{"id":28,"date":"2019-08-27T15:59:30","date_gmt":"2019-08-27T19:59:30","guid":{"rendered":"https:\/\/sciencescosmaincms.cm.ucf.edu\/chemistry\/lee\/?page_id=28"},"modified":"2026-04-03T11:00:44","modified_gmt":"2026-04-03T15:00:44","slug":"publications","status":"publish","type":"page","link":"https:\/\/sciences.ucf.edu\/chemistry\/lee\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"\n

Patents:<\/h2>\n\n\n\n

6.<\/strong> \u201cMethod of preparing organosiloxane compound via dehydrogenative silylation\u201d
K. L. Lee, J. Lee, N. Swann, J. Choi and D. Katsoulis
2025<\/strong>, US Patent application<\/em> 63\/804,949
<\/p>\n\n\n\n

5.<\/strong> \u201cMethod of preparing organosilicon compound via dehydrogenative silylation\u201d
K. L. Lee, S. A. Shetu, J. Choi and D. Katsoulis
2025<\/strong>, US Patent application<\/em> 63\/804,937
<\/p>\n\n\n\n

4.<\/strong> \u201cCurable Silicone-Acrylate Compositions, Conductive Materials Prepared Therewith, and Related Methods\u201d
R. Cooper, J. M. Mecca, K. Lee, D. Ahn, S. Mangold, D. Zhao, K. McDonald, J. Sootsman
2021<\/strong>, <\/a>WO 2021150666 A1<\/a> <\/em><\/p>\n\n\n\n

3.<\/strong> \u201cSilicone-Acrylate, Copolymers, and Related Methods and Compositions\u201d
E. B. Vogel, R. E. Drumright, R. Cooper, J. M. Mecca, K. Lee, M. Lee, M. Jeletic, D. Ahn
2021<\/strong>, <\/a>WO 2021150667 A1<\/a><\/em><\/p>\n\n\n\n

2.<\/strong> \u201cSilicone-Acrylate Polymers, Copolymers, and Related Methods and Compositions\u201d
E. B. Vogel, R. E. Drumright, W. Sattler, T. Kuo, J. M. Mecca, K. Lee
2021<\/strong>, <\/a>WO 2021150668 A1<\/a><\/em><\/p>\n\n\n\n

1.<\/strong> \u201cMethod for Preparing Arylalkoxysilanes by Dehydrogenative Silylation\u201d
J. Choi, D. Katsoulis, K. Lee
2020<\/strong>, <\/a><\/strong>US Patent, <\/em>20200123181 A1<\/a><\/p>\n\n\n\n

Research articles:<\/h2>\n\n\n\n

19.<\/strong> \u201cTBA\u201d
S. A. Shetu, J. Choi, D, Katsoulis and K. L. Lee*
2026<\/strong>, Manuscript in preparation<\/em><\/em><\/p>\n\n\n\n

<\/p>\n\n\n\n

18.<\/strong> \u201cTBA\u201d
M. Flannagan,\u2021<\/sup> J. Lee,\u2021<\/sup> N. Swann, M. Domin, and K. L. Lee*
2026<\/strong>, Manuscript in preparation<\/em><\/em><\/em><\/em><\/em><\/em><\/p>\n\n\n\n

17.<\/strong> \u201cC\u2013H Silyl Polymerization: One-step Synthesis of Silarylene\u2013Siloxane Copolymers\u201d
J. Lee, N. Swann, J. Nam, J. Choi, D, Katsoulis and K. L. Lee*
2026<\/strong>, Submitted<\/em><\/p>\n\n\n\n

16.<\/strong> \u201cDirect Access of Heteroaryl Difunctional Monomers for Arene-enriched Polysiloxane Synthesis.\u201d
S. A. Shetu,\u2021<\/sup> J. Nam, J.\u2021<\/sup> Choi, D, Katsoulis, M. Domin, and K. L. Lee*
Org. Lett<\/em><\/em>. 2025<\/strong>, 27<\/em>, 6830\u20136835<\/a><\/p>\n\n\n\n

