{"id":77,"date":"2016-07-07T14:17:18","date_gmt":"2016-07-07T18:17:18","guid":{"rendered":"https:\/\/sites.berry.edu\/mturlington\/?page_id=77"},"modified":"2025-05-28T11:03:34","modified_gmt":"2025-05-28T15:03:34","slug":"group-publications","status":"publish","type":"page","link":"https:\/\/sites.berry.edu\/mturlington\/group-publications\/","title":{"rendered":"Group Publications"},"content":{"rendered":"<p>13. Hammers, G. O.; Reddersen, H. M.; Taylor, H. W.; Jarrell, A. K.; Toole, I. K.; Price, D. V.; Buller, C. E.; Turlington, M.; Turlington, C. R. Metallopolymers in Minutes via Organocatalysis: Methods and Structure-Property Relationships. <em> Polym. J.<\/em> <strong>2025<\/strong>, <em>228<\/em>, 113840.<\/p>\n<p style=\"text-align: center\"><img loading=\"lazy\" decoding=\"async\" class=\"size-full wp-image-930\" src=\"https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2025\/05\/website-scheme2-1.jpg\" alt=\"\" width=\"794\" height=\"184\" srcset=\"https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2025\/05\/website-scheme2-1.jpg 794w, https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2025\/05\/website-scheme2-1-300x70.jpg 300w, https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2025\/05\/website-scheme2-1-768x178.jpg 768w\" sizes=\"auto, (max-width: 794px) 100vw, 794px\" \/><\/p>\n<p>Read the <a style=\"font-size: revert\" href=\"https:\/\/www.sciencedirect.com\/science\/article\/abs\/pii\/S0014305725001284\">article<\/a><span style=\"font-size: revert\">.<\/span><\/p>\n<p>12. Nelson, S. E.; Tucker, J. R.; Prado, M. G.; Tierney, L. C.; Quigley, S. L.; Lumpkin, A. T.; Dodd, C. J.; Hasko, V.; Howie, S. L.; Aastha; Ody, B. K.; Yin, J.; Heemstra, J. M.; Turlington, M. Development of Dual Aurora-A and Aurora-B Degrading PROTACs for MYCN-Amplified Neuroblastoma. <em>ChemMedChem<\/em> <strong>2025<\/strong>, <em>20<\/em> (5), e202400703.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"size-full wp-image-912 aligncenter\" src=\"https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2025\/05\/Abstract-Image.jpg\" alt=\"\" width=\"597\" height=\"123\" srcset=\"https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2025\/05\/Abstract-Image.jpg 597w, https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2025\/05\/Abstract-Image-300x62.jpg 300w\" sizes=\"auto, (max-width: 597px) 100vw, 597px\" \/><\/p>\n<p>Read the <a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/10.1002\/cmdc.202400703\">article<\/a>.<\/p>\n<p>11.\u00a0 Ody, B. K.; Zhang, J.; Nelson, S. E.; Xie, Y.; Liu, R.; Dodd, C. J.; Jacobs, S. E.; Whitzel, S. L.; Williams, L. A.; Gozem, S.; Turlington, M.; Yin, J. Synthesis and Evaluation of Cereblon-Recruiting HaloPROTACs. <em>ChemBioChem<\/em> <strong>2023<\/strong>, <em>24<\/em> (21), e202300498.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-833 aligncenter\" src=\"https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2024\/02\/ChemBioChem-Abstract-png-1.png\" alt=\"\" width=\"641\" height=\"166\" srcset=\"https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2024\/02\/ChemBioChem-Abstract-png-1.png 687w, https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2024\/02\/ChemBioChem-Abstract-png-1-300x78.png 300w\" sizes=\"auto, (max-width: 641px) 100vw, 641px\" \/><\/p>\n<p>Read the <a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/full\/10.1002\/cbic.202300498\">article<\/a>.<\/p>\n<p>10. Lester, A.; Sandman, M.; Herring, C.; Girard, C.; Dixon, B.; Ramsdell, H.; Reber, C.; Poulos, J.; Mitchell, A.; Spinney, A.; Henager, M. E.; Evans, C. N.; Turlington, M.; Johnson, Q. R. Computational Exploration of Potential CFTR Binding Sites for Type I Corrector Drugs. <em>Biochemistry<\/em> <strong>2023<\/strong>, <em>62<\/em> (16), 2503\u20132515.