{"id":52,"date":"2021-08-13T23:20:12","date_gmt":"2021-08-13T23:20:12","guid":{"rendered":"https:\/\/kaviaari.kapsi.fi\/wordpress\/?page_id=52"},"modified":"2021-10-28T14:56:20","modified_gmt":"2021-10-28T14:56:20","slug":"publications","status":"publish","type":"page","link":"https:\/\/kaviaari.kapsi.fi\/wordpress\/publications\/","title":{"rendered":"Publications"},"content":{"rendered":"\n<h4 class=\"wp-block-heading\"><strong>Independent career<\/strong><\/h4>\n\n\n\n<p>4. Nurmi, T.*;&nbsp;<strong>Siitonen, J. H.* <\/strong>&#8220;Upper Secondary School and University Level Students\u2019 Perceptions of Extractions in Context: Experiences from a Simple Laboratory Experiment&#8221;,<strong>&nbsp;<\/strong><a href=\"https:\/\/doi.org\/10.33774\/chemrxiv-2021-wdrwc\">ChemRxiv preprint<\/a>, <strong>2021.<\/strong><\/p>\n\n\n\n<p>3. Serna, A. V.; K\u00fcrti, L.*,\u00a0<strong>Siitonen, J. H.*\u00a0<\/strong>\u201cTotal Synthesis of (\u00b1)-Setigerumine I: Biosynthetic Origins of the Elusive Racemic\u00a0<em>Papaveracaea<\/em>\u00a0Isoxazolidine Alkaloids\u201d, <em>Angew. Chem. Int. Ed.<\/em>\u00a0<strong>2021<\/strong>, Accepted. (<a href=\"https:\/\/doi.org\/10.1002\/anie.202111049\">DOI<\/a>).<\/p>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter size-large is-resized\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/kaviaari.kapsi.fi\/wordpress\/wp-content\/uploads\/2021\/08\/setigerumine_TOC-1024x311.png\" alt=\"\" class=\"wp-image-35\" width=\"768\" height=\"233\" srcset=\"https:\/\/kaviaari.kapsi.fi\/wordpress\/wp-content\/uploads\/2021\/08\/setigerumine_TOC-1024x311.png 1024w, https:\/\/kaviaari.kapsi.fi\/wordpress\/wp-content\/uploads\/2021\/08\/setigerumine_TOC-300x91.png 300w, https:\/\/kaviaari.kapsi.fi\/wordpress\/wp-content\/uploads\/2021\/08\/setigerumine_TOC-768x233.png 768w, https:\/\/kaviaari.kapsi.fi\/wordpress\/wp-content\/uploads\/2021\/08\/setigerumine_TOC-1536x466.png 1536w, https:\/\/kaviaari.kapsi.fi\/wordpress\/wp-content\/uploads\/2021\/08\/setigerumine_TOC-2048x621.png 2048w\" sizes=\"auto, (max-width: 768px) 100vw, 768px\" \/><\/figure><\/div>\n\n\n\n<p>2. Kattamuri, P. V.;&nbsp;<strong>Siitonen, J. H.*<\/strong>; Morgan, N. Ess, D. H.*, K\u00fcrti, L.*&nbsp;<em>Submitted<\/em>,<em> <\/em><strong>2021<\/strong>.<\/p>\n\n\n\n<p>1.<strong>&nbsp;Siitonen, J. H.<\/strong>*; Lira, S.; Youssufuddin, M.; K\u00fcrti, L.* \u201cTotal Synthesis of Isatindigotindoline C\u201d,&nbsp;<em>Org. Biomol. Chem.<\/em>&nbsp;<strong>2020<\/strong>,&nbsp;<em>18<\/em>, 2051&nbsp;<a href=\"https:\/\/doi.org\/10.1039\/D0OB00270D\">(DOI)<\/a><em>.<\/em>&nbsp;Featured in&nbsp;<a href=\"https:\/\/www.organic-chemistry.org\/Highlights\/2020\/16November.shtm\">Org. Chem. Highlights: Alkaloid Synthesis<\/a>.