Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Ethel Garnier"'
Autor:
Stefka Gyoneva, Lauren Shapiro, Carlos Lazo, Ethel Garnier-Amblard, Yoland Smith, Gary W. Miller, Stephen F. Traynelis
Publikováno v:
Neurobiology of Disease, Vol 67, Iss , Pp 191-202 (2014)
Microglia, the immune cells of the central nervous system, constantly survey the parenchyma in the healthy brain to maintain homeostasis. When a disturbance, such as cell death, results in ATP release in vivo, microglial processes respond by utilizin
Externí odkaz:
https://doaj.org/article/6fff32c1eda048309711f94e97987885
Autor:
Christian Jarry, Ivan Rodriguez, Paul Caubere, Jean-Michel Léger, Ethel Garnier, Stéphanie Blanchard, Gérald Guillaumet
Publikováno v:
Synthesis. :2033-2040
Several 2-aryl and 2-heteroaryloxazolo[4,5-b]pyridines were synthesised in high yields from zwitterion or hydroxyamidine derivatives by heating in dimethylacetamide. These intermediates were generated via hetarynic reaction with the complex base NaNH
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bf0d156c23286fb197f0d236cfe84340
https://doi.org/10.1055/s-2003-41052
https://doi.org/10.1055/s-2003-41052
Publikováno v:
Synlett. 2006:0472-0474
The synthesis of several novel polynitrogen materials based on fused 1,2,4-triazines is described. A powerful palladium-catalyzed N-heteroarylation strategy followed by a cyclization provides a straightforward one-pot reaction to these tricyclic mate
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8efa1c0a6292133cb00993821fdd4e23
https://doi.org/10.1055/s-2006-926242
https://doi.org/10.1055/s-2006-926242
Autor:
Stefka, Gyoneva, Dimitrios, Davalos, Dipankar, Biswas, Sharon A, Swanger, Ethel, Garnier-Amblard, Francis, Loth, Katerina, Akassoglou, Stephen F, Traynelis
Publikováno v:
Glia. 62(8)
Microglia, the resident immune cells of the central nervous system, exist in either a “resting” state associated with physiological tissue surveillance or an “activated” state in neuroinflammation. We recently showed that ATP is the primary c
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::adb70666796fe9828c4c83b77c68ddcc
https://pubmed.ncbi.nlm.nih.gov/24807189
https://pubmed.ncbi.nlm.nih.gov/24807189
Autor:
Paul Caubere, Christian Jarry, Adriana-Luminita Finaru, Irina-Claudia Grig-Alexa, Jean-Michel Léger, Lucia Ivan, Gérald Guillaumet, Ethel Garnier
Publikováno v:
ChemInform. 36
New dihydrodiquinolinopyrazines (DHDQP) were easily obtained by hetarynic dimerization of 2-alkylamino-3-bromo-quinolines in the presence of complex base NaNH 2 -t-BuONa. Functionalization and derivatization of these new heterocycles are described.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a25b60b7bc4b5a7825fe7ea51985749c
https://doi.org/10.1002/chin.200505142
https://doi.org/10.1002/chin.200505142
Autor:
Gérald Guillaumet, Bruno Lebret, Eric Pasquinet, Jerome Audoux, Didier Poullain, Franck Suzenet, Ethel Garnier
Publikováno v:
The Journal of organic chemistry. 69(23)
In this paper, N-arylations between two heteroaryl compounds were studied. Conditions were found to generate selectively either 3- or 5-heteroarylamino-1,2,4-triazines by investigating anionic processes (use of bases such as 2,2',6,6'-tetramethylpipe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7abc24e3a28e2f970f2e338ab047b7ed
https://pubmed.ncbi.nlm.nih.gov/15527255
https://pubmed.ncbi.nlm.nih.gov/15527255
Autor:
Eric Pasquinet, Didier Poullain, Jerome Guillard, Gérald Guillaumet, Jean‐Michel Leger, Christian Jarry, Franck Suzenet, Bruno Lebret, Ethel Garnier
Publikováno v:
Organic letters. 5(24)
[reaction: see text] The first examples of C(6)-substituted 7-hydroxy-6,7-dihydro-5H-imidazo[1,2-b][1,2,4]triazines have been prepared by ring closure of different 5(2H)-1,2,4-triazin-3-ones 1a-c with 40% aqueous glyoxal and various nucleophiles (alc
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0b947c191fea321f7a774e4ec34be75c
https://pubmed.ncbi.nlm.nih.gov/14627392
https://pubmed.ncbi.nlm.nih.gov/14627392