Zobrazeno 1 - 10
of 30
pro vyhledávání: '"Adriana-Luminita Finaru"'
Publikováno v:
Horticulturae, Vol 10, Iss 5, p 504 (2024)
Origanum vulgare L. is ethnomedicinally valuable against various diseases. In Romania, attention for the oregano extracts such as infusions, decoctions, or tinctures, which are very popular among consumers, is constantly increasing, mainly as an impo
Externí odkaz:
https://doaj.org/article/63152bb697b94d04a165db78e8e46e64
Autor:
Andreea Hortolomeu, Diana Carmen Mirila, Ana-Maria Roșu, Florin Marian Nedeff, Iuri Scutaru, Dorel Ureche, Rodica Sturza, Adriana-Luminița Fînaru, Ileana Denisa Nistor
Publikováno v:
Nanomaterials, Vol 14, Iss 7, p 588 (2024)
During the manufacturing process of white wine, various physicochemical reactions can occur and can affect the quality of the finished product. For this reason, it is necessary to apply different treatments to minimize distinct factors such as protei
Externí odkaz:
https://doaj.org/article/57befa403f15481caae912888a8bdd78
Autor:
Anca Sandu-Bălan (Tăbăcariu), Irina-Loredana Ifrim, Oana-Irina Patriciu, Ioana-Adriana Ștefănescu, Adriana-Luminița Fînaru
Publikováno v:
Molecules, Vol 29, Iss 2, p 498 (2024)
A current alternative for sustainable development through green chemistry is the replacement of synthetic compounds with natural ones through the superior capitalization of natural resources, with numerous applications in different fields. The benefi
Externí odkaz:
https://doaj.org/article/6b2c72eaf830451db702d8751f8888a1
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:
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::745c4f21ed0ea2ded7854be953198f52
https://doi.org/10.1016/j.tetlet.2012.01.084
https://doi.org/10.1016/j.tetlet.2012.01.084
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,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fbc457ddb6e571b3c71d15b55492edc6
https://doi.org/10.1016/j.jchromb.2011.01.036
https://doi.org/10.1016/j.jchromb.2011.01.036
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fe5746ed19497e2a0b74d99e5cc643b3
https://doi.org/10.1016/j.chroma.2010.03.001
https://doi.org/10.1016/j.chroma.2010.03.001
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d3641dbd7bc0f0c7d0ed053fabaebbfd
https://doi.org/10.1002/ejoc.200900191
https://doi.org/10.1002/ejoc.200900191
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
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::25f6e371f0c99a5155d228706e7575ee
https://doi.org/10.1055/s-2007-990896
https://doi.org/10.1055/s-2007-990896
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
