Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Carlotta, Figliola"'
Autor:
Carlotta Figliola, Halina Anton, Christophe Sutter, Camille Chériaux, Alexandra Sutter, Valérie Mazan, Mourad Elhabiri, Pascal Didier, Denis Jacquemin, Gilles Ulrich
Publikováno v:
ChemBioChem.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::4da562651fd4b067d0b1ed2f05fe6508
https://doi.org/10.1002/cbic.202300139
https://doi.org/10.1002/cbic.202300139
Autor:
Kesar, Jagdev, Damiano, Tanini, Jack W, Lownes, Carlotta, Figliola, Louise, Male, Antonella, Capperucci, Richard S, Grainger
Publikováno v:
Organicbiomolecular chemistry. 19(48)
Glutathione peroxidase (GPx) regulates cellular peroxide levels through glutathione oxidation. GPx-mimics based on 4,5-disubstituted fluorene diselenides, their oxides, and ditellurides show catalytic activities consistent with conformational restric
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::f598d173eda4feaed3403c150e4dd41e
https://pubmed.ncbi.nlm.nih.gov/34846405
https://pubmed.ncbi.nlm.nih.gov/34846405
Autor:
Damiano Tanini, Antonella Capperucci, Louise Male, Carlotta Figliola, Jack W. Lownes, Richard S. Grainger, Kesar Jagdev
Publikováno v:
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2021, 19 (48), pp.10565-10569. ⟨10.1039/D1OB02153B⟩
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2021, 19 (48), pp.10565-10569. ⟨10.1039/D1OB02153B⟩
International audience; Glutathione peroxidase (GPx) regulates cellular peroxide levels through glutathione oxidation. GPx-mimics based on 4,5-disubstituted fluorene diselenides, their oxides, and ditellurides show catalytic activities consistent wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5768e1760200c52d514bc12ec02e664e
http://hdl.handle.net/2158/1253656
http://hdl.handle.net/2158/1253656
Publikováno v:
Chemical Reviews
Chemical Reviews, American Chemical Society, 2021, 121 (12), pp.6718-6743. ⟨10.1021/acs.chemrev.0c00806⟩
Chemical Reviews, 2021, 121 (12), pp.6718-6743. ⟨10.1021/acs.chemrev.0c00806⟩
Chemical Reviews, American Chemical Society, 2021, 121 (12), pp.6718-6743. ⟨10.1021/acs.chemrev.0c00806⟩
Chemical Reviews, 2021, 121 (12), pp.6718-6743. ⟨10.1021/acs.chemrev.0c00806⟩
International audience; Click and bioorthogonal reactions are dominated by cycloaddition reactions in general and 1,3-dipolar cycloadditions in particular. Among the dipoles routinely used for click chemistry, azides, nitrones, isonitriles and nitril
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::8e59fd3b2c3bc949d3c520b1c720fe53
https://pubmed.ncbi.nlm.nih.gov/33238101
https://pubmed.ncbi.nlm.nih.gov/33238101
Publikováno v:
Organic & Biomolecular Chemistry. 15:5410-5427
We report the synthesis of the first click-appended prodigiosene conjugates. Four prodigiosene conjugates of estradiol functionalised at the 7α-position were prepared, as were three prodigiosene conjugates of tamoxifen. The coupling between a prodig
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a3927ae4bde679e31f972767d80dab62
https://doi.org/10.1039/c7ob00943g
https://doi.org/10.1039/c7ob00943g
Autor:
Béatrice Tuccio, Jean-Luc Parrain, Carlotta Figliola, Olivier Chuzel, Gaëlle Chouraqui, Paola Nava, Amel Abdou Mohamed, Clara Aupic
Publikováno v:
Chemical Science
Chemical Science, 2019, 10 (26), pp.6524-6530. ⟨10.1039/C9SC01454C⟩
Chemical Science, The Royal Society of Chemistry, 2019, 10 (26), pp.6524-6530. ⟨10.1039/C9SC01454C⟩
Chemical Science, 2019, 10 (26), pp.6524-6530. ⟨10.1039/C9SC01454C⟩
Chemical Science, The Royal Society of Chemistry, 2019, 10 (26), pp.6524-6530. ⟨10.1039/C9SC01454C⟩
Stereogenic main group elements, a promising strategy for metal-free enantioselective catalysis.
