Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Fabrice Bisaro"'
Autor:
Fabrice Bisaro, Alya Inial, Jérémie Gatignol, Florent Allix, Aurélie Stallivieri, Jean-Luc Renaud, Lynda Achouri, Marian Parlog, Franck Delaunay, Thi-Nhàn Pham, Matthieu Hamel, Sylvain Gaillard
Publikováno v:
Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment
Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment, 2022, 1030, pp.166469. ⟨10.1016/j.nima.2022.166469⟩
Nuclear Instruments and Methods in Physics Research Section A: Accelerators, Spectrometers, Detectors and Associated Equipment, 2022, 1030, pp.166469. ⟨10.1016/j.nima.2022.166469⟩
International audience; The development of highly efficient plastic scintillators for neutron/gamma pulse shape discrimination is a matter of current interest. This is generally achieved using two fluorophores, with one of them being added to the pol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::79bbc4c9df5b142a66ddefdc3bf3dcf8
https://cea.hal.science/cea-04026308/file/article_FabriceBisaro.pdf
https://cea.hal.science/cea-04026308/file/article_FabriceBisaro.pdf
Autor:
Fabrice Bisaro, Veronique Gouverneur
Substituted vinyl and allyl phosphine oxides have been prepared by olefin cross-metathesis providing exclusive E olefin stereochemistry. The methodology has been successfully extended to the preparation of various bis-phosphine oxides. © 2003 Elsevi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4d969ad7898bec0782c21e34ac536bd9
https://doi.org/10.1016/s0040-4039(03)01842-2
https://doi.org/10.1016/s0040-4039(03)01842-2
Autor:
Fabrice Bisaro, Pascal Le Floch
Publikováno v:
Synlett. 2010:3081-3085
A tyrosine derivative with a phosphole moiety covalently attached to the phenolic hydroxy group was successfully prepared through P-0 bond-forming reaction, via a nucleophilic substitution reaction at the phosphorus, by slow addition of N-CBz-protect
Publikováno v:
Scopus-Elsevier
ResearcherID
ResearcherID
The acid mediated reaction between active methylenes and benzhydryl alcohols, or their derivatives, is reported. Ethyl acetoacetate, acetylacetone, and N,N-dibenzyl-malonamic acid methyl ester are benzhydrylated in quantitative yields in the presence
Autor:
Christopher J. Richards, Nathalie Dendele, Fabrice Bisaro, Annie-Claude Gaumont, Stéphane Perrio
Publikováno v:
Chemical communications (Cambridge, England). 48(14)
Kinetic resolution of racemic 4-N,N-dimethylaminomethyl[2.2]paracyclophane with 50% sodium tetrachloropalladate and (R)-N-acetylphenylalanine under basic conditions resulted in the formation of a (Sp)-planar chiral palladacycle (35%, >99% ee). Simila
Autor:
Sébastien Comesse, Fabrice Bisaro, Catherine Kadouri-Puchot, Rémy Morgentin, Sebastien J. J. Guesné, Claude Agami
Publikováno v:
ChemInform. 33
(2R,4R)-4-Methylpipecolic acid and (2S,4R)-4-hydroxypipecolic acid, two biologically active amino acids, were synthesized using the same strategy. A third amino acid, obtained in a protected form, was also obtained in the same way. The key step of th
Autor:
Fabrice Bisaro, Catherine S. J. Cazin, Cécilia A. Citadelle, Erwan Le Nouy, Alexandra M. Z. Slawin
Publikováno v:
Dalton transactions (Cambridge, England : 2003). 39(19)
A novel synthetic route leading to N-heterocyclic carbene copper complexes has been developed by using air-stable and commercially available copper(I) oxide and imidazolium salts starting materials.
Publikováno v:
ChemInform. 41
The hydrodehalogenation of polychlorinated phenyls and biphenyls (PCBs), catalysed by palladium N-heterocyclic carbene complexes, proceeds with excellent yields, at very low catalyst loadings and at room temperature, using isopropanol as the hydrogen
Publikováno v:
The Journal of organic chemistry. 70(26)
[reaction: see text] The preparation of phosphorus-containing trienes featuring two diastereotopic vinyl moieties followed by a diastereoselective ring-closing metathesis is described. This methodology allowed for the synthesis of novel highly functi
Autor:
Veronique Gouverneur, Fabrice Bisaro
Publikováno v:
ChemInform. 36
Desymmetrization of prochiral di- and trialkenyl phosphine oxides by cross-metathesis with various olefinic partners allowed direct access to novel racemic P-stereogenic products featuring two or three different alkenyl groups. The excellent control