Aerobic oxidation of cyclopentane-1,2-diols to cyclopentane-1,2-diones on Pt/C catalystReile, Indrek; Paju, Anne; Eek, Margus; Pehk, Tõnis; Lopp, MargusSynlett2008 / 3, p. 347-350 https://www.thieme-connect.com/products/ejournals/abstract/10.1055/s-2008-1032056

Asymmetric organocatalytic [2,3]-Wittig rearrangement of cyclohexanone derivativesKimm, Mariliis; Järving, Ivar; Ošeka, Maksim; Kanger, TõnisEuropean journal of organic chemistry2021 / p. 3113−3120 : ill https://doi.org/10.1002/ejoc.202100435 Journal metrics at Scopus Article at Scopus Journal metrics at WOS Article at WOS

Asymmetric organocatalytic [2,3]-Wittig rearrangement of cyclohexanone derivativesKimm, Mariliis; Ošeka, Maksim; Kanger, TõnisGSFMT Scientific Conference 2021 : Tartu, June 14-15, 2021 : abstracts2021 / P 41 https://fmtdk.ut.ee/wp-content/uploads/2021/06/GSFMT_abstractbook_2021.pdf

Asymmetric oxidation of ketonesLopp, Margus; Paju, Anne; Kanger, Tõnis; Kriis, Kadri; Ilmarinen, Kaja; Pehk, TõnisProceedings of the Estonian Academy of Sciences. Chemistry2001 / 3, p. 124-137

Asymmetric oxidation of prochiral and racemic ketones by using Sharpless catalystPaju, Anne2001 https://digi.lib.ttu.ee/i/?4206 https://www.ester.ee/record=b1551339*est

Asymmetric synthesis of 2-amino-8-oxo-9,10-epoxydeacnoic acid via cyclopropane cleavage strategy [Online resource]Elek, Gabor Zoltan; Koppel, Kaur; Borovkov, Victor; Lopp, Margus; Kananovich, DzmitryTartu 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/

Asymmetric synthesis of C2-symmetric bimorpholines and their application as chiral ligands in the transfer hydrogenation of aromatic ketonesKriis, Kadri2003 https://digi.lib.ttu.ee/i/?4204

Asymmetric transfer hydrogenation of aromatic ketones by Rh/bimorpholine complexesKriis, Kadri; Kanger, Tõnis; Lopp, MargusInternational Conference on Organic Synthesis : June 27-July 1, 2004, Riga, Latvia : program & abstracts2004 / p. 93 https://www.sciencedirect.com/science/article/pii/S0957416604005245

Asymmetric transfer hydrogenation of aromatic ketones by Rh(I)/bimorpholine complexesKriis, Kadri; Kanger, Tõnis; Lopp, MargusTetrahedron : Asymmetry2004 / p. 2687-2691 https://www.sciencedirect.com/science/article/pii/S0957416604005245

CE separation of various analytes of biological origin using polyether ether ketone capillaries and contactless conductivity detectionKnjazeva, Tatjana; Kulp, Maria; Kaljurand, MihkelElectrophoresis2009 / p. 424-430 https://www.researchgate.net/profile/Mihkel-Kaljurand/publication/23995365_CE_separation_of_various_analytes_of_biological_origin_using_polyether_ether_ketone_capillaries_and_contactless_conductivity_detection/links/5e50f603299bf1cdb93cf3a5/CE-separation-of-various-analytes-of-biological-origin-using-polyether-ether-ketone-capillaries-and-contactless-conductivity-detection.pdf

Diastereoselective [2,3]-sigmatropic rearrangement of N-allyl ammonium ylidesMurre, Aleksandra; Erkman, Kristin; Kaabel, Sandra; Järving, Ivar; Kanger, TõnisSynthesis2019 / p. 4183–4197 https://doi.org/10.1055/s-0039-1690185 Journal metrics at Scopus Article at Scopus Journal metrics at WOS Article at WOS

Direct asymmetric [alfa]-hydroxylation of 2-hydroxymethyl ketonesPaju, Anne; Kanger, Tõnis; Pehk, Tõnis; Lopp, MargusTetrahedron2002 / p. 7321-7326

Direct asymmetric alpha-hydroxylation of beta-hydroxyketonesLopp, Margus; Paju, Anne; Kanger, Tõnis; Pehk, Tõnis23rd Estonian Chemistry Days : abstracts of scientific conference1997 / p. 79