Stereogenic main group elements are clearly generating interest in the enantioselective catalysis field. Surprisingly, while chiral organoboron reag
Stereogenic main group elements are clearly generating interest in the enantioselective catalysis field. Surprisingly, while chiral organoboron reag
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9370bc45bfc4f60ae924b27c87078fc0
https://hal.science/hal-02149393
https://hal.science/hal-02149393
Publikováno v:
RSC Advances
RSC Advances, Royal Society of Chemistry, 2019, 9 (25), pp.14078-14092. ⟨10.1039/C9RA01435G⟩
RSC Advances, Royal Society of Chemistry, 2019, 9 (25), pp.14078-14092. ⟨10.1039/C9RA01435G⟩
Despite the vast literature that describes reacting folic acid with a pharmacophore, this route is ineffective in providing the correct regioisomer of the resulting conjugate. We herein present a step-wise route to the preparation of nine folate conj
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7fed8e9f4f4bd23669b85eae1fe7b74b
https://pubmed.ncbi.nlm.nih.gov/35519339
https://pubmed.ncbi.nlm.nih.gov/35519339
Autor:
Alison Thompson, Bry W. Crabbe, Carlotta Figliola, Estelle Marchal, Geniece L. Hallett-Tapley, Huguette Savoie, Ross W. Boyle
Publikováno v:
Photochemical & Photobiological Sciences
Photochemical & Photobiological Sciences, Royal Society of Chemistry, 2018, ⟨10.1039/C8PP00060C⟩
Photochemical & Photobiological Sciences, Royal Society of Chemistry, 2018, ⟨10.1039/C8PP00060C⟩
International audience; The photo-induced cytotoxicity of prodigiosenes is reported. One prodigiosene represents a synthetic analogue of the natural product prodigiosin, and two are conjugated to molecules that target the estrogen receptor (ER). A co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::d95cff5bc8c4a760ad62e350b4c1d1fc
https://hal.archives-ouvertes.fr/hal-01950232/file/PhotochemPhotobiol_before-edit.pdf
https://hal.archives-ouvertes.fr/hal-01950232/file/PhotochemPhotobiol_before-edit.pdf
Autor:
Alison Thompson, Carlotta Figliola, Kate-lyn A. R. Lund, Ann E. Johnsen, Aleksandra K. Kajetanowicz, Michael H. R. Beh, Elise M. Aronitz
Publikováno v:
Canadian Journal of Chemistry
Canadian Journal of Chemistry, NRC Research Press, 2018, ⟨10.1139/cjc-2017-0662⟩
Canadian Journal of Chemistry, NRC Research Press, 2018, ⟨10.1139/cjc-2017-0662⟩
International audience; The synthesis of symmetric α-free meso-H-dipyrrin hydrobromides from 5-H-2-formyl pyrroles was investigated. The self-condensation produces regioisomeric dipyrrins through adoption of two mechanistic pathways. The key differe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::54d33cfd73fe8e6bcc3f3ce65e07b367
https://hal.archives-ouvertes.fr/hal-01950271/document
https://hal.archives-ouvertes.fr/hal-01950271/document
Publikováno v:
Canadian Journal of Chemistry
Canadian Journal of Chemistry, NRC Research Press, 2018, ⟨10.1139/cjc-2017-0402⟩
Canadian Journal of Chemistry, NRC Research Press, 2018, ⟨10.1139/cjc-2017-0402⟩
International audience; Palladium-catalyzed decarboxylative arylation is reported using pyrroles N-protected with the 2-(trimethylsilyl)ethoxymethyl (SEM) group and featuring 2-, 3-, and 4-substituents about the pyrrolic framework. In contrast to N-p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::079da3b09d19365a5e9aeaea88cb6e23
https://hal.archives-ouvertes.fr/hal-01950253/document
https://hal.archives-ouvertes.fr/hal-01950253/document