Zobrazeno 1 - 10
of 20
pro vyhledávání: '"Guillaume Levitre"'
Autor:
Júlia Viñas-Lóbez, Guillaume Levitre, Adiran de Aguirre, Céline Besnard, Amalia I. Poblador-Bahamonde, Jérôme Lacour
Publikováno v:
ACS Organic & Inorganic Au, Vol 1, Iss 1, Pp 11-17 (2021)
Externí odkaz:
https://doaj.org/article/36203cc0b9c0441db3686ce24c4173dc
Publikováno v:
Accounts of Chemical Research. 56:385-401
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::108232a80a72cb95b847ca4883ede487
https://doi.org/10.1021/acs.accounts.2c00778
https://doi.org/10.1021/acs.accounts.2c00778
Publikováno v:
Green Chemistry. 25:560-565
An operationally simple method providing access to valuable chlorinated organic backbones is reported. The transformation transpires via a sustainable photoinduced halodecarboxylative halogen-atom transfer protocol.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f5cc6e39599668d141fde2f1852c5e89
https://doi.org/10.1039/d2gc04578h
https://doi.org/10.1039/d2gc04578h
Autor:
Longbo Li, Bianca Matsuo, Guillaume Levitre, Edward J. McClain, Eric A. Voight, Erika A. Crane, Gary A. Molander
Publikováno v:
Chemical Science. 14:2713-2720
Diverse DNA-encoded libraries of complex and novel sp3-rich spirocycles were achieved using a versatile and operationally simple visible light-mediated intermolecular [2 + 2] cycloaddition.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ca9f354518d32b785d8ddc6a587a4d4b
https://doi.org/10.1039/d3sc00144j
https://doi.org/10.1039/d3sc00144j
Autor:
Expédite Yen-Pon, Longbo Li, Guillaume Levitre, Jadab Majhi, Edward J. McClain, Eric A. Voight, Erika A. Crane, Gary A. Molander
Publikováno v:
Journal of the American Chemical Society. 144:12184-12191
DNA-encoded libraries have proven their tremendous value in the identification of new lead compounds for drug discovery. To access libraries in new chemical space, many methods have emerged to transpose traditional mol-scale reactivity to nmol-scale,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7bb4dda02c8cc1d32a7f8a6798a63669
https://doi.org/10.1021/jacs.2c03025
https://doi.org/10.1021/jacs.2c03025
Publikováno v:
Organic Letters.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::f66d8aa93513446fac6ae98389839c9e
https://doi.org/10.1021/acs.orglett.3c01223
https://doi.org/10.1021/acs.orglett.3c01223
Publikováno v:
Organic Letters. 24:3194-3198
The development of mild and practical conditions for the fluoroalkylation of arenes is an ongoing challenge in chemical organic synthesis. Herein, we report a metallaphotoredox method for the preparation of fluoroalkyl arenes based on the synergistic
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::409dfc924b8284de84a3bc86d995fa1f
https://doi.org/10.1021/acs.orglett.2c00969
https://doi.org/10.1021/acs.orglett.2c00969
Autor:
Céline Besnard, Jérôme Lacour, Adiran de Aguirre, Guillaume Levitre, Amalia I. Poblador-Bahamonde, Júlia Viñas-Lóbez
Publikováno v:
ACS Organic & Inorganic Au, Vol 1, Iss 1, Pp 11-17 (2021)
ACS Organic & Inorganic Au, Vol. 1, No 1 (2021) pp. 11-17
ACS Organic & Inorganic Au, Vol. 1, No 1 (2021) pp. 11-17
Malonate enol ethers are afforded in one step by condensation of cyclic ketones with α-diazomalonates under [CpRu(CH3CN)3][BArF] catalysis. The dual reactivity of these 2-vinyloxymalonates can be used to expand the classical range of cyclizations de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f5df5218f3f0a3e05795a8a8bea3086d
https://doi.org/10.1021/acsorginorgau.1c00006
https://doi.org/10.1021/acsorginorgau.1c00006
Autor:
Elsa Anselmi, Guillaume Levitre, Géraldine Masson, Béatrice Tuccio, Guillaume Dagousset, Emmanuel Magnier
Publikováno v:
Organic Letters
Organic Letters, American Chemical Society, 2019, 21 (15), pp.6005-6010. ⟨10.1021/acs.orglett.9b02152⟩
Organic Letters, 2019, 21 (15), pp.6005-6010. ⟨10.1021/acs.orglett.9b02152⟩
Organic Letters, American Chemical Society, 2019, 21 (15), pp.6005-6010. ⟨10.1021/acs.orglett.9b02152⟩
Organic Letters, 2019, 21 (15), pp.6005-6010. ⟨10.1021/acs.orglett.9b02152⟩
We report herein an efficient four-component photoredox-catalyzed reaction. Under the optimized conditions using [Ru(bpy)3(PF6)2] as the photocatalyst, a wide range of terminal and internal alkenes...
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2f409d77c5f19b9fc908dc86222109e4
https://doi.org/10.1021/acs.orglett.9b02152
https://doi.org/10.1021/acs.orglett.9b02152
Autor:
Pascal Retailleau, Géraldine Masson, Guillaume Levitre, Armen Panossian, Frédéric R. Leroux, Audrey Dumoulin
Publikováno v:
Journal of Organic Chemistry
Journal of Organic Chemistry, American Chemical Society, 2017, 82 (22), pp.11877-11883. ⟨10.1021/acs.joc.7b01597⟩
Journal of Organic Chemistry, American Chemical Society, 2017, 82 (22), pp.11877-11883. ⟨10.1021/acs.joc.7b01597⟩
An enantioselective direct oxygenation of propiophenone derivatives mediated by a catalytic or stoichiometric amount of new chiral non-C2-symmetric iodoarenes(III) is reported. The reaction gives an easy entry to optically active α-sulfonyl- and α-
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cd6044f9910cdd9b0e1af91157fd2e12
https://doi.org/10.1021/acs.joc.7b01597
https://doi.org/10.1021/acs.joc.7b01597