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\" wp-image-837 aligncenter\" src=\"https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2024\/02\/computatonal-abstract-image.gif\" alt=\"\" width=\"216\" height=\"244\" \/><\/p>\n<p>Read the <a href=\"https:\/\/pubs.acs.org\/doi\/full\/10.1021\/acs.biochem.3c00165\">article<\/a>.<\/p>\n<p>9. Ramey, E. E.; Whitman, E. ; Buller, C. E.; Tucker, J. R.; Jolly, C. S.; Oberle, K. G.; Becksvoort, A. J.; Turlington, M.; Turlington, C. R. A Biodegradable, Polymer-Supported Oxygen Atom Transfer Reagent. <em>Polymers<\/em> <strong>2023<\/strong>, <em>15<\/em> (9), 2052.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-785 \" src=\"https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2023\/06\/polymers-abstract-image-300x238.png\" alt=\"\" width=\"251\" height=\"199\" srcset=\"https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2023\/06\/polymers-abstract-image-300x238.png 300w, https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2023\/06\/polymers-abstract-image-1024x811.png 1024w, https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2023\/06\/polymers-abstract-image-768x608.png 768w, https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2023\/06\/polymers-abstract-image-1536x1217.png 1536w, https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2023\/06\/polymers-abstract-image.png 1568w\" sizes=\"auto, (max-width: 251px) 100vw, 251px\" \/><\/p>\n<p>Read the <a href=\"https:\/\/www.mdpi.com\/2073-4360\/15\/9\/2052#\">article<\/a>.<\/p>\n<p>8. Oberle, K. G.; Whitman, E. L.; Jolly, C. S.; Webster, K. A.; Marx, B. S.; Howard, C. M.; Hanger, C. A.; Ramey, E. E.; Zou, Y.; Lowe, J. C.; Turlington, M.; Turlington C. R. Metallopolymers in minutes via organocatalysis at room temperature. <em>Polym<\/em>. <em>Chem. <\/em><strong>2022<\/strong>, <em>13<\/em>, 4747-4751.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-717 aligncenter\" src=\"https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2023\/05\/metallopolymer-abstract-image.png\" alt=\"\" width=\"589\" height=\"185\" srcset=\"https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2023\/05\/metallopolymer-abstract-image.png 1662w, https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2023\/05\/metallopolymer-abstract-image-300x94.png 300w, https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2023\/05\/metallopolymer-abstract-image-1024x322.png 1024w, https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2023\/05\/metallopolymer-abstract-image-768x241.png 768w, https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2023\/05\/metallopolymer-abstract-image-1536x482.png 1536w\" sizes=\"auto, (max-width: 589px) 100vw, 589px\" \/><\/p>\n<p>Read the <a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2022\/py\/d2py00747a\">article<\/a>.<\/p>\n<p>7.\u00a0 Jolly, C. S.; Kochanowski, E.; Dodd, C. J.; Post, S. J.; Hill, H. M.; Turlington, M. Diastereoselective Synthesis of Terminal Bromo-Substituted Propargylamines via Generation of Lithium Bromoacetylide and Addition to Chiral N-Tert-Butanesulfinyl Aldimines. <em>J. Org. Chem.<\/em> <strong>2021<\/strong>, <em>86<\/em> (3), 2667\u20132681. https:\/\/doi.org\/10.1021\/acs.joc.0c02697.<\/p>\n<p style=\"text-align: center\"><img loading=\"lazy\" decoding=\"async\" class=\"alignnone size-full wp-image-630\" src=\"https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2021\/02\/bromoalkyne-figure.jpg\" alt=\"\" width=\"727\" height=\"139\" srcset=\"https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2021\/02\/bromoalkyne-figure.jpg 727w, https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2021\/02\/bromoalkyne-figure-300x57.jpg 300w\" sizes=\"auto, (max-width: 727px) 100vw, 727px\" \/><\/p>\n<p>Read the <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.joc.0c02697\">article<\/a>.