15.<\/strong> \u201cOne-step Synthesis of Aryl Monomers for Silicones enabled by Mechanistic Study of Intermolecular Dehydrogenative C\u2013H Silylations\u201d
S. Som, J. Nam, A. O. Farah, L. Borrego-Castaneda, S. A. Shetu, M. G. Flannagan, J. Lee, J. Choi, D. Katsoulis, B. Vanchura, M. Domin, T. E. Shaw, S. A. Kozimor, D. L. Gray, P. H.-Y. Cheong* and K. L. Lee*
ACS Catal<\/em>. 2025<\/strong>, 15<\/em>, 15444\u201315458<\/a>
<\/p>\n\n\n\n

14.<\/strong> \u201cIntermolecular C\u2013H Silylations of Arenes and Heteroarenes with Mono-, Bis-, and Tris(trimethylsiloxy)hydrosilanes: Control of Silane Redistribution under Operationally Diverse Approaches\u201d
N. Swann, K. Tang,\u2021<\/sup> J. Nam, J.\u2021<\/sup> Lee, M. Domin, T. E. Shaw, S. A. Kozimor, S. Som, and K. L. Lee*
Chem. Sci.<\/em> <\/em>2024<\/strong>, 15<\/em>, <\/em>11912\u201311918<\/a> <\/a><\/em> (1st<\/sup> & 2nd<\/sup> authors: undergraduate researchers)<\/em>
<\/p>\n\n\n\n

13.<\/strong> \u201cA Direct Method to Access Various Functional Arylalkoxysilanes by Rh-catalysed Intermolecular C\u2013H Silylation of Alkoxysilanes\u201d
S. Som, J. Choi, D. Katsoulis, and K. L. Lee*
Chem. Sci.<\/em> 2022<\/strong>, 13<\/em>, 10759\u201310764 <\/a><\/p>\n\n\n\n

12.<\/strong> \u201c(Aminomethyl)pyridine Complexes for the Co-catalyzed Anti-Markovnikov Hydrosilylation of Alkoxy- or Siloxy(vinyl)silanes with Alkoxy- or Siloxyhydrosilanes\u201d
K. L. Lee*
Angew. Chem., Int. Ed.<\/a> <\/em>2017<\/a><\/strong>, <\/a>56<\/a><\/em>, 3665\u20133669<\/a><\/p>\n\n\n\n

11.<\/strong> \u201cIntermolecular C\u2013H Silylation of Arenes and Heteroarenes with HSiEt3<\/sub> under Operationally Diverse Conditions: Neat\/Stoichiometric and Acceptor\/Acceptorless\u201d
K. Lee,* D. Katsoulis, J. Choi*
ACS Catal.<\/a> <\/em>2016<\/a><\/strong>, <\/a>6, <\/a><\/em>1493\u20131496<\/a><\/p>\n\n\n\n

\u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013 \u2013
<\/p>\n\n\n\n

10.<\/strong> \u201cNHC\u2013Cu-Catalyzed Silyl Conjugate Additions to Acyclic and Cyclic Dienones and Dienoates. Efficient Site-, Diastereo- and Enantioselective Synthesis of Carbonyl-Containing Allylsilanes\u201d
K. Lee, H. Wu, F. Haeffner, A. H. Hoveyda*
Organometallics<\/a> <\/em>2012<\/a><\/strong>, <\/a>31, <\/a><\/em>7823\u20137826<\/a><\/p>\n\n\n\n

9.<\/strong> \u201cEnantioselective Synthesis of Boron-Substituted Quaternary Carbons by NHC\u2013Cu-Catalyzed Boronate Conjugate Additions to Unsaturated Carboxylic Esters, Ketones, or Thioesters\u201d
J. M. O\u2019Brien, K. Lee, A. H. Hoveyda*
J. Am. Chem. Soc.<\/a> <\/em>2010<\/a><\/strong>, <\/a>132<\/a><\/em>, 10630\u201310633 <\/a> (Highlighted in Synfacts<\/em>, 2010<\/strong>, 1272)<\/p>\n\n\n\n

