• Anchimeric assistance in the case of vicinal dimesylate : formation of enantiomeric or meso-biomorpholineKanger, Tõnis; Laars, Marju; Kriis, Kadri; Kailas, Tiiu; Müürisepp, Aleksander-Mati; Pehk, Tõnis; Lopp, MargusSynthesis2006 / 11, p. 1853-1857 https://www.researchgate.net/publication/239729268_Anchimeric_Assistance_in_the_Case_of_Vicinal_Dimesylate_Formation_of_Enantiomeric_or_meso_-Bimorpholine
• Asymmetric aminocatalytic Michael addition of cyclopropane-containing aldehydes to nitroalkenesReitel, Kärt; Lippur, Kristin; Järving, Ivar; Kudrjašova, Marina; Lopp, Margus; Kanger, TõnisSynthesis2013 / p. 2679-2683 : ill https://doi.org/10.1055/s-0033-1338704 https://www.scopus.com/sourceid/26508 https://www.scopus.com/record/display.uri?eid=2-s2.0-84885022359&origin=resultslist&sort=plf-f&src=s&sot=b&sdt=b&s=DOI%2810.1055%2Fs-0033-1338704%29&sessionSearchId=842eff8fafa5da0f4673a77a0030efbc https://jcr.clarivate.com/jcr-jp/journal-profile?journal=SYNTHESIS-STUTTGART&year=2013 https://www.webofscience.com/wos/woscc/full-record/WOS:000325146200007
• Asymmetric Kulinkovich hydroxycyclopropanation of alkenes mediated by titanium(IV) TADDOLate complexesIskryk, Marharyta; Barysevich, Maryia; Ošeka, Maksim; Adamson, Jasper; Kananovich, DzmitrySynthesis2019 / p. 1935-1948 : ill https://doi.org/10.1055/s-0037-1611709 https://www.scopus.com/sourceid/26508 https://www.scopus.com/record/display.uri?eid=2-s2.0-85064490954&origin=inward&txGid=446feebfae2a7985de89bd56317dd3c7 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=SYNTHESIS-STUTTGART&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000465925200006
• Asymmetric organocatalytic aza-Michael reactions of isatin derivativesŽari, Sergei; Metsala, Andrus; Kudrjašova, Marina; Kaabel, Sandra; Järving, Ivar; Kanger, TõnisSynthesis2015 / p. 875-886 : ill
• Asymmetric organocatalytic cascade synthesis of tetrahydro­furanyl spirooxindolesTrubitsõn, Dmitri; Žari, Sergei; Kaabel, Sandra; Kudrjašova, Marina; Kriis, Kadri; Järving, Ivar; Pehk, Tõnis; Kanger, TõnisSynthesis2018 / p. 314-322 : ill https://doi.org/10.1055/s-0036-1590918 https://www.scopus.com/sourceid/26508 https://www.scopus.com/record/display.uri?eid=2-s2.0-85029671403&origin=inward&txGid=d1e1621f4ac22afe42b117bb2cbe6bb4 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=SYNTHESIS-STUTTGART&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000419348600012
• Asymmetric organocatalytic Michael addition–cyclisation cascade of cyclopentane-1,2-dione with alkylidene malononitrilesSilm, Estelle; Kaabel, Sandra; Järving, Ivar; Kanger, TõnisSynthesis2019 / p. 4198-4204 https://doi.org/10.1055/s-0039-1690484 https://www.scopus.com/sourceid/26508 https://www.scopus.com/record/display.uri?eid=2-s2.0-85074693980&origin=inward&txGid=68c26e72a5f83f62de749055df2a84b5 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=SYNTHESIS-STUTTGART&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000494735800008
• Asymmetric organocatalytic Michael Addition-cyclization cascade of cyclopentane-1,2-dione with substituted α,β-unsaturated aldehydesPreegel, Gert; Silm, Estelle; Kaabel, Sandra; Järving, Ivar; Rissanen, Kari; Lopp, MargusSynthesis2017 / p. 3118-3125 : ill https://doi.org/10.1055/s-0036-1588787 https://www.scopus.com/sourceid/26508 https://www.scopus.com/record/display.uri?eid=2-s2.0-85017654012&origin=inward&txGid=f54f351892007adcdb55271eacee54aa https://jcr.clarivate.com/jcr-jp/journal-profile?journal=SYNTHESIS-STUTTGART&year=2017 https://www.webofscience.com/wos/woscc/full-record/WOS:000406066800008
• Asymmetric organocatalytic synthesis of spiro-cyclopropaneoxindolesNoole, Artur; Malkov, Andrei; Kanger, TõnisSynthesis2013 / p. 2520-2524 : ill https://doi.org/10.1055/s-0033-1338505 https://www.scopus.com/sourceid/26508 https://www.scopus.com/record/display.uri?eid=2-s2.0-84883745179&origin=resultslist&sort=plf-f&src=s&sot=b&sdt=b&s=DOI%2810.1055%2Fs-0033-1338505%29&sessionSearchId=e9e33931daa5dfb8bafcb40c010d364a https://jcr.clarivate.com/jcr-jp/journal-profile?journal=SYNTHESIS-STUTTGART&year=2013 https://www.webofscience.com/wos/woscc/full-record/WOS:000323936400004
