang SW, Lee SY, Kang SK, Kum KY, Kim EC. In vitro biocompatibility, inflammatory response, and osteogenic potential of 4 root canal sealers: Sealapex, Sankin apatite root sealer, MTA Fillapex, and iRoot SP root canal sealer. Journal of Endodontics. 40: 1642-8. PMID 25260738 DOI: 10.1016/j.joen.2014.04.006  0.32
2014 Kang T, Kim H, Kim JG, Chang S. Synthesis of 1,2-amino alcohols via catalytic C-H amidation of sp(3) methyl C-H bonds. Chemical Communications (Cambridge, England). 50: 12073-5. PMID 25164364 DOI: 10.1039/C4Cc05655H  0.779
2014 Gwon D, Lee D, Kim J, Park S, Chang S. Iridium(III)-catalyzed C-H amidation of arylphosphoryls leading to a P-stereogenic center. Chemistry (Weinheim An Der Bergstrasse, Germany). 20: 12421-5. PMID 25145858 DOI: 10.1002/Chem.201404151  0.514
2014 Jeong J, Patel P, Hwang H, Chang S. Rhodium(III)-catalyzed C-C bond formation of quinoline N-oxides at the C-8 position under mild conditions. Organic Letters. 16: 4598-601. PMID 25141216 DOI: 10.1021/Ol502173D  0.38
2014 Chang SW, Lee SY, Ann HJ, Kum KY, Kim EC. Effects of calcium silicate endodontic cements on biocompatibility and mineralization-inducing potentials in human dental pulp cells. Journal of Endodontics. 40: 1194-200. PMID 25069932 DOI: 10.1016/j.joen.2014.01.001  0.313
2014 Hwang H, Kim J, Jeong J, Chang S. Regioselective introduction of heteroatoms at the C-8 position of quinoline N-oxides: remote C-H activation using N-oxide as a stepping stone. Journal of the American Chemical Society. 136: 10770-6. PMID 25029667 DOI: 10.1021/Ja5053768  0.367
2014 Baek JH, Ha K, Yatham LN, Chang JS, Ha TH, Jeon HJ, Hong KS, Chang SM, Ahn YM, Cho HS, Moon E, Cha B, Choi JE, Joo YH, Joo EJ, et al. Pattern of pharmacotherapy by episode types for patients with bipolar disorders and its concordance with treatment guidelines. Journal of Clinical Psychopharmacology. 34: 577-87. PMID 25006813 DOI: 10.1097/JCP.0000000000000175  0.317
2014 Kim H, Shin K, Chang S. Iridium-catalyzed C-H amination with anilines at room temperature: compatibility of iridacycles with external oxidants. Journal of the American Chemical Society. 136: 5904-7. PMID 24702587 DOI: 10.1021/Ja502270Y  0.514
2014 Li B, Lee S, Shin K, Chang S. Chelation-assisted hydroesterification of alkenes: new ruthenium catalyst systems and ligand effects. Organic Letters. 16: 2010-3. PMID 24673469 DOI: 10.1021/Ol500579N  0.335
2014 Yang SY, Cha BK, Kim G, Lee HW, Kim JG, Chang SK, Kim HJ. Dermatomyositis associated with hepatitis B virus-related hepatocellular carcinoma. The Korean Journal of Internal Medicine. 29: 231-5. PMID 24648807 DOI: 10.3904/kjim.2014.29.2.231  0.393
2014 Shin K, Ryu J, Chang S. Orthogonal reactivity of acyl azides in C-H activation: dichotomy between C-C and C-N amidations based on catalyst systems. Organic Letters. 16: 2022-5. PMID 24628106 DOI: 10.1021/Ol500602B  0.329
2014 Kang T, Kim Y, Lee D, Wang Z, Chang S. Iridium-catalyzed intermolecular amidation of sp³ C-H bonds: late-stage functionalization of an unactivated methyl group. Journal of the American Chemical Society. 136: 4141-4. PMID 24580093 DOI: 10.1021/Ja501014B  0.567
2014 Kim J, Chang S. Iridium-catalyzed direct C-H amidation with weakly coordinating carbonyl directing groups under mild conditions. Angewandte Chemie (International Ed. in English). 53: 2203-7. PMID 24470125 DOI: 10.1002/Anie.201310544  0.391
2014 Li B, Park Y, Chang S. Regiodivergent access to five- and six-membered benzo-fused lactams: Ru-catalyzed olefin hydrocarbamoylation. Journal of the American Chemical Society. 136: 1125-31. PMID 24410349 DOI: 10.1021/Ja411913E  0.438
2014 Kim HJ, Ajitha MJ, Lee Y, Ryu J, Kim J, Lee Y, Jung Y, Chang S. Hydrogen-bond-assisted controlled C-H functionalization via adaptive recognition of a purine directing group. Journal of the American Chemical Society. 136: 1132-40. PMID 24377460 DOI: 10.1021/Ja4118472  0.343
2014 Chang SW, Lee SY, Kum KY, Kim EC. Effects of ProRoot MTA, Bioaggregate, and Micromega MTA on odontoblastic differentiation in human dental pulp cells. Journal of Endodontics. 40: 113-8. PMID 24332001 DOI: 10.1016/j.joen.2013.09.036  0.322
2014 Pawar AB, Chang S. Catalytic cyanation of aryl iodides using DMF and ammonium bicarbonate as the combined source of cyanide: a dual role of copper catalysts. Chemical Communications (Cambridge, England). 50: 448-50. PMID 24253075 DOI: 10.1039/C3Cc47926A  0.34
2014 Park JH, Baek EK, Choi CH, Lee KH, Kim BJ, Kim JW, Kim JG, Chang SK. Comparison of the efficacy of 4- and 8-week lansoprazole treatment for ESD-induced gastric ulcers: a randomized, prospective, controlled study. Surgical Endoscopy. 28: 235-41. PMID 23996340 DOI: 10.1007/s00464-013-3177-z  0.408
2014 Figg TM, Park S, Park J, Chang S, Musaev DG. Comparative investigations of cp*-based group 9 metal-catalyzed direct C-H amination of benzamides Organometallics. 33: 4076-4085. DOI: 10.1021/Om5005868  0.575
2014 Park SH, Park Y, Chang S. Rhodium-catalyzed direct amination of arene c-h bonds using azides as the nitrogen source Organic Syntheses. 52-59. DOI: 10.1002/0471264229.Os091.05  0.402
