| Year |
Citation |
Score |
| 2023 |
Jeong S, Park E, Kim J, Park SB, Kim SH, Choe W, Kim J, Park YS. Increasing Chemical Diversity of B2N2 Anthracene Derivatives by Introducing Continuous Multiple Boron-Nitrogen Units. Angewandte Chemie (International Ed. in English). e202314148. PMID 37874975 DOI: 10.1002/anie.202314148 |
0.301 |
|
| 2021 |
Kim J, Umerani MJ, Kurakake R, Qin H, Ziller JW, Gorodetsky AA, Park YS. An aza-Diels-Alder approach to chlorinated quinolines, benzoquinolines, and polybenzoquinolines. Rsc Advances. 11: 13722-13730. PMID 35423954 DOI: 10.1039/d0ra06744j |
0.761 |
|
| 2020 |
Pati PB, Jin E, Kim Y, Kim Y, Mun J, Kim SJ, Kang SJ, Choe W, Lee G, Shin HJ, Park YS. Unveiling 79-Year-Old Ixene and its BN-Doped Derivative. Angewandte Chemie (International Ed. in English). PMID 32410277 DOI: 10.1002/Anie.202004049 |
0.354 |
|
| 2018 |
Shih F, Tian S, Gallagher N, Park YS, Grubbs RB. ipso-Arylative polymerization as a route to π-conjugated polymers: synthesis of poly(3-hexylthiophene) Polymer Chemistry. 9: 3223-3231. DOI: 10.1039/C8Py00605A |
0.667 |
|
| 2016 |
Park YS, Dibble DJ, Kim J, Lopez RC, Vargas E, Gorodetsky AA. Synthesis of Nitrogen-Containing Rubicene and Tetrabenzopentacene Derivatives. Angewandte Chemie (International Ed. in English). PMID 26834003 DOI: 10.1002/Anie.201510320 |
0.78 |
|
| 2015 |
Mazaheripour A, Dibble DJ, Umerani MJ, Park YS, Lopez R, Laidlaw D, Vargas E, Ziller JW, Gorodetsky AA. An Aza-Diels-Alder Approach to Crowded Benzoquinolines. Organic Letters. PMID 26705096 DOI: 10.1021/Acs.Orglett.5B02939 |
0.73 |
|
| 2015 |
Kim BS, Park YS, Yook JH, Oh ST, Kim BS. Differing Clinical Courses and Prognoses in Patients With Gastric Neuroendocrine Tumors Based on the 2010-WHO Classification Scheme. Medicine. 94: e1748. PMID 26554772 DOI: 10.1097/MD.0000000000001748 |
0.372 |
|
| 2015 |
Lee SH, Jung JT, Lee DW, Ha CY, Park KS, Lee SH, Yang CH, Park YS, Jeon SW. [Comparison on Endoscopic Hemoclip and Hemoclip Combination Therapy in Non-variceal Upper Gastrointestinal Bleeding Patients Based on Clinical Practice Data: Is There Difference between Prospective Cohort Study and Randomized Study?]. The Korean Journal of Gastroenterology = Taehan Sohwagi Hakhoe Chi. 66: 85-91. PMID 26289241 DOI: 10.4166/kjg.2015.66.2.85 |
0.337 |
|
| 2015 |
Yang HM, Jeon SW, Jung JT, Lee DW, Ha CY, Park KS, Lee SH, Yang CH, Park JH, Park YS. Comparison of scoring systems for nonvariceal upper gastrointestinal bleeding: A multicenter prospective cohort study. Journal of Gastroenterology and Hepatology. PMID 26211939 DOI: 10.1111/jgh.13057 |
0.31 |
|
| 2015 |
Dibble DJ, Park YS, Mazaheripour A, Umerani MJ, Ziller JW, Gorodetsky AA. Synthesis of polybenzoquinolines as precursors for nitrogen-doped graphene nanoribbons. Angewandte Chemie (International Ed. in English). 54: 5883-7. PMID 25823492 DOI: 10.1002/Anie.201411740 |
0.735 |
|
| 2015 |