<\/p>\n<p>6. Doiron, J. E.; Le, C. A.; Bacsa, J.; Breton, G. W.; Martin, K. L.; Aller, S. G.; Turlington, M. Structural Consequences of the 1,2,3-Triazole as an Amide Bioisostere in Analogues of the Cystic Fibrosis Drugs VX-809 and VX-770. <em>ChemMedChem<\/em> <strong>2020<\/strong>, <em>15<\/em> (18), 1720\u20131730. https:\/\/doi.org\/10.1002\/cmdc.202000220.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"size-full wp-image-622 aligncenter\" src=\"https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2020\/09\/ChemMedChem-Abstract.jpg\" alt=\"\" width=\"852\" height=\"124\" srcset=\"https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2020\/09\/ChemMedChem-Abstract.jpg 852w, https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2020\/09\/ChemMedChem-Abstract-300x44.jpg 300w, https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2020\/09\/ChemMedChem-Abstract-768x112.jpg 768w\" sizes=\"auto, (max-width: 852px) 100vw, 852px\" \/><\/p>\n<p>Read the <a href=\"https:\/\/chemistry-europe.onlinelibrary.wiley.com\/doi\/10.1002\/cmdc.202000220\">article<\/a>.<\/p>\n<p>5.\u00a0Doiron, J. E.; Le, C. A.; Ody, B. K.; Brace, J. B.; Post, S. J.; Thacker, N. L.; Hill, H. M.; Breton, G. W.; Mulder, M. J.; Chang, S.; Bridges, T. M.; Tang, L.; Wang, W.; Rowe, S. M.; Aller, S. G.; Turlington, M. Evaluation of 1,2,3-Triazoles as Amide Bioisosteres In Cystic Fibrosis Transmembrane Conductance Regulator Modulators VX-770 and VX-809. <em>Chem.\u00a0Eur. J.<\/em> <strong>2019<\/strong>, <em>25<\/em>, 3662-3674.<span class=\"current-selection\">\u00a0DOI: 10.1002\/chem.201805919<\/span><\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-492 size-large\" src=\"https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2019\/03\/website-chem-eur-j-image-1024x126.jpg\" alt=\"\" width=\"1024\" height=\"126\" srcset=\"https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2019\/03\/website-chem-eur-j-image-1024x126.jpg 1024w, https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2019\/03\/website-chem-eur-j-image-300x37.jpg 300w, https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2019\/03\/website-chem-eur-j-image-768x95.jpg 768w, https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2019\/03\/website-chem-eur-j-image.jpg 1289w\" sizes=\"auto, (max-width: 1024px) 100vw, 1024px\" \/><\/p>\n<div>Read the <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/chem.201805919\">article.<\/a><\/div>\n<p>4.\u00a0Prince, C. E.; Turlington, M. Nitration of 2-tert-Butylaniline: Preparation of an Intermediate Used in the Development of the Cystic Fibrosis Drug Ivacaftor. <em>Chem. Educator<\/em> \u00a0<strong>2018<\/strong>, <em>23<\/em>, 124-128.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-491\" src=\"https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2019\/03\/website-chem-ed-image.jpg\" alt=\"\" width=\"640\" height=\"148\" srcset=\"https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2019\/03\/website-chem-ed-image.jpg 838w, https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2019\/03\/website-chem-ed-image-300x69.jpg 300w, https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2019\/03\/website-chem-ed-image-768x178.jpg 768w\" sizes=\"auto, (max-width: 640px) 100vw, 640px\" \/>Read the <a href=\"http:\/\/chemeducator.org\/papers\/0023001\/23180124.pdf\">article.<\/a><\/p>\n<p>3. \u00a0Penk, D. N.; Robinson, N. A.; Hill, H. M.; Turlington, M. \u00a0&#8220;A flexible method for the synthesis of 2-substituted 1,2,5,6-tetrahydropyridines and piperidines from chloro-containing propargylamines.&#8221;\u00a0<em>Tetrahedron Lett.\u00a0<\/em><strong>2017<\/strong>, <i>58<\/i>, 470-473.