{"id":31,"date":"2017-02-09T10:38:59","date_gmt":"2017-02-09T15:38:59","guid":{"rendered":"https:\/\/sciencescosmaincms.cm.ucf.edu\/chemistry\/yuanlab\/?page_id=31"},"modified":"2024-02-23T12:54:59","modified_gmt":"2024-02-23T17:54:59","slug":"work-completed-at-ucf","status":"publish","type":"page","link":"https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/work-completed-at-ucf\/","title":{"rendered":"Work Completed at UCF"},"content":{"rendered":"<h4>Selected Journal Articles<\/h4>\n<p>Bobek, K. B.; Ezzat, N. S.; Jones, B. S.; Bian, Y.; Shaw, T. E.; Jurca, T.; Li, H.*; Yuan, Y.*, Total Synthesis of Polysubstituted \u03b3-Butyrolactone Lignans (\u2212)-Hinokinin, (\u2212)-Bicubebin B, and (\u2212)-Isodeoxypodophyllotoxin via Oxime Carbonate Formation. <em>Org. Lett.<\/em> <strong>2023<\/strong>, 25, 31. <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.2c03727\">Link<\/a><\/p>\n<p><img decoding=\"async\" class=\"alignnone size-medium wp-image-174 lazyload\" data-src=\"https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/23\/2023\/01\/images_large_jm2c01300_0010-1-300x65.jpeg\" alt=\"\" width=\"300\" height=\"65\" data-srcset=\"https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/23\/2023\/01\/images_large_jm2c01300_0010-1-300x65.jpeg 300w, https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/23\/2023\/01\/images_large_jm2c01300_0010-1-768x167.jpeg 768w, https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/23\/2023\/01\/images_large_jm2c01300_0010-1.jpeg 888w\" data-sizes=\"(max-width: 300px) 100vw, 300px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 300px; --smush-placeholder-aspect-ratio: 300\/65;\" \/><\/p>\n<p>Bian, Y.; Alem, D.; Beato, F.; Hogenson, T. L.; Yang, X.; Jiang, K.; Cai, J.; Ma, W. W.; Fernandez-Zapico, M.; Tan, A. C.; Lawrence, N. J.; Fleming, J. B.; Yuan, Y.*; Xie, H.*, Development of SOS1 Inhibitor-Based Degraders to Target KRAS-Mutant Colorectal Cancer. <em>J. Med. Chem.<\/em> <strong>2022<\/strong>, 65, 16432. <a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.jmedchem.2c01300\">Link<\/a><\/p>\n<p><img decoding=\"async\" class=\"alignnone size-medium wp-image-173 lazyload\" data-src=\"https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/23\/2023\/01\/images_large_jm2c01300_0010-300x160.jpeg\" alt=\"\" width=\"300\" height=\"160\" data-srcset=\"https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/23\/2023\/01\/images_large_jm2c01300_0010-300x160.jpeg 300w, https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/23\/2023\/01\/images_large_jm2c01300_0010-768x409.jpeg 768w, https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/23\/2023\/01\/images_large_jm2c01300_0010.jpeg 1000w\" data-sizes=\"(max-width: 300px) 100vw, 300px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 300px; --smush-placeholder-aspect-ratio: 300\/160;\" \/><\/p>\n<p>Huang, G., Solano, C.M., Melendez, J., Yu-Alfonzo, S., Boonhok, R., Min, H., Miao, J., Chakrabarti, D.*, Yuan, Y.* Discovery of Fast-Acting Dual-Stage Antimalarial Agents by Profiling Pyridylvinylquinoline Chemical Space via Copper Catalyzed Azide-Alkyne Cycloadditions, <em>Eur. J. Med. Chem.