• Chiral auxiliaries and chirogenesis iiSymmetry2021 / art. 1157 https://doi.org/10.3390/sym13071157 https://www.scopus.com/sourceid/21100201542 https://www.scopus.com/record/display.uri?eid=2-s2.0-85109362079&origin=resultslist&sort=plf-f&src=s&sid=c2a7dd19290d895742350a0da52ae0da&sot=b&sdt=b&s=DOI%2810.3390%2Fsym13071157%29&sl=31&sessionSearchId=c2a7dd19290d895742350a0da52ae0da&relpos=0 https://jcr.clarivate.com/jcr-jp/journal-profile?journal=SYMMETRY-BASEL&year=2022 https://www.webofscience.com/wos/woscc/full-record/WOS:000677085600001
• Comparison between 2D and 3D-QSAR approaches to correlate inhibitor activity for a series of indole amide hydroxamic acidKatritzky, Alan R.; Slavov, Svetoslav; Dobchev, Dimitar; Karelson, MatiQSAR & combinatorial science2007 / 3, p. 333-345 https://onlinelibrary.wiley.com/doi/abs/10.1002/qsar.200630021
• 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 N-functionalization of indole derivativesTrubitsõn, Dmitri; Kanger, TõnisGSFMT Scientific Conference 2020 : Tallinn, February 4-5, 2020 : abstracts2020 / p. 84 : ill http://fmtdk.ut.ee/wp-content/uploads/2020/01/GSFMT2020.pdf
• Enantioselective organocatalytic Michael addition to unsaturated indolyl ketonesTrubitsõn, Dmitri; Martõnova, Jevgenija; 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
• Indooli derivaatide enantioselektiivne N-alküleerimineTrubitsõn, Dmitri; Kudrjašova, Marina; Kanger, TõnisXXXIV Eesti keemiapäevad : 100. aastapäeva teaduskonverentsi teesid2019 / lk. 42 : ill https://www.ester.ee/record=b5208044*est
• Organocatalytic asymmetric synthesis of trisubstituted pyrrolidines via a cascade reactionNoole, Artur; Pehk, Tõnis; Järving, Ivar; Lopp, Margus; Kanger, TõnisTetrahedron : asymmetry2012 / p. 188-198 : ill https://www.sciencedirect.com/science/article/pii/S0957416612000912
• Organocatalytic asymmetric synthesis of trisubstituted pyrrolidines via a cascade reactionNoole, Artur; Pehk, Tõnis; Lopp, Margus; Kanger, TõnisBOS 2012 : International Conference on Organic Synthesis : July 1-4, 2012, Tallinn, Estonia : program and abstracts2012 / p. 144 https://www.sciencedirect.com/science/article/pii/S0957416612000912
• Organocatalytic enantioselective synthesis of N-alkylated indoles = Organokatalüütiline enantioselektiivne N-alküleeritud indoolide sünteesTrubitsõn, Dmitri2021 https://www.ester.ee/record=b5459634*est https://digikogu.taltech.ee/et/Item/0f4eb334-fce4-4178-9d7c-eac98677e646 https://doi.org/10.23658/taltech.46/2021