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pro vyhledávání: '"Aurélie Claraz"'
Autor:
Aurélie Claraz
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 20, Iss 1, Pp 1988-2004 (2024)
Hydrazones are important structural motifs in organic synthesis, providing a useful molecular platform for the construction of valuable compounds. Electrooxidative transformations of hydrazones constitute an attractive opportunity to take advantage o
Externí odkaz:
https://doaj.org/article/89c24d0634c74db3b94285ceeabd83de
Autor:
Aurélie Claraz, Géraldine Masson
Publikováno v:
ACS Organic & Inorganic Au, Vol 2, Iss 2, Pp 126-147 (2021)
Externí odkaz:
https://doaj.org/article/51f3e5ad88064c3e8cfe94a8862e1a0b
Publikováno v:
Synlett. 33:177-181
Efficient photocatalytic aerobic oxidative dehydrogenation reactions of N,N-disubstituted hydroxylamines to nitrones were developed with an in situ generated photocatalyst based on commercially available 3,6-dichlorotetrazine. This process affords a
Publikováno v:
Organicbiomolecular chemistry.
Dimeric cyclization reactions show great potential to rapidly form highly substituted complex cyclic molecules from simple starting materials. However, such an appealing process is often hampered by the lack of selectivity. Herein we report two diver
Publikováno v:
Organic Chemistry Frontiers
Organic Chemistry Frontiers, Royal Society of Chemistry, 2021, 8, pp.288. ⟨10.1039/D0QO01307B⟩
Organic Chemistry Frontiers, Royal Society of Chemistry, 2021, 8, pp.288. ⟨10.1039/D0QO01307B⟩
International audience; An electrochemical tandem radical trifluoromethylation of allylamines/formal (3+2)-cycloaddition with nitrile and carbonyl compounds has been developed under mild and environmentally benign reaction conditions. Such multicompo
Publikováno v:
RSC Advances. 11:36663-36669
A new family of chiral chimeric photo-organocatalysts derived from phosphoric acid were synthesized and their spectroscopic and electrochemical properties were investigated. Then, the ability of these photo-activable molecules to catalyse an asymmetr
Autor:
Aurélie Claraz
Publikováno v:
Comprehensive Heterocyclic Chemistry IV
Comprehensive Heterocyclic Chemistry IV, 11, Elsevier, pp.802-858, 2022, ⟨10.1016/B978-0-12-818655-8.00086-X⟩
Comprehensive Heterocyclic Chemistry IV ISBN: 9780128186565
Comprehensive Heterocyclic Chemistry IV, 11, Elsevier, pp.802-858, 2022, ⟨10.1016/B978-0-12-818655-8.00086-X⟩
Comprehensive Heterocyclic Chemistry IV ISBN: 9780128186565
International audience; Bicyclic 5-6 systems with one ring junction nitrogen atom and two extra heteroatoms (nitrogen, sulfur and oxygen) in both cycles are reviewed in this chapter. Literature data from 2007 to 2019 are considered. Among all the pos
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::24a81e763ec4f14c5e3fe71e012e6630
https://hal.archives-ouvertes.fr/hal-03452150/file/CH0000_UN-194_Claraz_revised_HAL.pdf
https://hal.archives-ouvertes.fr/hal-03452150/file/CH0000_UN-194_Claraz_revised_HAL.pdf
Publikováno v:
Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, In press, ⟨10.1002/chem.202103337⟩
Chemistry-A European Journal, Wiley-VCH Verlag, In press, ⟨10.1002/chem.202103337⟩
International audience; An electroreductive access to gem-difluoroalkenes has been developed through the decarboxylative/defluorinative coupling of N-hydroxyphtalimides esters and α-trifluoromethyl alkenes. The electrolysis is performed under very s
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7583c18a53f97e23e4adefe5ca335263
https://hal.archives-ouvertes.fr/hal-03452288/document
https://hal.archives-ouvertes.fr/hal-03452288/document
Publikováno v:
Organic Letters
Organic Letters, American Chemical Society, 2020, 22 (8), pp.3010-3013. ⟨10.1021/acs.orglett.0c00772⟩
Organic Letters, American Chemical Society, 2020, 22 (8), pp.3010-3013. ⟨10.1021/acs.orglett.0c00772⟩
A concise enantio- and stereocontrolled synthesis of (+)-lycoperdic acid is presented. The stereochemical control is based on iminium-catalyzed Mukaiyama–Michael reaction and enamine-catalyzed organocatalytic α-chlorination steps. The amino group
Publikováno v:
Organic letters. 22(4)
An electrochemical intramolecular oxytrifluoromethylation of