Kim JH, Lee SM, Myung CH, Lee KR, Hyun SM, Lee JE, Park YS, Jeon SR, Park JI, Chang SE, Hwang JS. Melanogenesis inhibition of β-lapachone, a natural product from Tabebuia avellanedae, with effective in vivo lightening potency. Archives of Dermatological Research. 307: 229-38. PMID 25663088 DOI: 10.1007/s00403-015-1543-5 |
0.32 |
|
| 2015 |
Dibble DJ, Umerani MJ, Mazaheripour A, Park YS, Ziller JW, Gorodetsky AA. An aza-Diels-Alder route to polyquinolines Macromolecules. 48: 557-561. DOI: 10.1021/Ma5020726 |
0.709 |
|
| 2014 |
Park YS, Wu Q, Nam CY, Grubbs RB. Polymerization of tellurophene derivatives by microwave-assisted palladium-catalyzed ipso-arylative polymerization. Angewandte Chemie (International Ed. in English). 53: 10691-5. PMID 25145499 DOI: 10.1002/Anie.201406068 |
0.67 |
|
| 2012 |
Nam CY, Qin Y, Park YS, Hlaing H, Lu X, Ocko BM, Black CT, Grubbs RB. Photo-cross-linkable azide-functionalized polythiophene for thermally stable bulk heterojunction solar cells Macromolecules. 45: 2338-2347. DOI: 10.1021/Ma3001725 |
0.665 |
|
| 2011 |
Boardman BM, Widawsky JR, Park YS, Schenck CL, Venkataraman L, Steigerwald ML, Nuckolls C. Conductance of single cobalt chalcogenide cluster junctions. Journal of the American Chemical Society. 133: 8455-7. PMID 21539375 DOI: 10.1021/Ja201334S |
0.609 |
|
| 2010 |
Parameswaran R, Widawsky JR, Vázquez H, Park YS, Boardman BM, Nuckolls C, Steigerwald ML, Hybertsen MS, Venkataraman L. Reliable formation of single molecule junctions with air-stable diphenylphosphine linkers Journal of Physical Chemistry Letters. 1: 2114-2119. DOI: 10.1021/Jz100656S |
0.635 |
|
| 2009 |
Park YS, Widawsky JR, Kamenetska M, Steigerwald ML, Hybertsen MS, Nuckolls C, Venkataraman L. Frustrated rotations in single-molecule junctions. Journal of the American Chemical Society. 131: 10820-1. PMID 19722660 DOI: 10.1021/Ja903731M |
0.622 |
|
| 2009 |
Kamenetska M, Koentopp M, Whalley AC, Park YS, Steigerwald ML, Nuckolls C, Hybertsen MS, Venkataraman L. Formation and evolution of single-molecule junctions. Physical Review Letters. 102: 126803. PMID 19392306 DOI: 10.1103/Physrevlett.102.126803 |
0.748 |
|
| 2008 |
Park YS, Little RD. Redox electron-transfer reactions: electrochemically mediated rearrangement, mechanism, and a total synthesis of daucene. The Journal of Organic Chemistry. 73: 6807-15. PMID 18665647 DOI: 10.1021/jo801199s |
0.313 |
|
| 2007 |
Park YS, Whalley AC, Kamenetska M, Steigerwald ML, Hybertsen MS, Nuckolls C, Venkataraman L. Contact chemistry and single-molecule conductance: a comparison of phosphines, methyl sulfides, and amines. Journal of the American Chemical Society. 129: 15768-9. PMID 18052282 DOI: 10.1021/Ja0773857 |
0.768 |
|
| 2007 |
Venkataraman L, Park YS, Whalley AC, Nuckolls C, Hybertsen MS, Steigerwald ML. Electronics and chemistry: varying single-molecule junction conductance using chemical substituents. Nano Letters. 7: 502-6. PMID 17253760 DOI: 10.1021/Nl062923J |
0.764 |
|
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