Direct asymmetric alpha-hydroxylation of beta-hydroxyketonesLopp, Margus; Paju, Anne; Kanger, Tõnis; Pehk, TõnisTetrahedron letters1997 / 28, p. 5051-5054

Direct asymmetric three-component Mannich reaction catalyzed by chiral counteranion-assisted silverYin, Zhongyou; Guo, Jianxin; Zhang, Rui; Borovkov, VictorThe journal of organic chemistry2020 / p. 10369−10377 : ill https://doi.org/10.1021/acs.joc.0c00031

Divergent access to histone deacetylase inhibitory cyclopeptides via a late-stage cyclopropane ring Cleavage strategy. Short synthesis of ChlamydocinElek, Gabor Zoltan; Koppel, Kaur; Zubrytski, Dzmitry M.; Konrad, Nele; Järving, Ivar; Lopp, Margus; Kananovich, DzmitryOrganic letters2019 / p. 8473-8478 : ill https://doi.org/10.1021/acs.orglett.9b03305 Journal metrics at Scopus Article at Scopus Journal metrics at WOS Article at WOS

Divergent access to histone deacetylase inhibitory cyclopeptides via a late-stage cyclopropane ring Cleavage strategy. Short synthesis of ChlamydocinElek, Gabor ZoltanESOC 2019 : 21st European Symposium on Organic Chemistry, July 14-18, 2019, Vienna, Austria : abstracts2019 / PO-381 ; p. 143 http://esoc2019.conf.tuwien.ac.at/fileadmin/ESOC2019/files/ESOC2019_web.pdf

Enantioselective one-pot synthesis of α,β-epoxy ketones via aerobic oxidation of cyclopropanolsElek, Gabor Zoltan; Borovkov, Victor; Lopp, Margus; Kananovich, DzmitryOrganic letters2017 / p. 3544-3547 : ill http://dx.doi.org/10.1021/acs.orglett.7b01519

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

Enantioselective synthesis of epoxyketones via aerobic oxidation of cyclopropanolsElek, Gabor Zoltan; Borovkov, Victor; Lopp, Margus; Kananovich, DzmitryOpen Readings 2017 : 60th International Conference for Students of Physics and Natural Sciences, March 14-17, 2017, Vilnius, Lithuania : programme and abstracts2017 / p. 140 : ill http://www.openreadings.eu/wp-content/uploads/2017/03/OR2017_abstracts_book.pdf

Enantioselective synthesis of Wieland-Miescher ketone through biomorpholine-catalyzed organocatalytic aldol condensationKriis, Kadri; Kanger, Tõnis; Laars, Marju; Kailas, Tiiu; Müürisepp, Aleksander-Mati; Pehk, Tõnis; Lopp, MargusSynlett2006 / 11, p. 1699-1702 https://www.researchgate.net/publication/237887633_Enantioselective_Synthesis_of_Wieland-Miescher_Ketone_through_Bimorpholine-Catalyzed_Organocatalytic_Aldol_Condensation

Extraction of total water-soluble alkylresorcinols from the tar water of the Kiviter process with methyl isobutyl ketoneBaerends, E. N.; Grigorieva, Larisa; Ostroukhov, NikolaiSolid fuel chemistry2021 / p. 177−186 https://doi.org/10.3103/S0361521921030046

Facile synthesis of distally fluorinated ketones by copper-mediated oxidative ring cleavage of cyclopropanolsKonik, Yulia A.; Zubrytski, Dzmitry M.; Gathergood, Nicholas; Kananovich, Dzmitry; Lopp, MargusBalticum Organicum Syntheticum : 3-6 July 2016, Riga, Latvia : program and abstracts2016 / p. 85 : ill http://www.boschem.eu/public/BOS2016/BOS-2016_Anstract-Book_Final.pdf

Highly chemoselective solvent-free synthesis of 1,3,5-triaryl-1,5- diketones: crystallographic investigation and intramolecular weak bifurcated H bonds involving aliphatic C-H groupYin, Zhongyou; Xiong, Changkun; Guo, Jianxin; Borovkov, VictorSynlett2019 / p. 2143−2147 https://doi.org/10.1055/s-0039-1690224