<\/p>\n<p class=\"ElsGraphAuthor\"><img loading=\"lazy\" decoding=\"async\" class=\"aligncenter wp-image-244 size-full\" src=\"https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2016\/07\/Piperidine-abstract.jpg\" width=\"650\" height=\"158\" srcset=\"https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2016\/07\/Piperidine-abstract.jpg 650w, https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2016\/07\/Piperidine-abstract-300x73.jpg 300w\" sizes=\"auto, (max-width: 650px) 100vw, 650px\" \/><\/p>\n<p class=\"ElsGraphAuthor\">Read the <a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040403916317166\" target=\"_blank\" rel=\"noopener noreferrer\">article<\/a>.<\/p>\n<p>2. Jordan, S.; Starks, S. A.; Whatley, M. F.; Turlington, M. &#8220;Highly Stereoselective Synthesis of Terminal Chloro-Substituted Propargylamines and Further Functionalization.&#8221;\u00a0<em>Org.\u00a0 Lett. <\/em><strong>2015<\/strong>, <em>17<\/em>, 4842-4845.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-119 size-full aligncenter\" src=\"https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2016\/07\/alkyne-scheme.jpg\" alt=\"alkyne scheme\" width=\"696\" height=\"167\" srcset=\"https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2016\/07\/alkyne-scheme.jpg 696w, https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2016\/07\/alkyne-scheme-300x72.jpg 300w, https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2016\/07\/alkyne-scheme-260x62.jpg 260w\" sizes=\"auto, (max-width: 696px) 100vw, 696px\" \/><\/p>\n<p>Read the <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.orglett.5b02408\" target=\"_blank\" rel=\"noopener noreferrer\">article<\/a>.<\/p>\n<p>1. Breton, G. W.; Turlington, M. &#8220;Alternative synthetic routes to N-methyl-1,2,4-triazoline-3,5-dione (MeTAD) and other triazolinedione derivatives.&#8221; \u00a0<em>Tetrahedron Lett. <\/em><strong>2014<\/strong>, <em>55<\/em>, 4661-4663.<\/p>\n<p><img loading=\"lazy\" decoding=\"async\" class=\"wp-image-159 size-full aligncenter\" src=\"https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2016\/07\/urazole-toc.jpg\" alt=\"urazole toc\" width=\"465\" height=\"101\" srcset=\"https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2016\/07\/urazole-toc.jpg 465w, https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2016\/07\/urazole-toc-300x65.jpg 300w, https:\/\/sites.berry.edu\/mturlington\/wp-content\/uploads\/sites\/55\/2016\/07\/urazole-toc-260x56.jpg 260w\" sizes=\"auto, (max-width: 465px) 100vw, 465px\" \/><\/p>\n<p>Read the <a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040403914011034\" target=\"_blank\" rel=\"noopener noreferrer\">article<\/a>.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>13. Hammers, G. O.; Reddersen, H. M.; Taylor, H. W.; Jarrell, A. K.; Toole, I. K.; Price, D. V.; Buller, C. E.; Turlington, M.; Turlington, C. R. Metallopolymers in Minutes [&hellip;]<\/p>\n","protected":false},"author":77,"featured_media":57,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"page-templates\/full-width.php","meta":{"footnotes":""},"class_list":["post-77","page","type-page","status-publish","has-post-thumbnail","hentry"],"_links":{"self":[{"href":"https:\/\/sites.berry.edu\/mturlington\/wp-json\/wp\/v2\/pages\/77","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/sites.berry.edu\/mturlington\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/sites.berry.edu\/mturlington\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/sites.berry.edu\/mturlington\/wp-json\/wp\/v2\/users\/77"}],"replies":[{"embeddable":true,"href":"https:\/\/sites.berry.edu\/mturlington\/wp-json\/wp\/v2\/comments?post=77"}],"version-history":[{"count":32,"href":"https:\/\/sites.berry.edu\/mturlington\/wp-json\/wp\/v2\/pages\/77\/revisions"}],"predecessor-version":[{"id":931,"href":"https:\/\/sites.berry.edu\/mturlington\/wp-json\/wp\/v2\/pages\/77\/revisions\/931"}],"wp:featuredmedia":[{"embeddable":true,"href":"https:\/\/sites.berry.edu\/mturlington\/wp-json\/wp\/v2\/media\/57"}],"wp:attachment":[{"href":"https:\/\/sites.berry.edu\/mturlington\/wp-json\/wp\/v2\/media?parent=77"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}