8.<\/strong> \u201cEnantioselective Conjugate Silyl Additions to Cyclic and Acyclic Unsaturated Carbonyls Catalyzed by Cu Complexes of Chiral N<\/em>-Heterocyclic Carbenes\u201d
K. Lee, A. H. Hoveyda*
J. Am. Chem. Soc<\/a>. <\/em>2010<\/a><\/strong>, <\/a>132<\/a><\/em>, 2898\u20132900<\/a> <\/p>\n\n\n\n

7.<\/strong> \u201cEfficient C\u2013B Bond Formation Promoted by N<\/em>-Heterocyclic Carbenes: Synthesis of Tertiary and Quaternary B-Substituted Carbons through Metal-Free Catalytic Boron Conjugate Additions to Cyclic and Acyclic a<\/em>,b<\/em>-Unsaturated Carbonyls\u201d
K. Lee, A. R. Zhugralin, A. H. Hoveyda*
J. Am. Chem. Soc.<\/a> <\/em>2009<\/a><\/strong>, <\/a>131<\/a><\/em>, 7253\u20137255<\/a> (Highlighted in Synfacts<\/em>, 2009<\/strong>, 898) <\/p>\n\n\n\n

6.<\/strong> \u201cMonodentate Non-C<\/em>2<\/sub>-Symmetric Chiral N-Heterocyclic Carbene Complexes for Enantioselective Synthesis. Cu-Catalyzed Conjugate Additions of Aryl- and Alkenylsilylfluorides to Cyclic Enones\u201d
K. Lee, A. H. Hoveyda*
J. Org. Chem.<\/a> <\/em>2009<\/a><\/strong>, <\/a>74<\/a><\/em>, 4455\u20134462<\/a>  (Highlighted in C&E<\/em> News<\/em> 2009<\/strong>, June 8<\/em>, 52<\/a> and in Synfacts<\/em>, 2009<\/strong>, 993)<\/p>\n\n\n\n

5.<\/strong> \u201cA Practical Method for Enantioselective Synthesis of All-Carbon Quaternary Stereogenic Centers through NHC\u2013Cu-Catalyzed Conjugate Additions of Alkyl- and Arylzinc Reagents to b<\/em>-Substituted Cyclic Enones\u201d
K. Lee, M. K. Brown, A. W. Hird, A. H. Hoveyda*
J. Am. Chem. Soc.<\/a> <\/em>2006<\/a><\/strong>, <\/a>128<\/a><\/em>, 7182\u20137184<\/a>  (Highlighted in Synfacts<\/em>, 2006<\/strong>, 913)<\/p>\n\n\n\n

4.<\/strong> \u201cCu(I) Mediated One-Pot Synthesis of Azobenzenes from Bis-Boc Aryl Hydrazines and Aryl Halides\u201d
K. Kim, J. Shin, K. Lee, C. Cho*
Tetrahedron Lett<\/a>. <\/em><\/a><\/a><\/a>2004<\/a><\/strong><\/a><\/a><\/a><\/a><\/a>, <\/a><\/a><\/a><\/a><\/a>45<\/a><\/em><\/a><\/a><\/a><\/a><\/a><\/a><\/a><\/a>, 117\u2013120<\/p>\n\n\n\n

3.<\/strong> \u201cNovel Route to Azobenzenes via Pd-Catalyzed Coupling Reactions of Aryl Hydrazides with Aryl Halides, Followed by Direct Oxidations\u201d
Y. Lim, K. Lee, C. Cho*
Org. Lett.<\/a> <\/em>2003<\/a><\/strong>, <\/a>5<\/a><\/em>, 979\u2013982<\/a><\/p>\n\n\n\n

2.<\/strong> \u201cAg+<\/sup> Mediated Deaminations of N-Boc Hydrazines for the Efficient Synthesis of N<\/em>-Boc Aryl Amines\u201d
K. Lee, Y. Lim, C. Cho*
Tetrahe<\/a>dron Le<\/a>tt<\/a>. <\/em>2002<\/a><\/strong>, <\/a>43<\/a><\/em>, 7463\u20137464<\/a><\/p>\n\n\n\n

