Zobrazeno 1 - 10
of 125
pro vyhledávání: '"Jacques Rouden"'
Autor:
Nesrine Harfouche, Philippe Marie, Diana Dragoe, Hung Le, Pascal Thébault, Christelle Bilot, Arnaud Fouchet, Jacques Rouden, Jérôme Baudoux, Bénédicte Lepoittevin
Publikováno v:
Materials, Vol 17, Iss 8, p 1775 (2024)
Antibacterial coatings are becoming increasingly attractive for application in the field of biomaterials. In this framework, we developed polymer coating zirconia with antibacterial activity using the “grafting from” methodology. First, 1-(4-viny
Externí odkaz:
https://doaj.org/article/8023e01649e54cb88d124b5af02f709f
Publikováno v:
Molecules, Vol 28, Iss 21, p 7333 (2023)
A simple and rapid access to fluorinated dithioesters was developed by a one-pot sequence corresponding to a Grignard reaction—Mitsunobu type substitution. These activated dithioesters have shown excellent reactivity in an aminolysis reaction from
Externí odkaz:
https://doaj.org/article/9764cdb13fdd4344bd5e8b9bd2dfccc8
Publikováno v:
Molbank, Vol 2022, Iss 3, p M1414 (2022)
Zwitterionic polymers emerge as very useful materials for applications in antifouling surfaces. The properties of these polymers can be tuned by variations of the chemical structure of the corresponding monomer. In this study, two zwitterionic ammoni
Externí odkaz:
https://doaj.org/article/89842fe3f0da4f9dacbcc3e33b697885
Publikováno v:
Molbank, Vol 2018, Iss 1, p M974 (2018)
The synthesis of 3-[2-(oxiran-2-yl)ethyl]-1-{4-[(2-oxiran-2-yl)ethoxy]benzyl}imidazolium bis(trifluoromethane)sulfonimide was achieved in seven steps with an overall yield of 63%. This ionic liquid monomer is based on an imidazolium core containing a
Externí odkaz:
https://doaj.org/article/c5269e65a02447268d0ffac6d6ea4463
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 9, Iss 1, Pp 1480-1486 (2013)
A concise and regioselective preparation of 2-heteroarylmethylene decorated N-arylpyrroles is described through a metal-free Mannich/Wittig/hydroamination sequence followed by isomerization of the N-arylpyrrolidine adducts. Furthermore, the C–H reg
Externí odkaz:
https://doaj.org/article/a56fb8f77f9c4f2aa7b16d8a60cbbd52
Autor:
Clément Dezanet, Diana Dragoe, Philippe Marie, Nesrine Harfouche, Sandrine Froissart, Arnaud Fouchet, Jacques Rouden, Jérôme Lecourt, Christelle Harnois, Pascal Thébault, Jérôme Baudoux, Bénédicte Lepoittevin
Publikováno v:
Progress in Organic Coatings
Progress in Organic Coatings, 2022, 173, pp.107202. ⟨10.1016/j.porgcoat.2022.107202⟩
Progress in Organic Coatings, 2022, 173, pp.107202. ⟨10.1016/j.porgcoat.2022.107202⟩
International audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c9c35231258bbf5bcca058ebbb3e13da
https://normandie-univ.hal.science/hal-03782186
https://normandie-univ.hal.science/hal-03782186
Publikováno v:
ChemSusChem. 15(14)
Ionic liquids have recently emerged as monomers to synthesize multifunctional polymeric materials. Among such species, ionic epoxy-based networks represent promising but underdeveloped materials that are hindered by tricky access to the functionalize
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::eafb86b54e75e3c0fe2660e87539799b
https://pubmed.ncbi.nlm.nih.gov/35499286
https://pubmed.ncbi.nlm.nih.gov/35499286
Publikováno v:
European Journal of Organic Chemistry. 2019:995-998
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d6fc6fb452d6fe7c96b4da0cf443740e
https://doi.org/10.1002/ejoc.201801528
https://doi.org/10.1002/ejoc.201801528
Publikováno v:
European Journal of Organic Chemistry. 2017:4319-4323
A new class of thioamide-substituted cinchona derivatives is reported. A convergent and practical approach was developed to insert the thioamide functional group onto the cinchonidine from readily available dithioesters. These organocatalysts were ef
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::64b7c7696a4e4e76f575afe1884ff757
https://doi.org/10.1002/ejoc.201700870
https://doi.org/10.1002/ejoc.201700870
Publikováno v:
European Journal of Organic Chemistry. 2017:3240-3243
A rapid and convenient method has been developed for the stereoselective synthesis of alpha,beta-diamino acid derivatives from amido-substituted Malonic Acid Half Oxyesters (MAHOs) and imines. The anti-products were obtained with a diastereomeric rat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4615b09227d0f9608f08fcfdbf403d7c
https://doi.org/10.1002/ejoc.201700468
https://doi.org/10.1002/ejoc.201700468