Year |
Citation |
Score |
2019 |
Dharmaratne NU, Pothupitiya JU, Kiesewetter MK. The mechanistic duality of (thio)urea organocatalysts for ring-opening polymerization. Organic & Biomolecular Chemistry. PMID 30834919 DOI: 10.1039/C8Ob03174F |
0.408 |
|
2019 |
Hewawasam RS, Kalana ULDI, Dharmaratne NU, Wright TJ, Bannin TJ, Kiesewetter ET, Kiesewetter MK. Bisurea and Bisthiourea H-Bonding Organocatalysts for Ring-Opening Polymerization: Cues for the Catalyst Design Macromolecules. 52: 9232-9237. DOI: 10.1021/Acs.Macromol.9B01875 |
0.437 |
|
2018 |
Coderre DN, Fastnacht KV, Wright TJ, Dharmaratne NU, Kiesewetter MK. H-Bonding Organocatalysts for Ring-Opening Polymerization at Elevated Temperatures Macromolecules. 51: 10121-10126. DOI: 10.1021/Acs.Macromol.8B02219 |
0.364 |
|
2018 |
Pothupitiya JU, Hewawasam RS, Kiesewetter MK. Urea and Thiourea H-Bond Donating Catalysts for Ring-Opening Polymerization: Mechanistic Insights via (Non)linear Free Energy Relationships Macromolecules. 51: 3203-3211. DOI: 10.1021/Acs.Macromol.8B00321 |
0.371 |
|
2018 |
Bannin TJ, Datta PP, Kiesewetter ET, Kiesewetter MK. Synthesizing Stilbene by Olefin Metathesis Reaction Using Guided Inquiry To Compare and Contrast Wittig and Metathesis Methodologies Journal of Chemical Education. 96: 143-147. DOI: 10.1021/Acs.Jchemed.8B00313 |
0.32 |
|
2017 |
Dharmaratne NU, Pothupitiya JU, Bannin TJ, Kazakov OI, Kiesewetter MK. Triclocarban: Commercial Antibacterial and Highly Effective H-Bond Donating Catalyst for Ring-Opening Polymerization Acs Macro Letters. 6: 421-425. DOI: 10.1021/Acsmacrolett.7B00111 |
0.347 |
|
2017 |
Pothupitiya JU, Dharmaratne NU, Jouaneh TMM, Fastnacht KV, Coderre DN, Kiesewetter MK. H-Bonding Organocatalysts for the Living, Solvent-Free Ring-Opening Polymerization of Lactones: Toward an All-Lactones, All-Conditions Approach Macromolecules. 50: 8948-8954. DOI: 10.1021/Acs.Macromol.7B01991 |
0.42 |
|
2017 |
Datta PP, Pothupitiya JU, Kiesewetter ET, Kiesewetter MK. Coupled equilibria in H-bond donating ring-opening polymerization: The effective catalyst-determined shift of a polymerization equilibrium European Polymer Journal. 95: 671-677. DOI: 10.1016/J.Eurpolymj.2017.05.018 |
0.4 |
|
2016 |
Datta PP, Kiesewetter MK. Controlled Organocatalytic Ring-Opening Polymerization of ε-Thionocaprolactone. Macromolecules. 49: 774-780. PMID 27182087 DOI: 10.1021/Acs.Macromol.6B00136 |
0.407 |
|
2016 |
Fastnacht KV, Spink SS, Dharmaratne NU, Pothupitiya JU, Datta PP, Kiesewetter ET, Kiesewetter MK. Bis- and Tris-Urea H-Bond Donors for Ring-Opening Polymerization: Unprecedented Activity and Control from an Organocatalyst Acs Macro Letters. 5: 982-986. DOI: 10.1021/Acsmacrolett.6B00527 |
0.394 |
|
2015 |
Spink SS, Kazakov OI, Kiesewetter ET, Kiesewetter MK. Rate Accelerated Organocatalytic Ring-Opening Polymerization of L-Lactide via the Application of a Bis(thiourea) H-bond Donating Cocatalyst. Macromolecules. 48: 6127-6131. PMID 27182086 DOI: 10.1021/Acs.Macromol.5B01320 |
0.381 |
|
2015 |
Bannin TJ, Kiesewetter MK. Poly(thioester) by Organocatalytic Ring-Opening Polymerization. Macromolecules. 48: 5481-5486. PMID 27182085 DOI: 10.1021/Acs.Macromol.5B01463 |
0.371 |
|
2015 |
Kazakov OI, Kiesewetter MK. Cocatalyst Binding Effects in Organocatalytic Ring-Opening Polymerization of l -Lactide Macromolecules. 48: 6121-6126. DOI: 10.1021/Acs.Macromol.5B01140 |
0.358 |
|
2014 |
Michaelis VK, Ong TC, Kiesewetter MK, Frantz DK, Walish JJ, Ravera E, Luchinat C, Swager TM, Griffin RG. Topical Developments in High-Field Dynamic Nuclear Polarization. Israel Journal of Chemistry. 54: 207-221. PMID 25977588 DOI: 10.1002/Ijch.201300126 |
0.383 |
|
2014 |
Kazakov OI, Datta PP, Isajani M, Kiesewetter ET, Kiesewetter MK. Cooperative Hydrogen-Bond Pairing in Organocatalytic Ring-Opening Polymerization. Macromolecules. 47: 7463-7468. PMID 25400295 DOI: 10.1021/Ma501847X |
0.383 |
|
2014 |
Kiesewetter MK, Michaelis VK, Walish JJ, Griffin RG, Swager TM. High field dynamic nuclear polarization NMR with surfactant sheltered biradicals. The Journal of Physical Chemistry. B. 118: 1825-30. PMID 24506193 DOI: 10.1021/Jp410387E |
