Alifaatse CC küllastamata sideme elektrofiilne alküleerimineMuks, ElviXVI Eesti keemiapäevad : teaduskonverentsi ettekannete referaadid = 16th Estonian chemistry days : abstracts of scientific conference1995 / lk. 83-85

Alkylation of phenols and resorcinolsLopušanskaja, Eleana; Paju, Anne; Lopp, MargusBalticum Organicum Syntheticum (BOS 2022) : program and abstract book2022 / p. 114 Kogumik

Asümmeetriliste alküleerimisreaktsioonide mehhanismi uurimine poolempiiriliste kvantkeemiliste arvutustega = Mechanistic studies of asymmetric alkylation reactions by semi-empirical quantum chemical calculationsMartin, Ivar; Parve, Omar; Vares, L.XVII Eesti keemiapäevad : teaduskonverentsi ettekannete referaadid = 17th Estonian Chemistry Days : abstracts of scientific conference1996 / lk. 109-110 https://www.ester.ee/record=b1070511*est

Dearomatization of naphtols via alkylationLarin, Anni; Lopp, MargusGSFMT Scientific Conference 2020 : Tallinn, February 4-5, 2020 : abstracts2020 / p. 51 : ill http://fmtdk.ut.ee/wp-content/uploads/2020/01/GSFMT2020.pdf

Development of dearomatization of phenols with alkyl electrophilesLopušanskaja, Eleana; Lopp, MargusGSFMT Scientific Conference 2020 : Tallinn, February 4-5, 2020 : abstracts2020 / p. 55 : ill http://fmtdk.ut.ee/wp-content/uploads/2020/01/GSFMT2020.pdf

Diastereoselective alkylation of (arene)tricarbonylchromium and ferrocene complexes using a chiral, C2-symmetrical 1,2-diamine as auxiliaryAlexakis, Alexandre; Tomassi, Axel; Andrey, Olivier; Aav, Riina; Bernardinelli, GeraldEuropean journal of organic chemistry2006 / 15, p. 3057 https://chemistry-europe.onlinelibrary.wiley.com/doi/full/10.1002/ejoc.200600425

Enantioselective N-alkylation of indole derivates [Online resource]Trubitsõn, Dmitri; 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/

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

Ortho-selective electrophilic substitution/addition to phenolatesLopušanskaja, EleanaGSFMT Scientific Conference 2021 : Tartu, June 14-15, 2021 : abstracts2021 / O 19 https://fmtdk.ut.ee/wp-content/uploads/2021/06/GSFMT_abstractbook_2021.pdf

A photochemical organocatalytic strategy for the α-alkylation of ketones by using radicalsSpinnato, Davide; Schweitzer-Chaput, Bertrand; Goti, Giulio; Ošeka, Maksim; Melchiorre, PaoloAngewandte Chemie international Edition2020 / p. 9485 - 9490 https://doi.org/10.1002/anie.201915814 Journal metrics at Scopus Article at Scopus Journal metrics at WOS Article at WOS

Selective C-alkylation of substituted naphthols under non-aqueous conditionsKooli, Anni; Shalima, Tatsiana; Lopušanskaja, Eleana; Paju, Anne; Lopp, MargusTetrahedron2021 / art. 132278, 8 p. : ill https://doi.org/10.1016/j.tet.2021.132278 Journal metics at Scopus Article at Scopus Journal metrics at WOS Article at WOS

Semiempirical AM1 calculations on the competing 1- and 4-alkylation of 2-methylbuta-1,3-diene with primary allylic cationsMartin, Ivar; Muks, ElviJournal of chemical research. Pt. S, Synopses1996 / p. 52-53

Semiempirical transition state modeling of asymmetric alkylation reactionMartin, Ivar; Parve, Omar; Vares, L.Japan-Northern Baltic Symposium on Synthetic Chemistry, Helsinki, Finland, June 25-26, 1996 : abstracts1996 / p. PL17

3-alkylcyclopentane-1,2-diones in asymmetric oxidation and alkylation reactions = 3-alküültsüklopentaan-1,2-dioonid asümmeetrilistes oksüdeerimis- ja alküleerimisreaktsioonidesReile, Indrek2012 http://www.ester.ee/record=b2756921*est

Towards ortho-selective electrophilic substitution/addition to phenolates in anhydrous solventsLopušanskaja, Eleana; Kooli, Anni; Paju, Anne; Järving, Ivar; Lopp, MargusTetrahedron2021 / art. 131935, 9 p https://doi.org/10.1016/j.tet.2021.131935 Journal metrics at Scopus Article at Scopus Journal metrics at WOS Article at WOS

[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

Uncommon reaction in 4-formyl phenols - substitution of the formyl groupLopušanskaja, Eleana; Paju, Anne; Lopp, MargusProceedings of the Estonian Academy of Sciences2024 / p. 1-5 https://doi.org/10.3176/proc.2024.1.01

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/

Wittigi [2,3]-ümberasetusreaktsioon kui α-hargnenud tsüklopentanoonide formaalne asümmeetriline alküleerimismeetodKimm, Mariliis; Ošeka, Maksim; Kanger, TõnisXXXIV Eesti keemiapäevad : 100. aastapäeva teaduskonverentsi teesid2019 / lk. 18 : ill

Закономерности экстракции алкилрезорциновRaude, Urmas; Kuslapuu, H.5-я республиканская конференция молодых ученых-химиков : [тезисы докладов]1983 / с. 223-224 https://www.ester.ee/record=b1312297*est

Закономерности экстракции алкилрезорциновRaude, UrmasXXVII студенческая научно-техническая конференция вузов Прибалтийских республик, Белорусской ССР и Молдавской ССР, 19-21 апреля 1983 г : тезисы докладов. Часть 21983 / с. 109 https://www.ester.ee/record=b1571566*est

Исследования в области алкилрезорцинов : автореферат ... доктора химических наук (05.17.07)Lille, Ülo1973 https://www.ester.ee/record=b1329657*est

Исследования в области алкилрезорцинов : диссертация на соискание ученой степени доктора химических наукLille, Ülo1973 https://www.ester.ee/record=b4432879*est https://digi.lib.ttu.ee/i/?7130

О синтезе алкилфенолов методом алкилрования в пристутствии ZnCl2Raudsepp, Hugo; Karolin, KaljuСборник статей по химии и химической технологии. 171967 / с. 67-73 https://www.ester.ee/record=b2182175*est https://digikogu.taltech.ee/et/Item/7729329c-fcb4-4227-8663-3a21bf5c78ff

Технологические основы выделения индивидуальных алкилрезорцинов из сложной смесиMölder, Leevi; Zabellevitš, I.V.; Kuslapuu, H.; Tamvelius, Hindrek; Tiikma, LaineРеспубликанская научная конференция "Химия и применение фенолальдегидных смол" : тезисы докладов1982 / с. 115-117 https://www.ester.ee/record=b1265870*est