2013 Lee D, Kim Y, Chang S. Iridium-catalyzed direct arene C-H bond amidation with sulfonyl- and aryl azides. The Journal of Organic Chemistry. 78: 11102-9. PMID 24079849 DOI: 10.1021/Jo4019683  0.398
2013 Ryu J, Kwak J, Shin K, Lee D, Chang S. Ir(III)-catalyzed mild C-H amidation of arenes and alkenes: an efficient usage of acyl azides as the nitrogen source. Journal of the American Chemical Society. 135: 12861-8. PMID 23957845 DOI: 10.1021/Ja406383H  0.427
2013 Shin K, Baek Y, Chang S. Direct C-H amination of arenes with alkyl azides under rhodium catalysis. Angewandte Chemie (International Ed. in English). 52: 8031-6. PMID 23788328 DOI: 10.1002/Anie.201302784  0.343
2013 Kim J, Kim J, Chang S. Ruthenium-catalyzed direct C-H amidation of arenes including weakly coordinating aromatic ketones. Chemistry (Weinheim An Der Bergstrasse, Germany). 19: 7328-33. PMID 23616285 DOI: 10.1002/Chem.201301025  0.361
2013 Lee SM, Song JY, Choi JY, Lee SY, Paik JS, Chang SI, Shim WS, Kim SH. Transcatheter closure of perimembranous ventricular septal defect using Amplatzer ductal occluder. Catheterization and Cardiovascular Interventions : Official Journal of the Society For Cardiac Angiography & Interventions. 82: 1141-6. PMID 23554093 DOI: 10.1002/ccd.24810  0.324
2013 Wang Z, Chang S. Copper-mediated transformation of organosilanes to nitriles with DMF and ammonium iodide. Organic Letters. 15: 1990-3. PMID 23541176 DOI: 10.1021/Ol400659P  0.351
2013 Lin CS, Wang LS, Chou TY, Hsu WH, Lin HC, Lee SY, Lee MH, Chang SC, Wei YH. Cigarette smoking and hOGG1 Ser326Cys polymorphism are associated with 8-OHdG accumulation on mitochondrial DNA in thoracic esophageal squamous cell carcinoma. Annals of Surgical Oncology. 20: S379-88. PMID 22941157 DOI: 10.1245/s10434-012-2576-z  0.303
2013 Kim J, Kim HJ, Chang S. Synthetic Uses of Ammonia in Transition‐Metal Catalysis European Journal of Organic Chemistry. 2013: 3201-3213. DOI: 10.1002/Ejoc.201300164  0.56
2012 Kim J, Kim HJ, Chang S. Synthesis of aromatic nitriles using nonmetallic cyano-group sources. Angewandte Chemie (International Ed. in English). 51: 11948-59. PMID 23132837 DOI: 10.1002/Anie.201206168  0.54
2012 Kwak J, Ohk Y, Jung Y, Chang S. Rollover cyclometalation pathway in rhodium catalysis: dramatic NHC effects in the C-H bond functionalization. Journal of the American Chemical Society. 134: 17778-88. PMID 23013604 DOI: 10.1021/Ja308205D  0.394
2012 Ryu J, Shin K, Park SH, Kim JY, Chang S. Rhodium-catalyzed direct C-H amination of benzamides with aryl azides: a synthetic route to diarylamines. Angewandte Chemie (International Ed. in English). 51: 9904-8. PMID 22936469 DOI: 10.1002/Anie.201205723  0.408
2012 Ryu BJ, Baek SH, Kim J, Bae SJ, Chang SY, Heo JN, Lee H, Lee SY, Kim SH. Anti-androgen receptor activity of apoptotic CK2 inhibitor CX4945 in human prostate cancer LNCap cells. Bioorganic & Medicinal Chemistry Letters. 22: 5470-4. PMID 22832316 DOI: 10.1016/j.bmcl.2012.07.031  0.326
2012 Kim J, Kim H, Chang S. Copper-mediated selective cyanation of indoles and 2-phenylpyridines with ammonium iodide and DMF. Organic Letters. 14: 3924-7. PMID 22794272 DOI: 10.1021/Ol301674M  0.675
2012 Kim JY, Park SH, Ryu J, Cho SH, Kim SH, Chang S. Rhodium-catalyzed intermolecular amidation of arenes with sulfonyl azides via chelation-assisted C-H bond activation. Journal of the American Chemical Society. 134: 9110-3. PMID 22624801 DOI: 10.1021/Ja303527M  0.566
2012 Lee HW, Kim HJ, Hong SP, Cha BK, Chang HY, Choi CH, Do JH, Kim JG, Chang SK. Simultaneous emergence of entecavir resistance mutations in a nucleoside-naive chronic hepatitis B patient. Intervirology. 55: 380-4. PMID 22538265 DOI: 10.1159/000336561  0.403
2012 Ryu J, Cho SH, Chang S. A versatile rhodium(I) catalyst system for the addition of heteroarenes to both alkenes and alkynes by a C-H bond activation. Angewandte Chemie (International Ed. in English). 51: 3677-81. PMID 22383453 DOI: 10.1002/Anie.201200120  0.534
2012 Kim HJ, Cho SH, Chang S. Intramolecular oxidative diamination and aminohydroxylation of olefins under metal-free conditions. Organic Letters. 14: 1424-7. PMID 22364422 DOI: 10.1021/Ol300166Q  0.521
2012 Kim J, Choi J, Shin K, Chang S. Copper-mediated sequential cyanation of aryl C-B and arene C-H bonds using ammonium iodide and DMF. Journal of the American Chemical Society. 134: 2528-31. PMID 22280330 DOI: 10.1021/Ja211389G  0.576
2012 Kim SH, Park SH, Chang S. Palladium-catalyzed oxidative alkynylation of arene C–H bond using the chelation-assisted strategy Tetrahedron. 68: 5162-5166. DOI: 10.1016/J.Tet.2012.04.003  0.384
2012 Kim J, Kim HJ, Chang S. Synthese aromatischer Nitrile mithilfe nichtmetallischer CN‐Quellen Angewandte Chemie. 124: 12114-12125. DOI: 10.1002/Ange.201206168  0.493
2011 Park MY, Kwon SU, Lee SY, Kang B, Kim HY, Cho YJ, Chang WI, Chang SH. Tricuspid valvular myxoma: unusual case of tricuspid valve myxoma mimicking thrombus after pulmonary artery embolectomy and tricuspid annuloplasty in pulmonary thromboembolism patient. Journal of Cardiovascular Ultrasound. 19: 207-10. PMID 22259666 DOI: 10.4250/jcu.2011.19.4.207  0.303