<\/em>, <strong>2021<\/strong>, 112889. <a href=\"https:\/\/www.sciencedirect.com\/science\/article\/pii\/S0223523420308618?via%3Dihub\">Link<\/a><\/p>\n<p><img decoding=\"async\" class=\"alignnone wp-image-170 lazyload\" data-src=\"https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/2\/sites\/23\/2020\/11\/click-300x119.png\" alt=\"\" width=\"492\" height=\"195\" data-srcset=\"https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/23\/2020\/11\/click-300x119.png 300w, https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/23\/2020\/11\/click-1024x407.png 1024w, https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/23\/2020\/11\/click-768x305.png 768w, https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/23\/2020\/11\/click-1536x610.png 1536w, https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/23\/2020\/11\/click-1600x636.png 1600w, https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/23\/2020\/11\/click.png 2016w\" data-sizes=\"(max-width: 492px) 100vw, 492px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 492px; --smush-placeholder-aspect-ratio: 492\/195;\" \/><\/p>\n<p>Huang, G., Solano, G.M., Melendez, J., Shaw, J., Collins, J., Banks, R., Arshadi, A.K., Boonhok, R., Min, H., Miao, J., Chakrabarti, D.*, Yuan, Y.* Synthesis, Structure\u2212Activity Relationship, and Antimalarial Efficacy of 6\u2011Chloro-2-arylvinylquinolines. <em>J. Med. Chem<\/em>., <strong>2020<\/strong>, 11756. <a href=\"https:\/\/pubs.acs.org\/doi\/pdf\/10.1021\/acs.jmedchem.0c00858\">Link<\/a><\/p>\n<p><img decoding=\"async\" class=\"alignnone wp-image-167 lazyload\" data-src=\"https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/2\/sites\/23\/2020\/11\/501-300x115.jpg\" alt=\"\" width=\"475\" height=\"182\" data-srcset=\"https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/23\/2020\/11\/501-300x115.jpg 300w, https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/23\/2020\/11\/501-1024x393.jpg 1024w, https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/23\/2020\/11\/501-768x295.jpg 768w, https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/23\/2020\/11\/501.jpg 1035w\" data-sizes=\"(max-width: 475px) 100vw, 475px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 475px; --smush-placeholder-aspect-ratio: 475\/182;\" \/><\/p>\n<p>Jin, K., Sam, I.H., Po, H.L., Lin, D., Ghazvini Zadeh, E.H., Chen, S*, Yuan, Y.*, Li, X.* Total Synthesis of Teixobactin. <em>Nat. Commun<\/em>.,\u00a0<strong>2016<\/strong>, 7:12394 doi: 10.1038\/ ncomms12394. <a href=\"http:\/\/www.nature.com\/ncomms\/2016\/160803\/ncomms12394\/full\/ncomms12394.html\" target=\"_blank\" rel=\"noopener noreferrer\">Link<\/a><\/p>\n<p><img decoding=\"async\" class=\"alignnone size-full wp-image-37 lazyload\" data-src=\"https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/2\/sites\/23\/2017\/02\/pub8.jpg\" alt=\"Publication 8 graphic\" width=\"440\" height=\"311\" data-srcset=\"https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/23\/2017\/02\/pub8.jpg 440w, https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/23\/2017\/02\/pub8-300x212.jpg 300w\" data-sizes=\"(max-width: 440px) 100vw, 440px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 440px; --smush-placeholder-aspect-ratio: 440\/311;\" \/><\/p>\n<p>Logan, M.W.; Yuen, A.L.; Zheng, Y.; Hall, E.A. Hettinger, M.A.; Marks, R.M.; Hosler, M.L.; Rossi, F.M.; Yuan, Y.*; Uribe-Romo, F.