Zobrazeno 1 - 10
of 75
pro vyhledávání: '"Florian Berthiol"'
Autor:
Florian Berthiol, Joseph Boissieras, Hugues Bonnet, Marie Pierrot, Christian Philouze, Jean-François Poisson, Anton Granzhan, Jérôme Dejeu, Eric Defrancq
Publikováno v:
Molecules, Vol 28, Iss 2, p 682 (2023)
During the last decade, the evidence for the biological relevance of i-motif DNA (i-DNA) has been accumulated. However, relatively few molecules were reported to interact with i-DNA, and a controversy concerning their binding mode, affinity, and sele
Externí odkaz:
https://doaj.org/article/62ab071e462643768462809c25a0471f
Autor:
Guanqi Wang, Yohann Moreau, Florian Berthiol, Christian Philouze, Olivier Jarjayes, Fabrice Thomas
Publikováno v:
European Journal of Inorganic Chemistry. 26
Publikováno v:
Synthesis. 54:2309-2329
Chiral α-tertiary amines, a motif present in α,α-disubstituted α-amino acids, in a wide range of natural products, and many drugs and drug candidates, are important targets in organic chemistry. Among the possible strategies, 1,2-addition to chir
Publikováno v:
European Journal of Inorganic Chemistry. 2021:1481-1489
Publikováno v:
Dalton Transactions
Dalton Transactions, Royal Society of Chemistry, 2020, 49 (37), pp.12990-13002. ⟨10.1039/d0dt02524k⟩
Dalton Transactions, Royal Society of Chemistry, 2020, 49 (37), pp.12990-13002. ⟨10.1039/d0dt02524k⟩
The sterically hindered salen ligands featuring biphenyl and tetramethyl putrescine linkers were synthesized and chelated to copper. The resulting complexes CuLbp,tBu, CuLbp,OMe, CuLpu,tBu and CuLpu,OMe were structurally characterized, showing a sign
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc91c32b165de2e5677e110c12147d80
https://hal.archives-ouvertes.fr/hal-02988221
https://hal.archives-ouvertes.fr/hal-02988221
Publikováno v:
European Journal of Organic Chemistry
European Journal of Organic Chemistry, Wiley-VCH Verlag, 2020, ⟨10.1002/ejoc.202000608⟩
European Journal of Organic Chemistry, Wiley-VCH Verlag, 2020, ⟨10.1002/ejoc.202000608⟩
International audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cdc70ed6865ae6a0ec6c0bf88b1b3664
https://hal.archives-ouvertes.fr/hal-02988213
https://hal.archives-ouvertes.fr/hal-02988213
Publikováno v:
Russian Journal of General Chemistry. 86:2881-2886
A convenient green procedure have been proposed for the synthesis of 6-(2-arylvinyl)-4-hydroxy-3-(phenylsulfanyl)-2H-pyran-2-ones by condensation of 6-(arylvinyl)-4-hydroxy-2H-pyran-2-ones with S-phenyl benzenesulfonothioate in aqueous potassium hydr
Publikováno v:
Tetrahedron Letters
Tetrahedron Letters, Elsevier, 2018, 59 (23), pp.2293-2295. ⟨10.1016/j.tetlet.2018.05.013⟩
Tetrahedron Letters, Elsevier, 2018, 59 (23), pp.2293-2295. ⟨10.1016/j.tetlet.2018.05.013⟩
An unprecedented 7-membered ring cyclization of an enamide to a phenol through hypervalent iodine phenolic oxidation was discovered. In the process a molecule of solvent is incorporated on the cycle forming an unusual and stable hemi-aminal ether.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c844db3c8effa7aecaf658b7ff6872b7
https://hal.archives-ouvertes.fr/hal-01846972
https://hal.archives-ouvertes.fr/hal-01846972
Autor:
Christian Philouze, Nicolas Leconte, Jules Moutet, Fabrice Thomas, Florian Berthiol, Amélie Kochem, Linus Chiang, Tim Storr, Laureline Lecarme
Publikováno v:
Inorganic Chemistry
Inorganic Chemistry, American Chemical Society, 2018, 57 (16), pp.9708-9719. ⟨10.1021/acs.inorgchem.8b00044⟩
Inorganic Chemistry, American Chemical Society, 2018, 57 (16), pp.9708-9719
Inorganic Chemistry, 2018, 57 (16), pp.9708-9719. ⟨10.1021/acs.inorgchem.8b00044⟩
Inorganic Chemistry, American Chemical Society, 2018, 57 (16), pp.9708-9719. ⟨10.1021/acs.inorgchem.8b00044⟩
Inorganic Chemistry, American Chemical Society, 2018, 57 (16), pp.9708-9719
Inorganic Chemistry, 2018, 57 (16), pp.9708-9719. ⟨10.1021/acs.inorgchem.8b00044⟩
The sterically hindered bis(phenol)–dipyrrin ligands HLH3 and PhLH3 were reacted with 1 equiv of copper(II) under ambient conditions to produce the copper radical complexes [Cu(HL)] and [Cu(PhL)]. Their X-ray crystal structures show relatively shor
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8a3489ea1f059d4d57c6c2e3cc4554b8
https://hal.archives-ouvertes.fr/hal-01846980
https://hal.archives-ouvertes.fr/hal-01846980
Autor:
Florian Berthiol, Christian Philouze, Amélie Kochem, Fabrice Thomas, Jennifer K. Molloy, Nicolas Leconte, Olivier Jarjayes, Gisèle Gellon
Publikováno v:
Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, 2017, 23 (56), pp.13929-13940. ⟨10.1002/chem.201702010⟩
Chemistry-A European Journal, 2017, 23 (56), pp.13929-13940. ⟨10.1002/chem.201702010⟩
Chemistry-A European Journal, Wiley-VCH Verlag, 2017, 23 (56), pp.13929-13940. ⟨10.1002/chem.201702010⟩
Chemistry-A European Journal, 2017, 23 (56), pp.13929-13940. ⟨10.1002/chem.201702010⟩
Three copper(II) complexes of the (R,R)-N,N'-Bis(3,5-di-tert-butyl-2-aminobenzylidene)-1,2-diaminocyclohexane, namely [Cu(NL)], [Cu(NLH)]+ and [Cu(NLH2)]2+, were prepared and structurally characterized. In [Cu(NLH2)]2+ the copper ion lies in an octah
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7aeb8b457dd3b37176af13a959b5df29
https://hal.archives-ouvertes.fr/hal-01636986
https://hal.archives-ouvertes.fr/hal-01636986