B
Béla Mátravölgyi
Researcher at Budapest University of Technology and Economics
Publications - 39
Citations - 342
Béla Mátravölgyi is an academic researcher from Budapest University of Technology and Economics. The author has contributed to research in topics: Enantioselective synthesis & Catalysis. The author has an hindex of 10, co-authored 35 publications receiving 283 citations. Previous affiliations of Béla Mátravölgyi include Hungarian Academy of Sciences.
Papers
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Journal ArticleDOI
Continuous end-to-end production of solid drug dosage forms: Coupling flow synthesis and formulation by electrospinning
Attila Balogh,András Domokos,Balázs Farkas,Attila Farkas,Zsolt Rapi,Domokos Kiss,Zoltán Nyiri,Zsuzsanna Eke,Györgyi Szarka,Róbert Örkényi,Béla Mátravölgyi,Ferenc Faigl,György Marosi,Zsombor Kristóf Nagy +13 more
TL;DR: In this article, an end-to-end benchtop device was developed unprecedented for the production of solid drug dosage forms by connecting flow synthesis and formulation via electrospinning (ES), together with the optimized two-step continuous-flow synthesis of acetylsalicylic acid (ASA) a water-soluble polymeric excipient (polyvinylpyrrolidone K30, PVPK30) was introduced.
Patent
Industrial process for the synthesis of ivabradine salts
Ujvari Viktor,József Bódi,Farago Janos,Katalin Szoeke,Ferenc Faigl,Nemet Zoltán,Krisztina Temesvári,Róbert Kiss,Béla Mátravölgyi,Ferencné Kassai,Dorottya Kiss-Bartos +10 more
TL;DR: In this article, the synthesis of Ivabradine salts of formula (I) the chemical name of which is: 3-{3-[((S)-3,4-dimethoxy-bicyclo[4.0]octa-1,3,5-triene- 7-ylmethyl)-methyl-amino]-propyl}-7,8-dimethyl-1.3, 4,5,tetrahydro-2H-3-benzazepine-2-one salts (HQ=HCl,
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A new pyrrolidine-derived atropisomeric amino alcohol as a highly efficient chiral ligand for the asymmetric addition of diethylzinc to aldehydes
TL;DR: A pyrrolidine-derived atropisomeric amino alcohol, (Sa)-1-[2-diphenylhydroxymethyl-6-(trifluoromethyl)phenyl]-2-(1-pyrrolido)methyl-1H-Pyrrole, has been synthesized as a chiral ligand for the enantioselective addition of diethylzinc to some prochiral aldehydes to afford (S)-alcohols.
Journal ArticleDOI
Synthesis and utilization of optically active α-aminophosphonate derivatives by Kabachnik-Fields reaction
Erika Bálint,Ádám Tajti,Dorottya Kalocsai,Béla Mátravölgyi,Konstantin Karaghiosoff,Mátyás Czugler,György Keglevich +6 more
TL;DR: In this paper, an optically active α-Phenylethylamine was used in the microwave-assisted Kabachnik-Fields condensation with paraformaldehyde and >P(O)H species.
Journal ArticleDOI
Resolution of 1-[2-carboxy-6-(trifluoromethyl)phenyl]-1H-pyrrole-2-carboxylic acid with methyl (R)-2-phenylglycinate, reciprocal resolution and second order asymmetric transformation
TL;DR: In this paper, a method was developed for the separation of the optical isomers of 1-[2-carboxy-6-(trifluoromethyl)phenyl]-1 H -pyrrole-2 carboxylic acid with methyl (R )-2-phenylglycinate.