Year |
Citation |
Score |
2023 |
Gallin CF, Lee WW, Byers JA. A Simple, Selective, and General Catalyst for Ring Closing Depolymerization of Polyesters and Polycarbonates for Chemical Recycling. Angewandte Chemie (International Ed. in English). e202303762. PMID 37093979 DOI: 10.1002/anie.202303762 |
0.326 |
|
2021 |
Wong AS, Zhang B, Li B, Neidig ML, Byers JA. Air-Stable Iron-Based Precatalysts for Suzuki-Miyaura Cross-Coupling Reactions between Alkyl Halides and Aryl Boronic Esters. Organic Process Research & Development. 25: 2461-2472. PMID 36340744 DOI: 10.1021/acs.oprd.1c00235 |
0.406 |
|
2021 |
Qi M, Zhang H, Dong Q, Li J, Musgrave RA, Zhao Y, Dulock N, Wang D, Byers JA. Electrochemically switchable polymerization from surface-anchored molecular catalysts. Chemical Science. 12: 9042-9052. PMID 34276933 DOI: 10.1039/d1sc02163j |
0.303 |
|
2021 |
Qi M, Zhang H, Dong Q, Li J, Musgrave RA, Zhao Y, Dulock N, Wang D, Byers JA. Electrochemically switchable polymerization from surface-anchored molecular catalysts. Chemical Science. 12: 9042-9052. PMID 34276933 DOI: 10.1039/d1sc02163j |
0.303 |
|
2021 |
Rayder TM, Bensalah AT, Li B, Byers JA, Tsung CK. Engineering Second Sphere Interactions in a Host-Guest Multicomponent Catalyst System for the Hydrogenation of Carbon Dioxide to Methanol. Journal of the American Chemical Society. PMID 33464883 DOI: 10.1021/jacs.0c08957 |
0.775 |
|
2020 |
Tyrol CC, Yone NS, Gallin CF, Byers JA. Iron-catalysed enantioconvergent Suzuki-Miyaura cross-coupling to afford enantioenriched 1,1-diarylalkanes. Chemical Communications (Cambridge, England). PMID 33155609 DOI: 10.1039/d0cc05003b |
0.379 |
|
2020 |
Crockett MP, Wong AS, Li B, Byers JA. Rational Design of an Iron-Based Catalyst for Suzuki-Miyaura Cross-Couplings Involving Heteroaromatic Boronic Esters and Tertiary Alkyl Electrophiles. Angewandte Chemie (International Ed. in English). PMID 32022394 DOI: 10.1002/Anie.201914315 |
0.515 |
|
2020 |
Rayder TM, Adillon EH, Byers JA, Tsung C. A Bioinspired Multicomponent Catalytic System for Converting Carbon Dioxide into Methanol Autocatalytically Chem. 6: 1742-1754. DOI: 10.1016/J.Chempr.2020.04.008 |
0.77 |
|
2019 |
Crockett MP, Zhang H, Thomas CM, Byers JA. Adding diffusion ordered NMR spectroscopy (DOSY) to the arsenal for characterizing paramagnetic complexes. Chemical Communications (Cambridge, England). PMID 31730148 DOI: 10.1039/C9Cc08229H |
0.364 |
|
2018 |
Crockett MP, Tyrol CC, Wong AS, Li B, Byers JA. Iron-Catalyzed Suzuki-Miyaura Cross-Coupling Reactions between Alkyl Halides and Unactivated Arylboronic Esters. Organic Letters. PMID 30132330 DOI: 10.1021/Acs.Orglett.8B02184 |
0.454 |
|
2018 |
Li Z, Rayder TM, Luo L, Byers JA, Tsung CK. Aperture-Opening Encapsulation of a Transition Metal Catalyst in a Metal-Organic Framework for CO Hydrogenation. Journal of the American Chemical Society. PMID 29909631 DOI: 10.1021/Jacs.8B04047 |
0.771 |
|
2018 |
Qi M, Dong Q, Wang D, Byers JA. Electrochemically switchable ring-opening polymerization of lactide and cyclohexene oxide. Journal of the American Chemical Society. PMID 29672028 DOI: 10.1021/Jacs.8B02171 |