2011 Kim HJ, Kim J, Cho SH, Chang S. Intermolecular oxidative C-N bond formation under metal-free conditions: control of chemoselectivity between aryl sp2 and benzylic sp3 C-H bond imidation. Journal of the American Chemical Society. 133: 16382-5. PMID 21928852 DOI: 10.1021/Ja207296Y  0.529
2011 Kim SH, Park SH, Choi JH, Chang S. Sulfonyl and phosphoryl azides: going further beyond the click realm of alkyl and aryl azides. Chemistry, An Asian Journal. 6: 2618-34. PMID 21748856 DOI: 10.1002/Asia.201100340  0.388
2011 Cho SH, Kim JY, Kwak J, Chang S. Recent advances in the transition metal-catalyzed twofold oxidative C-H bond activation strategy for C-C and C-N bond formation. Chemical Society Reviews. 40: 5068-83. PMID 21643614 DOI: 10.1039/C1Cs15082K  0.557
2011 Kim J, Ohk Y, Park SH, Jung Y, Chang S. Intramolecular aromatic carbenoid insertion of biaryldiazoacetates for the regioselective synthesis of fluorenes. Chemistry, An Asian Journal. 6: 2040-7. PMID 21567971 DOI: 10.1002/Asia.201100142  0.586
2011 Chang SK, Noss EH, Chen M, Gu Z, Townsend K, Grenha R, Leon L, Lee SY, Lee DM, Brenner MB. Cadherin-11 regulates fibroblast inflammation. Proceedings of the National Academy of Sciences of the United States of America. 108: 8402-7. PMID 21536877 DOI: 10.1073/Pnas.1019437108  0.306
2011 Kim HJ, Kim M, Chang S. Rhodium(NHC)-catalyzed O-arylation of aryl bromides. Organic Letters. 13: 2368-71. PMID 21469715 DOI: 10.1021/Ol200603C  0.387
2011 Park SH, Kim JY, Chang S. Rhodium-catalyzed selective olefination of arene esters via C-H bond activation. Organic Letters. 13: 2372-5. PMID 21469713 DOI: 10.1021/Ol200600P  0.415
2011 Kim J, Yoo E, Chang S, Lee YS. Electronic and chelation effects on the unusual C2-methylation of N-(para-substituted)phenylaziridines with lithium organocuprates. Journal of Computational Chemistry. 32: 1859-68. PMID 21455961 DOI: 10.1002/Jcc.21768  0.337
2011 Cho SH, Yoon J, Chang S. Intramolecular oxidative C-N bond formation for the synthesis of carbazoles: comparison of reactivity between the copper-catalyzed and metal-free conditions. Journal of the American Chemical Society. 133: 5996-6005. PMID 21446710 DOI: 10.1021/Ja111652V  0.575
2011 Kwak J, Kim M, Chang S. Rh(NHC)-catalyzed direct and selective arylation of quinolines at the 8-position. Journal of the American Chemical Society. 133: 3780-3. PMID 21355550 DOI: 10.1021/Ja111670S  0.433
2011 Kim SH, Yoon J, Chang S. Palladium-catalyzed oxidative alkynylation of heterocycles with terminal alkynes under air conditions. Organic Letters. 13: 1474-7. PMID 21348492 DOI: 10.1021/Ol200154S  0.37
2011 Lee GE, Lee WG, Lee SY, Lee CR, Park CS, Chang S, Park SG, Song MR, Kim YC. Characterization of protoberberine analogs employed as novel human P2X7 receptor antagonists. Toxicology and Applied Pharmacology. 252: 192-200. PMID 21320518 DOI: 10.1016/j.taap.2011.02.009  0.324
2011 Kim CY, Park HW, Ko SK, Chang SI, Moon HB, Kim YY, Cho SH. The financial burden of asthma: a nationwide comprehensive survey conducted in the republic of Korea. Allergy, Asthma & Immunology Research. 3: 34-8. PMID 21217923 DOI: 10.4168/aair.2011.3.1.34  0.352
2011 Lee SY, Park JM, Lee JH, Chang ST, Park JS, Kim YH, Min J. Interaction of transcriptional repressor ArgR with transcriptional regulator FarR at the argB promoter region in Corynebacterium glutamicum. Applied and Environmental Microbiology. 77: 711-8. PMID 21115700 DOI: 10.1128/AEM.01610-10  0.303
2011 So KH, Han YJ, Park HY, Kim JG, Sung DJ, Bae YM, Yang BC, Park SB, Chang SK, Kim EY, Park SP. Generation of functional cardiomyocytes from mouse induced pluripotent stem cells. International Journal of Cardiology. 153: 277-85. PMID 20870305 DOI: 10.1016/j.ijcard.2010.08.052  0.4
2011 Park GH, Rhee DY, Bak H, Chang SE, Lee MW, Choi JH, Moon KC, Bang JS, Kim BJ, Kim MN, Lee SY. Treatment of atrophic scars with fractional photothermolysis: short-term follow-up. The Journal of Dermatological Treatment. 22: 43-8. PMID 20653485 DOI: 10.3109/09546630903473552  0.311
2011 Kim JY, Cho SH, Joseph J, Chang S. Cobalt- and Manganese-Catalyzed Direct Amination of Azoles Synfacts. 2011: 312-312. DOI: 10.1055/S-0030-1259419  0.367
2010 Kim JY, Cho SH, Joseph J, Chang S. Cobalt- and manganese-catalyzed direct amination of azoles under mild reaction conditions and the mechanistic details. Angewandte Chemie (International Ed. in English). 49: 9899-903. PMID 21105037 DOI: 10.1002/Anie.201005922  0.513
2010 Yoo KH, Jeong JW, Yoon HJ, Chang SI, Moon HB, Choi BH, Kim YY, Cho SH. Customized Asthma Control Test with reflection on sociocultural differences. Journal of Korean Medical Science. 25: 1134-9. PMID 20676322 DOI: 10.3346/jkms.2010.25.8.1134  0.359
2010 Kim J, Chang S. A new combined source of "CN" from N,N-dimethylformamide and ammonia in the palladium-catalyzed cyanation of aryl C-H bonds. Journal of the American Chemical Society. 132: 10272-4. PMID 20662510 DOI: 10.1021/Ja104917T  0.558
