{"id":53,"date":"2017-01-05T19:58:12","date_gmt":"2017-01-05T19:58:12","guid":{"rendered":"http:\/\/pcr550.chem.elte.hu\/wordpress\/?page_id=53"},"modified":"2025-12-05T09:44:36","modified_gmt":"2025-12-05T09:44:36","slug":"publications","status":"publish","type":"page","link":"http:\/\/tolnai.chem.elte.hu\/?page_id=53","title":{"rendered":"Publications"},"content":{"rendered":"\n<hr class=\"wp-block-separator has-css-opacity\"\/>\n\n\n\n<h6 class=\"wp-block-heading\"><a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/full\/10.1002\/anie.202424425\">17. Guideline for Analysis and Prevention of Contamination Catalysis.<\/a><\/h6>\n\n\n\n<figure class=\"wp-block-image size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"932\" height=\"847\" src=\"http:\/\/tolnai.chem.elte.hu\/wp-content\/uploads\/2025\/12\/ACIE_TOC_Guideline250414b.png\" alt=\"\" class=\"wp-image-921\" srcset=\"http:\/\/tolnai.chem.elte.hu\/wp-content\/uploads\/2025\/12\/ACIE_TOC_Guideline250414b.png 932w, http:\/\/tolnai.chem.elte.hu\/wp-content\/uploads\/2025\/12\/ACIE_TOC_Guideline250414b-300x273.png 300w, http:\/\/tolnai.chem.elte.hu\/wp-content\/uploads\/2025\/12\/ACIE_TOC_Guideline250414b-768x698.png 768w\" sizes=\"auto, (max-width: 932px) 100vw, 932px\" \/><\/figure>\n\n\n\n<p>Daru, J.; Gonda, Z.; May, Z.; Nov\u00e1k, Z.; Tolnai, G. L.,<\/p>\n\n\n\n<p><em>Angew. Chem. Int. Ed.<\/em> <strong>2025<\/strong>, 64 (<em>26<\/em>), e202424425.<\/p>\n\n\n\n<h6 class=\"wp-block-heading\"><a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.orglett.4c00511\">16. Photoinduced Decarboxylative Borylation of <em>N<\/em>-Hydroxyphthalimide Esters with Hypoboric Acid<\/a><\/h6>\n\n\n\n<figure class=\"wp-block-image size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"717\" height=\"385\" src=\"http:\/\/tolnai.chem.elte.hu\/wp-content\/uploads\/2025\/12\/abstract5.jpg\" alt=\"\" class=\"wp-image-920\" srcset=\"http:\/\/tolnai.chem.elte.hu\/wp-content\/uploads\/2025\/12\/abstract5.jpg 717w, http:\/\/tolnai.chem.elte.hu\/wp-content\/uploads\/2025\/12\/abstract5-300x161.jpg 300w\" sizes=\"auto, (max-width: 717px) 100vw, 717px\" \/><\/figure>\n\n\n\n<p>Nagy, B.; Gonda, Z.; F\u00f6ldesi, T.; Feh\u00e9r, P. P.; Stirling, A.; Tolnai, G. L.; Nov\u00e1k, Z.,<\/p>\n\n\n\n<p><em>Org. Lett.<\/em> <strong>2024<\/strong>, 26 (<em>11<\/em>), 2292-2296.<\/p>\n\n\n\n<h6 class=\"wp-block-heading\" id=\"15-synthesis-and-use-of-bicyclo-1-1-1-pentylaldehyde-building-blocks\">15. <a href=\"https:\/\/pubs.acs.org\/doi\/full\/10.1021\/acs.joc.1c02267\" target=\"_blank\" rel=\"noreferrer noopener\">Synthesis and Use of Bicyclo[1.1.1]pentylaldehyde Building Blocks<\/a><\/h6>\n\n\n\n<figure class=\"wp-block-image size-full\"><img loading=\"lazy\" decoding=\"async\" width=\"747\" height=\"387\" src=\"http:\/\/tolnai.chem.elte.hu\/wp-content\/uploads\/2022\/01\/Aldehid-TOC_2.jpg\" alt=\"\" class=\"wp-image-852\" srcset=\"http:\/\/tolnai.chem.elte.hu\/wp-content\/uploads\/2022\/01\/Aldehid-TOC_2.jpg 