1.<\/strong> \u201cOverman Rearrangement of Aryl Crotyl Alcohols: Effects of Aryl Substituents\u201d
C. Cho,* Y. Lim, K. Lee, I. Jung, M. Yoon
Synth. Commun.<\/a> <\/em>2000<\/a><\/strong>, <\/a>30<\/a><\/em>, 1643\u20131650.<\/a><\/p>\n\n\n\n

Book Chapter:<\/h2>\n\n\n\n

1.<\/strong> \u201cActivation of B\u2013B and B\u2013Si Bonds and Synthesis of Organoboron and Organosilicon Compounds through Lewis Base-Catalyzed Transformations (n\u2192n*)\u201d
A. H. Hoveyda, H. Wu, S. Radomkit, J. M. Garcia, F. Haeffner, K. Lee
\u201cLewis Base Catalysis in Organic Synthesis\u201d<\/a><\/em> E. Vedejs, S. E. Denmark, Eds; Wiley-VCH, Verlag GmbH & Co., 2016; pp. 967\u00ad\u20131010<\/a><\/p>\n\n\n\n

<\/p>\n","protected":false},"excerpt":{"rendered":"

Patents: 6. \u201cMethod of preparing organosiloxane compound via dehydrogenative silylation\u201d K. L. Lee, J. Lee, N. Swann, J. Choi and D. Katsoulis 2025, US Patent application 63\/804,949 5. \u201cMethod of preparing organosilicon compound via dehydrogenative silylation\u201d K. L. Lee, S. A. Shetu, J. Choi and D. Katsoulis 2025, US Patent application 63\/804,937 4. \u201cCurable Silicone-Acrylate
+ Read More<\/a><\/p>\n","protected":false},"author":42,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":"","_links_to":"","_links_to_target":""},"class_list":["post-28","page","type-page","status-publish","hentry"],"yoast_head":"\nPublications - Lee Research Group<\/title>\n<meta name=\"robots\" content=\"noindex, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Publications - Lee Research Group\" \/>\n<meta property=\"og:description\" content=\"Patents: 6. \u201cMethod of preparing organosiloxane compound via dehydrogenative silylation\u201d K. L. Lee, J. Lee, N. Swann, J. Choi and D. Katsoulis 2025, US Patent application 63\/804,949 5. \u201cMethod of preparing organosilicon compound via dehydrogenative silylation\u201d K. L. Lee, S. A. Shetu, J. Choi and D. Katsoulis 2025, US Patent application 63\/804,937 4. \u201cCurable Silicone-Acrylate+ Read More\" \/>\n<meta property=\"og:url\" content=\"https:\/\/sciences.ucf.edu\/chemistry\/lee\/publications\/\" \/>\n<meta property=\"og:site_name\" content=\"Lee Research Group\" \/>\n<meta property=\"article:modified_time\" content=\"2026-04-03T15:00:44+00:00\" \/>\n<meta name=\"twitter:card\" content=\"summary_large_image\" \/>\n<meta name=\"twitter:label1\" content=\"Est. reading time\" \/>\n\t<meta name=\"twitter:data1\" content=\"4 minutes\" \/>\n<script type=\"application\/ld+json\" class=\"yoast-schema-graph\">{\"@context\":\"https:\/\/schema.org\",\"@graph\":[{\"@type\":\"WebPage\",\"@id\":\"https:\/\/sciences.ucf.edu\/chemistry\/lee\/publications\/\",\"url\":\"https:\/\/sciences.ucf.edu\/chemistry\/lee\/publications\/\",\"name\":\"Publications - Lee Research Group\",\"isPartOf\":{\"@id\":\"https:\/\/sciences.ucf.edu\/chemistry\/lee\/#website\"},\"datePublished\":\"2019-08-27T19:59:30+00:00\",\"dateModified\":\"2026-04-03T15:00:44+00:00\",\"inLanguage\":\"en-US\",\"potentialAction\":[{\"@type\":\"ReadAction\",\"target\":[\"https:\/\/sciences.ucf.edu\/chemistry\/lee\/publications\/\"]}]},{\"@type\":\"WebSite\",\"@id\":\"https:\/\/sciences.ucf.edu\/chemistry\/lee\/#website\",\"url\":\"https:\/\/sciences.ucf.edu\/chemistry\/lee\/\",\"name\":\"Lee Research Group\",\"description\":\"Department of Chemistry\",\"potentialAction\":[{\"@type\":\"SearchAction\",\"target\":{\"@type\":\"EntryPoint\",\"urlTemplate\":\"https:\/\/sciences.ucf.edu\/chemistry\/lee\/?s={search_term_string}\"},\"query-input\":{\"@type\":\"PropertyValueSpecification\",\"valueRequired\":true,\"valueName\":\"search_term_string\"}}],\"inLanguage\":\"en-US\"}]}<\/script>\n<!