Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Anikó Nemes"'
Autor:
Dénes Szabó, D. Costa, Anton Kokalj, Jernej Iskra, József Rábai, Dolores Zimerl, Philippe Marcus, Matic Poberznik, Antoine Seyeux, Anikó Nemes, Charly Carrière, Ingrid Milošev, Sandrine Zanna
Publikováno v:
Journal of The Electrochemical Society
Journal of The Electrochemical Society, Electrochemical Society, 2021
Journal of The Electrochemical Society, Electrochemical Society, 2021
The ability of surfactant-like compounds to inhibit the corrosion of aluminum in NaCl solution was systematically investigated. The basic idea of this study was to scrutinize the effect of type of backbone chain (alkyl and perfluoroalkyl), length of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b37b55d55d32bd84b5360d183f576f2
https://hal.archives-ouvertes.fr/hal-03453311
https://hal.archives-ouvertes.fr/hal-03453311
Publikováno v:
Helvetica Chimica Acta. 103
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7b0518745ddc3949033676acf227e9b8
https://doi.org/10.1002/hlca.202000081
https://doi.org/10.1002/hlca.202000081
Publikováno v:
Chemical Papers. 73:47-54
Racemic 2-iodomandelic acid 1 was synthesized from commercially available 2-iodobenzoic acid 2. Acyl chloride 3 was reacted with diethyl malonate, then the formed diester was hydrolysed and decarboxylated in a one-pot reaction. The obtained 2-iodoace
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::daad46c8c53a18a903cb8c81528da8df
https://doi.org/10.1007/s11696-018-0568-6
https://doi.org/10.1007/s11696-018-0568-6
Publikováno v:
Journal of Fluorine Chemistry. 210:70-77
Convenient and robust synthesis of (perfluoroalkyl)alkane thiols [(CnF2n+1(CH2)mSH); m/n = 3/4,6,8,10, 4a-d; m/n = 2/6, 8; m/n = 1/1,2,3,7,8H, 12a-e] was developed starting from commercially available fluorous alcohols (1a-d, 5, 9a-e). The intermedia
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::aa85b37ffb655b22d54cb5028a45a3ac
https://doi.org/10.1016/j.jfluchem.2018.02.014
https://doi.org/10.1016/j.jfluchem.2018.02.014
Publikováno v:
SynOpen, Vol 02, Iss 01, Pp 0064-0071 (2018)
The reaction of aryl iodides, 3-mercaptopropionic acid, and Cu2O in refluxing pyridine resulted in the formation of 3-(arylthio)propionic acids in good to excellent yield. The latter 3-(arylthio)propionic acids — as novel aryl mercaptan equivalents
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7b1376645757cf681c27fec457d0859f
http://www.thieme-connect.de/DOI/DOI?10.1055/s-0036-1591771
http://www.thieme-connect.de/DOI/DOI?10.1055/s-0036-1591771
Publikováno v:
Journal of Fluorine Chemistry. 203:75-80
Based on the unusual reactivity of trifluoromethyl groups in nitrogen containing heterocycles, we synthesized the appropriate porphyrin mono-, di-, tri- or tetra-carboxylic ester derivatives by treatment of the precursor meso-tetrakis(trifluoromethyl
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6573ea8d178f357c2664acbbf4182b7d
https://doi.org/10.1016/j.jfluchem.2017.05.009
https://doi.org/10.1016/j.jfluchem.2017.05.009
Publikováno v:
Tetrahedron: Asymmetry. 28:1078-1082
Despite of the fact that resolution is an extremely important process in the pharmaceutical and agrochemical industries, the development of the separation of enantiomers is still based on trial-and-error experiments. In order to compare the different
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d8cb9b301dc699a70df207fbc4be31e9
https://doi.org/10.1016/j.tetasy.2017.07.001
https://doi.org/10.1016/j.tetasy.2017.07.001
Publikováno v:
Journal of Fluorine Chemistry. 196:57-62
The reaction of F- alkylation reagents including (perfluoroalkyl)alkyl halides and sulfonates [R fn (CH 2 ) m X (X = Br, I, OTs, OTf)], and a slight excess of NaN 3 in DMSO at 100 °C for 5 h, followed by steam distillation, allowed the isolation of
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ac9706efd0a2b7bd4f943a5516a4c6e
https://doi.org/10.1016/j.jfluchem.2016.08.005
https://doi.org/10.1016/j.jfluchem.2016.08.005
Autor:
Bálint Menczinger, Dénes Szabó, Tamás Jernei, Gitta Schlosser, József Rábai, Anikó Nemes, Antal Csámpai
Publikováno v:
Journal of Fluorine Chemistry. 231:109464
Aryl 2,2,2-trifluoroethyl sulfides were synthesized by copper(I)-catalyzed nucleophilic aromatic substitution reaction (Goldberg-Ullmann coupling). The method requires aryl iodides and 2,2,2-trifluoroethyl thioacetate as starting materials, benzylami
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::637fc2e19288acdf8730d9afb55cbe29
https://doi.org/10.1016/j.jfluchem.2020.109464
https://doi.org/10.1016/j.jfluchem.2020.109464
Publikováno v:
Tetrahedron Letters. 54:1730-1733
Three novel α-(nonafluoro-tert-butoxy)carboxylic esters were synthesized by two methods: the Mitsunobu reaction of optically active (S)-α-hydroxycarboxylic esters and the Williamson synthesis starting from the corresponding O-mesyl derivatives. Bot
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::bb4b6dceda5ca4cb2039bda78a4dd693
https://doi.org/10.1016/j.tetlet.2013.01.072
https://doi.org/10.1016/j.tetlet.2013.01.072