2010 Lee SY, Kim BN, Han JH, Chang ST, Choi YW, Kim YH, Min J. Treatment of phenol-contaminated soil by Corynebacterium glutamicum and toxicity removal evaluation. Journal of Hazardous Materials. 182: 937-40. PMID 20638173 DOI: 10.1016/j.jhazmat.2010.06.092  0.325
2010 Cho SH, Jeong JW, Park HW, Pyun BY, Chang SI, Moon HB, Kim YY, Choi BW. Effectiveness of a computer-assisted asthma management program on physician adherence to guidelines. The Journal of Asthma : Official Journal of the Association For the Care of Asthma. 47: 680-6. PMID 20632781 DOI: 10.3109/02770903.2010.481342  0.359
2010 Oh SH, Kim KM, Kim DY, Lee YJ, Rhee KW, Jang JY, Chang SH, Lee SY, Kim JS, Choi BH, Park SJ, Yoon CH, Ko GY, Sung KB, Hwang GS, et al. Long-term outcomes of pediatric living donor liver transplantation at a single institution. Pediatric Transplantation. 14: 870-8. PMID 20609169 DOI: 10.1111/j.1399-3046.2010.01357.x  0.31
2010 Husmann R, Na YS, Bolm C, Chang S. Copper-catalyzed one-pot synthesis of alpha-functionalized imidates. Chemical Communications (Cambridge, England). 46: 5494-6. PMID 20577668 DOI: 10.1039/C0Cc00941E  0.31
2010 Kim KS, Moon HJ, Choi CH, Baek EK, Lee SY, Cha BK, Lee HW, Kim HJ, Do JH, Chang SK. The Frequency and Risk Factors of Colorectal Adenoma in Health-Check-up Subjects in South Korea: Relationship to Abdominal Obesity and Age. Gut and Liver. 4: 36-42. PMID 20479911 DOI: 10.5009/gnl.2010.4.1.36  0.307
2010 Lee SY, Le TH, Chang ST, Park JS, Kim YH, Min J. Utilization of phenol and naphthalene affects synthesis of various amino acids in Corynebacterium glutamicum. Current Microbiology. 61: 596-600. PMID 20443004 DOI: 10.1007/s00284-010-9658-6  0.381
2010 Kim SH, Chang S. Highly efficient and versatile pd-catalyzed direct alkynylation of both azoles and azolines. Organic Letters. 12: 1868-71. PMID 20337427 DOI: 10.1021/Ol100488V  0.325
2010 Kim M, Chang S. Rhodium(NHC)-catalyzed amination of aryl bromides. Organic Letters. 12: 1640-3. PMID 20205466 DOI: 10.1021/Ol100437J  0.456
2010 Lee MY, Kim MH, Kim J, Kim SH, Kim BT, Jeong IH, Chang S, Kim SH, Chang SY. Synthesis and SAR of sulfonyl- and phosphoryl amidine compounds as anti-resorptive agents. Bioorganic & Medicinal Chemistry Letters. 20: 541-5. PMID 20005100 DOI: 10.1016/J.Bmcl.2009.11.104  0.517
2010 Kim YJ, Kim JG, Chang SH, Shim JC, Kim SB, Lee MY. Posterior root tear of the medial meniscus in multiple knee ligament injuries. The Knee. 17: 324-8. PMID 19914834 DOI: 10.1016/j.knee.2009.10.001  0.393
2010 Han H, Chang S. Metal-Free Conversion of Carboxamides to Ureas Using Tertiary Amines and Iodosylmesitylene Bulletin of the Korean Chemical Society. 31: 746-748. DOI: 10.5012/Bkcs.2010.31.03.746  0.338
2010 CHANG S, GRUBBS RH. ChemInform Abstract: A Highly Efficient and Practical Synthesis of Chromene Derivatives Using Ring-Closing Olefin Metathesis. Cheminform. 29: no-no. DOI: 10.1002/chin.199826171  0.399
2010 Yuan Y, Thomé I, Kim SH, Chen D, Beyer A, Bonnamour J, Zuidema E, Chang S, Bolm C. Dimethyl Sulfoxide/Potassium Hydroxide: A Superbase for the Transition Metal-Free Preparation of Cross-Coupling Products Advanced Synthesis & Catalysis. 352: 2892-2898. DOI: 10.1002/Adsc.201000575  0.305
2009 Lee J, Kim M, Chang S, Lee HY. Anhydrous hydration of nitriles to amides using aldoximes as the water source. Organic Letters. 11: 5598-601. PMID 19911824 DOI: 10.1021/Ol902309Z  0.529
2009 Cho SH, Kim JY, Lee SY, Chang S. Silver-mediated direct amination of benzoxazoles: tuning the amino group source from formamides to parent amines. Angewandte Chemie (International Ed. in English). 48: 9127-30. PMID 19856358 DOI: 10.1002/Anie.200903957  0.565
2009 Kim M, Kwak J, Chang S. Rhodium/N-heterocyclic carbene catalyzed direct intermolecular arylation of sp2 and sp3 C-H bonds with chelation assistance. Angewandte Chemie (International Ed. in English). 48: 8935-9. PMID 19856352 DOI: 10.1002/Anie.200903500  0.396
2009 Hwang SJ, Kim HJ, Chang S. Highly efficient and versatile synthesis of polyarylfluorenes via Pd-catalyzed C-H bond activation. Organic Letters. 11: 4588-91. PMID 19754073 DOI: 10.1021/Ol901854F  0.385
2009 Bak H, Kim BJ, Lee WJ, Bang JS, Lee SY, Choi JH, Chang SE. Treatment of striae distensae with fractional photothermolysis. Dermatologic Surgery : Official Publication For American Society For Dermatologic Surgery [Et Al.]. 35: 1215-20. PMID 19438664 DOI: 10.1111/j.1524-4725.2009.01221.x  0.303
2009 Lee IK, Kim do H, Gorden DL, Lee YS, Jung SE, Oh ST, Kim JG, Jeon HM, Kim EK, Chang SK. Selective laparoscopic management of adhesive small bowel obstruction using CT guidance. The American Surgeon. 75: 227-31. PMID 19350858  0.408
2009 Do MY, Lee YC, Choi CH, Kim SJ, Mun CS, Moon HJ, Lee HW, Oh HC, Kim HJ, Kim JW, Do JH, Kim JG, Chang SK. [The changes in prevalence and the related factors of Helicobacter pylori infection in Korean health check-up subjects during 8 years]. The Korean Journal of Gastroenterology = Taehan Sohwagi Hakhoe Chi. 53: 76-83. PMID 19237832  0.413
2009 Yoo EJ, Park SH, Lee SH, Chang S. A new entry of copper-catalyzed four-component reaction: facile access to alpha-aryl beta-hydroxy imidates. Organic Letters. 11: 1155-8. PMID 19209900 DOI: 10.1021/Ol900023T  0.596
