• A DFT study of an organocatalytic enantioselective Mannich Reaction reveals that the enantiodeterming step is associated with the torsional degrees of freedomMetsala, Andrus; Kriis, Kadri; Kaasik, Mikk; Kanger, TõnisBalticum Organicum Syntheticum (BOS 2024) : Book of Abstracts2024 / art. P83, p. 102 https://boschem.eu/bos2024/wp-content/uploads/sites/5/2024/07/BOS2024_Abstract-Book.pdf
• Enantioselective [8+2] cycloadditions of photogenerated ketenesKaasik, Mikk; Anker Jørgensen, K.; Eugui, M.Balticum Organicum Syntheticum (BOS 2024) : Book of Abstracts2024 / art. P47, p. 66 https://boschem.eu/bos2024/wp-content/uploads/sites/5/2024/07/BOS2024_Abstract-Book.pdf
• Enantioselective Michael addition to vinyl phosphonates via hydrogen bond-enhanced halogen bond catalysisKaasik, Mikk; Martõnova, Jevgenija; Erkman, Kristin; Metsala, Andrus; Järving, Ivar; Kanger, TõnisChemical science2021 / p. 7561-7568 https://doi.org/10.1039/D1SC01029H https://www.scopus.com/sourceid/19700200838 https://www.scopus.com/record/display.uri?eid=2-s2.0-85107299099&origin=inward&txGid=888bb2f1ebc5c907d4276fb626991dd9 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=CHEM%20SCI&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000646815100001
• Halo-1,2,3-triazolium salts as halogen bond donors for the activation of imines in dihydropyridinone synthesisKaasik, Mikk; Metsala, Andrus; Kaabel, Sandra; Kriis, Kadri; Järving, Ivar; Kanger, TõnisJournal of organic chemistry2019 / p. 4294–4303 : ill https://doi.org/10.1021/acs.joc.9b00248 https://www.scopus.com/sourceid/25896 https://www.scopus.com/record/display.uri?eid=2-s2.0-85063388030&origin=inward&txGid=7eef36f373f16fd6c1ec07847121c190 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=J%20ORG%20CHEM&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000464250800052
• Halogeenside võib võimendada kaugete aatomite interaktsiooneMetsala, Andrus; Kaasik, Mikk; Kanger, Tõnis; Lopp, MargusXXXIV Eesti keemiapäevad : 100. aastapäeva teaduskonverentsi teesid2019 / lk. 28 https://www.ester.ee/record=b5208044*est
• Halogen-Bonding Organocatalysis - New Opportunities for Asymmetric SynthesisKaasik, Mikk; Kanger, TõnisAsymmetric Organocatalysis: New Strategies, Catalysts, and Opportunities. Vol. 12022 / p. 203-224 https://doi.org/10.1002/9783527832217.ch6
• Halotriazolium salts as organocatalysts in aza-Diels-Alder reaction [Online resource]Kaasik, Mikk; Kriis, Kadri; Kanger, TõnisTartu Ülikooli ASTRA projekt PER ASPERA : Funktsionaalsed materjalid ja tehnoloogiad : [7-8 märtsil 2018, Tallinn : teesid] GSFMT Scientific Conference 2018 : Tallinn, March 7-8, 2018 : abstracts2018 / 1 p http://fmtdk.ut.ee/teesid-2018/
• Kas Eesti on teadustalentidele ahvatlev sihtkoht?Vaaks, EveliisTrialoog2025 https://trialoog.taltech.ee/kas-eesti-on-teadustalentidele-ahvatlev-sihtkoht/
• Multifunctional catalysts in the asymmetric Mannich reaction of malononitrile with N-Phosphinoylimines : coactivation by halogen bonding versus hydrogen bondingKriis, Kadri; Martõnov, Harry; Miller, Annette; Erkman, Kristin; Järving, Ivar; Kaasik, Mikk; Kanger, TõnisThe journal of organic chemistry2022 / p. 7422-7435 : ill https://doi.org/10.1021/acs.joc.2c00674 https://www.scopus.com/sourceid/25896 https://www.scopus.com/record/display.uri?eid=2-s2.0-85133034533&origin=inward&txGid=6708ff02dbf67af90550965187e93803 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=J%20ORG%20CHEM&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000809765000037
• Organocatalytic conjugate addition of cyclopropylacetaldehyde derivatives to nitro olefins : en route to β- and γ-amino acidsKaasik, Mikk; Noole, Artur; Reitel, Kärt; Järving, Ivar; Kanger, TõnisEuropean journal of organic chemistry2015 / p. 1745-1753 : ill https://doi.org/10.1002/ejoc.201403387 https://www.scopus.com/sourceid/25853 https://www.scopus.com/record/display.uri?eid=2-s2.0-85027918297&origin=inward&txGid=61223f1041600a31384517cea489e15e https://jcr.clarivate.com/jcr-jp/journal-profile?journal=EUR%20J%20ORG%20CHEM&year=2015 https://www.webofscience.com/wos/woscc/full-record/WOS:000351054500013
