É
Éva Szabó
Researcher at Budapest University of Technology and Economics
Publications - 15
Citations - 94
Éva Szabó is an academic researcher from Budapest University of Technology and Economics. The author has contributed to research in topics: One-pot synthesis & Enone. The author has an hindex of 5, co-authored 15 publications receiving 69 citations.
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Journal ArticleDOI
A facile synthesis of two isomeric components of San Jose scale pheromone
Journal ArticleDOI
Computer-aided spectrophotometric determination of multicomponent drugs
Judit Géher,Éva Szabó +1 more
TL;DR: The conditions of least squares deconvolution by linear combination have been investigated in three- component systems and the content of active ingredients of three-component injections was determined by means of computer-aided evaluation of UV-spectra in systems that fulfilled these conditions.
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Validation of microplastic sample preparation method for freshwater samples.
Áron Mári,Gábor Bordós,Szilveszter Gergely,Mónika Büki,Judit Háhn,Zoltán Palotai,Gabriella Besenyő,Éva Szabó,András Salgó,Balázs Kriszt,Sándor Szoboszlay +10 more
TL;DR: In this paper, the Small Volume Glass Separator (SVMGS) is proposed to isolate microplastics from freshwater samples and concentrate the treated sample in a small volume, thus reducing the brine solution use and the sample transfer steps.
Journal ArticleDOI
Validation of pressurized fractionated filtration microplastic sampling in controlled test environment.
Gábor Bordós,Szilveszter Gergely,Judit Háhn,Zoltán Palotai,Éva Szabó,Gabriella Besenyő,András Salgó,Péter Harkai,Balázs Kriszt,Sándor Szoboszlay +9 more
TL;DR: It is concluded, that surface sampling is more efficient than sampling in a deeper layer of the water column and validating the efficiency of the whole sampling process from the environment is more important than measuring only the filtration device's recovery.
Journal ArticleDOI
Synthesis of novel HMG-CoA reductase inhibitors. I: Naphthalene analogs of mevinolin
Lajos Novák,János Rohály,László Poppe,Gábor Hornyánszky,Pál Kolonits,István Zelei,Imre Fehér,Jeno Fekete,Éva Szabó,Uwe I. Záhorszky,András Jávor,Csaba Szántay +11 more
TL;DR: In this article, the title compounds 2 and their corresponding epimers 18 are prepared in several steps by starting with chiral formyl ester 5, and α-tetralones 10: coupling reaction with the ylide generated from 11 to yield unsaturated ester 13, reduction to the corresponding alcohol 14, addition of the Grignard reagent derived from 14 to formyl Ester 5 to afford the hydroxy esters 16 and 17, and lactonization.