0.429 |
|
2018 |
Ortuño MA, Dereli B, Chiaie KRD, Biernesser AB, Qi M, Byers JA, Cramer CJ. The Role of Alkoxide Initiator, Spin State, and Oxidation State in Ring-Opening Polymerization of ε-Caprolactone Catalyzed by Iron Bis(imino)pyridine Complexes. Inorganic Chemistry. PMID 29381341 DOI: 10.1021/Acs.Inorgchem.7B02964 |
0.464 |
|
2017 |
Delle Chiaie KR, Biernesser AB, Ortuño MA, Dereli B, Iovan DA, Wilding MJT, Li B, Cramer CJ, Byers JA. The role of ligand redox non-innocence in ring-opening polymerization reactions catalysed by bis(imino)pyridine iron alkoxide complexes. Dalton Transactions (Cambridge, England : 2003). 46: 12971-12980. PMID 28932853 DOI: 10.1039/C7Dt03067C |
0.476 |
|
2016 |
Biernesser AB, Delle Chiaie KR, Curley JB, Byers JA. Block Copolymerization of Lactide and an Epoxide Facilitated by a Redox Switchable Iron-Based Catalyst. Angewandte Chemie (International Ed. in English). PMID 26991820 DOI: 10.1002/Anie.201511793 |
0.497 |
|
2016 |
Kaplan HZ, Mako TL, Wilding MJT, Li B, Byers JA. Electron-donating capabilities and evidence for redox activity in low oxidation state iron complexes bearing bis(amidine)pyrimidylidene ligands Journal of Coordination Chemistry. 69: 2047-2058. DOI: 10.1080/00958972.2016.1176158 |
0.783 |
|
2016 |
Delle Chiaie KR, Yablon LM, Biernesser AB, Michalowski GR, Sudyn AW, Byers JA. Redox-triggered crosslinking of a degradable polymer Polymer Chemistry. 7: 4675-4681. DOI: 10.1039/C6Py00975A |
0.79 |
|
2016 |
Mako TL, Byers JA. Recent advances in iron-catalysed cross coupling reactions and their mechanistic underpinning Inorganic Chemistry Frontiers. 3: 766-790. DOI: 10.1039/C5Qi00295H |
0.359 |
|
2016 |
Baker TM, Mako TL, Vasilopoulos A, Li B, Byers JA, Neidig ML. Magnetic Circular Dichroism and Density Functional Theory Studies of Iron(II)-Pincer Complexes: Insight into Electronic Structure and Bonding Effects of Pincer N-Heterocyclic Carbene Moieties Organometallics. 35: 3692-3700. DOI: 10.1021/Acs.Organomet.6B00651 |
0.749 |
|
2015 |
Manna CM, Kaur A, Yablon LM, Haeffner F, Li B, Byers JA. Stereoselective Catalysis Achieved through in Situ Desymmetrization of an Achiral Iron Catalyst Precursor. Journal of the American Chemical Society. PMID 26509216 DOI: 10.1021/Jacs.5B09966 |
0.809 |
|
2015 |
Drake JL, Kaplan HZ, Wilding MJ, Li B, Byers JA. Spin transitions in bis(amidinato)-N-heterocyclic carbene iron(ii) and iron(iii) complexes. Dalton Transactions (Cambridge, England : 2003). 44: 16703-7. PMID 26365530 DOI: 10.1039/C5Dt02440D |
0.739 |
|
2014 |
Morabito JV, Chou LY, Li Z, Manna CM, Petroff CA, Kyada RJ, Palomba JM, Byers JA, Tsung CK. Molecular encapsulation beyond the aperture size limit through dissociative linker exchange in metal-organic framework crystals. Journal of the American Chemical Society. 136: 12540-3. PMID 25144760 DOI: 10.1021/Ja5054779 |
0.606 |
|
2014 |
Tamburini F, Kelly T, Weerapana E, Byers JA. Paper to Plastics: An Interdisciplinary Summer Outreach Project in Sustainability Journal of Chemical Education. 91: 1574-1579. DOI: 10.1021/Ed400892T |
0.53 |
|
2014 |