<\/p>\n\n\n\n<div class=\"wp-block-image\"><figure class=\"aligncenter size-large is-resized\"><img loading=\"lazy\" decoding=\"async\" src=\"https:\/\/kaviaari.kapsi.fi\/wordpress\/wp-content\/uploads\/2021\/10\/isatindigotindoline_c_toc-1024x354.png\" alt=\"\" class=\"wp-image-317\" width=\"768\" height=\"266\" srcset=\"https:\/\/kaviaari.kapsi.fi\/wordpress\/wp-content\/uploads\/2021\/10\/isatindigotindoline_c_toc-1024x354.png 1024w, https:\/\/kaviaari.kapsi.fi\/wordpress\/wp-content\/uploads\/2021\/10\/isatindigotindoline_c_toc-300x104.png 300w, https:\/\/kaviaari.kapsi.fi\/wordpress\/wp-content\/uploads\/2021\/10\/isatindigotindoline_c_toc-768x266.png 768w, https:\/\/kaviaari.kapsi.fi\/wordpress\/wp-content\/uploads\/2021\/10\/isatindigotindoline_c_toc-1536x532.png 1536w, https:\/\/kaviaari.kapsi.fi\/wordpress\/wp-content\/uploads\/2021\/10\/isatindigotindoline_c_toc-2048x709.png 2048w\" sizes=\"auto, (max-width: 768px) 100vw, 768px\" \/><\/figure><\/div>\n\n\n\n<h4 class=\"wp-block-heading\"><strong>Mentored career<\/strong><\/h4>\n\n\n\n<p>13. Paudyal, M. P.; Wang, M.;&nbsp;<strong>Siitonen, J. H.<\/strong>;&nbsp; Hu, Y.; Yousufuddin, M.; Shen, H. C.*; Falck, J. R.* K\u00fcrti, L.* \u201cIntramolecular&nbsp;<em>N<\/em>-Me and&nbsp;<em>N<\/em>-H Aminoetherification for the Synthesis of&nbsp;<em>N<\/em>-Unprotected 3-Amino-<em>O<\/em>-Heterocycles\u201d&nbsp;<em>Org. Biomol. Chem.<\/em>&nbsp;<strong>2021<\/strong>,&nbsp;<em>19<\/em>, 557. (<a href=\"https:\/\/pubs.rsc.org\/en\/content\/articlelanding\/2021\/ob\/d0ob02122a#!divAbstract\">DOI<\/a>).<\/p>\n\n\n\n<p>12.<strong>&nbsp;Siitonen, J. H.;<\/strong>&nbsp;Cs\u00f3k\u00e1s, D.; Papai, I.*; Pihko, P. M.* \u201cTotal Synthesis of Stemoamide, 9a-<em>epi<\/em>-Stemoamide and 9a,10-<em>epi<\/em>-Stemoamide: Divergent Stereochemistry of the Final Methylation Steps\u201d,&nbsp;<em>Synlett<\/em>,&nbsp;<strong>2020<\/strong><em>, 31<\/em>, 1581 (<a href=\"http:\/\/dx.doi.org\/10.1055\/s-0040-1707201\">DOI<\/a>).<\/p>\n\n\n\n<p>11. Behnke, N. E.;&nbsp;<strong>Siitonen, J. H.<\/strong>; Chamness, S. A.; K\u00fcrti, L.* \u201cSynthesis of Highly-Substituted Cyclopropanes&nbsp;<em>via<\/em>&nbsp;the Quasi-Favorskii Rearrangement of&nbsp;<em>\u03b1<\/em>,<em>\u03b1<\/em>-Dichlorocyclobutanols\u201d,&nbsp;<em>Org. Lett.<\/em>&nbsp;<strong>2020<\/strong>,&nbsp;<em>22<\/em>, 15, 5715 (<a href=\"http:\/\/dx.doi.org\/10.1021\/acs.orglett.0c01229\">DOI<\/a>)<em>.&nbsp;<\/em>Featured cover.<\/p>\n\n\n\n<p>10. Cs\u00f3k\u00e1s, D.;&nbsp;<strong>Siitonen, J. H.<\/strong>; Pihko, P. M.*; Papai, I.