- 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
- 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 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 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 with titanacyclopropane reagents : From early results to the recent achievementsKonik, Yulia A.; Kananovich, DzmitryTetrahedron letters2020 / art. 152036, 12 p. : ill https://doi.org/10.1016/j.tetlet.2020.152036 https://www.scopus.com/sourceid/26514 https://www.scopus.com/record/display.uri?eid=2-s2.0-85085060293&origin=inward&txGid=ec76785aaadec19b82c62c480851a12e https://jcr.clarivate.com/jcr-jp/journal-profile?journal=TETRAHEDRON%20LETT&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000540277100006
- Chiral ionic liquids : effect of symmetry and stereochemistry on toxicity and biodegradationGathergood, NicholasSymmetry : culture and science2017 / p. 179-182 : ill http://journal-scs.symmetry.hu/content-pages/volume-28-number-2-pages-161-240-2017/
- 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 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 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
- 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
- Insight into the mechanism and stereochemistry of the transformations of alkyltitanium ate-complexes. An enhanced enantioselectivity in the cyclopropanation of the carboxylic esters with titanacyclopropane reagentsKulinkovich, Oleg G.; Kananovich, Dzmitry G.; Lopp, Margus; Snieckus, VictorAdvanced synthesis and catalysis2014 / p. 3615-3626 : ill https://doi.org/10.1002/adsc.201400480 https://www.scopus.com/sourceid/22669 https://www.scopus.com/record/display.uri?eid=2-s2.0-84915757732&origin=inward&txGid=18406ec98c06449a64098607d8a3bde4 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=ADV%20SYNTH%20CATAL&year=2014 https://www.webofscience.com/wos/woscc/full-record/WOS:000345312500014
- 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