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• ChemEASTry Europe, the status of the chemical sciences in a growing regionGryko, Dorota; Szumna, Agnieszka; Aav, Riina; Soos, TiborOrganic letters2023 / p. 6237-6239 https://doi.org/10.1021/acs.orglett.3c02621 https://www.scopus.com/sourceid/26396 https://www.scopus.com/record/display.uri?eid=2-s2.0-85169381019&origin=inward&txGid=1a266ce28c59169fd8a7490eebe0b179 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=ORG%20LETT&year=2023 https://www.webofscience.com/wos/woscc/full-record/WOS:001061542100001
• Divergent access to histone deacetylase inhibitory cyclopeptides via a late-stage cyclopropane ring Cleavage strategy. Short synthesis of ChlamydocinElek, Gabor Zoltan; Koppel, Kaur; Zubrytski, Dzmitry M.; Konrad, Nele; Järving, Ivar; Lopp, Margus; Kananovich, DzmitryOrganic letters2019 / p. 8473-8478 : ill https://doi.org/10.1021/acs.orglett.9b03305 https://www.scopus.com/sourceid/26396 https://www.scopus.com/record/display.uri?eid=2-s2.0-85073100249&origin=inward&txGid=5360ee176044cdd8271fc261862badb7 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=ORG%20LETT&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000492114600068
• Enantioselective one-pot synthesis of α,β-epoxy ketones via aerobic oxidation of cyclopropanolsElek, Gabor Zoltan; Borovkov, Victor; Lopp, Margus; Kananovich, DzmitryOrganic letters2017 / p. 3544-3547 : ill https://doi.org/10.1021/acs.orglett.7b01519 https://www.scopus.com/sourceid/26396 https://www.scopus.com/record/display.uri?eid=2-s2.0-85022335376&origin=inward&txGid=6482d206067f1dc75b8bd3ca5b318383 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=ORG%20LETT&year=2023 https://www.webofscience.com/wos/woscc/full-record/WOS:000405358300054
• Enantioselective organocatalytic Michael addition to unsaturated indolyl ketonesTrubitsõn, Dmitri; Martõnova, Jevgenia; Kudrjašova, Marina; Erkman, Kristin; Järving, Ivar; Kanger, TõnisOrganic letters2021 / p. 1820-1824 https://doi.org/10.1021/acs.orglett.1c00222 https://www.scopus.com/sourceid/26396 https://www.scopus.com/record/display.uri?eid=2-s2.0-85102604896&origin=inward&txGid=5380d070312ee927de594770565b93c1 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=ORG%20LETT&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000626844800055
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• Organocatalytic asymmetric synthesis of 3-chlorooxindoles bearing adjacent quaternary–tertiary centersNoole, Artur; Järving, Ivar; Werner, Franz; Lopp, Margus; Malkov, Andrei; Kanger, TõnisOrganic letters2012 / p. 4922-4925 : ill https://pubs.acs.org/doi/10.1021/ol302245b
• Remote activation of the nucleophilicity of isatinŽari, Sergei; Kudrjašova, Marina; Pehk, Tõnis; Lopp, Margus; Kanger, TõnisOrganic letters2014 / p. 1740-1743 : ill https://doi.org/10.1021/ol500421k https://www.scopus.com/sourceid/26396 https://www.scopus.com/record/display.uri?eid=2-s2.0-84896992268&origin=inward&txGid=f7e4e57d7616f8ebef10259420e40e70 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=ORG%20LETT&year=2014 https://www.webofscience.com/wos/woscc/full-record/WOS:000333477400052
• Site-selective and stereoselective C–H functionalization of N-Cyclopropylamides via a directed remote metalation strategyErmolovich, Yuri; Barysevich, Maryia V.; Adamson, Jasper; Rogova, Oksana; Kaabel, Sandra; Järving, Ivar; Gathergood, Nicholas; Kananovich, DzmitryOrganic letters2019 / p. 969-973 : ill https://doi.org/10.1021/acs.orglett.8b03955 https://www.scopus.com/sourceid/26396 https://www.scopus.com/record/display.uri?eid=2-s2.0-85061234275&origin=inward&txGid=0dd4ac6548033304adb3a8e89900a7c9 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=ORG%20LETT&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000459366800026
• Tailor-made supramolecular chirogenic system based on Cs-symmetric rigid organophosphoric acid host and amino alcohols : mechanistic studies, bulkiness effect, and chirality sensingHasan, Mohammed; Khose, Vaibhav N.; Pandey, Anita D.; Borovkov, Victor; Karnik, Anil V.Organic Letters2016 / p. 440 - 443 https://doi.org/10.1021/acs.orglett.5b03477 https://www.scopus.com/sourceid/26396 https://www.scopus.com/record/display.uri?eid=2-s2.0-84957927742&origin=resultslist&sort=plf-f&src=s&sid=741f751a3d10533043b019afc943a063&sot=b&sdt=b&s=DOI%2810.1021%2Facs.orglett.5b03477%29&sl=32&sessionSearchId=741f751a3d10533043b019afc943a063&relpos=0 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=ORG%20LETT&year=2016 https://www.webofscience.com/wos/woscc/full-record/WOS:000369771800025
• [2,3]-Wittig rearrangement as a formal asymmetric alkylation of α-branched ketonesKimm, Mariliis; Ošeka, Maksim; Kaabel, Sandra; Metsala, Andrus; Järving, Ivar; Kanger, TõnisOrganic letters2019 / p. 4976-4980 https://doi.org/10.1021/acs.orglett.9b01495 https://www.scopus.com/sourceid/26396 https://www.scopus.com/record/display.uri?eid=2-s2.0-85068002193&origin=inward&txGid=2d21bf04b0a24ef04d69e5fa5bf63140 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=ORG%20LETT&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000474795200012