2009 Chang S, Kim J, Lee S, Lee J, Do Y. Utility of Ammonium Salts for the Synthesis of Amidines Synfacts. 2009: 0255-0255. DOI: 10.1055/S-0028-1087796  0.308
2009 Kim M, Lee J, Lee H, Chang S. Significant Self-Acceleration Effects of Nitrile Additives in the Rhodium-Catalyzed Conversion of Aldoximes to Amides: A New Mechanistic Aspect Advanced Synthesis & Catalysis. 351: 1807-1812. DOI: 10.1002/Adsc.200900251  0.451
2008 Park EJ, Kim SH, Chang S. Copper-catalyzed reaction of alpha-aryldiazoesters with terminal alkynes: a formal [3 + 2] cycloaddition route leading to indene derivatives. Journal of the American Chemical Society. 130: 17268-9. PMID 19053444 DOI: 10.1021/Ja808080H  0.377
2008 Hwang SJ, Cho SH, Chang S. Synthesis of condensed pyrroloindoles via Pd-catalyzed intramolecular C-H bond functionalization of pyrroles. Journal of the American Chemical Society. 130: 16158-9. PMID 18998684 DOI: 10.1021/Ja806897H  0.553
2008 Kim J, Lee SY, Lee J, Do Y, Chang S. Synthetic utility of ammonium salts in a Cu-catalyzed three-component reaction as a facile coupling partner. The Journal of Organic Chemistry. 73: 9454-7. PMID 18956843 DOI: 10.1021/Jo802014G  0.642
2008 Lee IK, Jung SE, Gorden DL, Lee YS, Jung DY, Oh ST, Kim JG, Jeon HM, Chang SK. The diagnostic criteria for right colonic diverticulitis: prospective evaluation of 100 patients. International Journal of Colorectal Disease. 23: 1151-7. PMID 18704462 DOI: 10.1007/s00384-008-0512-2  0.394
2008 Kim J, Chang S. Ammonium salts as an inexpensive and convenient nitrogen source in the Cu-catalyzed amination of aryl halides at room temperature. Chemical Communications (Cambridge, England). 3052-4. PMID 18688345 DOI: 10.1039/B804637A  0.536
2008 Cho SH, Hwang SJ, Chang S. Palladium-catalyzed C-H functionalization of pyridine N-oxides: highly selective alkenylation and direct arylation with unactivated arenes. Journal of the American Chemical Society. 130: 9254-6. PMID 18582040 DOI: 10.1021/Ja8026295  0.544
2008 Yoo EJ, Ahlquist M, Bae I, Sharpless KB, Fokin VV, Chang S. Mechanistic studies on the Cu-catalyzed three-component reactions of sulfonyl azides, 1-alkynes and amines, alcohols, or water: dichotomy via a common pathway. The Journal of Organic Chemistry. 73: 5520-8. PMID 18557650 DOI: 10.1021/Jo800733P  0.671
2008 Lee SH, Kim HJ, Mun JS, Oh HC, Lee HW, Choi CH, Kim JW, Do JH, Kim JG, Chang SK, Kim MK. A case of primary hepatic Burkitt's lymphoma. The Korean Journal of Gastroenterology = Taehan Sohwagi Hakhoe Chi. 51: 259-64. PMID 18516006  0.399
2008 Lee JM, Park EJ, Cho SH, Chang S. Cu-facilitated C-O bond formation using N-hydroxyphthalimide: efficient and selective functionalization of benzyl and allylic C-H bonds. Journal of the American Chemical Society. 130: 7824-5. PMID 18512912 DOI: 10.1021/Ja8031218  0.572
2008 Han H, Park SB, Kim SK, Chang S. Copper-nitrenoid formation and transfer in catalytic olefin aziridination utilizing chelating 2-pyridylsulfonyl moieties. The Journal of Organic Chemistry. 73: 2862-70. PMID 18327956 DOI: 10.1021/Jo800134J  0.508
2008 Cho SH, Chang S. Room temperature copper-catalyzed 2-functionalization of pyrrole rings by a three-component coupling reaction. Angewandte Chemie (International Ed. in English). 47: 2836-9. PMID 18318034 DOI: 10.1002/Anie.200705940  0.523
2008 Yoo EJ, Chang S. A new route to indolines by the Cu-catalyzed cyclization reaction of 2-ethynylanilines with sulfonyl azides. Organic Letters. 10: 1163-6. PMID 18288852 DOI: 10.1021/Ol800049B  0.615
2008 Park K, Kim WJ, Cho YH, Lee YI, Lee H, Jeong S, Cho ES, Chang SI, Moon SK, Kang BS, Kim YJ, Cho SH. Cancer gene therapy using adeno-associated virus vectors. Frontiers in Bioscience : a Journal and Virtual Library. 13: 2653-9. PMID 17981740 DOI: 10.2741/2872  0.362
2008 Hwang SJ, Cho SH, Chang S. Evaluation of catalytic activity of copper salts and their removal processes in the three-component coupling reactions Pure and Applied Chemistry. 80: 873-879. DOI: 10.1351/Pac200880050873  0.536
2008 Kim JY, Kim SH, Chang S. Highly efficient synthesis of α-amino amidines from ynamides by the Cu-catalyzed three-component coupling reactions Tetrahedron Letters. 49: 1745-1749. DOI: 10.1016/J.Tetlet.2008.01.073  0.342
2008 Cho SH, Hwang SJ, Chang S. Copper‐Catalyzed Three‐Component Reaction of 1‐Alkynes, Sulfonyl Azides, and Water: N‐(4‐Acetamidophenylsulfonyl)‐2‐Phenylacetamide Organic Syntheses. 85: 131-137. DOI: 10.1002/0471264229.Os085.14  0.531
2007 Choi BW, Yoo KH, Jeong JW, Yoon HJ, Kim SH, Park YM, Kim WK, Oh JW, Rha YH, Pyun BY, Chang SI, Moon HB, Kim YY, Cho SH. Easy diagnosis of asthma: computer-assisted, symptom-based diagnosis. Journal of Korean Medical Science. 22: 832-8. PMID 17982231 DOI: 10.3346/jkms.2007.22.5.832  0.357
2007 Kim SH, Jung DY, Chang S. Phosphoryl azides as versatile new reaction partners in the Cu-catalyzed three-component couplings. The Journal of Organic Chemistry. 72: 9769-71. PMID 17979288 DOI: 10.1021/Jo7016247  0.335