0.4 |
|
2012 |
Edward JA, Kiesewetter MK, Kim H, Flanagan JC, Hedrick JL, Waymouth RM. Organocatalytic synthesis of quinine-functionalized poly(carbonate)s. Biomacromolecules. 13: 2483-9. PMID 22849552 DOI: 10.1021/Bm300718B |
0.616 |
|
2012 |
Geihe EI, Cooley CB, Simon JR, Kiesewetter MK, Edward JA, Hickerson RP, Kaspar RL, Hedrick JL, Waymouth RM, Wender PA. Designed guanidinium-rich amphipathic oligocarbonate molecular transporters complex, deliver and release siRNA in cells. Proceedings of the National Academy of Sciences of the United States of America. 109: 13171-6. PMID 22847412 DOI: 10.1073/Pnas.1211361109 |
0.492 |
|
2012 |
Kiesewetter MK, Corzilius B, Smith AA, Griffin RG, Swager TM. Dynamic nuclear polarization with a water-soluble rigid biradical. Journal of the American Chemical Society. 134: 4537-40. PMID 22372769 DOI: 10.1021/Ja212054E |
0.387 |
|
2011 |
Kiesewetter MK, Edward JA, Kim H, Waymouth RM. Polycondensation of butenediol: synthesis of telechelic 2-butene-1,4-diol oligomers. Journal of the American Chemical Society. 133: 16390-3. PMID 21939269 DOI: 10.1021/Ja207465H |
0.646 |
|
2010 |
Kiesewetter MK, Waymouth RM. Kinetics of an air- and water-stable ruthenium(IV) catalyst for the deprotection of allyl alcohol in water Organometallics. 29: 6051-6056. DOI: 10.1021/Om100892V |
0.541 |
|
2010 |
Kiesewetter MK, Shin EJ, Hedrick JL, Waymouth RM. Organocatalysis: Opportunities and challenges for polymer synthesis Macromolecules. 43: 2093-2107. DOI: 10.1021/Ma9025948 |
0.558 |
|
2009 |
Kiesewetter MK, Scholten MD, Kirn N, Weber RL, Hedrick JL, Waymouth RM. Cyclic guanidine organic catalysts: what is magic about triazabicyclodecene? The Journal of Organic Chemistry. 74: 9490-6. PMID 19928812 DOI: 10.1021/Jo902369G |
0.548 |
|
2009 |
Cooley CB, Trantow BM, Nederberg F, Kiesewetter MK, Hedrick JL, Waymouth RM, Wender PA. Oligocarbonate molecular transporters: oligomerization-based syntheses and cell-penetrating studies. Journal of the American Chemical Society. 131: 16401-3. PMID 19860416 DOI: 10.1021/Ja907363K |
0.484 |
|
2007 |
Coulembier O, Kiesewetter MK, Mason A, Dubois P, Hedrick JL, Waymouth RM. A distinctive organocatalytic approach to complex macromolecular architectures. Angewandte Chemie (International Ed. in English). 46: 4719-21. PMID 17506056 DOI: 10.1002/Anie.200700522 |
0.61 |
|
2006 |
Kiesewetter MK, Gard MN, Reiter RC, Stevenson CD. Reactions involving di-trans-[12]annulenes. Journal of the American Chemical Society. 128: 15618-24. PMID 17147369 DOI: 10.1021/Ja062846U |
0.363 |
|
2006 |
Stevenson CD, Kiesewetter MK, Reiter RC, Chebny VJ, Rathore R. Selective intercalation of Cs+ in the "V"-shaped cavity of a bichromophoric anion radical: Cs+ assisted pi-s-pi-delocalization of an electron. The Journal of Physical Chemistry. A. 110: 9602-6. PMID 16884193 DOI: 10.1021/Jp0624653 |
0.309 |
|
2005 |
Kiesewetter MK, Reiter RC, Stevenson CD. The capture of sym-[8]annuldiyne: the cyclooctadienyne-eta2-ynyl potassium zwitterionic radical. Organic Letters. 7: 2623-6. PMID 15957906 DOI: 10.1021/Ol050795K |
0.362 |
|
2005 |
Stevenson CD, Kiesewetter MK, Reiter RC, Abdelwahed SH, Rathore R. Intramolecular C-H/C-D exchange in cofacially stacked polyfluorenes via electron-induced bond activation. Journal of the American Chemical Society. 127: 5282-3. PMID 15826141 DOI: 10.1021/Ja0432261 |
0.318 |
|
2005 |
Kiesewetter MK, Reiter RC, Stevenson CD. The second cyclopropannulene: cycloprop-[8]annulene. Journal of the American Chemical Society. 127: 1118-9. PMID 15669848 DOI: 10.1021/Ja044278T |
0.353 |
|
2004 |
Kiesewetter MK, Reiter RC, Stevenson CD. The second triannulenylene: tri-[8]annulenylene. Journal of the American Chemical Society. 126: 8884-5. PMID 15264805 DOI: 10.1021/Ja049020H |
0.333 |
|
2003 |
Peters SJ, Turk MR, Kiesewetter MK, Stevenson CD. Single-electron entrapment of [8]annulyne, biannulenylenes, and an annulenoannulene. Journal of the American Chemical Society. 125: 11264-8. PMID 16220947 DOI: 10.1021/Ja035062E |
0.32 |
|
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