• Quantum chemical calculation procedure for the c-c bond forming reactionsMetsala, Andrus; Kaasik, Mikk; Kriis, Kadri; Kanger, Tõnis; Kimm, MariliisBalticum Organicum Syntheticum (BOS 2022) : program and abstract book2022 / p. 127 https://ortus.rtu.lv/science/lv/publications/35091/attachments/7168
• Supramolecular halogen bonds in asymmetric catalysisKaasik, Mikk; Kanger, TõnisFrontiers in chemistry2020 / art. 599064, 18 p. : ill https://doi.org/10.3389/fchem.2020.599064 https://www.scopus.com/sourceid/21100461983 https://www.scopus.com/record/display.uri?eid=2-s2.0-85094973114&origin=inward&txGid=591eb471bf48f0323a569d1f91614b09 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=FRONT%20CHEM&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000584528800001
• Synthesis and characterisation of chiral triazole-based halogen-bond donors: halogen bonds in the solid state and in solutionKaasik, Mikk; Kaabel, Sandra; Kriis, Kadri; Järving, Ivar; Aav, Riina; Rissanen, Kari; Kanger, TõnisChemistry - a European journal2017 / p. 7337-7344 : ill https://doi.org/10.1002/chem.201700618 https://www.scopus.com/sourceid/23392 https://www.scopus.com/record/display.uri?eid=2-s2.0-85019100418&origin=inward&txGid=e5fe9d7f0bed2028bcc729d0b2459a12 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=CHEM-EUR%20J&year=2017 https://www.webofscience.com/wos/woscc/full-record/WOS:000402640600026
• Synthesis and characterization of chiral triazole-based halogen bond donors [Online resource]Kaasik, Mikk; Kaabel, Sandra; Kriis, Kadri; Järving, Ivar; Aav, Riina; Rissanen, Kari; Kanger, TõnisTartu Ülikooli ASTRA projekt PER ASPERA : Funktsionaalsed materjalid ja tehnoloogiad : [7-8 märts 2017, Tartu : teesid]2017 / [1] p. : ill http://fmtdk.ut.ee/teesid/
• Synthesis of chiral triazole-based halogen bond donorsKaasik, Mikk; Kaabel, Sandra; Kriis, Kadri; Järving, Ivar; Kanger, TõnisSynthesis2019 / p. 2128-2135 : ill https://doi.org/10.1055/s-0037-1610864 https://www.scopus.com/sourceid/26508 https://www.scopus.com/record/display.uri?eid=2-s2.0-85064605644&origin=inward&txGid=a0a162b4787f71e480f9faf0acd13d5b https://jcr.clarivate.com/jcr-jp/journal-profile?journal=SYNTHESIS-STUTTGART&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000467273700008
• Synthesis of triazole-based halogen-bond donorsKaasik, Mikk; Kriis, Kadri; Kaabel, Sandra; Kanger, TõnisBalticum Organicum Syntheticum : 3-6 July 2016, Riga, Latvia : program and abstracts2016 / p. 81 : ill http://www.boschem.eu/public/BOS2016/BOS-2016_Anstract-Book_Final.pdf
• Synthesis, characterisation and catalytic activity of enantiopure triazole based halogen bond donors = Enantiomeerselt puhaste triasooli-põhiste halogeensideme doonorite süntees, iseloomustamine ja katalüütiline aktiivsusKaasik, Mikk2020 https://digikogu.taltech.ee/et/Item/4a5fa759-84c8-45b0-ade1-a1a887b8e91b
• Synthesis, characterization and catalytic activity of enantiopure triazole-based halogen bond donorsKaasik, Mikk; Kaabel, Sandra; Metsala, Andrus; Peterson, Anna; Kriis, Kadri; Järving, Ivar; Aav, Riina; Rissanen, Kari; Adamson, Jasper; Kanger, TõnisGSFMT Scientific Conference 2020 : Tallinn, February 4-5, 2020 : abstracts2020 / p. 35 : ill http://fmtdk.ut.ee/wp-content/uploads/2020/01/GSFMT2020.pdf
• Triazole-based XB donors in solution and applications in catalysisKaasik, MikkFrontiers in Organic Synthesis : Dedicated to the 70th birthday of Professor Margus Lopp, Tallinn, 15th November 20192019 http://fmtdk.ut.ee/2019/11/05/seminar-frontiers-in-organic-synthesis/
• Tunable chiral triazole-based halogen bond donors : assessment of donor strength in solution with nitrogen-containing acceptorsPeterson, Anna; Kaasik, Mikk; Metsala, Andrus; Järving, Ivar; Adamson, Jasper; Kanger, TõnisRSC advances2019 / p. 11718–11721 : ill https://doi.org/10.1039/c9ra01692a https://www.scopus.com/sourceid/21100199840 https://www.scopus.com/record/display.uri?eid=2-s2.0-85064620017&origin=inward&txGid=044b24f19857fa474d4b49de027d4887 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=RSC%20ADV&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000466757100016