* \u201cConformationally Locked Pyramidality Explains the Methylation Stereochemistry of&nbsp;<em>trans<\/em>-Fused Butyrolactones\u201d,&nbsp;<em>Org. Lett.<\/em>&nbsp;<strong>2020<\/strong>, 22,&nbsp;<em>12<\/em>, 4597 (<a href=\"https:\/\/pubs.acs.org\/doi\/abs\/10.1021\/acs.orglett.0c01008\">DOI<\/a>). Featured cover.<\/p>\n\n\n\n<p>9.<strong>&nbsp;Siitonen, J. H.<\/strong>; Kattamuri, P. V.; Yousufuddin, M.; K\u00fcrti, L.* \u201cArylboronic Acid-Catalyzed&nbsp;<em>C<\/em>-Allylation of Unprotected Oximes: Total Synthesis of&nbsp;<em>N<\/em>-Me-Euphococcine\u201d,&nbsp;<em>Org. Lett.<\/em>&nbsp;<strong>2020<\/strong>,&nbsp;22,&nbsp;<em>6<\/em>, 2486<em>&nbsp;<\/em>(<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.0c00727\">DOI<\/a>).<\/p>\n\n\n\n<p>8. Cheng, Q.-Q.; Zhou, Z.; Jiang, H.;&nbsp;<strong>Siitonen, J. H.;<\/strong>&nbsp;Ess, D. H.*; Zhang X.; K\u00fcrti, L.* \u201cOrganocatalytic nitrogen-transfer to unactivated olefins&nbsp;<em>via<\/em>&nbsp;transient oxaziridines\u201d,&nbsp;<em>Nature Catalysis<\/em>&nbsp;<strong>2020<\/strong>,&nbsp;<em>3<\/em>, 386.&nbsp;<a href=\"https:\/\/doi.org\/10.1038\/s41929-020-0430-4\">(DOI)<\/a>. Highligted by&nbsp;<a href=\"https:\/\/cen.acs.org\/synthesis\/catalysis\/make-aziridines-olefins-without-expensive\/98\/web\/2020\/02\">C&amp;EN<\/a>&nbsp;and&nbsp;<a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/html\/10.1055\/s-0040-1707448\">SynFacts<\/a>.<\/p>\n\n\n\n<p>7. Urmibhusan, B.; Kattamuri, P. V.;&nbsp;<strong>Siitonen, J. H.<\/strong>; Alemany, L. B.; K\u00fcrti, L.* \u201cEnantioselective Catalytic Allylboration of Acyclic Ketiminoesters\u201d,&nbsp;<em>Org. Lett.<\/em>&nbsp;<strong>2019<\/strong>,&nbsp;<em>21<\/em>, 9208&nbsp;<a href=\"https:\/\/pubs.acs.org\/doi\/10.1021\/acs.orglett.9b03574\">(DOI)<\/a>.<\/p>\n\n\n\n<p>6.&nbsp;<strong>Siitonen, J. H.<\/strong>&nbsp;\u201cSynthetic Studies on 1-Azabicyclo[5.3.0]decane Alkaloids\u201d,&nbsp;<a href=\"https:\/\/jyx.jyu.fi\/handle\/123456789\/59525\">PhD thesis,&nbsp;<strong>2018<\/strong><\/a>.<\/p>\n\n\n\n<p>5.&nbsp;<strong>Siitonen, J. H.<\/strong>; Yu, L.; Danielsson, J.; Di Gregorio, G.; Somfai, P.* \u201cFormal synthesis of&nbsp;<em>ent<\/em>-Cephalotaxine using a one-pot Parham\u2013aldol sequence\u201d,&nbsp;<em>J. Org. Chem.<\/em>&nbsp;<strong>2018<\/strong>,&nbsp;<em>18<\/em>, 11318&nbsp;<a href=\"http:\/\/dx.doi.org\/10.1021\/acs.joc.8b01540\">(DOI)<\/a>.<\/p>\n\n\n\n<p>4. K\u00e4rki, K.;&nbsp;<strong>Siitonen, J. H.<\/strong>; Kortet, S.; Cederstr\u00f6m M.; Pihko, P. M.* \u201cEnzymatic Resolution of 3-oxodicyclopentadiene on a Decagram Scale\u201d,&nbsp;<em>Synlett<\/em>&nbsp;<strong>2018<\/strong>,&nbsp;<em>29<\/em>, 1723&nbsp;<a href=\"http:\/\/dx.doi.org\/10.1055\/s-0037-1610109\">(DOI)<\/a>.