• 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 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 Reactions of Cyclopentane-1,2-dione = Tsüklopentaan-1,2-diooni asümmeetrilised organokatalüütilised reaktsioonidSilm, Estelle2022 https://doi.org/10.23658/taltech.23/2022 https://digikogu.taltech.ee/et/Item/106a2384-0619-453b-bd4d-4a6e6d237368 https://www.ester.ee/record=b5499810*est
• Catalysts derived from sustainable natural and value added alkaloids from poppiesSilm, Estelle; Pata, Pille; Kruis, Jaqueline Cecilia; Sikerina, Anastassia; Pata, Illar; Kanger, Tõnis; Gathergood, NicholasIUPAC Postgraduate Summer School on Green Chemistry : 7-13 July 2018, Venice - Italy : book of abstracts2018 / p. 24 https://www.unive.it/pag/fileadmin/user_upload/extra/SSGC/documenti/Book_of_abstracts_per_website_23_July.pdf
• Catalysts derived from sustainable natural and value added alkaloids from poppies [Online resource]Silm, Estelle; Pata, Pille; Kruis, Jaqueline Cecilia; Sikerina, Anastassia; Pata, Illar; Kanger, Tõnis; Gathergood, NicholasTartu Ülikooli ASTRA projekt PER ASPERA : Funktsionaalsed materjalid ja tehnoloogiad : [7-8 märtsil 2018, Tallinn : teesid] GSFMT Scientific Conference 2018 : Tallinn, March 7-8, 2018 : abstracts2018 / 1 p http://fmtdk.ut.ee/teesid-2018/
• Catalysts derived from sustainable natural and value added alkaloids from poppies [Online resource]Silm, Estelle; Kanger, Tõnis; Gathergood, NicholasTartu Ülikooli ASTRA projekt PER ASPERA : Funktsionaalsed materjalid ja tehnoloogiad : [7-8 märts 2017, Tartu : teesid]2017 / [1] p. : ill http://fmtdk.ut.ee/teesid/
• Cyclopentane-1,2-dione and cyclopent-2-en-1-one in asymmetric organocatalytic reactionsPreegel, Gert; Mose, Rasmus; Silm, Estelle; Lopp, MargusBalticum Organicum Syntheticum : 3-6 July 2016, Riga, Latvia : program and abstracts2016 / p. 133 http://www.boschem.eu/public/BOS2016/BOS-2016_Anstract-Book_Final.pdf
• Kerox technology: potential of piloting the production of medium chain dicarboxylic acids from kerogen in a continuous-flow oxidation reactorReinaas, Maria; Kaldas, Kristiina; Muldma, Kati; Uustalu, Jaan Mihkel; Koern, Villem Ödner; Siirde, Kaarel; Silm, Estelle; Mets, Birgit; Kimm, Mariliis; Rõuk, KristiFuture Frontiers : PhD Conference on Emerging Technologies : Book of Abstracts2025 / p. 29 https://tuit.ut.ee/sites/default/files/2025-05/PhD%20Conference%202025%20Book%20of%20Abstracts_pub3.pdf
• Methylation of phenolsSilm, Estelle; Närep, Angelica; Kimm, Mariliis; Kaldas, Kristiina; Lopp, MargusBalticum Organicum Syntheticum (BOS 2024) : Book of Abstracts2024 / art. 126, p. 145 https://boschem.eu/bos2024/wp-content/uploads/sites/5/2024/07/BOS2024_Abstract-Book.pdf
• Michael-addition/cyclization of cyclopentane-1,2-dione to alkylidenemalononitriles [Online resource]Silm, Estelle; Kanger, TõnisTartu Ülikooli ASTRA projekt PER ASPERA : Funktsionaalsed materjalid ja tehnoloogiad : [4.-5. veebr. 2019, Tartu : teesid]2019 / 1 p.: ill http://fmtdk.ut.ee/teesid-2019/
• Potential of producing medium chain dicarboxylic acids from kerogen in kukersite in a continuous-flow oxidation reactorReinaas, Maria; Kaldas, Kristiina; Muldma, Kati; Uustalu, Jaan Mihkel; Koern, Villem Ödner; Siirde, Kaarel; Silm, Estelle; Mets, Birgit; Kimm, Mariliis; Rõuk, KristiISCRE 28 Abstracts2024 / 2 p https://www.iscre28.org/abstracts/abstract_587_517_1.pdf
• Tsüklopentaan-1,2-diooni asümmeetriline organokatalüütiline Michaeli liitumise/tsükliseerimise kaskaadreaktsioon alkülideenmalononitriilideleSilm, Estelle; Kanger, TõnisXXXIV Eesti keemiapäevad : 100. aastapäeva teaduskonverentsi teesid2019 / lk. 38 https://www.ester.ee/record=b5208044*est