* Heterogeneous Photoredox Synthesis of N-hydroxy-oxazolidinones Catalyzed by Metal-Organic Frameworks<em>. Catal. Sci. Technol<\/em>.,\u00a0<strong>2016<\/strong>, 5647-5655. <a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2016\/cy\/c6cy00054a#!divAbstract\" target=\"_blank\" rel=\"noopener noreferrer\">Link<\/a><\/p>\n<p><img decoding=\"async\" class=\"alignnone size-full wp-image-35 lazyload\" data-src=\"https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/2\/sites\/23\/2017\/02\/pub4.gif\" alt=\"\" width=\"378\" height=\"156\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 378px; --smush-placeholder-aspect-ratio: 378\/156;\" \/><\/p>\n<p>Zheng, Y.; Zadeh, E.H.G.; Yuan, Y.* One-Pot, Enantioselective Synthesis of 2,3-Dihydroazulen-6(1H)-one: A Concise Access to the Core Structure of Cephalotaxus Norditerpenes. \u200e<em>Eur. J. Org. Chem<\/em>.\u00a0<strong>2016<\/strong><span lang=\"ZH-CN\">\uff0c<\/span>2115-2119. <a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/ejoc.201600321\/abstract\" target=\"_blank\" rel=\"noopener noreferrer\">Link<\/a><\/p>\n<p><img decoding=\"async\" class=\"alignnone size-full wp-image-36 lazyload\" data-src=\"https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/2\/sites\/23\/2017\/02\/pub5.jpg\" alt=\"\" width=\"336\" height=\"300\" data-srcset=\"https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/23\/2017\/02\/pub5.jpg 336w, https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/23\/2017\/02\/pub5-300x268.jpg 300w\" data-sizes=\"(max-width: 336px) 100vw, 336px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 336px; --smush-placeholder-aspect-ratio: 336\/300;\" \/><\/p>\n<p>Craig, W.; Chen, J. Richardson, D.; Thorpe, R., Yuan, Y.* A Highly Stereoselective and Scalable Synthesis of L-allo-Enduracididine. <em>Org. Lett.,<\/em><strong>2015<\/strong>, 17, 4620-4623. <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.orglett.5b02362\" target=\"_blank\" rel=\"noopener noreferrer\">Link<\/a><\/p>\n<p><img decoding=\"async\" class=\"alignnone size-full wp-image-32 lazyload\" data-src=\"https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/2\/sites\/23\/2017\/02\/pub1.jpg\" alt=\"\" width=\"255\" height=\"142\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 255px; --smush-placeholder-aspect-ratio: 255\/142;\" \/><\/p>\n<p>Zheng, Y.; Cleaveland, J.; Richardson, D.; Yuan, Y.* An Organocatalysis Based Carbocyclic Spiroindoline Synthesis Enables Facile Structure\u2212Activity Relationship (SAR) Study at C2 Position. <em>Org. Lett.,<\/em> <strong>2015<\/strong>, 17, 4240-4243. <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.orglett.5b02031\" target=\"_blank\" rel=\"noopener noreferrer\">Link<\/a><\/p>\n<p><img decoding=\"async\" class=\"alignnone size-full wp-image-33 lazyload\" data-src=\"https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/2\/sites\/23\/2017\/02\/pub2.jpg\" alt=\"\" width=\"338\" height=\"126\" data-srcset=\"https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/23\/2017\/02\/pub2.jpg 338w, https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/wp-content\/uploads\/sites\/23\/2017\/02\/pub2-300x112.jpg 300w\" data-sizes=\"(max-width: 338px) 100vw, 338px\" src=\"data:image\/svg+xml;base64,PHN2ZyB3aWR0aD0iMSIgaGVpZ2h0PSIxIiB4bWxucz0iaHR0cDovL3d3dy53My5vcmcvMjAwMC9zdmciPjwvc3ZnPg==\" style=\"--smush-placeholder-width: 338px; --smush-placeholder-aspect-ratio: 338\/126;\" \/><\/p>\n<h4>Book Chapter<\/h4>\n<p>1. Yuan, Y.*; Wang, W. Post-Synthetic Chemical Modification of Oligonucleotides. Volume 9, <em>Comprehensive Organic Synthesis, Ed.