Year |
Citation |
Score |
2021 |
Mikula P, Mlnaříková M, Nadres ET, Takahashi H, Babica P, Kuroda K, Bláha L, Sovadinová I. Synthetic Biomimetic Polymethacrylates: Promising Platform for the Design of Anti-Cyanobacterial and Anti-Algal Agents. Polymers. 13. PMID 33810255 DOI: 10.3390/polym13071025 |
0.436 |
|
2019 |
Takahashi H, Yumoto K, Yasuhara K, Nadres ET, Kikuchi Y, Buttitta L, Taichman RS, Kuroda K. Author Correction: Anticancer polymers designed for killing dormant prostate cancer cells. Scientific Reports. 9: 17455. PMID 31767898 DOI: 10.1038/S41598-019-53859-Y |
0.481 |
|
2019 |
Takahashi H, Yumoto K, Yasuhara K, Nadres ET, Kikuchi Y, Taichman RS, Kuroda K. Anticancer polymers designed for killing dormant prostate cancer cells. Scientific Reports. 9: 1096. PMID 30705336 DOI: 10.1038/S41598-018-36608-5 |
0.508 |
|
2017 |
Nguyen HN, Nadres ET, Alamani BG, Rodrigues DF. Designing polymeric adhesives for antimicrobial materials: poly(ethylene imine) polymer, graphene, graphene oxide and molybdenum trioxide - a biomimetic approach. Journal of Materials Chemistry. B. 5: 6616-6628. PMID 32264424 DOI: 10.1039/C7Tb00722A |
0.312 |
|
2017 |
Hong S, Takahashi H, Nadres ET, Mortazavian H, Caputo GA, Younger JG, Kuroda K. A Cationic Amphiphilic Random Copolymer with pH-Responsive Activity against Methicillin-Resistant Staphylococcus aureus. Plos One. 12: e0169262. PMID 28060853 DOI: 10.1371/Journal.Pone.0169262 |
0.499 |
|
2016 |
Takahashi H, Nadres ET, Kuroda K. Cationic Amphiphilic Polymers with Antimicrobial Activity for Oral Care Applications: Eradication of S. mutans Biofilm. Biomacromolecules. PMID 27992189 DOI: 10.1021/Acs.Biomac.6B01598 |
0.528 |
|
2016 |
Nadres ET, Takahashi H, Kuroda K. Radical-medicated end-group transformation of amphiphilic methacrylate random copolymers for modulation of antimicrobial and hemolytic activities Journal of Polymer Science Part a: Polymer Chemistry. 55: 304-312. DOI: 10.1002/Pola.28384 |
0.527 |
|
2014 |
Nadres ET, Santos GIF, Shabashov D, Daugulis O. ChemInform Abstract: Scope and Limitations of Auxiliary-Assisted, Palladium-Catalyzed Arylation of Alkylation and sp2and sp3C-H Bonds. Cheminform. 45: no-no. DOI: 10.1002/chin.201409040 |
0.677 |
|
2013 |
Nadres ET, Santos GI, Shabashov D, Daugulis O. Scope and limitations of auxiliary-assisted, palladium-catalyzed arylation and alkylation of sp2 and sp3 C-H bonds. The Journal of Organic Chemistry. 78: 9689-714. PMID 24090404 DOI: 10.1021/Jo4013628 |
0.678 |
|
2013 |
Zhang D, Nadres ET, Brookhart M, Daugulis O. Synthesis of highly branched polyethylene using "sandwich" (8-p-tolyl naphthyl α-diimine)nickel(II) catalysts Organometallics. 32: 5136-5143. DOI: 10.1021/Om400704H |
0.643 |
|
2012 |
Nadres ET, Daugulis O. Heterocycle synthesis via direct C-H/N-H coupling. Journal of the American Chemical Society. 134: 7-10. PMID 22206416 DOI: 10.1021/Ja210959P |
0.629 |
|
2011 |
Nadres ET, Lazareva A, Daugulis O. Palladium-catalyzed indole, pyrrole, and furan arylation by aryl chlorides. The Journal of Organic Chemistry. 76: 471-83. PMID 21192652 DOI: 10.1021/Jo1018969 |
0.676 |
|
Show low-probability matches. |