- Aerobic oxidations in asymmetric synthesis : catalytic strategies and recent developmentsKananovich, Dzmitry; Elek, Gabor Zoltan; Lopp, Margus; Borovkov, VictorFrontiers in chemistry2021 / art. 614944 https://doi.org/10.3389/fchem.2021.614944 https://www.scopus.com/sourceid/21100461983 https://www.scopus.com/record/display.uri?eid=2-s2.0-85104128108&origin=inward&txGid=f36f26c77ee83fef33d860da354212ac https://jcr.clarivate.com/jcr-jp/journal-profile?journal=FRONT%20CHEM&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000639425500001
- Aminocatalysts are more environmentally friendly than hydrogen-bonding catalystsSihtmäe, Mariliis; Silm, Estelle; Kriis, Kadri; Kahru, Anne; Kanger, TõnisChemSusChem2022 / art. e202201045, 5 p. : ill https://doi.org/10.1002/cssc.202201045 https://www.scopus.com/sourceid/12000154478 https://www.scopus.com/record/display.uri?eid=2-s2.0-85133484436&origin=inward&txGid=89fa33edcc50dd67c6ee8e9f841e5ab7 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=CHEMSUSCHEM&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000820655200001
- 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 diastereoselective synthesis of spirocyclopropane derivatives of oxindoleOšeka, Maksim; Noole, Artur; Žari, Sergei; Öeren, Mario; Järving, Ivar; Lopp, Margus; Kanger, TõnisEuropean journal of organic chemistry2014 / p. 3599-3606 : ill https://doi.org/10.1002/ejoc.201402061 https://www.scopus.com/sourceid/25853 https://www.scopus.com/record/display.uri?eid=2-s2.0-84901848714&origin=inward&txGid=326593326ca1d31e7a7b1b79bfa070f4 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=EUR%20J%20ORG%20CHEM&year=2014 https://www.webofscience.com/wos/woscc/full-record/WOS:000337693500014
- 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 of cyclopentane-1,2-dione to alkylidene oxindoleSilm, Estelle; Järving, Ivar; Kanger, TõnisBeilstein Journal of Organic Chemistry2022 / p. 167-173 https://doi.org/10.3762/bjoc.18.18 https://www.scopus.com/sourceid/4400151742 https://www.scopus.com/record/display.uri?eid=2-s2.0-85125118030&origin=inward&txGid=f83ed63aabbd769f9d675999a25d2438 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=BEILSTEIN%20J%20ORG%20CHEM&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000751890600001
- 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
- Aza-Michael reactions of isatin imines : deeper insight and origin of the stereoselectivityMetsala, Andrus; Žari, Sergei; Kanger, TõnisChemCatChem2016 / p. 2961-2967 : ill https://doi.org/10.1002/cctc.201600584 https://www.scopus.com/sourceid/19900191733 https://www.scopus.com/record/display.uri?eid=2-s2.0-84982217573&origin=inward&txGid=602911bad3d963dfdaba7f67d0ddfcb0 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=CHEMCATCHEM&year=2016 https://www.webofscience.com/wos/woscc/full-record/WOS:000386919300016
- Challenges in mechanistic investigation of a flexible aminocatalyst as demonstrated through enamine formationOsadchuk, Irina; Kanger, TõnisChemistryOpen2025 / art. 2500116 https://doi.org/10.1002/open.202500116 https://chemistry-europe.onlinelibrary.wiley.com/doi/10.1002/open.202500116
- Cyclopentane-1,2-dione bis(tert-butyldimethylsilyl) enol ether in asymmetric organocatalytic Mukaiyama–Michael reactionsReile, Indrek; Paju, Anne; Kanger, Tõnis; Järving, Ivar; Lopp, MargusTetrahedron letters2012 / p. 1476-1478 : ill https://www.sciencedirect.com/science/article/pii/S0040403912000767
- A DFT study of an organocatalytic enantioselective Mannich reaction under the sway of noncovalent interactionsMetsala, Andrus; Kriis, Kadri; Kanger, TõnisJournal of computational chemistry2025 / art. e70159 https://doi.org/10.1002/jcc.70159
- Enantioselective catalytic synthesis of N-alkylated indolesTrubitsõn, Dmitri; Kanger, TõnisChiral Auxiliaries and Chirogenesis II2021 / p. 1-30 https://doi.org/10.3390/sym12071184 https://doi.org/10.3390/books978-3-0365-1155-9
- Enantioselective Catalytic Synthesis of N-alkylated IndolesTrubitsõn, Dmitri; Kanger, TõnisSymmetry2020 / art. 1184 ; 30 p.: ill https://doi.org/10.3390/sym12071184 https://www.scopus.com/sourceid/21100201542 https://www.scopus.com/record/display.uri?eid=2-s2.0-85088513402&origin=inward&txGid=f25ecd60dc754006b7c05ed3cb404414 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=SYMMETRY-BASEL&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000557238800001
- 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 https://doi.org/10.1055/s-0035-1560347 https://www.scopus.com/sourceid/26508 https://www.scopus.com/record/display.uri?eid=2-s2.0-84947804430&origin=inward&txGid=7bcc08685d2ba12d41bc3095812c4371 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=SYNTHESIS-STUTTGART&year=2015 https://www.webofscience.com/wos/woscc/full-record/WOS:000365304000020
- 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
- Highly enantio- and diastereoselective generation of two quaternary centers in spirocyclopropanation of oxindole derivatiesNoole, Artur; Sucman, Natalia S.; Kabeshov, Mikhail A.; Kanger, Tõnis; Macaev, Fliur Z.; Malkov, AndreiChemistry : a European journal2012 / p. 14929–14933 : ill https://pubmed.ncbi.nlm.nih.gov/23112107/
- Organocatalytic asymmetric addition of malonates to unsaturated 1,4-diketonesŽari, Sergei; Kailas, Tiiu; Kudrjašova, Marina; Öeren, Mario; Järving, Ivar; Tamm, Toomas; Lopp, Margus; Kanger, TõnisBeilstein journal of organic chemistry2012 / p. 1452-1457 : ill https://pubmed.ncbi.nlm.nih.gov/23019480/
- 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
- 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
- 3-Chlorooxindoles : versatile starting materials for asymmetric organocatalytic synthesis of spirooxindolesNoole, Artur; Ošeka, Maksim; Pehk, Tõnis; Öeren, Mario; Järving, Ivar; Elsegood, Mark R. J.; Malkov, Andrei; Lopp, Margus; Kanger, TõnisAdvanced synthesis and catalysis2013 / p. 829-835 : ill https://www.scopus.com/sourceid/22669 https://www.scopus.com/record/display.uri?eid=2-s2.0-84875476598&origin=resultslist&sort=plf-f&src=s&sot=b&sdt=b&s=DOI%2810.1002%2Fadsc.201300019%29&sessionSearchId=627c52b3557ef2545451d137647da466 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=ADV%20SYNTH%20CATAL&year=2013 https://www.webofscience.com/wos/woscc/full-record/WOS:000316808200001