Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Laëtitia Chausset-Boissarie"'
Autor:
Nassim El Achi, Youssef Bakkour, Wissal Adhami, Julien Molina, Maël Penhoat, Nathalie Azaroual, Laëtitia Chausset-Boissarie, Christian Rolando
Publikováno v:
Frontiers in Chemistry, Vol 8 (2020)
ATRP of methyl methacrylate catalyzed by Eosin Y, an inexpensive and an environmental benign dye, was performed in a continuous flow reactor made of FEP tubing and irradiated by visible light green LEDs. The reaction under flow conditions was signifi
Externí odkaz:
https://doaj.org/article/0161751d938043468558d17fa835b83d
Publikováno v:
Molecules, Vol 25, Iss 23, p 5532 (2020)
Monofluoroalkenes are versatile fluorinated synthons in organic synthesis, medicinal chemistry and materials science. In light of the importance of alkyl-substituted monofluoroalkenes efficient synthesis of these moieties still represents a synthetic
Externí odkaz:
https://doaj.org/article/999e291aae6c48f5be8108a11d6f40c6
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.
Autor:
Mélanie Roseau, Laëtitia Chausset-Boissarie, Sylvain Gremetz, Philippe M. C. Roth, Maël Penhoat
Publikováno v:
Photochemical & Photobiological Sciences
Photochemical & Photobiological Sciences, 2022, 21 (3), pp.421-432. ⟨10.1007/s43630-022-00171-w⟩
Photochemical & Photobiological Sciences, 2022, 21 (3), pp.421-432. ⟨10.1007/s43630-022-00171-w⟩
International audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24ed9cb04a8bea439e72a85bb3d2d63d
https://hal.science/hal-03861787
https://hal.science/hal-03861787
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
Autor:
Mélanie, Roseau, Laëtitia, Chausset-Boissarie, Sylvain, Gremetz, Philippe M C, Roth, Maël, Penhoat
Publikováno v:
Photochemicalphotobiological sciences : Official journal of the European Photochemistry Association and the European Society for Photobiology. 21(3)
The characterization of commercially available Corning
Autor:
Xavier Trivelli, François Xavier Cantrelle, Laëtitia Chausset-Boissarie, Maël Penhoat, Mélanie Roseau, Vincent De Waele
Publikováno v:
Helvetica Chimica Acta
Helvetica Chimica Acta, Wiley, 2021, 104 (7), pp.e2100071. ⟨10.1002/hlca.202100071⟩
Helvetica Chimica Acta, 2021, 104 (7), pp.e2100071. ⟨10.1002/hlca.202100071⟩
Helvetica Chimica Acta, Wiley, 2021, 104 (7), pp.e2100071. ⟨10.1002/hlca.202100071⟩
Helvetica Chimica Acta, 2021, 104 (7), pp.e2100071. ⟨10.1002/hlca.202100071⟩
International audience; (E)-Azobenzene is introduced as a suitable chemical actinometer in the visible spectral range (440–540 nm) for photon flux determination of fluidic microphotoreactors or for assessing efficiency of visible light photo-induce
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::21d26c1f86b41f8ff127f2982498ef1c
https://hal.archives-ouvertes.fr/hal-03440224
https://hal.archives-ouvertes.fr/hal-03440224
Publikováno v:
Molecules, Vol 25, Iss 5532, p 5532 (2020)
Molecules
Molecules, MDPI, 2020, 25 (23), pp.5532. ⟨10.3390/molecules25235532⟩
Molecules, 2020, 25 (23), pp.5532. ⟨10.3390/molecules25235532⟩
Molecules
Molecules, MDPI, 2020, 25 (23), pp.5532. ⟨10.3390/molecules25235532⟩
Molecules, 2020, 25 (23), pp.5532. ⟨10.3390/molecules25235532⟩
International audience; Monofluoroalkenes are versatile fluorinated synthons in organic synthesis, medicinal chemistry and materials science. In light of the importance of alkyl-substituted monofluoroalkenes efficient synthesis of these moieties stil
Autor:
Maël Penhoat, Nathalie Azaroual, Youssef Bakkour, Christian Rolando, Wissal Adhami, Nassim El Achi, Julien Molina, Laëtitia Chausset-Boissarie
Publikováno v:
Frontiers in Chemistry
Frontiers in Chemistry, Frontiers Media, 2020, 8, ⟨10.3389/fchem.2020.00740⟩
Frontiers in Chemistry, 2020, 8, ⟨10.3389/fchem.2020.00740⟩
Frontiers in Chemistry, Vol 8 (2020)
Frontiers in Chemistry, Frontiers Media, 2020, 8, ⟨10.3389/fchem.2020.00740⟩
Frontiers in Chemistry, 2020, 8, ⟨10.3389/fchem.2020.00740⟩
Frontiers in Chemistry, Vol 8 (2020)
ATRP of methyl methacrylate catalyzed by Eosin Y, an inexpensive and an environmental benign dye, was performed in a continuous flow reactor made of FEP tubing and irradiated by visible light green LEDs. The reaction under flow conditions was signifi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::befdf8c58064d6b6bc06964c49ae2ed7
https://hal.archives-ouvertes.fr/hal-03060626/document
https://hal.archives-ouvertes.fr/hal-03060626/document
Autor:
Clothilde Le Guen, Patricia Melnyk, Christian Rolando, Laëtitia Chausset-Boissarie, Ahmed Mazzah, Maël Penhoat
Publikováno v:
Synthesis: Journal of Synthetic Organic Chemistry
Synthesis: Journal of Synthetic Organic Chemistry, 2020, 53 (6), pp.1157-1162. ⟨10.1055/s-0040-1706482⟩
SYNTHESIS
SYNTHESIS, Georg Thieme Verlag, 2020, 53 (6), pp.1157-1162. ⟨10.1055/s-0040-1706482⟩
Synthesis: Journal of Synthetic Organic Chemistry, 2020, 53 (6), pp.1157-1162. ⟨10.1055/s-0040-1706482⟩
SYNTHESIS
SYNTHESIS, Georg Thieme Verlag, 2020, 53 (6), pp.1157-1162. ⟨10.1055/s-0040-1706482⟩
Herein, a regioselective and direct monofluorination strategy of pyridylic and quinolinic C(sp3)–H bonds was developed under transition-metal-free conditions with Selectfluor. The reaction was performed under smooth conditions and afforded fluorina
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::35c214efd27d814864ff0ae188c2754b
https://hal.science/hal-03061701
https://hal.science/hal-03061701