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pro vyhledávání: '"F, Guillier"'
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Autor:
Yacine Nia, Frédéric Auvray, Laurent Guillier, Jacques-Antoine Hennekinne, S. Messio, L. Neveux, Isabelle Mutel, F. Guillier, Bertrand Lombard, Sylvie Pairaud, Sabine Herbin, S. Gentil
Publikováno v:
International Journal of Food Microbiology. 354:109319
In the frame of the CEN Mandate M/381 from the European Commission to CEN (European Committee for Standardization), a method for the detection of staphylococcal enterotoxins in foodstuffs has been developed, validated and standardized. An extraction
Autor:
Annick Ostyn, A.-L. Prufer, S. Krys, Jacques-Antoine Hennekinne, I. Papinaud, B. Lombard, Sabine Messio, F. Guillier
Publikováno v:
Letters in Applied Microbiology. 52:468-474
Aim: To determine the performance of the Ridascreen® SET Total kit, after sample extraction and concentration by dialysis, with regard to its use in official controls for staphylococcal enterotoxins under European Regulation (EC) No. 2073/2005 modif
Autor:
P. Rocca, Guy Quéguiner, F. Nivoliers, F. Guillier, Francis Marsais, A. Godard, Guillaume Albert Jacques Duvey
Publikováno v:
Canadian Journal of Chemistry. 79:1754-1761
Connection between ortho-directed metallation of π-deficient heterocycles and Suzuki cross-coupling reactions provides a very efficient and fruitful strategy to polycyclic molecules of biological interest. The methodology is used to synthesize alkal
Publikováno v:
Journal of Heterocyclic Chemistry. 36:1157-1165
A methodical investigation on functionalization by carbonylated groups in position 4 and 5 of the benzo[c][2,7]naphthyridine skeleton has been undertaken. In particular the study has shown the complex influence of these two sites on each other. A car
Publikováno v:
Synthetic Communications. 26:4421-4436
A short and efficient synthesis of 8H-pyrido[4,3,2-mn]acridone is described. The strategy involves the preparation of 4-chloro-5-methylbenzo[c][2,7]naphtyridine, as key intermediate, by metalation and Palladium catalyzed cross-coupling reaction. A se
Publikováno v:
Tetrahedron Letters. 35:6489-6492
A short new route to 4,5-disubstituted-benzo[c]-2,7-naphthyridines has been developed. The strategy involves directed ortho metalation of pyridines following by an halogen dance reaction and biaryl cross-coupling as key steps. A concise and efficient
Autor:
A, Ostyn, F, Guillier, A-L, Prufer, I, Papinaud, S, Messio, S, Krys, B, Lombard, J-A, Hennekinne
Publikováno v:
Letters in applied microbiology. 52(5)
To determine the performance of the Ridascreen® SET Total kit, after sample extraction and concentration by dialysis, with regard to its use in official controls for staphylococcal enterotoxins under European Regulation (EC) No. 2073/2005 modified.
Autor:
J. F. Guillier, M. Poloujadoff
Publikováno v:
International Journal of Modelling and Simulation. 13:20-24
Autor:
F. Guillier, Alain Godard, Jean Bourguignon, Francis Marsais, Guy Quéguiner, Georges Dupas, F. Nivoliers
Publikováno v:
ChemInform. 24
The first total synthesis of the naturally occuring cerpegin is described. Metalation of a pyridine derivative has been used in the key step.