-- \/ Yoast SEO plugin. -->","yoast_head_json":{"title":"Publications - Lee Research Group","robots":{"index":"noindex","follow":"follow","max-snippet":"max-snippet:-1","max-image-preview":"max-image-preview:large","max-video-preview":"max-video-preview:-1"},"og_locale":"en_US","og_type":"article","og_title":"Publications - Lee Research Group","og_description":"Patents: 6. \u201cMethod of preparing organosiloxane compound via dehydrogenative silylation\u201d K. L. Lee, J. Lee, N. Swann, J. Choi and D. Katsoulis 2025, US Patent application 63\/804,949 5. \u201cMethod of preparing organosilicon compound via dehydrogenative silylation\u201d K. L. Lee, S. A. Shetu, J. Choi and D. Katsoulis 2025, US Patent application 63\/804,937 4. \u201cCurable Silicone-Acrylate+ Read More","og_url":"https:\/\/sciences.ucf.edu\/chemistry\/lee\/publications\/","og_site_name":"Lee Research Group","article_modified_time":"2026-04-03T15:00:44+00:00","twitter_card":"summary_large_image","twitter_misc":{"Est. reading time":"4 minutes"},"schema":{"@context":"https:\/\/schema.org","@graph":[{"@type":"WebPage","@id":"https:\/\/sciences.ucf.edu\/chemistry\/lee\/publications\/","url":"https:\/\/sciences.ucf.edu\/chemistry\/lee\/publications\/","name":"Publications - Lee Research Group","isPartOf":{"@id":"https:\/\/sciences.ucf.edu\/chemistry\/lee\/#website"},"datePublished":"2019-08-27T19:59:30+00:00","dateModified":"2026-04-03T15:00:44+00:00","inLanguage":"en-US","potentialAction":[{"@type":"ReadAction","target":["https:\/\/sciences.ucf.edu\/chemistry\/lee\/publications\/"]}]},{"@type":"WebSite","@id":"https:\/\/sciences.ucf.edu\/chemistry\/lee\/#website","url":"https:\/\/sciences.ucf.edu\/chemistry\/lee\/","name":"Lee Research Group","description":"Department of Chemistry","potentialAction":[{"@type":"SearchAction","target":{"@type":"EntryPoint","urlTemplate":"https:\/\/sciences.ucf.edu\/chemistry\/lee\/?s={search_term_string}"},"query-input":{"@type":"PropertyValueSpecification","valueRequired":true,"valueName":"search_term_string"}}],"inLanguage":"en-US"}]}},"_links":{"self":[{"href":"https:\/\/sciences.ucf.edu\/chemistry\/lee\/wp-json\/wp\/v2\/pages\/28","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/sciences.ucf.edu\/chemistry\/lee\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/sciences.ucf.edu\/chemistry\/lee\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/sciences.ucf.edu\/chemistry\/lee\/wp-json\/wp\/v2\/users\/42"}],"replies":[{"embeddable":true,"href":"https:\/\/sciences.ucf.edu\/chemistry\/lee\/wp-json\/wp\/v2\/comments?post=28"}],"version-history":[{"count":116,"href":"https:\/\/sciences.ucf.edu\/chemistry\/lee\/wp-json\/wp\/v2\/pages\/28\/revisions"}],"predecessor-version":[{"id":681,"href":"https:\/\/sciences.ucf.edu\/chemistry\/lee\/wp-json\/wp\/v2\/pages\/28\/revisions\/681"}],"wp:attachment":[{"href":"https:\/\/sciences.ucf.edu\/chemistry\/lee\/wp-json\/wp\/v2\/media?parent=28"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}