Zobrazeno 1 - 5
of 5
pro vyhledávání: '"Laetitia Mistico"'
Autor:
Ming-Qiang Zheng, Vincent M. Carroll, Cedric Tresse, John Seibyl, Laetitia Mistico, Cristian Constantinescu, Olivier Barret, David Alagille, Alexandra Gouasmat, Christine M. Sandiego, Kenneth Marek, Gilles Tamagnan, Caroline Papin
Publikováno v:
Molecular Imaging and Biology. 21:509-518
Synaptic vesicle protein 2A (SV2A) serves as a biomarker of synaptic density and positron emission tomography (PET) imaging of SV2A could provide a tool to assess progression of neurodegenerative diseases. Two tracers have primarily been reported and
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c7163821fa77e00d198de09e8d20c12c
https://doi.org/10.1007/s11307-018-1260-5
https://doi.org/10.1007/s11307-018-1260-5
Autor:
Cyril François, Laetitia Mistico, Lieven Meerpoel, Patrick René Angibaud, Olivier Alexis Georges Querolle, Thomas Boddaert, Muriel Durandetti, Jacques Maddaluno
Publikováno v:
Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, 2014, 20 (32), pp.10131-10139. ⟨10.1002/chem.201402597⟩
Chemistry-A European Journal, Wiley-VCH Verlag, 2014, 20 (32), pp.10131-10139. ⟨10.1002/chem.201402597⟩
A simple access to silylated and germylated binuclear heterocycles, based on an original anionic rearrangement, is described. A set of electron-rich and electron-poor silylated aromatic and heteroaromatic substrates were tested to understand the mech
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6749f9386419eec080167bd42f92d660
https://doi.org/10.1002/chem.201402597
https://doi.org/10.1002/chem.201402597
Autor:
Guillaume Prestat, Laetitia Mistico, Giovanni Poli, Emel Ay, Julie Oble, Vaizanne Huynh, Fabrice Chemla, Alejandro Perez-Luna, Franck Ferreira, Aurelie Bourderioux
Publikováno v:
Journal of Organometallic Chemistry
Journal of Organometallic Chemistry, Elsevier, 2014, 760, pp.124--129. ⟨10.1016/j.jorganchem.2013.11.026⟩
Journal of Organometallic Chemistry, Elsevier, 2014, 760, pp.124--129. 〈10.1016/j.jorganchem.2013.11.026〉
Journal of Organometallic Chemistry, 2014, 760, pp.124--129. ⟨10.1016/j.jorganchem.2013.11.026⟩
Journal of Organometallic Chemistry, Elsevier, 2014, 760, pp.124--129. ⟨10.1016/j.jorganchem.2013.11.026⟩
Journal of Organometallic Chemistry, Elsevier, 2014, 760, pp.124--129. 〈10.1016/j.jorganchem.2013.11.026〉
Journal of Organometallic Chemistry, 2014, 760, pp.124--129. ⟨10.1016/j.jorganchem.2013.11.026⟩
The performance of tert-butanesulfinamides as nitrogen nucleophiles in Pd(0)-catalyzed allylic substitution reactions has been investigated. Metalated N-alkyl and N-acetyl sulfinamides have been identified as suitable partners for the reaction with
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f769ad76e9e0c7db2330fa648e6b9fbc
https://doi.org/10.1016/j.jorganchem.2013.11.026
https://doi.org/10.1016/j.jorganchem.2013.11.026
Autor:
Olivier Alexis Georges Querolle, Muriel Durandetti, Patrick René Angibaud, Jacques Maddaluno, Lieven Meerpoel, Laetitia Mistico
Publikováno v:
Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, 2016, 22 (28), pp.9687-9692. ⟨10.1002/chem.201601533⟩
Chemistry-A European Journal, Wiley-VCH Verlag, 2016, 22 (28), pp.9687-9692. ⟨10.1002/chem.201601533⟩
International audience; A simple and efficient approach to new silylated heterocycles of potential interest in medicinal chemistry is presented. A set of bromophenyl trimethylsilyl pyrazole intermediates can be transformed by direct organometallic ro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::86c69e17eb7681cb1d7f46bf625ffbfd
https://hal.archives-ouvertes.fr/hal-02019187
https://hal.archives-ouvertes.fr/hal-02019187
Autor:
Aurelie Bourderioux, Laetitia Mistico, Emel Ay, Fabrice Chemla, Julie Oble, Vaizanne Huynh, Alejandro Perez-Luna, Guillaume Prestat, Franck Ferreira, Giovanni Poli
Publikováno v:
ChemInform. 45
The process can not be applied to 1,1′,2-trisubstituted alkenes such as prenyl carbonate which does not react.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::68a88dd62488a23b56119ff097e9b2b7
https://doi.org/10.1002/chin.201440060
https://doi.org/10.1002/chin.201440060