Zobrazeno 1 - 10 of 18 pro vyhledávání: '"Péter Slégel"'
1
Synthesis of 1′-Aryl-1,3′-bi-β-carbolines and Their Saturated Counterparts
Autor: Mátyás Milen, Balázs Volk, Péter Slégel, Péter Ábrányi-Balogh, András Dancsó
Publikováno v: Polycyclic Aromatic Compounds. 38:131-140
1-Aryl-β-carboline-3-carbaldehyde building blocks have been used as the starting materials for the synthesis of novel bis-β-carboline derivatives. In the two-step synthesis the Pictet–Spengler reaction was used before the dehydrogenation of the p
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::d7b08dc7b914c7eb223b932f0bda2552
https://doi.org/10.1080/10406638.2016.1173073
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2
Propylphosphonic anhydride (T3P®) mediated one-pot three-component synthesis of racemic dialkyl (2-substituted-3-oxo-2,3-dihydro-1H-isoindol-1-yl)phosphonates
Autor: Tamás Földesi, András Dancsó, Péter Slégel, Mátyás Milen, Balázs Volk
Publikováno v: Tetrahedron. 72:5091-5099
A practical and efficient synthesis of racemic dialkyl (2-substituted-3-oxo-2,3-dihydro-1H-isoindol-1-yl) phosphonates has been developed via the three-component reaction of 2-formylbenzoic acid, various primary amines and trialkyl phosphites, using
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::9d21b2fc291e7e17c93be012065b073c
https://doi.org/10.1016/j.tet.2016.06.074
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3
Efficient synthesis of N b -thioacyltryptamine derivatives by a three-component Willgerodt–Kindler reaction, and their transformation to 1-substituted-3,4-dihydro-β-carbolines
Autor: Mátyás Milen, Péter Slégel, Balázs Volk, Péter Keglevich, Gyula Simig, Gyoergy Keglevich
Publikováno v: Tetrahedron Letters. 56:5697-5700
A practical and efficient synthesis of Nb-thioacyltryptamines has been developed via the three-component reaction of tryptamine, various aldehydes and elemental sulfur. The products were obtained in moderate to excellent yields and proved to be valua
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::91099d6b7159a848f34466e42b93f252
https://doi.org/10.1016/j.tetlet.2015.09.007
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4
Synthesis of new tricyclic imidazotriazepine derivatives condensed with various heterocycles
Autor: Balázs Volk, Mátyás Milen, András Dancsó, Tamás Földesi, Péter Slégel
Publikováno v: Molecular diversity. 21(4)
Previously synthesized 9-aryl-5H-imidazo[2,1-d][1,2,5]triazepin-6(7H)-ones have been used as starting materials for the synthesis of three new tricyclic ring systems, where an imidazotriazepine is condensed with an imidazole, triazole or tetrazole ri
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc3e686b6c6b74dc2f803abf05867625
https://pubmed.ncbi.nlm.nih.gov/28726025
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5
New Synthetic Approach for the Preparation of 1-Aryl-3,4-dihydro­isoquinolines by Liebeskind–Srogl Reaction
Autor: Mátyás Milen, Balázs Volk, Péter Slégel, Péter Ábrányi-Balogh, László Pongó
Publikováno v: Synlett. 25:2574-2578
An efficient synthetic methodology has been developed to construct 1-aryl-3,4-dihydroisoquinoline derivatives. The reaction was performed under neutral conditions by a palladium-catalyzed desulfitative carbon–carbon cross-coupling protocol.
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::be7910caf13f7235716691d0edb2d28e
https://doi.org/10.1055/s-0034-1379109
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6
ChemInform Abstract: Efficient Synthesis of Nb-Thioacyltryptamine Derivatives by a Three-Component Willgerodt-Kindler Reaction, and Their Transformation to 1-Substituted-3,4-dihydro-β-carbolines
Autor: Péter Keglevich, Balázs Volk, Gyula Simig, Mátyás Milen, Péter Slégel, Gyoergy Keglevich
Publikováno v: ChemInform. 47
A practical and efficient synthesis of Nb-thioacyltryptamines has been developed via the three-component reaction of tryptamine, various aldehydes and elemental sulfur. The products were obtained in moderate to excellent yields and proved to be valua
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::56a8f6f95ef218ea006920b5e9c9c60c
https://doi.org/10.1002/chin.201607179
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10
New chromatographic hydrophobicity index (ϕ0) based on the slope and the intercept of the log k′ versus organic phase concentration plot
Autor: Péter Slégel, Klára Valkó
Publikováno v: Journal of Chromatography A. 631:49-61
A new chromatographic hydrophobicity index (ϕ 0 ) is suggested as a measure of the lipophilic character of compounds in reversed-phase high-performance liquid chromatography (RP-HPLC). The parameter ϕ 0 is defined as the organic phase concentration
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::f3d898bfb7a1a2a3a850842c6476797d
https://doi.org/10.1016/0021-9673(93)80506-4
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