Zobrazeno 1 - 10
of 12
pro vyhledávání: '"Mathéo Berthet"'
Synthesis of stable cerium oxide nanoparticles coated with phosphonic acid-based functional polymers
Autor:
Ameni Dhouib, Braham Mezghrani, Giusy Finocchiaro, Rémi Le Borgne, Mathéo Berthet, Bénédicte Daydé-Cazals, Alain Graillot, Xiaohui Ju, Jean-François Berret
Functional polymers, such as poly(ethylene glycol) (PEG) terminated with a single phosphonic acid, hereafter PEGik-Ph are often applied to coat metal oxide surfaces during post synthesis steps, but are not sufficient to stabilize sub-10 nm particles
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4175839a5521bc6217cdc058c4ca4543
http://arxiv.org/abs/2305.10179
http://arxiv.org/abs/2305.10179
Autor:
Sofia Barluenga, Quentin Laurent, Stefan Matile, Mathéo Berthet, Yangyang Cheng, Naomi Sakai, Nicolas Winssinger
Publikováno v:
ChemBioChem, Vol. 21, No 1-2 (2020) pp. 69-73
Cellular uptake mediated by cyclic oligochalcogenides (COCs) is emerging as a conceptually innovative method to penetrate mammalian cells. Their mode of action is based on dynamic covalent oligochalcogenide exchange with cellular thiols. To test thio
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ac3bb76a01d13ed0283d94c4c6a1a330
https://archive-ouverte.unige.ch/unige:129267
https://archive-ouverte.unige.ch/unige:129267
Publikováno v:
Organic Letters. 19:492-495
A stereoconservative three-step synthesis to access to 1,2,4-oxadiazine-3,6-dione is presented. This underexplored platform could be considered as a constrained oxy-azapeptide or an aza-diketomorpholine, the methodology being then successfully applie
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::492029d4b505f0b2f8228f7129c419a9
https://doi.org/10.1021/acs.orglett.6b03656
https://doi.org/10.1021/acs.orglett.6b03656
Publikováno v:
Chemical Reviews. 116:15235-15283
The isoxazolidine ring represents one of the privileged structures in medicinal chemistry, and there have been an increasing number of studies on isoxazolidine and isoxazolidine-containing compounds. Optimization of the 1,3-dipolar cycloaddition (1,3
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::31c06b1330a09f5d01d9d85f59ed2848
https://doi.org/10.1021/acs.chemrev.6b00543
https://doi.org/10.1021/acs.chemrev.6b00543
Autor:
Alice Beauseigneur, Vincent Dalla, Mathéo Berthet, Charlotte Moine, Mohamed Othman, Catherine Taillier
Publikováno v:
Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, 2018, 24 (6), pp.1278-1282. ⟨10.1002/chem.201705949⟩
Chemistry-A European Journal, Wiley-VCH Verlag, 2018, 24 (6), pp.1278-1282. ⟨10.1002/chem.201705949⟩
International audience; Heavy silyl enol ethers (mostly TIPS and TBS) combine with cyclic N-alkenyl N-acyliminium salts generated in situ from their N,O-acetal precursors, to furnish highly functionalized indolizidines through an unprecedented double
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2c7ce1e04ee32b9b9dd1b3a9551de69b
https://hal-normandie-univ.archives-ouvertes.fr/hal-02413309
https://hal-normandie-univ.archives-ouvertes.fr/hal-02413309
Publikováno v:
Tetrahedron, Vol. 74, No 41 (2018) pp. 6012-6021
The sesquiterpene lactones cover a diverse and pharmacologically important diversity space. In particular, the electrophilic α-exo-methylene-γ-butyrolactone moiety that is preponderant in this natural product family has been shown to readily engage
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::baf03edb455815bd43ee571a2182ec19
https://archive-ouverte.unige.ch/unige:107781
https://archive-ouverte.unige.ch/unige:107781
Autor:
Jean Martinez, Guillaume Cazals, Aurélien Lebrun, Isabelle Parrot, Mathéo Berthet, Morgane Pasco, Guilhem Chaubet
Publikováno v:
Letters in Organic Chemistry
Letters in Organic Chemistry, Bentham Science Publishers, 2018, 15 (12), pp.1046-1055. ⟨10.2174/1570178615666180326160131⟩
Letters in Organic Chemistry, Bentham Science Publishers, 2018, 15 (12), pp.1046-1055. ⟨10.2174/1570178615666180326160131⟩
International audience; A new ring contraction of fused bis-lactams into spirolactams is presented here. In the presence of a triflate catalyst in various solvents under microwave irradiation, this rearrangement allows a clean conversion of some fuse
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ca2bdee7e381b62903b4b6432958877d
https://hal.archives-ouvertes.fr/hal-02388789
https://hal.archives-ouvertes.fr/hal-02388789
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2017, 82 (18), pp.9916-9922. ⟨10.1021/acs.joc.7b01828⟩
Journal of Organic Chemistry, American Chemical Society, 2017, 82 (18), pp.9916-9922. ⟨10.1021/acs.joc.7b01828⟩
International audience; A completely regioselective and challenging gold(I)-catalyzed ring-opening of cyclic 1,3-dioxolanes and dioxanes by trimethylsilyl alkynes to set diol-derived propargyl trimethylsilyl bis-ethers is reported. This unprecedented
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::467f1bf5af78abd4fe5b25f5711d275c
https://pubmed.ncbi.nlm.nih.gov/28812891
https://pubmed.ncbi.nlm.nih.gov/28812891
Autor:
Isabelle Parrot, Mathéo Berthet, Arnaud Martel, Jean Martinez, Thomas Cheviet, Aurélien Lebrun
Publikováno v:
ChemistrySelect
ChemistrySelect, Wiley, 2017, 2 (21), pp.5824-5827. ⟨10.1002/slct.201701393⟩
ChemistrySelect, Wiley, 2017, 2 (21), pp.5824-5827. ⟨10.1002/slct.201701393⟩
International audience; An improvement of the 1,2,5‐oxadiazine‐3,6‐diones (Oxd) synthesis and reactivity is described in this paper. The methodology has been successfully applied to produce a library of this poorly studied scaffold, which can b
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::986ee9eaee75bf2a1c1fa36cfb5f4be4
https://hal-univ-lemans.archives-ouvertes.fr/hal-02313808
https://hal-univ-lemans.archives-ouvertes.fr/hal-02313808
Autor:
Baptiste Legrand, Jean-Louis Bantignies, Jean Martinez, Muriel Amblard, Vincent Martin, Gilles Subra, Monique Calmes, Lubomir Vezenkov, Mathéo Berthet
Publikováno v:
Angewandte Chemie International Edition
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2015, 54 (47), pp.13966-13970. ⟨10.1002/anie.201506955⟩
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2015, 54 (47), pp.13966-13970. ⟨10.1002/anie.201506955⟩
The conformational control of molecular scaffolds allows the display of functional groups in defined spatial arrangement. This is of considerable interest for developing fundamental and applied systems in both the fields of biology and material scien
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::09ecd3d8ff8b5abb78f2f96d1cc8faed
https://hal.archives-ouvertes.fr/hal-01946536
https://hal.archives-ouvertes.fr/hal-01946536