2007 Cho SH, Chang S. Rate-accelerated nonconventional amide synthesis in water: a practical catalytic aldol-surrogate reaction. Angewandte Chemie (International Ed. in English). 46: 1897-900. PMID 17450617 DOI: 10.1002/Anie.200604358  0.519
2007 Yoo EJ, Ahlquist M, Kim SH, Bae I, Fokin VV, Sharpless KB, Chang S. Copper-catalyzed synthesis of N-sulfonyl-1,2,3-triazoles: controlling selectivity. Angewandte Chemie (International Ed. in English). 46: 1730-3. PMID 17397087 DOI: 10.1002/CHIN.200724118  0.675
2007 Lee IK, Sung NY, Lee YS, Lee SC, Kang WK, Cho HM, Ahn CH, Lee do S, Oh ST, Kim JG, Jeon HM, Chang SK. The survival rate and prognostic factors in 26 perforated colorectal cancer patients. International Journal of Colorectal Disease. 22: 467-73. PMID 16947042 DOI: 10.1007/s00384-006-0184-8  0.398
2006 Lee JM, Ahn DS, Jung DY, Lee J, Do Y, Kim SK, Chang S. Hydrogen-bond-directed highly stereoselective synthesis of Z-enamides via Pd-catalyzed oxidative amidation of conjugated olefins. Journal of the American Chemical Society. 128: 12954-62. PMID 17002392 DOI: 10.1021/Ja0639315  0.524
2006 Chang S, Lee M, Jung DY, Yoo EJ, Cho SH, Han SK. Catalytic one-pot synthesis of cyclic amidines by virtue of tandem reactions involving intramolecular hydroamination under mild conditions. Journal of the American Chemical Society. 128: 12366-7. PMID 16984157 DOI: 10.1021/Ja064788I  0.69
2006 Park EJ, Lee JM, Han H, Chang S. Halide ions as a highly efficient promoter in the Ru-catalyzed hydroesterification of alkenes and alkynes. Organic Letters. 8: 4355-8. PMID 16956225 DOI: 10.1021/Ol061753E  0.385
2006 Kang B, Kim M, Lee J, Do Y, Chang S. Trimanganese complexes bearing bidentate nitrogen ligands as a highly efficient catalyst precursor in the epoxidation of alkenes. The Journal of Organic Chemistry. 71: 6721-7. PMID 16930020 DOI: 10.1021/Jo060709+  0.406
2006 Yoo EJ, Bae I, Cho SH, Han H, Chang S. A facile access to N-sulfonylimidates and their synthetic utility for the transformation to amidines and amides. Organic Letters. 8: 1347-50. PMID 16562888 DOI: 10.1021/Ol060056J  0.69
2006 Lee SY, Dancer GI, Chang SS, Rhee MS, Kang DH. Efficacy of chlorine dioxide gas against Alicyclobacillus acidoterrestris spores on apple surfaces. International Journal of Food Microbiology. 108: 364-8. PMID 16466821 DOI: 10.1016/j.ijfoodmicro.2005.11.023  0.335
2006 Lee CH, Lee K, Chang S, Park JT, Kim B. Highly efficient MCM-48-based template synthesis of osmium and platinum 3-D nanonetworks Bulletin of the Korean Chemical Society. 27: 130-132. DOI: 10.5012/Bkcs.2006.27.1.130  0.319
2006 Chang S, Lee M, Jung D, Yoo E, Cho S, Han S. Synthesis of Cyclic Amidines via Ru-Catalyzed Hydroamination Synfacts. 2006: 1210-1210. DOI: 10.1055/S-2006-955574  0.594
2006 Lee JM, Chang S. Pt-Catalyzed sp3 C–H bond activation of o-alkyl substituted aromatic carboxylic acid derivatives for the formation of aryl lactones Tetrahedron Letters. 47: 1375-1379. DOI: 10.1016/J.Tetlet.2005.12.104  0.383
2005 Cho SH, Yoo EJ, Bae I, Chang S. Copper-catalyzed hydrative amide synthesis with terminal alkyne, sulfonyl azide, and water. Journal of the American Chemical Society. 127: 16046-7. PMID 16287290 DOI: 10.1021/Ja056399E  0.695
2005 Koo DH, Kim M, Chang S. WO3 nanoparticles on MCM-48 as a highly selective and versatile heterogeneous catalyst for the oxidation of olefins, sulfides, and cyclic ketones. Organic Letters. 7: 5015-8. PMID 16235946 DOI: 10.1021/Ol052019I  0.379
2005 Park SJ, Rim SH, Kim KM, Lee JH, Choi BH, Lee SY, Chang SH, Lee YJ, Lee SG. Long-term growth of pediatric patients following living-donor liver transplantation. Journal of Korean Medical Science. 20: 835-40. PMID 16224159 DOI: 10.3346/jkms.2005.20.5.835  0.302
2005 Hwang LK, Na Y, Lee J, Do Y, Chang S. Tetraarylphosphonium halides as arylating reagents in Pd-catalyzed Heck and cross-coupling reactions. Angewandte Chemie (International Ed. in English). 44: 6166-9. PMID 16175530 DOI: 10.1002/Anie.200501582  0.305
2005 Paik KH, Song SM, Ki CS, Yu HW, Kim JS, Min KH, Chang SH, Yoo EJ, Lee IJ, Kwan EK, Han SJ, Jin DK. Identification of mutations in the GNPTA (MGC4170) gene coding for GlcNAc-phosphotransferase alpha/beta subunits in Korean patients with mucolipidosis type II or type IIIA. Human Mutation. 26: 308-14. PMID 16116615 DOI: 10.1002/humu.20205  0.45
2005 Bae I, Han H, Chang S. Highly efficient one-pot synthesis of N-sulfonylamidines by Cu-catalyzed three-component coupling of sulfonyl azide, alkyne, and amine. Journal of the American Chemical Society. 127: 2038-9. PMID 15713069 DOI: 10.1021/Ja0432968  0.382
2004 Ann JY, Kim SJ, Han SP, Kim JW, Kim HJ, Do JH, Kim JG, Chang SK, Jeon WK. [Effect of glutamine on the non-steroidal anti-inflammatory drug-induced bacterial translocation]. The Korean Journal of Gastroenterology = Taehan Sohwagi Hakhoe Chi. 44: 252-8. PMID 15564804  0.393
2004 Kang B, Lee JM, Kwak J, Lee YS, Chang S. Substituent effects on the Z/E-selectivity in cross-metathesis of conjugated enynes. The Journal of Organic Chemistry. 69: 7661-4. PMID 15497994 DOI: 10.1021/Jo048883Q  0.338