<\/p>\n\n\n\n<p>3. M\u00e4kinen, M E; Mallik R.;&nbsp;<strong>Siitonen, J. H.<\/strong>; K\u00e4rki K.; Pihko, P. M.* \u201cTowards Waltheriones C and D: Synthesis of the Oxabicyclic Core\u201d,&nbsp;<em>Synlett<\/em>&nbsp;<strong>2017<\/strong>,&nbsp;<em>18<\/em>, 1209&nbsp;<a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0036-1588150\">(DOI)<\/a>. Featured on cover of Synlett 10\/2017.<\/p>\n\n\n\n<p>2. Claraz, A.;&nbsp;<strong>Siitonen, J. H.<\/strong>; Pihko, P. M.* In&nbsp;<em>Lewis Base Catalysis in Organic Synthesis<\/em>; Vedjes, E.; Denmark, S.; Eds.; Wiley-VCH Verlag GmbH: Weinheim, Germany,&nbsp;<a href=\"https:\/\/books.google.com\/books?id=02jWCgAAQBAJ&amp;pg=PA805#v=onepage&amp;q&amp;f=false\"><strong>2016<\/strong>, Vol. 2, Chapter 16: \u2018Iminium catalysis (n\u2192\u03c0*)\u2019<\/a>.<\/p>\n\n\n\n<p>1.&nbsp;<strong>Siitonen, J. H.<\/strong>; Pihko, P. M.*, \u201cTotal Synthesis of (+)-Greek Tobacco Lactone\u201d,&nbsp;<em>Synlett<\/em>&nbsp;<strong>2014<\/strong>,&nbsp;<em>25<\/em>, 1888&nbsp;<a href=\"https:\/\/www.thieme-connect.com\/products\/ejournals\/abstract\/10.1055\/s-0034-1378273\">(DOI)<\/a>. Highlighted in ChemInform Abstract.<\/p>\n","protected":false},"excerpt":{"rendered":"<p>Independent career 4. Nurmi, T.*;&nbsp;Siitonen, J. H.* &#8220;Upper Secondary School and University Level Students\u2019 Perceptions of Extractions in Context: Experiences from a Simple Laboratory Experiment&#8221;,&nbsp;ChemRxiv preprint, 2021. 3. Serna, A. V.; K\u00fcrti, L.*,\u00a0Siitonen, J. H.*\u00a0\u201cTotal Synthesis of (\u00b1)-Setigerumine I: Biosynthetic&#8230;<\/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-52","page","type-page","status-publish","hentry"],"_links":{"self":[{"href":"https:\/\/kaviaari.kapsi.fi\/wordpress\/wp-json\/wp\/v2\/pages\/52","targetHints":{"allow":["GET"]}}],"collection":[{"href":"https:\/\/kaviaari.kapsi.fi\/wordpress\/wp-json\/wp\/v2\/pages"}],"about":[{"href":"https:\/\/kaviaari.kapsi.fi\/wordpress\/wp-json\/wp\/v2\/types\/page"}],"author":[{"embeddable":true,"href":"https:\/\/kaviaari.kapsi.fi\/wordpress\/wp-json\/wp\/v2\/users\/1"}],"replies":[{"embeddable":true,"href":"https:\/\/kaviaari.kapsi.fi\/wordpress\/wp-json\/wp\/v2\/comments?post=52"}],"version-history":[{"count":27,"href":"https:\/\/kaviaari.kapsi.fi\/wordpress\/wp-json\/wp\/v2\/pages\/52\/revisions"}],"predecessor-version":[{"id":326,"href":"https:\/\/kaviaari.kapsi.fi\/wordpress\/wp-json\/wp\/v2\/pages\/52\/revisions\/326"}],"wp:attachment":[{"href":"https:\/\/kaviaari.kapsi.fi\/wordpress\/wp-json\/wp\/v2\/media?parent=52"}],"curies":[{"name":"wp","href":"https:\/\/api.w.org\/{rel}","templated":true}]}}