747w, http:\/\/tolnai.chem.elte.hu\/wp-content\/uploads\/2022\/01\/Aldehid-TOC_2-300x155.jpg 300w\" sizes=\"auto, (max-width: 747px) 100vw, 747px\" \/><\/figure>\n\n\n\n<p>D\u00e1niel Las\u00e1nyi, D\u00e1niel M\u00e1th, Gergely L. Tolnai*<\/p>\n\n\n\n<p><em>J. Org. Chem. 2022<\/em>, 87, 5, 2393\u20132401<\/p>\n\n\n\n<h6 class=\"wp-block-heading\" id=\"14-revisiting-the-amine-catalysed-cross-coupling\">14. <a href=\"https:\/\/www.nature.com\/articles\/s41929-021-00709-8\">Revisiting the amine-catalysed cross-coupling<\/a><\/h6>\n\n\n\n<p>Zolt\u00e1n Nov\u00e1k, R\u00e9ka Adamik, J\u00e1nos T Csenki, Ferenc B\u00e9ke, Regina Gavaldik, B\u00e1lint Varga, B\u00e1lint Nagy, Zolt\u00e1n May, J\u00e1nos Daru, Zsombor Gonda, Gergely L Tolnai<\/p>\n\n\n\n<p><em>Nature Catalysis<\/em> 2021, 4, 991.<\/p>\n\n\n\n<h6 class=\"wp-block-heading\" id=\"13-synthesis-and-biological-studiesof-o3-arylgalactosides-as-galectin-inhibitors\">13. <a href=\"https:\/\/onlinelibrary.wiley.com\/doi\/epdf\/10.1002\/hlca.202000220\" target=\"_blank\" rel=\"noreferrer noopener\">Synthesis and Biological Studiesof O3-ArylGalactosides as Galectin Inhibitors<\/a><\/h6>\n\n\n\n<p>Gabriella Kervefors, Kumar Bhaskar Pal, Gergely L Tolnai, Mukul Mahanti, Hakon Leffler, Ulf J Nilsson, Berit Olofsson*<\/p>\n\n\n\n<p><em>Helv. Chim. Acta <\/em>2021, 104, e2000220.<\/p>\n\n\n\n<h6 class=\"wp-block-heading\" id=\"12-copper-catalyzed-ring-opening-of-1-1-1-propellane-with-alkynes-synthesis-of-exocyclic-allenic-cyclobutanes\">12. <a rel=\"noreferrer noopener\" aria-label=\" (opens in a new tab)\" href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.orglett.9b03999\" target=\"_blank\">Copper-Catalyzed Ring Opening of [1.1.1]Propellane with Alkynes: Synthesis of Exocyclic Allenic Cyclobutanes<\/a><\/h6>\n\n\n\n<p>Las\u00e1nyi, D; Tolnai, G. L.*<br><em>Org. Lett.<\/em> 2019, 21, 24, 10057-10062 <\/p>\n\n\n\n<figure class=\"wp-block-image size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"614\" height=\"82\" src=\"http:\/\/tolnai.chem.elte.hu\/wp-content\/uploads\/2019\/12\/Cyclobut_graph_abs.jpg\" alt=\"\" class=\"wp-image-760\" srcset=\"http:\/\/tolnai.chem.elte.hu\/wp-content\/uploads\/2019\/12\/Cyclobut_graph_abs.jpg 614w, http:\/\/tolnai.chem.elte.hu\/wp-content\/uploads\/2019\/12\/Cyclobut_graph_abs-300x40.jpg 300w\" sizes=\"auto, (max-width: 614px) 100vw, 614px\" \/><\/figure>\n\n\n\n<h6 class=\"wp-block-heading\" id=\"11-transition-metal-catalyzed-reactions-with-iodine-iii-reagents\">11. <a rel=\"noreferrer noopener\" href=\"https:\/\/onlinelibrary.wiley.com\/doi\/abs\/10.1002\/9780470682531.pat0961\" target=\"_blank\">TRANSITION METAL-CATALYZED REACTIONS WITH IODINE(III) REAGENTS<\/a><\/h6>\n\n\n\n<p>Gergely L. Tolnai, Zsombor Gonda, and Zolt\u00e1n Nov\u00e1k<br>pp 919<br>in <em>The Chemistry of Hypervalent Halogen Compounds<\/em><br>edited by Olofsson, Marek, Rappoport<\/p>\n\n\n\n<h6 class=\"wp-block-heading\" id=\"10-catalytic-activation-of-trimethylsilylacetylenes-a-one-pot-route-to-unsymmetrical-acetylenes-and-heterocycles\">10.