<\/em> 2, 463-493, <strong>2014<\/strong>. <a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/B9780080977423009083\" target=\"_blank\" rel=\"noopener noreferrer\">Link<\/a>.<\/p>\n<h3>Prior to UCF<\/h3>\n<h4>Journal Articles<\/h4>\n<p>24. Zewge, D.; Gosselin, F.; Tellers, D.M.; Davies, I.W.; Jadhav, V.; Nerurkar, S.S.; Yuan, Y.; Li, J.; Flanagan, W.M., Kenski, D.M. High-Throughput Chemical Modification of Oligonucleotides for Systematic Structure-Activity Relationship Evaluation. <em>Bioconjugate Chem.<\/em>, 2014, 25, 2222.<\/p>\n<p>23. Janout, V.; Cline, L.L.; Feuston, B.P.; Klein, L.; O&#8217;Brien, A.; Tucker, T.; Yuan, Y.; O&#8217;Neill-Davis, L.A.; Peiffer, R.L.; Nerurkar, S.S.; Jadhav, V.; Tellers, D.M., Regen, S.L. Molecular Umbrella Conjugate for the Ocular Delivery of siRNA. <em>Bioconjugate Chem.<\/em>, 2014, 25, 197.<\/p>\n<p>22. Wang, P.; Li, X.; Zhu, J.; Chen, J.; Yuan, Y.; Wu, X., Danishefsky, S.J. Encouraging Progress in the omega-Aspartylation of Complex Oligosaccharides as a General Route to beta-N-Linked Glycopolypeptides. <em>J. Am. Chem. Soc.<\/em>, 2011, 133, 1597.<\/p>\n<p>21. Aaronson, J.G.; Klein, L.J.; Momose, A.A.; O&#8217;Brien, A.M.; Shaw, A.W.; Tucker, T.J.; Yuan, Y., Tellers, D.M. Rapid HATU-Mediated Solution Phase siRNA Conjugation. <em>Bioconjugate Chem.<\/em>, 2011, 22, 1723.<\/p>\n<p>20. Yuan, Y.; Chen, J.; Wan, Q.; Wilson, R.M., Danishefsky, S.J. Toward Fully Synthetic, Homogeneous Glycoproteins: Advances in Chemical Ligation. <em>Biopolymers<\/em>, 2010, 94, 373.<\/p>\n<p>19. Joo, J.M.; David, R.A.; Yuan, Y., Lee, C. Concise Synthesis of the Erythrina Alkaloid 3-Demethoxyerythratidinone via Combined Rhodium Catalysis. <em>Org. Lett.<\/em>, 2010, 12, 5704.<\/p>\n<p>18. Yuan, Y.; Zhu, J.; Li, X.; Wu, X., Danishefsky, S.J. Preparation and reactions of Nthioformyl peptides from amino thioacids and isonitriles. <em>Tetrahedron Lett.<\/em>, 2009, 50, 2329.<\/p>\n<p>17. Yuan, Y.; Chen, J.; Wan, Q.; Tan, Z.; Chen, G.; Kan, C., Danishefsky, S.J. Toward Homogeneous Erythropoietin: Fine Tuning of the C-Terminal Acyl Donor in the Chemical Synthesis of the Cys(29)-Gly(77) Glycopeptide Domain. <em>J. Am. Chem. Soc.<\/em>, 2009, 131, 5432.<\/p>\n<p>16. Wu, X.; Yuan, Y.; Li, X., Danishefsky, S.J. Thio-mediated synthesis of derivatized N-linked glycopeptides using isonitrile chemistry. <em>Tetrahedron Lett.<\/em>, 2009, 50, 4666.<\/p>\n<p>15. Wang, P.; Zhu, J.; Yuan, Y., Danishefsky, S.J. Total Synthesis of the 2,6-Sialylated Immunoglobulin G Glycopeptide Fragment in Homogeneous Form. <em>J. Am. Chem. Soc.<\/em>, 2009, 131, 16669.<\/p>\n<p>14. Tan, Z.; Shang, S.; Halkina, T.; Yuan, Y., Danishefsky, S.J. Toward Homogeneous Erythropoietin: Non-NCL-Based Chemical Synthesis of the Gln(78)-Arg(166) Glycopeptide Domain. <em>J. Am. Chem. Soc.<\/em>, 2009, 131, 5424.<\/p>\n<p>13. Kan, C.; Trzupek, J.D.; Wu, B.; Chen, G.; Tan, Z.; Yuan, Y., Danishefsky, S.J. Toward Homogeneous Erythropoietin: Chemical Synthesis of the Ala(1)-Gly(28) Glycopeptide Domain by &#8220;Alanine&#8221; Ligation. <em>J. Am. Chem. Soc.<\/em>, 2009, 131, 5438.<\/p>\n<p>12. Wan, Q.; Chen, J.; Yuan, Y., Danishefsky, S.J. Oxo-ester Mediated Native Chemical Ligation: Concept and Applications. <em>J. Am. Chem. Soc.<\/em>, 2008, 130, 15814.