• 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
• 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/
• 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