<a rel=\"noreferrer noopener\" href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.joc.8b00998\" target=\"_blank\">Catalytic Activation of Trimethylsilylacetylenes: A \u201cOne \u2013Pot\u201d Route to Unsymmetrical Acetylenes and Heterocycles<\/a><\/h6>\n\n\n\n<p> Las\u00e1nyi D., M\u00e9sz\u00e1ros \u00c1, Nov\u00e1k Z, and Tolnai G. L.*<br> J. Org. Chem., <strong>2018<\/strong>, <em>83<\/em>, 8281 <\/p>\n\n\n\n<figure class=\"wp-block-image size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"904\" height=\"140\" src=\"http:\/\/tolnai.chem.elte.hu\/wp-content\/uploads\/2019\/12\/Cat_desilyl_Graph_abd.jpg\" alt=\"\" class=\"wp-image-761\" srcset=\"http:\/\/tolnai.chem.elte.hu\/wp-content\/uploads\/2019\/12\/Cat_desilyl_Graph_abd.jpg 904w, http:\/\/tolnai.chem.elte.hu\/wp-content\/uploads\/2019\/12\/Cat_desilyl_Graph_abd-300x46.jpg 300w, http:\/\/tolnai.chem.elte.hu\/wp-content\/uploads\/2019\/12\/Cat_desilyl_Graph_abd-768x119.jpg 768w\" sizes=\"auto, (max-width: 904px) 100vw, 904px\" \/><\/figure>\n\n\n\n<h6 class=\"wp-block-heading\" id=\"9-gold-catalyzed-direct-alkynylation-of-azulenes\">9.<a rel=\"noreferrer noopener\" href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.orglett.7b00259\" target=\"_blank\">Gold-Catalyzed Direct Alkynylation of Azulenes<\/a><\/h6>\n\n\n\n<p>Sz\u00e9kely, A.,&nbsp; P\u00e9ter \u00c1., Aradi, K., Tolnai, G. L.,* Nov\u00e1k, Z.*<br>Org. Lett.,<strong> 2017<\/strong>, <em>19<\/em>, 954<\/p>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"484\" height=\"190\" src=\"http:\/\/tolnai.chem.elte.hu\/wp-content\/uploads\/2019\/12\/azulene_graph_abs.jpg\" alt=\"\" class=\"wp-image-763\" srcset=\"http:\/\/tolnai.chem.elte.hu\/wp-content\/uploads\/2019\/12\/azulene_graph_abs.jpg 484w, http:\/\/tolnai.chem.elte.hu\/wp-content\/uploads\/2019\/12\/azulene_graph_abs-300x118.jpg 300w\" sizes=\"auto, (max-width: 484px) 100vw, 484px\" \/><\/figure><\/div>\n\n\n<h6 class=\"wp-block-heading\" id=\"8-efficient-o-functionalization-of-carbohydrates-with-electrophilic-reagents\">8. <a rel=\"noreferrer noopener\" href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/anie.201605999\/abstract\" target=\"_blank\">Efficient O-Functionalization of Carbohydrates with Electrophilic Reagents<\/a><\/h6>\n\n\n\n<p>Tolnai, G. L., Nilsson, U. J., Olofsson, B.*<br><em>Angew. Chem. Int. Ed.<\/em> <strong>2016,<\/strong> <em>55<\/em><strong>, <\/strong>11226.<br><em>Angew. Chem.<\/em> <strong>2016,<\/strong> <em>128<\/em>, 11392.