| Year |
Citation |
Score |
| 2019 |
Won SY, Kim SE, Kwon YJ, Shin I, Ham J, Kim WS. Chan-Lam coupling reaction of sulfamoyl azides with arylboronic acids for synthesis of unsymmetrical -arylsulfamides. Rsc Advances. 9: 2493-2497. PMID 35520509 DOI: 10.1039/c8ra09219b |
0.511 |
|
| 2017 |
Kwon YJ, Jeon YK, Sim HB, Oh IY, Shin I, Kim WS. 3-Hydroxy-2-(trialkylsilyl)phenyl Triflate: A Benzyne Precursor Triggered via 1,3-C-sp(2)-to-O Silyl Migration. Organic Letters. PMID 29112429 DOI: 10.1021/acs.orglett.7b03160 |
0.493 |
|
| 2016 |
Hyun SS, Han H, Kim W. A Model of Patrons’ Impulsive Ordering Behaviors in Luxury Restaurants Asia Pacific Journal of Tourism Research. 21: 541-569. DOI: 10.1080/10941665.2015.1062403 |
0.394 |
|
| 2016 |
Han HS, Park N, Suh JY, Nam HS, Seok HK, Kim WT, Kim YC, Cha PR. Reassessing the atomic size effect on glass forming ability: Effect of atomic size difference on thermodynamics and kinetics Intermetallics. 69: 123-127. DOI: 10.1016/J.Intermet.2015.10.021 |
0.394 |
|
| 2015 |
Kim WH, Park JY, Ok SH, Shin IW, Sohn JT. Association Between the Neutrophil/Lymphocyte Ratio and Acute Kidney Injury After Cardiovascular Surgery: A Retrospective Observational Study. Medicine. 94: e1867. PMID 26512598 DOI: 10.1097/MD.0000000000001867 |
0.426 |
|
| 2015 |
Moon SY, Kim UB, Sung DB, Kim WS. A synthetic approach to N-aryl carbamates via copper-catalyzed Chan-Lam coupling at room temperature. The Journal of Organic Chemistry. 80: 1856-65. PMID 25584697 DOI: 10.1021/Jo502828R |
0.346 |
|
| 2014 |
Moon SY, Nam J, Rathwell K, Kim WS. Copper-catalyzed Chan-Lam coupling between sulfonyl azides and boronic acids at room temperature. Organic Letters. 16: 338-41. PMID 24404934 DOI: 10.1021/Ol403717F |
0.327 |
|
| 2012 |
Smith AB, Hoye AT, Martinez-Solorio D, Kim WS, Tong R. Unification of anion relay chemistry with the Takeda and Hiyama cross-coupling reactions: identification of an effective silicon-based transfer agent. Journal of the American Chemical Society. 134: 4533-6. PMID 22352347 DOI: 10.1021/Ja2120103 |
0.314 |
|
| 2011 |
Smith AB, Tong R, Kim WS, Maio WA. Anion relay chemistry: Access to the type II ARC reaction manifold through a fundamentally different reaction pathway exploiting 1-oxa-2-silacyclopentanes and related congeners Angewandte Chemie - International Edition. 50: 8904-8907. PMID 21834108 DOI: 10.1002/Anie.201103886 |
0.66 |
|
| 2011 |
Smith AB, Han H, Kim WS. Diversity-oriented synthesis of 2,4,6-trisubstituted piperidines via type II anion relay chemistry. Organic Letters. 13: 3328-31. PMID 21644563 DOI: 10.1021/Ol2010598 |
0.544 |
|
| 2011 |
Smith AB, Kim WS. Diversity-oriented synthesis leads to an effective class of bifunctional linchpins uniting anion relay chemistry (ARC) with benzyne reactivity. Proceedings of the National Academy of Sciences of the United States of America. 108: 6787-92. PMID 21245309 DOI: 10.1073/Pnas.1015265108 |
0.336 |
|
| 2010 |
Smith AB, Kim WS, Tong R. Uniting anion relay chemistry with Pd-mediated cross coupling: design, synthesis and evaluation of bifunctional aryl and vinyl silane linchpins. Organic Letters. 12: 588-91. PMID 20028107 DOI: 10.1021/Ol902784Q |
0.31 |
|
| 2009 |
Devarie-Baez NO, Kim WS, Smith AB, Xian M. Multicomponent type II anion relay chemistry (ARC): one-pot syntheses of 2,3-disubstituted furans and thiophenes. Organic Letters. 11: 1861-4. PMID 19301924 DOI: 10.1021/Ol900434K |
0.526 |
|
| 2008 |
Smith AB, Kim WS, Wuest WM. Ortho-TMS benzaldehyde: an effective linchpin for type II anion relay chemistry (ARC). Angewandte Chemie (International Ed. in English). 47: 7082-6. PMID 18666303 DOI: 10.1002/Anie.200802301 |
0.613 |
|
| 2006 |
Smith AB, Xian M, Kim WS, Kim DS. The [1,5]-Brook rearrangement: an initial application in anion relay chemistry. Journal of the American Chemical Society. 128: 12368-9. PMID 16984158 DOI: 10.1021/Ja065033E |
0.601 |
|
| 2003 |
Kim WS, Kim HJ, Cho CG. Regioselectivity in the Stille coupling reactions of 3,5-dibromo-2-pyrone. Journal of the American Chemical Society. 125: 14288-9. PMID 14624572 DOI: 10.1021/Ja037043A |
0.319 |
|
| 2002 |
Kim W, Kim H, Cho C. Regioselective Stille coupling reactions of 3,5-dibromo-2-pyrone with various aryl and vinyl stannanes Tetrahedron Letters. 43: 9015-9017. DOI: 10.1016/S0040-4039(02)02305-5 |
0.36 |
|
| 2002 |
Lee J, Kim W, Lee YY, Cho C. Stille couplings of 3-(trimethylstannyl)-5-bromo-2-pyrone for the syntheses of 3-aryl-5-bromo-2-pyrones and their ambident dienyl characters Tetrahedron Letters. 43: 5779-5782. DOI: 10.1016/S0040-4039(02)01182-6 |
0.351 |
|
| Show low-probability matches. |