Manna CM, Kaplan HZ, Li B, Byers JA. High molecular weight poly(lactic acid) produced by an efficient iron catalyst bearing a bis(amidinato)-N-heterocyclic carbene ligand Polyhedron. 84: 160-167. DOI: 10.1016/J.Poly.2014.07.002 |
0.802 |
|
2013 |
Biernesser AB, Li B, Byers JA. Redox-controlled polymerization of lactide catalyzed by bis(imino)pyridine iron bis(alkoxide) complexes. Journal of the American Chemical Society. 135: 16553-60. PMID 24073988 DOI: 10.1021/Ja407920D |
0.561 |
|
2013 |
Byers JA, Jamison TF. Entropic factors provide unusual reactivity and selectivity in epoxide-opening reactions promoted by water. Proceedings of the National Academy of Sciences of the United States of America. 110: 16724-9. PMID 24046369 DOI: 10.1073/Pnas.1311133110 |
0.568 |
|
2013 |
Drake JL, Manna CM, Byers JA. Enhanced carbon dioxide hydrogenation facilitated by catalytic quantities of bicarbonate and other inorganic salts Organometallics. 32: 6891-6894. DOI: 10.1021/Om401057P |
0.759 |
|
2012 |
Kaplan HZ, Li B, Byers JA. Synthesis and characterization of a bis(imino)-N-heterocyclic carbene analogue to bis(imino)pyridine iron complexes Organometallics. 31: 7343-7350. DOI: 10.1021/Om300885D |
0.78 |
|
2011 |
Morten CJ, Byers JA, Jamison TF. Evidence that epoxide-opening cascades promoted by water are stepwise and become faster and more selective after the first cyclization. Journal of the American Chemical Society. 133: 1902-8. PMID 21235230 DOI: 10.1021/Ja1088748 |
0.575 |
|
2009 |
Morten CJ, Byers JA, Van Dyke AR, Vilotijevic I, Jamison TF. The development of endo-selective epoxide-opening cascades in water. Chemical Society Reviews. 38: 3175-92. PMID 19847350 DOI: 10.1039/B816697H |
0.731 |
|
2009 |
Byers JA, Jamison TF. On the synergism between H2O and a tetrahydropyran template in the regioselective cyclization of an epoxy alcohol. Journal of the American Chemical Society. 131: 6383-5. PMID 19385615 DOI: 10.1021/Ja9004909 |
0.521 |
|
2008 |
Min EYJ, Byers JA, Bercaw JE. Catalyst site epimerization during the kinetic resolution of chiral α-olefins by polymerization Organometallics. 27: 2179-2188. DOI: 10.1021/Om700778E |
0.564 |
|
2006 |
Byers JA, Bercaw JE. Kinetic resolution of racemic alpha-olefins with ansa-zirconocene polymerization catalysts: Enantiomorphic site vs. chain end control. Proceedings of the National Academy of Sciences of the United States of America. 103: 15303-8. PMID 17032768 DOI: 10.1073/Pnas.0603071103 |
0.462 |
|
2003 |
Bolton DH, Goetz JM, Gan D, Byers JA, Poliks B, Wooley KL, Schaefer J. Chain dynamics in linear and hyperbranched phenol-polycarbonates Macromolecules. 36: 2368-2373. DOI: 10.1021/Ma021648U |
0.358 |
|
2002 |
O'Connor RD, Poliks B, Bolton DH, Goetz JM, Byers JA, Wooley KL, Schaefer J. Chain packing in linear phenol-polycarbonate by 13C{2H} REDOR Macromolecules. 35: 2608-2617. DOI: 10.1021/Ma010919I |
0.402 |
|
2002 |
O'Connor RD, Byers JA, Arnold WD, Oldfield E, Wooley KL, Schaefer J. Chain packing in ethoxyphenyl-polycarbonate by 13C{2H} REDOR Macromolecules. 35: 2618-2623. DOI: 10.1021/Ma010918Q |
0.387 |
|
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