<\/p>\n\n\n\n<figure class=\"wp-block-image size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"620\" height=\"619\" src=\"http:\/\/tolnai.chem.elte.hu\/wp-content\/uploads\/2019\/12\/TOC0717.jpg\" alt=\"\" class=\"wp-image-767\" srcset=\"http:\/\/tolnai.chem.elte.hu\/wp-content\/uploads\/2019\/12\/TOC0717.jpg 620w, http:\/\/tolnai.chem.elte.hu\/wp-content\/uploads\/2019\/12\/TOC0717-300x300.jpg 300w, http:\/\/tolnai.chem.elte.hu\/wp-content\/uploads\/2019\/12\/TOC0717-150x150.jpg 150w\" sizes=\"auto, (max-width: 620px) 100vw, 620px\" \/><\/figure>\n\n\n\n<h6 class=\"wp-block-heading\" id=\"7-gold-catalyzed-direct-alkynylation-of-tryptophan-in-peptides-using-tips-ebx\">7. <a rel=\"noreferrer noopener\" href=\"http:\/\/www.beilstein-journals.org\/bjoc\/single\/articleFullText.htm?publicId=1860-5397-12-74\" target=\"_blank\">Gold-catalyzed direct alkynylation of tryptophan in peptides using TIPS-EBX<\/a><\/h6>\n\n\n\n<p>Tolnai, G. L., Brand, J., Waser, J.*<br><em>Beilstein J. Org. Chem.<\/em>, <strong>2016<\/strong>, <em>12,<\/em> 745<\/p>\n\n\n<div class=\"wp-block-image\">\n<figure class=\"aligncenter size-large\"><img loading=\"lazy\" decoding=\"async\" width=\"480\" height=\"164\" src=\"http:\/\/tolnai.chem.elte.hu\/wp-content\/uploads\/2019\/12\/Beilstein_JOC_PeptideGraph_abs.jpg\" alt=\"\" class=\"wp-image-774\" srcset=\"http:\/\/tolnai.chem.elte.hu\/wp-content\/uploads\/2019\/12\/Beilstein_JOC_PeptideGraph_abs.jpg 480w, http:\/\/tolnai.chem.elte.hu\/wp-content\/uploads\/2019\/12\/Beilstein_JOC_PeptideGraph_abs-300x103.jpg 300w\" sizes=\"auto, (max-width: 480px) 100vw, 480px\" \/><\/figure><\/div>\n\n<h6>6. <a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0035-1561369\" target=\"_blank\" rel=\"noopener noreferrer\">Diaryliodonium Salts in Organic Syntheses:<\/a><br \/><a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0035-1561369\" target=\"_blank\" rel=\"noopener noreferrer\">A Useful Compound Class for Novel Arylation Strategies<\/a><\/h6>\n<p style=\"padding-left: 30px;\">Aradi, K.; T\u00f3th, B.; Tolnai, G. L.; Nov\u00e1k, Z.*<br \/><em>Synlett<\/em>, <strong>2016<\/strong>, <em>27,<\/em> 1456<\/p>\n<h6>5. <a href=\"http:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2015\/cc\/c5cc00519a#!divAbstract\" target=\"_blank\" rel=\"noopener noreferrer\">Efficient direct 2,2,2-trifluoroethylation of indoles via C-H functionalization<\/a><\/h6>\n<p style=\"padding-left: 30px;\">Tolnai, G. L.; Sz\u00e9kely, A.,; Mako, Z.; Gati, T; Daru, J; Bihari, T; Stirling, A;* Nov\u00e1k, Z.*<br \/><em>Chem. Commun. <\/em><strong>2015<\/strong>, <em>51<\/em>, 4488.<\/p>\n<h6>4. <a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/adsc.201300687\/abstract;jsessionid=C3EEEE173D63E8EFB9967AB0CEFAE564.f02t04\" target=\"_blank\" rel=\"noopener noreferrer\">Palladium-Catalyzed Methoxylation of Aromatic Chlorides with Borate Salts<\/a><\/h6>\n<p style=\"padding-left: 30px;\">Tolnai, G. L.; Peth\u0151, B.; Kr\u00e1ll, P.; Nov\u00e1k, Z.*<br \/><em>Adv. Synth. Catal.<\/em> <strong>2014<\/strong>, <em>356<\/em>, 125.