• An NMR and MD modeling insight into nucleation of 1,2-alkanediols : selective crystallization of lipase-catalytically resolved enantiomers from the reaction mixturesParve, Omar; Reile, Indrek; Parve, Jaan; Kasvandik, Sergo; Kudrjašova, Marina; Tamp, Sven; Metsala, Andrus; Villo, Ly; Pehk, Tõnis; Jarvet, Jüri; Vares, LauriJournal of organic chemistry2013 / p. 12795-12801 : ill https://doi.org/10.1021/jo402189e https://www.scopus.com/sourceid/25896 https://www.scopus.com/record/display.uri?eid=2-s2.0-84890893626&origin=resultslist&sort=plf-f&src=s&sot=b&sdt=b&s=DOI%2810.1021%2Fjo402189e%29&sessionSearchId=16314ced3f93db00e1cd16f9eeb5fc34 https://www.webofscience.com/wos/woscc/full-record/WOS:000329077900049 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=J%20ORG%20CHEM&year=2013
• Asymmetric synthesis of congested spiro-cyclopentaneoxindoles via an organocatalytic cascade reactionNoole, Artur; Ilmarinen, Kaja; Järving, Ivar; Lopp, Margus; Kanger, TõnisJournal of organic chemistry2013 / p. 8117-8122 : ill https://doi.org/10.1021/jo4008223 https://www.scopus.com/sourceid/25896 https://www.scopus.com/record/display.uri?eid=2-s2.0-84882390637&origin=resultslist&sort=plf-f&src=s&sot=b&sdt=b&s=DOI%2810.1021%2Fjo4008223%29&sessionSearchId=c42962733a94ae09ac921c72c691ac9c&relpos=0 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=J%20ORG%20CHEM&year=2013 https://www.webofscience.com/wos/woscc/full-record/WOS:000323362600031
• Benzyne-mediated nonconcerted pathway toward synthesis of sterically crowded [5]- and [7]oxahelicenoids, stereochemical and theoretical studies, and optical resolution of helicenoidsGawade, Prashant M.; Khose, Vaibhav N.; Badani, Purav M.; Kaabel, Sandra; Borovkov, VictorJournal of organic chemistry2019 / p. 860-868 : ill https://doi.org/10.1021/acs.joc.8b02507 https://www.scopus.com/sourceid/25896 https://www.scopus.com/record/display.uri?eid=2-s2.0-85060026679&origin=inward&txGid=a93a50f57430c38e6afce832cde8e042 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=J%20ORG%20CHEM&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000456632800036
• Bimorpholine-mediated enantioselective intramolecular and intermolecular aldol condensationKanger, Tõnis; Kriis, Kadri; Laars, Marju; Kailas, Tiiu; Müürisepp, Aleksander-Mati; Pehk, Tõnis; Lopp, MargusJournal of organic chemistry2007 / p. 5168-5173 https://pubs.acs.org/doi/10.1021/jo070524i
• CaCl₂, bisoxazoline, and malonate : a protocol for an asymmetric Michael reactionLippur, Kristin; Kaabel, Sandra; Järving, Ivar; Rissanen, Kari; Kanger, TõnisJournal of organic chemistry2015 / p. 6336-6341 : ill https://doi.org/10.1021/acs.joc.5b00769 https://www.scopus.com/sourceid/25896 https://www.scopus.com/record/display.uri?eid=2-s2.0-84934889823&origin=inward&txGid=500c7a513ca8269c44ef7f42fac73cd5 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=J%20ORG%20CHEM&year=2015 https://www.webofscience.com/wos/woscc/full-record/WOS:000356845800034
• Directional Approach to Enantiomerically Enriched Functionalized [7]Oxa-helicenoids and Groove-Based Selective Cyanide SensingKhose, Vaibhav N.; Hasan, Mohammed; Khot, Sushil C.; Mobin, Shaikh M.; Borovkov, Victor; Karnik, Anil V.Journal of organic chemistry2019 / p. 1847−1860 : ill https://doi.org/10.1021/acs.joc.9b02100
• 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
• Interplay of monosaccharide configurations on the deacetylation with Candida Antarctica Lipase-mHunt, Kaarel Erik; Miller, Annette; Liias, Kristin; Jarg, Tatsiana; Kriis, Kadri; Kanger, TõnisJournal of organic chemistry2025 / p. 663-671 https://doi.org/10.1021/acs.joc.4c02582
• Stereospecific synthesis of cyclic sulfite esters with sulfur-centered chirality via diastereoselective strategy and intramolecular H-Bonding assistanceHu, Xiaoyun; Yin, Zhongyou; Guo, Jianxin; Adamson, Jasper; Fujiki, Michiya; Borovkov, VictorJournal of Organic Chemistry2021 / p. 379 - 387 https://doi.org/10.1021/acs.joc.0c02147 https://www.scopus.com/sourceid/25896 https://www.scopus.com/record/display.uri?eid=2-s2.0-85097825283&origin=resultslist&sort=plf-f&src=s&sid=4e20fc566512faafe6a1b2ec2b66583e&sot=b&sdt=b&s=DOI%2810.1021%2Facs.joc.0c02147%29&sl=25&sessionSearchId=4e20fc566512faafe6a1b2ec2b66583e&relpos=0 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=J%20ORG%20CHEM&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000606840200029
• Synthesis of deoxy sugar esters : a chemoenzymatic stereoselective approach affording deoxy sugar derivatives also in the form of aldehydeVillo, Ly; Danilas, Kady; Metsala, Andrus; Kreen, Malle; Vallikivi, Imre; Vija, Sirje; Pehk, Tõnis; Luciano, Saso; Parve, OmarJournal of organic chemistry2007 / p. 5813-5816 https://pubs.acs.org/doi/10.1021/jo062640b
• Two catalytic methods of an asymmetric wittig [2,3]-rearrangementOšeka, Maksim; Kimm, Mariliis; Järving, Ivar; Lippur, Kristin; Kanger, TõnisJournal of organic chemistry2017 / p. 2889-2897 : ill https://doi.org/10.1021/acs.joc.6b02786 https://www.scopus.com/sourceid/25896 https://www.scopus.com/record/display.uri?eid=2-s2.0-85015630067&origin=inward&txGid=64c8012b4b0a4e48ddce4e5e1b16b72b https://jcr.clarivate.com/jcr-jp/journal-profile?journal=J%20ORG%20CHEM&year=2017 https://www.webofscience.com/wos/woscc/full-record/WOS:000397077500010