Zobrazeno 1 - 4
of 4
pro vyhledávání: '"Mathieu Beaucamp"'
Autor:
Elise Leclercq, Aurélien Moncomble, Céline Debavelaere, Mathieu Beaucamp, Maël Penhoat, Laëtitia Chausset-Boissarie
Publikováno v:
Green Chemistry
Green Chemistry, 2022, 24 (19), pp.7388-7394. ⟨10.1039/D2GC02326A⟩
Green Chemistry, 2022, 24 (19), pp.7388-7394. ⟨10.1039/D2GC02326A⟩
International audience; An environmentally friendly electrochemical process for the direct trifluoromethylation of 2-pyridones with a broad substrate scope has been developed.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::272221d21c13b9b48ccf06c52a0f4430
https://doi.org/10.1039/d2gc02326a
https://doi.org/10.1039/d2gc02326a
Autor:
Katerina Bretosh, Mathieu Beaucamp, Florine Toulotte, Jinyi Yuan, Philippe Hapiot, Maël Penhoat
Publikováno v:
Journal of flow chemistry
Journal of flow chemistry, 2023, ⟨10.1007/s41981-022-00245-x⟩
Journal of flow chemistry, 2023, ⟨10.1007/s41981-022-00245-x⟩
International audience; Water soluble biomimetic models of Riboflavin (B2 vitamin) and Folic acid (B8 vitamin) demonstrated to be good oxidant of formic acid at various pH. Their usage as anolyte mediators in a flow fuel cell to convert formic acid (
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3264e4043b2d92ec735ab2a0ef9afcea
https://hal.science/hal-03969077/document
https://hal.science/hal-03969077/document
Publikováno v:
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2021, 19 (43), pp.9379-9385. ⟨10.1039/D1OB01822A⟩
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry, 2021, 19 (43), pp.9379-9385. ⟨10.1039/D1OB01822A⟩
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2021, 19 (43), pp.9379-9385. ⟨10.1039/D1OB01822A⟩
Organic & Biomolecular Chemistry
Organic & Biomolecular Chemistry, 2021, 19 (43), pp.9379-9385. ⟨10.1039/D1OB01822A⟩
An efficient and versatile protocol for the C–H sulfonylation of imidazoheterocycles via electrochemical activation was established under batch and flow conditions. The selective C–H bond functionalization proceeded under catalyst- and oxidant-fr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c43c063e10e67869996de2538a473652
https://hal.archives-ouvertes.fr/hal-03440235
https://hal.archives-ouvertes.fr/hal-03440235
Publikováno v:
ChemPhotoChem. 3:198-203
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::3fe41dd8f77353526cb9004eab6ceb84
https://doi.org/10.1002/cptc.201800236
https://doi.org/10.1002/cptc.201800236