<\/p>\n<h6>3. <a href=\"http:\/\/pubs.acs.org\/doi\/abs\/10.1021\/ol3031389?journalCode=orlef7&amp;quickLinkVolume=15&amp;quickLinkPage=112&amp;selectedTab=citation&amp;volume=15\" target=\"_blank\" rel=\"noopener noreferrer\">C2 Selective Direct Alkynylation of Indoles<\/a><\/h6>\n<p style=\"padding-left: 30px;\">Tolnai, G. L.; Ganss, S.; Brand, J. P.; Waser, J.*<br \/><em>Org. Lett.<\/em>, <strong>2013<\/strong>, <em>15<\/em>, 112<\/p>\n<h6>2. <a href=\"http:\/\/onlinelibrary.wiley.com\/doi\/10.1002\/chem.201001880\/abstract;jsessionid=57000E473F2CEAB657E657796C0C421E.f02t03\">Dramatic Impact of ppb Levels of Palladium on the \u201cCopper-Catalyzed\u201d Sonogashira Coupling<\/a><\/h6>\n<p style=\"padding-left: 30px;\">Tolnai, G. L.; Gonda, Z.; Nov\u00e1k, Z.*<br \/><em>Chem. Eur J<\/em>., <strong>2010<\/strong>, <em>16<\/em>, 11822.<\/p>\n<h6>1. <a href=\"http:\/\/www.sciencedirect.com\/science\/article\/pii\/S0040403908019126\" target=\"_blank\" rel=\"noopener noreferrer\">Copper-free Sonogashira coupling in amine-water solvent mixtures<\/a><\/h6>\n<p style=\"padding-left: 30px;\">Kom\u00e1romi, A.; Tolnai, G. L.; Nov\u00e1k, Z.*<br \/><em>Tetrahedron Lett.<\/em>, <strong>2008<\/strong>, <em>49<\/em>, 7294.<\/p>","protected":false},"excerpt":{"rendered":"<p>17. Guideline for Analysis and Prevention of Contamination Catalysis. Daru, J.; Gonda, Z.; May, Z.; Nov\u00e1k, Z.; Tolnai, G. L., Angew. Chem. Int. Ed. 2025, 64 (26), e202424425. 16. Photoinduced Decarboxylative Borylation of N-Hydroxyphthalimide Esters with Hypoboric Acid Nagy, B.; Gonda, Z.; F\u00f6ldesi, T.; Feh\u00e9r, P. P.; Stirling, A.; Tolnai, G. L.; Nov\u00e1k, Z., Org. &hellip; <a href=\"http:\/\/tolnai.chem.elte.hu\/?page_id=53\" class=\"more-link\">Continue reading <span class=\"screen-reader-text\">Publications<\/span><\/a><\/p>\n","protected":false},"author":1,"featured_media":0,"parent":0,"menu_order":0,"comment_status":"closed","ping_status":"closed","template":"","meta":{"footnotes":""},"class_list":["post-53","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"http:\/\/tolnai.chem.elte.hu\/index.php?rest_route=\/wp\/v2\/pages\/53","targetHints":{"allow":["GET"]}}],"collection":[{"href":"http:\/\/tolnai.chem.elte.hu\/index.php?rest_route=\/wp\/v2\/pages"}],"about":[{"href":"http:\/\/tolnai.chem.elte.hu\/index.php?rest_route=\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"http:\/\/tolnai.chem.elte.hu\/index.php?rest_route=\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"http:\/\/tolnai.chem.elte.hu\/index.php?rest_route=%2Fwp%2Fv2%2Fcomments&post=53"}],"version-history":[{"count":23,"href":"http:\/\/tolnai.chem.elte.hu\/index.php?rest_route=\/wp\/v2\/pages\/53\/revisions"}],"predecessor-version":[{"id":926,"href":"http:\/\/tolnai.chem.elte.hu\/index.php?rest_route=\/wp\/v2\/pages\/53\/revisions\/926"}],"wp:attachment":[{"href":"http:\/\/tolnai.chem.elte.hu\/index.php?rest_route=%2Fwp%2Fv2%2Fmedia&parent=53"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}