Zobrazeno 1 - 10 of 20 pro vyhledávání: '"Sylvie MOEBS-SANCHEZ"'
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Akademický článek
Identifying Potent Nonsense-Mediated mRNA Decay Inhibitors with a Novel Screening System
Autor: Julie Carrard, Fiona Ratajczak, Joséphine Elsens, Catherine Leroy, Rebekah Kong, Lucie Geoffroy, Arnaud Comte, Guy Fournet, Benoît Joseph, Xiubin Li, Sylvie Moebs-Sanchez, Fabrice Lejeune
Publikováno v: Biomedicines, Vol 11, Iss 10, p 2801 (2023)
Nonsense-mediated mRNA decay (NMD) is a quality control mechanism that degrades mRNAs carrying a premature termination codon. Its inhibition, alone or in combination with other approaches, could be exploited to develop therapies for genetic diseases
Externí odkaz: https://doaj.org/article/05e2ba02ef9c46fb8388786117f2811b
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2
Akademický článek
Nitrogen-functionalized Isohexides in Asymmetric Induction
Autor: Marine Janvier, Sylvie Moebs-Sanchez, Florence Popowycz
Publikováno v: CHIMIA, Vol 70, Iss 1-2 (2016)
Biosourced isohexides have attracted the considerable attention of both the academic and industrial chemistry communities over the last 50 years. This highlight focuses on the synthesis of nitrogen-containing isohexides and their applications in asym
Externí odkaz: https://doaj.org/article/9bf2e013517e4182a41cd3bd1802627c
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4
Catalytic access to anhydrohexitols and their isomerization
Autor: Mathieu Sauthier, Isabelle Suisse, Florence Popowycz, Sylvie Moebs-Sanchez, Maïwenn Jacolot
Publikováno v: Carbohydrate Chemistry
Carbohydrate Chemistry, 45, Royal Society of Chemistry, pp.305-335, 2021, Carbohydrate Chemistry, ⟨10.1039/9781839164538-00305⟩
International audience
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::15b17ae28cdeb05c5892c1c317632e43
https://hal.science/hal-03543793
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5
Design and synthesis of 3, 5- hetero diesters of 4-deoxy quinic acid and their aphicidal activity against Acyrthosiphon pisum
Autor: Pedro da Silva, Sylvie Moebs-Sanchez, Xiubin Li, Catherine Sivignon, Yvan Rahbé, Yves Queneau
Publikováno v: Tetrahedron
Tetrahedron, Elsevier, 2021, pp.131982. ⟨10.1016/j.tet.2021.131982⟩
International audience; our analogs of 3,5-dicaffeoylquinic acid, including a new heterodiester of 4-deoxyquinic acid, were found toxic against the pea aphid. Several 4-deoxy quinic analogs featuring two different hydroxyl cinnamoyl moieties in posit
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b80ad4884adfdb2ff98f375582f9ce91
https://hal.archives-ouvertes.fr/hal-03126097/document
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6
Bio-Based Amides from Renewable Isosorbide by a Direct and Atom-Economic Boric Acid Amidation Methodology
Autor: Sylvie Moebs-Sanchez, Florence Popowycz, Marine Janvier
Publikováno v: European Journal of Organic Chemistry
European Journal of Organic Chemistry, Wiley-VCH Verlag, 2016, 2016 (13), pp.2308-2318. ⟨10.1002/ejoc.201600186⟩
International audience; The functionalization of bio-sourced isohexides has proved challenging over the last number of years, especially in polymer and medicinal chemistry. We report herein the synthesis of bio-based amido-isohexides by the known bor
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5cf522ca2451a341cf26e932af50e0bc
https://doi.org/10.1002/ejoc.201600186
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7
The Piancatelli reaction and its variants: recent applications to high added-value chemicals and biomass valorization
Autor: Florence Popowycz, Yves Queneau, Sylvie Moebs-Sanchez, Charlie Verrier
Publikováno v: Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2018, 77, pp.215-222. ⟨10.1039/c7ob02962d⟩
The Piancatelli reaction, also called the Piancatelli rearrangement, consists in the direct conversion of furfuryl alcohols to cyclopentenone derivatives through a furan ring opening-electrocyclization process. Discovered in the late 70's, this react
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d2949daef059ac28528baa5aaedbe80b
https://pubmed.ncbi.nlm.nih.gov/29362755
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9
Ring opening of epoxidized methyl or ethyl oleate by alkyl glycosides
Autor: Yves Queneau, Carine Alfos, Cédric Epoune Lingome, Sylvie Moebs-Sanchez, Benoit Gadenne
Publikováno v: European Journal of Lipid Science and Technology
European Journal of Lipid Science and Technology, Wiley-VCH Verlag, 2017, 119 (7), pp.1600413. ⟨10.1002/ejlt.201600413⟩
Epoxidized methyl or ethyl oleate were used as models of FAtty Methyl Esters to explore their functionalization via ring opening of the internal epoxide by alkyl glycosides. Overcoming solubility issues, medium to long-chain alkyl glucosides gave bet
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ed3301767176791ac79e99040b15a854
https://hal-udl.archives-ouvertes.fr/hal-02193024
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10
Synthesis and biological evaluation of C-3 aliphatic coumarins as vitamin K antagonists
Autor: Manon Boulven, Claire Hascoët, Maïwenn Jacolot, Etienne Benoit, Virginie Lattard, Florence Popowycz, Abdessalem Hammed, Marc Lemaire, Adrien Montagut-Romans, Stéphane Besse, Sylvie Moebs-Sanchez
Publikováno v: Bioorganic and Medicinal Chemistry Letters
Bioorganic and Medicinal Chemistry Letters, Elsevier, 2017, 27 (7), pp.1598-1601. ⟨10.1016/j.bmcl.2017.02.017⟩
Since the discovery of Warfarin in the 1940s, the design of new warfarin-derived anticoagulants for rodent management has been challenging, with mainly structural modifications performed on the C3 position of the coumarin skeleton. In order to better
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1b427e15b7b038dfa89d0c74e81f0b21
https://hal.archives-ouvertes.fr/hal-01606714
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