2004 Han H, Bae I, Yoo EJ, Lee J, Do Y, Chang S. Notable coordination effects of 2-pyridinesulfonamides leading to efficient aziridination and selective aziridine ring opening. Organic Letters. 6: 4109-12. PMID 15496111 DOI: 10.1021/Ol0481784  0.615
2004 Lee JM, Na Y, Han H, Chang S. Cooperative multi-catalyst systems for one-pot organic transformations. Chemical Society Reviews. 33: 302-12. PMID 15272370 DOI: 10.1039/B309033G  0.314
2004 Lee Y, Seomoon D, Kim S, Han H, Chang S, Lee PH. Highly efficient iridium-catalyzed oxidation of organosilanes to silanols. The Journal of Organic Chemistry. 69: 1741-3. PMID 14987039 DOI: 10.1021/Jo035647R  0.492
2004 Lyu YY, Yi SH, Shon JK, Chang S, Pu LS, Lee SY, Yie JE, Char K, Stucky GD, Kim JM. Highly stable mesoporous metal oxides using nano-propping hybrid gemini surfactants. Journal of the American Chemical Society. 126: 2310-1. PMID 14982427 DOI: 10.1021/Ja0390348  0.381
2004 Na Y, Park S, Han SB, Han H, Ko S, Chang S. Ruthenium-catalyzed Heck-type olefination and Suzuki coupling reactions: studies on the nature of catalytic species. Journal of the American Chemical Society. 126: 250-8. PMID 14709090 DOI: 10.1021/Ja038742Q  0.376
2004 Na Y, Lee C, Pak JY, Lee KH, Chang S. Electrochemistry as a correlation tool candidate with catalytic activities in Ru-catalyzed hydrolytic oxidation of organosilane Tetrahedron Letters. 45: 7863-7865. DOI: 10.1016/J.Tetlet.2004.08.154  0.339
2004 Kang B, Chang S. A facile synthetic route to (+)-allosedamine via hydrolytic kinetic resolution and olefin metathesis Tetrahedron. 60: 7353-7359. DOI: 10.1016/J.Tet.2004.05.054  0.359
2004 Park S, Kim M, Koo DH, Chang S. Use of Ruthenium/Alumina as a Convenient Catalyst for Copper‐Free Sonogashira Coupling Reactions Advanced Synthesis & Catalysis. 346: 1638-1640. DOI: 10.1002/Adsc.200404189  0.417
2003 Do JH, Chang SK, Ahnn JY, Cha BK, Cheong SM, Kim DW, Cheong HR, Kim HJ, Kim JG, Lee TJ, Park ES, Park SM. [Is immunohistochemistry for MLH1 and MSH2 proteins a useful method for detection of microsatellite instability in sporadic colorectal cancer?]. The Korean Journal of Gastroenterology = Taehan Sohwagi Hakhoe Chi. 42: 369-76. PMID 14646573  0.415
2003 Park S, Choi YA, Han H, Yang SH, Chang S. Rh-catalyzed one-pot and practical transformation of aldoximes to amides. Chemical Communications (Cambridge, England). 1936-7. PMID 12932041 DOI: 10.1039/B305268K  0.303
2003 Kang B, Kim DH, Do Y, Chang S. Conjugated enynes as a new type of substrates for olefin metathesis. Organic Letters. 5: 3041-3. PMID 12916976 DOI: 10.1021/Ol035014Z  0.386
2003 Ko S, Han H, Chang S. Ru-catalyzed hydroamidation of alkenes and cooperative aminocarboxylation procedure with chelating formamide. Organic Letters. 5: 2687-90. PMID 12868890 DOI: 10.1021/Ol034862R  0.353
2003 Lee K, Kim YH, Han SB, Kang H, Park S, Seo WS, Park JT, Kim B, Chang S. Osmium replica of mesoporous silicate MCM-48: efficient and reusable catalyst for oxidative cleavage and dihydroxylation reactions. Journal of the American Chemical Society. 125: 6844-5. PMID 12783518 DOI: 10.1021/Ja034137B  0.351
2003 Ko S, Lee C, Choi MG, Na Y, Chang S. Chelation-accelerated sequential decarbonylation of formate and alkoxycarbonylation of aryl halides using a combined Ru and Pd catalyst. The Journal of Organic Chemistry. 68: 1607-10. PMID 12585917 DOI: 10.1021/Jo026591O  0.304
2003 Kim KS, Hong YK, Joe YA, Lee Y, Shin JY, Park HE, Lee IH, Lee SY, Kang DK, Chang SI, Chung SI. Anti-angiogenic activity of the recombinant kringle domain of urokinase and its specific entry into endothelial cells. The Journal of Biological Chemistry. 278: 11449-56. PMID 12529357 DOI: 10.1074/Jbc.M212358200  0.318
2003 Na Y, Ko S, Hwang LK, Chang S. Ruthenium-catalyzed hydroesterification of alkynes and dienes based on a chelation-approach Tetrahedron Letters. 44: 4475-4478. DOI: 10.1016/S0040-4039(03)01016-5  0.329
2002 Kim YK, Kim SH, Tak YJ, Jee YK, Lee BJ, Kim SH, Park HW, Jung JW, Bahn JW, Chang YS, Choi DC, Chang SI, Min KU, Kim YY, Cho SH. High prevalence of current asthma and active smoking effect among the elderly. Clinical and Experimental Allergy : Journal of the British Society For Allergy and Clinical Immunology. 32: 1706-12. PMID 12653160 DOI: 10.1046/j.1365-2222.2002.01524.x  0.357
2002 Choi E, Lee C, Na Y, Chang S. [RuCl(2)(p-cymene)](2) on carbon: an efficient, selective, reusable, and environmentally versatile heterogeneous catalyst. Organic Letters. 4: 2369-71. PMID 12098249 DOI: 10.1021/Ol0260977  0.314
2002 Ko S, Na Y, Chang S. A novel chelation-assisted hydroesterification of alkenes via ruthenium catalysis. Journal of the American Chemical Society. 124: 750-1. PMID 11817940 DOI: 10.1021/Ja017076V  0.406
2002 Chang S, Lee M, Ko S, Lee PH. RUTHENIUM-CATALYZED FACILE AEROBIC OXIDATION OF α-HYDROXYCARBONYLS TO 1,2-DICARBONYL COMPOUNDS Synthetic Communications. 32: 1279-1284. DOI: 10.1081/Scc-120003622  0.45
2002 Lee PH, Sung S, Lee K, Chang S. Palladium-Catalyzed Allylic Substitution Using in Situ Generated Allylindium Reagents Synlett. 2002: 0146-0148. DOI: 10.1055/S-2002-19357  0.502