• Asymmetric synthesis of 2,3,4-trisubstituted piperidinesKriis, Kadri; Melnik, Triin; Lips, Kristiina; Juhanson, Ilona; Kaabel, Sandra; Järving, Ivar; Kanger, TõnisSynthesis2017 / p. 604-614 : ill https://doi.org/10.1055/s-0036-1588299 https://www.scopus.com/sourceid/26508 https://www.scopus.com/record/display.uri?eid=2-s2.0-84986559267&origin=inward&txGid=810c640b7b897c86e62b4517401192a1 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=SYNTHESIS-STUTTGART&year=2017 https://www.webofscience.com/wos/woscc/full-record/WOS:000393233000020
• Asymmetric synthesis of 2-aryl-5-oxotetrahydrofuran-2-carboxylic acidsJõgi, Artur; Paju, Anne; Pehk, Tõnis; Kailas, Tiiu; Müürisepp, Aleksander-Mati; Kanger, Tõnis; Lopp, MargusSynthesis2006 / 18, p. 3031-3036 : ill https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-2006-950193
• Diastereoselective [2,3]-sigmatropic rearrangement of N-allyl ammonium ylidesMurre, Aleksandra; Erkman, Kristin; Kaabel, Sandra; Järving, Ivar; Kanger, TõnisSynthesis2019 / p. 4183–4197 https://doi.org/10.1055/s-0039-1690185 https://www.scopus.com/sourceid/26508 https://www.scopus.com/record/display.uri?eid=2-s2.0-85074698649&origin=inward&txGid=d630c99870ba593f8c86e2d507d2e801 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=SYNTHESIS-STUTTGART&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000494735800007
• Enantioselective N-Alkylation of Nitroindoles under Phase-Transfer CatalysisTrubitsõn, Dmitri; Martõnova, Jevgenia; Erkman, Kristin; Metsala, Andrus; Saame, Jaan; Köster, Kristjan; Järving, Ivar; Leito, Ivo; Kanger, TõnisSynthesis2020 / p. 1047-1059 https://doi.org/10.1055/s-0039-1690751 https://www.scopus.com/sourceid/26508 https://www.scopus.com/record/display.uri?eid=2-s2.0-85082490126&origin=inward&txGid=a2d59f80f36413d4b971486dea4b59e1 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=SYNTHESIS-STUTTGART&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000526537000009
• Enantioselective organocatalytic Michael addition of cyclopentane-1,2-diones to nitroolefinsPreegel, Gert; Noole, Artur; Ilmarinen, Kaja; Järving, Ivar; Kanger, Tõnis; Pehk, Tõnis; Lopp, MargusSynthesis2014 / p. 2595-2600 : ill https://doi.org/10.1055/s-0034-1378374 https://www.scopus.com/sourceid/26508 https://www.scopus.com/record/display.uri?eid=2-s2.0-84947750562&origin=inward&txGid=5a9295efa1eb86f98b9eedf0a8f86293 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=SYNTHESIS-STUTTGART&year=2014 https://www.webofscience.com/wos/woscc/full-record/WOS:000342568800012
• Enantioselective organocatalytic Michael addition–cyclization cascade of cyclopentane-1,2-dione with substituted (E)-2-oxobut-3-enoatesPreegel, Gert; Ilmarinen, Kaja; Järving, Ivar; Kanger, Tõnis; Pehk, Tõnis; Lopp, MargusSynthesis2015 / p. 3805-3812 : ill
• Novel, efficient and regiospecific alkylation/arylation/heteroarylation of unsymmetrical azo compoundsTšubrik, Olga; Sillard, Rannar; Mäeorg, UnoSynthesis2006 / p. 843-846 https://www.researchgate.net/publication/239239897_Novel_Efficient_and_Regiospecific_AlkylationArylationHeteroarylation_of_Unsymmetrical_Azo_Compounds
• Synthesis and derivatization of bis-nor Wieland-Miescher ketoneKanger, Tõnis; Raudla, Kristin; Aav, Riina; Müürisepp, Aleksander-Mati; Pehk, Tõnis; Lopp, MargusSynthesis2005 / p. 3147-3151 https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-2005-916025
• Synthesis and use of 3,3'-bimorpholine derivatives in asymmetric Michael addition and intramolecular aldol reactionSulzer-Mosse, Sarah; Laars, Marju; Kriis, Kadri; Kanger, Tõnis; Alexakis, AlexandreSynthesis2007 / 11, p. 1729-1732 https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-2007-965966
• 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 cyclic 3-aryl-substituted 1,2-dicarbonyl compounds via Suzuki cross-coupling reactionsLopušanskaja, Eleana; Paju, Anne; Järving, Ivar; Lopp, MargusSynthesis2018 / p. 1883-1890 : ill https://doi.org/10.1055/s-0036-1591543 https://www.scopus.com/sourceid/26508 https://www.scopus.com/record/display.uri?eid=2-s2.0-85041905274&origin=inward&txGid=9baa4ccd792a6e2f56f2064d3a849445 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=SYNTHESIS-STUTTGART&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000430349100015