<\/p>\n<p>11. Li, X.; Yuan, Y.; Kan, C., Danishefsky, S.J. Addressing Mechanistic Issues in the Coupling of Isonitriles and Carboxylic Acids: Potential Routes to Peptidic Constructs. <em>J. Am. Chem. Soc.<\/em>, 2008, 130, 13225.<\/p>\n<p>10. Li, X.; Yuan, Y.; Berkowitz, W.F.; Todaro, L.J., Danishefsky, S.J. On the TwoComponent Microwave-Mediated Reaction of Isonitriles with Carboxylic Acids: Regarding Alleged Formimidate Carboxylate Mixed Anhydrides. <em>J. Am. Chem. Soc.<\/em>, 2008, 130, 13222.<\/p>\n<p>9. Chen, J.; Wan, Q.; Yuan, Y.; Zhu, J., Danishefsky, S.J. Native Chemical Ligation at Valine: A Contribution to Peptide and Glycopeptide Synthesis. <em>Angew. Chem., Int. Ed.<\/em>, 2008, 47, 8521.<\/p>\n<p>8. Yuan, Y.; Lai, A.J.; Kraml, C.M., Lee, C. A highly Enantio- and Diastereoselective 1,3-Dimethylallylation of Aldehydes. <em>Tetrahedron<\/em>, 2006, 62, 11391.<\/p>\n<p>7. Joo, J.M.; Yuan, Y., Lee, C. Tandem Cyclization of Alkynes via Rhodium Alkynyl and Alkenylidene Catalysis. <em>J. Am. Chem. Soc.<\/em>, 2006, 128, 14818.<\/p>\n<p>6. Yuan, Y.; Men, H.B., Lee, C.B. Total Synthesis of Kendomycin: A Macro-CGlycosidation Approach. <em>J. Am. Chem. Soc.<\/em>, 2004, 126, 14720.<\/p>\n<h4>Patents<\/h4>\n<p>5. Danishefsky, S. J.; David, J. D.; Chen, J.; Wu, B.; Chen, G.; Wan, Q.; Tan, Z.; Kan, C.; Yuan, Y.; Hua, Z.; Ranganathan, K.; Trzupek, J. D. Preparation of Homogeneous Erythropoietin and Other Peptides and Proteins. WO 2007\/120614 A2 20071025<\/p>\n<p>4. Aaronson, J.G.; Barnett, S.F.; Bartz, R.; Colletti, S.L.; Jadhav, V.R.; Momose, A.A.; Shaw, A.W.; Tellers, D.M.; Tucker, T.J.; Wang, W.; Yuan, Y. Novel Single Chemical Entities and Methods for Delivery of Oligonucleotides. WO 2011\/126974<\/p>\n<p>3. Colletti, S.L.; Gosselin, F.; Jadhav, V.R.; Shaw, A.W.; Tellers, D.M.; Tucker, T.J.; Yuan, Y.; Zewge, D. Novel Single Chemical Entities and Methods for Delivery of Oligonucleotides. WO 2012\/030683<\/p>\n<p>2. Tellers, D. M.; Colletti, S. L.; Dudkin, V.; Aaronson, J.; Momose, A.; Tucker, T. J.; Yuan, Y.; Calati, K. B.; Tian, L.; Parmar, R. G.; Shaw, A. W.; Wang, W.; Storr, R. A.; Busuek, M.; Kowtoniuk, R. A. Novel TetraGalNAc and Peptide Containing Conjugates and Methods for Delivery of Oligonucleotides. WO 2013166155<\/p>\n<p>1. Tellers, D. M.; Colletti, S. L.; Dudkin, V.; Ikemoto, N.; Liao, H.; Parish, C.; Pei, T.; Shaw, A. W.; Truong, Q.; Wang, L.; Yuan, Y.; Zhu, M. Novel TetraGalNAc Containing Conjugates and Methods for Delivery of Oligonucleotides. WO 2013166121<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Selected Journal Articles Bobek, K. B.; Ezzat, N. S.; Jones, B. S.; Bian, Y.; Shaw, T. E.; Jurca, T.; Li,&hellip;<\/p>\n","protected":false},"author":3,"featured_media":87,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":"","_links_to":"","_links_to_target":""},"class_list":["post-31","page","type-page","status-publish","has-post-thumbnail","hentry"],"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v27.2 - https:\/\/yoast.com\/product\/yoast-seo-wordpress\/ -->\n<title>Work Completed at UCF - The Yuan Lab<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/sciences.ucf.edu\/chemistry\/yuanlab\/work-completed-at-ucf\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Work Completed at UCF - The Yuan Lab\" \/>\n<meta property=\"og:description\" content=\"Selected Journal Articles Bobek, K. 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