Isobaric vapor-liquid equilibria of the ternary system methylbutyl ketone+1-pentanol+anisoleKirss, Helle; Kuus, Mati; Siimer, EnnJournal of chemical and engineering data2009 / p. 2128-2131 : ill https://pubs.acs.org/doi/10.1021/je900058p

Ketoonide faasidevahelise jaotumise uuriminePajula, S.; Toomet, P.; Mikkal, Maret-EloXXIX vabariiklik üliõpilaste teaduslik- tehniline konverents 30. märtsist - 1. aprillini 1977 : ettekannete teesid1977 / lk. 93 https://www.ester.ee/record=b2449987*est

Ketoonide hüdriidülekandega taandamine Rh(I)/kiraalne diamiin kompleksi manuluselKriis, Kadri; Kanger, Tõnis; Lopp, MargusXXIX Eesti keemiapäevad : teaduskonverentsi ettekannete teesid = 29th Estonian Chemistry Days : abstracts of scientific conference2005 / lk. 44

Otsene beeta-hüdroksüketoonide asümmeetriline alfa-hüdroksüleerimineLopp, Margus; Paju, Anne; Kanger, Tõnis; Pehk, TõnisXXIII Eesti keemiapäevad : teaduskonverentsi ettekannete referaadid1997 / lk. 70

Phosphine-free nonaromatic catalytic system for asymmetric transfer reduction of aromatic ketonesKanger, Tõnis; Kriis, Kadri; Lopp, MargusConference on Knowledge-based Materials and Technologies for Sustainable Chemistry : 1-5 June 2005, Tallinn, Estonia : abstract book2005 / p. 26

Simple access to β-trifluoromethyl-substituted ketones via copper-catalyzed ring-opening trifluoromethylation of substituted cyclopropanolsKananovich, Dzmitry; Konik, Yulia A.; Zubrytski, Dzmitry M.; Järving, Ivar; Lopp, MargusChemical communications2015 / p. 8349-8352 : ill

Small rings in action: organic synthesis with activated cyclopropanesKananovich, DzmitryBalticum Organicum Syntheticum 2018, 1-4 July 2018 : program and abstracts2018 / 1 p. : ill https://boschem.eu/bos2018/

Synthesis of cyclic 3-aryl-substituted 1,2-dicarbonyl compounds via Suzuki cross-coupling reactionsLopušanskaja, Eleana; Paju, Anne; Järving, Ivar; Lopp, MargusSynthesis2018 / p. 1883-1890 : ill https://doi.org/10.1055/s-0036-1591543 Journal metrics at Scopus Article at Scopus Journal metrics at WOS Article at WOS

Synthesis of cyclic 3-aryl-substituted 1,2-dicarbonyl compounds via Suzuki cross-coupling reactions [Online resource]Lopušanskaja, Eleana; Paju, Anne; Lopp, MargusTartu 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/

Synthesis of γ-keto sulfones by copper-catalyzed oxidative sulfonylation of tertiary cyclopropanolsKonik, Yulia A.; Elek, Gabor Zoltan; Kaabel, Sandra; Järving, Ivar; Lopp, Margus; Kananovich, DzmitryOrganic & biomolecular chemistry2017 / p. 8334-8340 : ill http://dx.doi.org/10.1039/C7OB01605K

Обесфеноливание подсмольной воды горючего сланца с помощью высококипящей фракции кетонов, выделенных из сланцевой подсмольной водыSiirde, Enno; Luhakooder, EdvardСборник статей по химии и технологии горючего сланца. 21955 / с. 169-179 https://www.ester.ee/record=b2180947*est https://digikogu.taltech.ee/et/Item/8f402223-246d-4b22-89fc-18b8d094db19

Tsükliliste ketoonide võrdlev Baeyer-Villiger'i asümmeetriline oksüdeerimineKriis, Kadri; Kanger, Tõnis; Paju, Anne; Ilmarinen, Kaja; Pehk, Tõnis; Lopp, MargusXXV Eesti keemiapäevad : teaduskonverentsi ettekannete referaadid = 25th Estonian Chemistry Days : abstracts of scientific conference1999 / lk. 58-59

[2,3]-Wittig rearrangement as a formal asymmetric alkylation of α-branched ketonesKimm, Mariliis; Ošeka, Maksim; Kaabel, Sandra; Metsala, Andrus; Järving, Ivar; Kanger, TõnisOrganic letters2019 / p. 4976-4980 https://doi.org/10.1021/acs.orglett.9b01495 Journal metrics at Scopus Article at Scopus Journal metrics at WOS Article at WOS

