| Cooperative multi-catalyst systems for one-pot organic transformations JM Lee, Y Na, H Han, S Chang Chemical Society Reviews 33 (5), 302-312, 2004 | 595 | 2004 |
| Highly Efficient One-Pot Synthesis of N-Sulfonylamidines by Cu-Catalyzed Three-Component Coupling of Sulfonyl Azide, Alkyne, and Amine I Bae, H Han, S Chang Journal of the American Chemical Society 127 (7), 2038-2039, 2005 | 520 | 2005 |
| A Facile Access to N-Sulfonylimidates and Their Synthetic Utility for the Transformation to Amidines and Amides EJ Yoo, I Bae, SH Cho, H Han, S Chang Organic Letters 8 (7), 1347-1350, 2006 | 230 | 2006 |
| Ruthenium-catalyzed Heck-type olefination and Suzuki coupling reactions: studies on the nature of catalytic species Y Na, S Park, SB Han, H Han, S Ko, S Chang Journal of the American Chemical Society 126 (1), 250-258, 2004 | 182 | 2004 |
| Enantioselective carbonyl reverse prenylation from the alcohol or aldehyde oxidation level employing 1, 1-dimethylallene as the prenyl donor SB Han, IS Kim, H Han, MJ Krische Journal of the American Chemical Society 131 (20), 6916-6917, 2009 | 168 | 2009 |
| Direct Generation of Acyclic Polypropionate Stereopolyads via Double Diastereo- and Enantioselective Iridium-Catalyzed Crotylation of 1,3-Diols: Beyond Stepwise … X Gao, H Han, MJ Krische Journal of the American Chemical Society 133 (32), 12795-12800, 2011 | 127 | 2011 |
| Ru-catalyzed hydroamidation of alkenes and cooperative aminocarboxylation procedure with chelating formamide S Ko, H Han, S Chang Organic Letters 5 (15), 2687-2690, 2003 | 125 | 2003 |
| Highly efficient iridium-catalyzed oxidation of organosilanes to silanols Y Lee, D Seomoon, S Kim, H Han, S Chang, PH Lee The Journal of Organic Chemistry 69 (5), 1741-1743, 2004 | 122 | 2004 |
| All-carbon quaternary centers via ruthenium-catalyzed hydroxymethylation of 2-substituted butadienes mediated by formaldehyde: beyond hydroformylation T Smejkal, H Han, B Breit, MJ Krische Journal of the American Chemical Society 131 (30), 10366-10367, 2009 | 117 | 2009 |
| Diastereo- and Enantioselective anti-Alkoxyallylation Employing Allylic gem-Dicarboxylates as Allyl Donors via Iridium-Catalyzed Transfer Hydrogenation SB Han, H Han, MJ Krische Journal of the American Chemical Society 132 (6), 1760-1761, 2010 | 86 | 2010 |
| Notable coordination effects of 2-pyridinesulfonamides leading to efficient aziridination and selective aziridine ring opening H Han, I Bae, EJ Yoo, J Lee, Y Do, S Chang Organic Letters 6 (22), 4109-4112, 2004 | 81 | 2004 |
| Copper− nitrenoid formation and transfer in catalytic olefin aziridination utilizing chelating 2-pyridylsulfonyl moieties H Han, SB Park, SK Kim, S Chang The Journal of Organic Chemistry 73 (7), 2862-2870, 2008 | 71 | 2008 |
| Isotope‐coded N‐terminal sulfonation of peptides allows quantitative proteomic analysis with increased de novo peptide sequencing capability YH Lee, H Han, SB Chang, SW Lee Rapid communications in mass spectrometry 18 (24), 3019-3027, 2004 | 57 | 2004 |
| Direct Ruthenium-Catalyzed C− C Coupling of Ethanol: Diene Hydro-hydroxyethylation To Form All-Carbon Quaternary Centers H Han, MJ Krische Organic letters 12 (12), 2844-2846, 2010 | 55 | 2010 |
| Method of forming magnetic patterns, and method of manufacturing magnetic memory devices HY Kim, JH Bae, H Han, WJ Lee, CK Lee, B Geun-Joo, J Jeon US Patent 10,062,837, 2018 | 53 | 2018 |
| Halide ions as a highly efficient promoter in the Ru-catalyzed hydroesterification of alkenes and alkynes EJ Park, JM Lee, H Han, S Chang Organic letters 8 (19), 4355-4358, 2006 | 48 | 2006 |
| Transition-metal-catalyzed asymmetric allylation of carbonyl compounds with unsaturated hydrocarbons PS Wang, ML Shen, LZ Gong Synthesis 50 (05), 956-967, 2018 | 46 | 2018 |
| Rh-Catalyzed one-pot and practical transformation of aldoximes to amides S Park, Y Choi, H Han, SH Yang, S Chang Chemical communications, 1936-1937, 2003 | 42 | 2003 |
| Org. Lett. H Han, JR Kong, MJ Krische | 32 | 2008 |
| Compositions for etching and methods of forming a semiconductor device using the same YT Hong, J Lee, J Lim, J Park, C Jeong, H Han, S Park, Y Lee, SW Bae, ... US Patent 8,940,182, 2015 | 25 | 2015 |
Sukbok ChangInstitute for Basic Science (IBS) and KAIST在 kaist.ac.kr 的电子邮件经过验证