2001 Yang SH, Chang S. Highly efficient and catalytic conversion of aldoximes to nitriles. Organic Letters. 3: 4209-4211. PMID 11784179 DOI: 10.1021/Ol0168768  0.329
2001 Lee PH, Lee K, Sung S, Chang S. The catalytic Sakurai reaction. The Journal of Organic Chemistry. 66: 8646-9. PMID 11735551 DOI: 10.1021/Jo0105641  0.48
2001 Chang S, Na Y, Choi E, Kim S. Catalytic and highly efficient 1,4-addition of terminal alkynes to conjugated enones by [RuCl(2)(p-cymene)]2/pyrrolidine. Organic Letters. 3: 2089-91. PMID 11418056 DOI: 10.1021/Ol016047M  0.495
2001 Lee PH, Bang K, Lee K, Sung S, Chang S. ULTRASOUND PROMOTED SYNTHESIS OF β-HYDROXYESTERS BY REFORMATSKY REACTION USING INDIUM METAL Synthetic Communications. 31: 3781-3789. DOI: 10.1081/Scc-100108228  0.487
2001 Lee PH, Lee K, Chang S. In-mediated allylation of alpha-keto esters with allyl halides Synthetic Communications. 31: 3189-3196. DOI: 10.1081/Scc-100105896  0.48
2001 Chang S, Lee M, Kim S. N-alkoxyimidoyl bromides as a new and efficient coupling partner in Pd-catalyzed Stille reaction Synlett. 2001: 1557-1558. DOI: 10.1055/S-2001-17480  0.451
2001 Park SH, Kang HJ, Ko S, Park S, Chang S. A short and concise synthetic route to (−)-coniceine Tetrahedron-Asymmetry. 12: 2621-2624. DOI: 10.1016/S0957-4166(01)00446-3  0.336
2001 Lee WW, Shin HJ, Chang S. A rapid formal synthesis of the macrolide (-)-A26771B Tetrahedron Asymmetry. 12: 29-31. DOI: 10.1016/S0957-4166(01)00004-0  0.356
2001 Chang S, Yang SH, Lee PH. Pd-catalyzed cross-coupling of alkynylsilanols with iodobenzenes Tetrahedron Letters. 42: 4833-4835. DOI: 10.1016/S0040-4039(01)00811-5  0.447
2000 Hong HJ, Lee JW, Park SS, Kang YJ, Chang SY, Kim KM, Kim JO, Murthy KK, Payne JS, Yoon SK, Park MJ, Kim IC, Kim JG, Kang CY. A humanized anti--4-1BB monoclonal antibody suppresses antigen-induced humoral immune response in nonhuman primates. Journal of Immunotherapy (Hagerstown, Md. : 1997). 23: 613-21. PMID 11186149 DOI: 10.1097/00002371-200011000-00002  0.4
2000 Na Y, Chang S. Highly Stereoselective and Efficient Hydrosilylation of Terminal Alkynes Catalyzed by [RuCl2(p-cymene)]2 Organic Letters. 2: 1887-1889. PMID 10891183 DOI: 10.1021/Ol0059697  0.36
2000 Ho Lee P, Bang K, Lee K, Lee C, Chang S. In-mediated synthesis of 2-(2-hydroxyethyl)homoallenylsilanes Tetrahedron Letters. 41: 7521-7524. DOI: 10.1016/S0040-4039(00)01290-9  0.309
2000 Lee M, Chang S. Highly efficient aerobic oxidation of benzylic and allylic alcohols by a simple catalyst system of [RuCl2(p-cymene)]2/Cs2CO3 Tetrahedron Letters. 41: 7507-7510. DOI: 10.1016/S0040-4039(00)01284-3  0.303
1999 Jo E, Na Y, Chang S. A highly efficient synthesis of (S)-(+)-N-Boc-coniine using ring- closing olefin metathesis (RCM) Tetrahedron Letters. 40: 5581-5582. DOI: 10.1016/S0040-4039(99)01081-3  0.333
1998 Chang S, Grubbs RH. A Highly Efficient and Practical Synthesis of Chromene Derivatives Using Ring-Closing Olefin Metathesis. The Journal of Organic Chemistry. 63: 864-866. PMID 11672084 DOI: 10.1021/Jo9712198  0.472
1998 Chang S, Jones L, Wang C, Henling LM, Grubbs RH. Synthesis and Characterization of New Ruthenium-Based Olefin Metathesis Catalysts Coordinated with Bidentate Schiff-Base Ligands Organometallics. 17: 3460-3465. DOI: 10.1021/Om970910Y  0.465
1998 Grubbs RH, Chang S. Recent advances in olefin metathesis and its application in organic synthesis Tetrahedron. 54: 4413-4450. DOI: 10.1016/S0040-4020(97)10427-6  0.496
1997 Lee CN, Chang SW, Cho NH, Cho SH. Nitrous oxide synthase expression in placenta of preeclampsia. Journal of Korean Medical Science. 12: 532-8. PMID 9443092  0.362
1997 Chang S, Grubbs RH. A simple method to polyhydroxylated olefinic molecules using ring-closing olefin metathesis Tetrahedron Letters. 38: 4757-4760. DOI: 10.1016/S0040-4039(97)01031-9  0.503
1997 Finney NS, Pospisil PJ, Chang S, Palucki M, Konsler RG, Hansen KB, Jacobsen EN. On the Viability of Oxametallacyclic Intermediates in the(salen)Mn-Catalyzed Asymmetric Epoxidation Angewandte Chemie International Edition in English. 36: 1720-1723. DOI: 10.1002/Anie.199717201  0.537
1997 Finney NS, Pospisil PJ, Chang S, Palucki M, Konsler RG, Hansen KB, Jacobsen EN. Zum Auftreten von oxametallacyclischen Intermediaten in der [Mn(salen)]-katalysierten asymmetrischen Epoxidierung Angewandte Chemie. 109: 1798-1801. DOI: 10.1002/Ange.19971091614  0.43
1994 Chang S, Galvin JM, Jacobsen EN. Effect of Chiral Quaternary Ammonium Salts on (salen)Mn-Catalyzed Epoxidation of cis-Olefins. A Highly Enantioselective, Catalytic Route to Trans-Epoxides Journal of the American Chemical Society. 116: 6937-6938. DOI: 10.1021/Ja00094A059  0.525
1994 Chang S, Heid RM, Jacobsen EN. Enantioselective epoxidation of cyclic 1,3-dienes catalyzed by a sterically and electronically optimized (salen)Mn complex Tetrahedron Letters. 35: 669-672. DOI: 10.1016/S0040-4039(00)75786-8  0.535
1993 Chang S, Lee NH, Jacobsen EN. Regio- and enantioselective catalytic epoxidation of conjugated polyenes. Formal synthesis of LTA4 methyl ester Journal of Organic Chemistry. 58: 6939-6941. DOI: 10.1021/Jo00077A001  0.568
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