Wittig [2,3]-rearrangement as a formal asymmetric alkylation of α-branched cyclopentanonesKimm, Mariliis; Ošeka, Maksim; Kanger, TõnisTartu Ülikooli ASTRA projekt PER ASPERA : Funktsionaalsed materjalid ja tehnoloogiad : [4.-5. veebr. 2019, Tartu : teesid]2019 / 1 p http://fmtdk.ut.ee/teesid-2019/

Выделение кетонов водными растворами двухатомных феноловAarna, Agu; Siimer, EnnСборник статей по химии и химической технологии. 121965 / с. 71-81 : илл https://www.ester.ee/record=b2182032*est https://digikogu.taltech.ee/et/Item/cc98a110-70ff-45fd-9a24-57acf33fc031

Выделение кетонов из углеводородных растворов при помощи молекулярных комплексовAarna, Agu; Siimer, EnnXX научная конференция, посвященная 25-летию Эстонской ССР 18-22 мая 1965 г. : тезисы и резюме1965 / с. 90 https://www.ester.ee/record=b1359832*est

Газохроматографическое определение термодинамических функций растворения кетонов и простых эфировAarna, Agu; Mölder, Leevi; Ebber, ArkadiЖурнал прикладной химии1979 / с. 1640-1642 https://www.ester.ee/record=b1182398*est

Использование модифицированной теории регулярных растворов для описания растворов кетонов в неполярных растворителяхAarna, Agu; Mölder, Leevi; Ebber, ArkadiЖурнал прикладной химии1980 / с. 156-158 : илл https://www.ester.ee/record=b1182398*est

Исследование взаимодействия некоторых фенолов с кетонамиAarna, Agu; Mölder, LeeviEesti NSV Teaduste Akadeemia toimetised. Füüsika, matemaatika ja tehnikateaduste seeria = Известия Академии наук Эстонской ССР. Серия физико-математических и технических наук1964 / lk. 10-14 ; 2 tab https://www.ester.ee/record=b1264320*est

Исследование взаимодействия фенолов с кетонами методом инфракрасной спектроскопииMölder, Leevi; Alev, MilviСборник статей по химии и химической технологии. 101964 / с. 75-81 : илл https://www.ester.ee/record=b2181961*est https://digikogu.taltech.ee/et/Item/9569e6db-150a-42c8-bf3b-765725dfd969

Исследование свойств молекулярных комплексных соединений калориметрическим методом (сообщение II)Aarna, Agu; Siimer, EnnСборник статей по химии и химической технологии. 111964 / с. 217-228 : илл https://www.ester.ee/record=b2181984*est https://digikogu.taltech.ee/et/Item/958b7e78-6cf4-425c-b75d-b028262eada8

Исследование свойств молекулярных комплексных соединений калориметрическим методом (сообщение III)Aarna, Agu; Siimer, EnnСборник статей по химии и химической технологии. 111964 / с. 229-235 : илл https://www.ester.ee/record=b2181984*est https://digikogu.taltech.ee/et/Item/958b7e78-6cf4-425c-b75d-b028262eada8

Корреляция предельных коэффициентов активности сложных эфиров и кетонов с характеристиками растворителейMakitra, R.G.; Mölder, Leevi; Pirig, J.N.; Ebber, ArkadiУкраинский химический журнал1983 / с. 367-372 : табл https://www.ester.ee/record=b1806971*est

О возможности выделения кетонов из сланцевой смолыAarna, Agu; Paluoja, Vilma; Kiisler, KarlСборник статей по химии и технологии горючего сланца. 51958 / с. 54-58 https://www.ester.ee/record=b2181274*est https://digikogu.taltech.ee/et/Item/d4787728-120d-40c7-8299-c6997abc3167

Предельные коэффициенты активности органических соединений в некоторых фенолах, кетонах и эфирахMölder, Leevi; Metlitskaja, OlgaЖурнал прикладной химии1985 / с. 1928-1930 https://www.ester.ee/record=b1182398*est

Экстракция суммарных водорастворимых алкилрезорцинов из подсмольной воды производства Kiviter метилизобутилкетономGrigorieva, Larisa; Baerends, E. N.; Ostroukhov, N. N.Химия твердого топлива2021 / с. 48-57 https://doi.org/10.31857/S002311772103004X