Zobrazeno 1 - 10
of 28
pro vyhledávání: '"ADRIANA LUMINITA FINARU"'
Autor:
Alina Mihaela (Maciuca) Birtea, Andra Poloboc, Nicolae Catalin Tampu, Raluca Ioana Tampu, Oana-Irina Patriciu, Bérengère Claude, Reine Nehmé, Adriana Luminita Finaru
Publikováno v:
Scientific Study & Research: Chemistry & Chemical Engineering, Biotechnology, Food Industry, Vol 21, Iss 2, Pp 279-288 (2020)
This paper presents a simple, ecofriendly, robust and inexpensive method for the preparation of radish (Raphanus sativus) and spinach (Spinacia oleracea) extracts that are destined to be tested as green corrosion inhibitors. The obtained extracts
Externí odkaz:
https://doaj.org/article/30fc9382234542f5979699ab963bc9d0
Autor:
IRINA-CLAUDIA ALEXA, PETRONEL PAVĂL, DANIELA NICUŢĂ, PETRONELA BRAN, OANA-IRINA PATRICIU, LUMINIŢA GROSU, ADRIANA LUMINITA FINARU
Publikováno v:
Scientific Study & Research: Chemistry & Chemical Engineering, Biotechnology, Food Industry, Vol 16, Iss 1, Pp 075-079 (2015)
The current study presented in vitro plant development of Calendula officinalis on MS (Murashige and Skoog) medium supplemented with different formula of hormones. The morphogenetic response was evaluated by recording the number of plantlets, the pla
Externí odkaz:
https://doaj.org/article/3c74b263ed7742e997d1dc4c575963d8
Autor:
Lavinia Misaila, Narcis Barsan, Florin Marian Nedeff, Dumitra Raducanu, Cristian Radu, Luminita Grosu, Oana-Irina Patriciu, Lucian Gavrila, Adriana-Luminita Finaru
Publikováno v:
Water, Vol 14, Iss 19, p 2942 (2022)
In the present study, using a combination of several analytical techniques such as conductometry/total dissolved solids (TDS), pH-metry, ICP-MS and UV-Vis spectrometry, 38 parameters (Na, K, Mg, Ca, Al, Fe, B, Li, Cr, Mn, Ni, Cu, Zn, Se, Sr, Ag, Cd,
Externí odkaz:
https://doaj.org/article/1c0d92f8d9d44279adc175b1de14ce65
Autor:
Irina-Claudia Grig-Alexa, Christian Jarry, Iuliana Simionescu, Oana-Irina Patriciu, Jean-Michel Léger, Stéphane Massip, Adriana-Luminita Finaru, Gérald Guillaumet
Publikováno v:
Tetrahedron Letters. 53:1885-1888
The formation of alkoxy substituted di(pyridin-2-yl)amines and N-arylpyridin-2-ylamines by nitro group reduction is described. Unexpected substitution of ortho with the amino at C-6 was observed during the reduction using SnCl2·2H2O in different alc
Publikováno v:
Journal of Chromatography B. 879:633-640
This paper evaluates the performances of reversed-phase (RPLC) and ion-pairing chromatography (IPLC) coupled with UV detection for the analysis of a set of 12 catecholamines and related compounds. Different chromatographic columns (porous C18-silica,
Publikováno v:
Journal of Chromatography A. 1217:3091-3104
This paper presents the comparison between 12 hydrophilic interaction liquid chromatography columns that are commercially available. The main factors influencing the retention and selectivity toward 12 neurotransmitters for these different HILIC syst
Publikováno v:
European Journal of Organic Chemistry. 2009:3619-3627
The synthesis of 3-amino-8-azachromans and 3-amino-7-azabenzofurans derivatives is reported. The synthetic strategy is based on an inverse electron demand Diels–Alder approach, which employs 1,2,4-triazines that are judiciously substituted with ami
Autor:
Adriana-Luminita Finaru, Gérald Guillaumet, Christelle Pillard, Oana-Irina Patriciu, Ioan Sandulescu
Publikováno v:
Synthesis. 2007:3868-3876
The amination of 3-nitropyridines with aromatic amides generated from various aminopyridine derivatives proceeded unexpectedly in the position PARA to the nitro group, giving the oxidative nucleophilic substitution of hydrogen (ONSH) derived compound
Autor:
Emmanuel Deau, Grzegorz Satała, Adriana-Luminita Finaru, Gérald Guillaumet, Andrzej J. Bojarski, Raluca Voinea, Gilles Tamagnan, Agnes Chartier, David Alagille, Franck Suzenet, Nathalie Percina, Elodie Robin, Séverine Morisset-Lopez
Publikováno v:
Journal of Medicinal Chemistry
Journal of Medicinal Chemistry, American Chemical Society, 2015, 58 (20), pp.8066-8096. ⟨10.1021/acs.jmedchem.5b00874⟩
Journal of Medicinal Chemistry, 2015, 58 (20), pp.8066-8096. ⟨10.1021/acs.jmedchem.5b00874⟩
Journal of Medicinal Chemistry, American Chemical Society, 2015, 58 (20), pp.8066-8096. ⟨10.1021/acs.jmedchem.5b00874⟩
Journal of Medicinal Chemistry, 2015, 58 (20), pp.8066-8096. ⟨10.1021/acs.jmedchem.5b00874⟩
International audience; We report the synthesis of 46 tertiary amine-bearing N-alkylated benzo[d]imidazol-2(3H)-ones, imidazo[4,5-b]pyridin-2(3H)-ones, imidazo[4,5-c]pyridin-2(3H)-ones, benzo[d]oxazol-2(3H)-ones, oxazolo[4,5-b]pyridin-2(3H)-ones and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8ad91d50e9dc985d392b70a081a500bb
https://hal-cnrs.archives-ouvertes.fr/hal-03082898
https://hal-cnrs.archives-ouvertes.fr/hal-03082898
Autor:
Adriana-Luminita Finaru, Gérald Guillaumet, Paul Caubere, Irina-Claudia Grig-Alexa, Lucia Ivan
Publikováno v:
Synthesis. 2006:619-628
A variety of3-bromo-2-[(N-substituted)amino]pyridines were obtained via two convenient methods and were used in the hetarynic synthesis of the corresponding N-substituted dihydro-dipyridopyrazines.