Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Nathalie Fresneau"'
Publikováno v:
Molecules, Vol 17, Iss 12, Pp 14409-14417 (2012)
Following our previous results on an environmentally benign one-pot Sonogashira-cyclization protocol to obtain substituted furopyrimidine nucleosides under aqueous conditions, we investigate herein the Suzuki-Miyaura cross-coupling reactions of aryl
Externí odkaz:
https://doaj.org/article/6d23e8482b9a48928a83a236d706b6f9
Autor:
Hélène Cazier, Carole Malgorn, Dominique Georgin, Nathalie Fresneau, Fabrice Beau, Kostas Kostarelos, Cyrill Bussy, Stéphane Campidelli, Mathieu Pinault, Martine Mayne-L'Hermite, Frédéric Taran, Christophe Junot, François Fenaille, Antoine Sallustrau, Benoit Colsch
Publikováno v:
Cazier, H, Malgorn, C, Georgin, D, Fresneau, N, Beau, F, Kostarelos, K, Bussy, C, Campidelli, S, Pinault, M, Mayne-L'hermite, M, Taran, F, Junot, C, Fenaille, F, Sallustrau, A & Colsch, B 2023, ' Correlative radioimaging and mass spectrometry imaging: a powerful combination to study 14 C-graphene oxide in vivo biodistribution ', Nanoscale, vol. 15, no. 11, pp. 5510-5518 . https://doi.org/10.1039/D2NR06753F
Research on graphene based nanomaterials has flourished in the last decade due their unique properties and emerging socio-economic impact. In the context of their potential exploitation for biomedical applications, there is a growing need for the dev
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::206fd036aac7edbe46d1e453c38cc044
https://research.manchester.ac.uk/en/publications/e536229c-7993-46a9-b902-3a0ce705732b
https://research.manchester.ac.uk/en/publications/e536229c-7993-46a9-b902-3a0ce705732b
Autor:
Benoit Colsch, François Fenaille, Antoine Sallustrau, Nathalie Fresneau, Dominique Georgin, Stéphane Campidelli, Hélène Cazier, Jean-Claude Tabet, Mathieu Pinault, Vincent Dive, Christophe Junot, Carole Malgorn, Frédéric Taran, Céline Chollet, Martine Mayne
Publikováno v:
Journal of The American Society for Mass Spectrometry
Journal of The American Society for Mass Spectrometry, Springer Verlag (Germany), 2020, 31 (5), pp.1025-1036. ⟨10.1021/jasms.9b00070⟩
Journal of The American Society for Mass Spectrometry, 2020, 31 (5), pp.1025-1036. ⟨10.1021/jasms.9b00070⟩
Journal of The American Society for Mass Spectrometry, Springer Verlag (Germany), 2020, 31 (5), pp.1025-1036. ⟨10.1021/jasms.9b00070⟩
Journal of The American Society for Mass Spectrometry, 2020, 31 (5), pp.1025-1036. ⟨10.1021/jasms.9b00070⟩
International audience; Graphene-based nanoparticles are continuously being developed for biomedical applications, and their use raises concerns about their environmental and biological impact. In the literature, some imaging techniques based on fluo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6a5f9943cabd772b22c2f9f2b2da713f
https://pubmed.ncbi.nlm.nih.gov/32223237
https://pubmed.ncbi.nlm.nih.gov/32223237
Publikováno v:
Tetrahedron
Tetrahedron, Elsevier, 2013, pp.5393-5400. ⟨10.1016/j.tet.2013.04.104⟩
Tetrahedron, Elsevier, 2013, pp.5393-5400. ⟨10.1016/j.tet.2013.04.104⟩
International audience; Substituted diazino[c]quinolin-5(6H)-ones and -isoquinolin-6(5H)-ones, diazino[c]naphthyridin-6(5H)- and -5(6H)-ones were obtained using two synthetic routes: one-pot cross-coupling/cyclization and two-step cross-coupling/KOH-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::13231bfedfd7172418cd9c6ee5faea3a
https://doi.org/10.1016/j.tet.2013.04.104
https://doi.org/10.1016/j.tet.2013.04.104
Publikováno v:
Tetrahedron Letters. 53:1760-1763
An environmentally benign one-pot protocol was herein reported to obtain different substituted furopyrimidine nucleosides in aqueous conditions with a low catalysts loading.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9dbb9aadbb6eadf81c69763c530e5199
https://doi.org/10.1016/j.tetlet.2012.01.106
https://doi.org/10.1016/j.tetlet.2012.01.106
Autor:
Céline Ballandonne, Frédéric Fabis, Noé Dumas, Philippe Millet, Aurélien Lesnard, Christine Fossey, Jean-Philippe Bouillon, Benjamin B. Tournier, Yves Charnay, Nathalie Fresneau, Thomas Cailly
Publikováno v:
European Journal of Medicinal Chemistry
European Journal of Medicinal Chemistry, Elsevier, 2015, 94, pp.386-396. ⟨10.1016/j.ejmech.2015.03.017⟩
European Journal of Medicinal Chemistry, Vol. 94 (2015) pp. 386-96
European Journal of Medicinal Chemistry, Elsevier, 2015, 94, pp.386-396. ⟨10.1016/j.ejmech.2015.03.017⟩
European Journal of Medicinal Chemistry, Vol. 94 (2015) pp. 386-96
International audience; With the aim to develop a suitable radiotracer for the brain imaging of the serotonin 4 receptor subtype (5-HT4R) using single photon emission computed tomography (SPECT), we synthesized and evaluated a library of di- and tria
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fcc02ee916395d5bf7992eb9f3bb1fd3
https://hal.archives-ouvertes.fr/hal-02011103
https://hal.archives-ouvertes.fr/hal-02011103
Publikováno v:
ChemInform. 44
via one-pot cross-coupling/cyclization or two-step cross-coupling/KOH-mediated anionic ring closure reactions
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::314bb75f87d2038f187e037dfa0f2234
https://doi.org/10.1002/chin.201345172
https://doi.org/10.1002/chin.201345172
Publikováno v:
ChemInform. 43
Under optimized conditions, the Sonogashira coupling of substrate (I) with alkynes is followed by cyclization.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::631f2e1413a93192217c4402f4cef7f4
https://doi.org/10.1002/chin.201230218
https://doi.org/10.1002/chin.201230218