Zobrazeno 1 - 10
of 107
pro vyhledávání: '"Luc Neuville"'
Autor:
Wei‐Yang Ma, Emeric Montinho‐Inacio, Bogdan I. Iorga, Pascal Retailleau, Xavier Moreau, Luc Neuville, Géraldine Masson
Publikováno v:
Advanced Synthesis & Catalysis. 364:1708-1715
Autor:
Coralie Gelis, Géraldine Masson, Luc Neuville, Damien Bouchet, Wei-Yang Ma, Pascal Retailleau, Xavier Moreau
Publikováno v:
Organic Letters
Organic Letters, American Chemical Society, 2021, 23 (2), pp.442-448. ⟨10.1021/acs.orglett.0c03947⟩
Organic Letters, American Chemical Society, 2021, 23 (2), pp.442-448. ⟨10.1021/acs.orglett.0c03947⟩
International audience; Highly enantio- and regioselective (3 + 2) formal cycloaddition of β-substituted ene- and thioenecarbamates as well as cyclic enamides with quinone diimides catalyzed by a BINOL- and SPINOL-derived phosphoric acid is reported
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:
Mateja Matišić, Géraldine Masson, Thomas Varlet, Luc Neuville, Vincent Gandon, Elsa Van Elslande
Publikováno v:
Journal of the American Chemical Society
Journal of the American Chemical Society, American Chemical Society, 2021, 143 (30), pp.11611-11619. ⟨10.1021/jacs.1c04648⟩
Journal of the American Chemical Society, American Chemical Society, 2021, 143 (30), pp.11611-11619. ⟨10.1021/jacs.1c04648⟩
International audience; A diastereodivergent and enantioselective synthesis of chiral spirocyclohexyl-indolenines with four contiguous stereogenic centers is achieved by a chiral phosphoric acid-catalyzed cycloaddition of 2-susbtituted 3-indolylmetha
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ef575e1ecb2c5ae954f3ff1c83b7bb8c
https://hal.archives-ouvertes.fr/hal-03329179/document
https://hal.archives-ouvertes.fr/hal-03329179/document
Publikováno v:
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2020, 18 (33), pp.6502-6508. ⟨10.1039/D0OB01502D⟩
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2020, 18 (33), pp.6502-6508. ⟨10.1039/D0OB01502D⟩
International audience; The combined Lewis acid catalytic system, generated from molecular iodine and tritylium tetrafluoroborate effectively catalyzed the Friedel−Crafts (FC) arylation of diarylmethyl sulfides providing an efficient access to vari
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0698e3e00870addd98ddd9f930d22904
https://hal.archives-ouvertes.fr/hal-03009611
https://hal.archives-ouvertes.fr/hal-03009611
Autor:
Luc Neuville, Coralie Gelis, Pascal Retailleau, Thomas Varlet, Guillaume Bernadat, Géraldine Masson
Publikováno v:
Angewandte Chemie International Edition
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2020, 59 (22), pp.8491-8496. ⟨10.1002/anie.202000838⟩
Angewandte Chemie International Edition, Wiley-VCH Verlag, 2020, 59 (22), pp.8491-8496. ⟨10.1002/anie.202000838⟩
International audience; An efficient enantioselective construction of tetrahydronaphthalene-1,4-diones as well as dihydronaphthalene-1,4-diols via a chiral phosphoric acid catalyzed quinone Diels-Alder reaction with dienecarbamate was reported. The n
Publikováno v:
Chem
Chem, Cell Press, 2020, 6 (8), pp.1855-1858. ⟨10.1016/j.chempr.2020.07.020⟩
Chem, Cell Press, 2020, 6 (8), pp.1855-1858. ⟨10.1016/j.chempr.2020.07.020⟩
International audience; Achieving high selectivity through multiple C-H functionalization is a challenging topic. In this issue of Chem, Lumb, Luan and co-workers disclose a clever strategy taking advantage of steric remote effects for the synthesis
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::2cf2c99b32cb0cf0debcbda7e2e1fe28
https://hal.archives-ouvertes.fr/hal-03009609/file/Masson-Chem-1.pdf
https://hal.archives-ouvertes.fr/hal-03009609/file/Masson-Chem-1.pdf
Autor:
Luc Neuville, Philippe Dauban, Yanis Lazib, Benjamin Darses, David Leboeuf, Julien Maury, Romain Rodrigues
Publikováno v:
Organic Chemistry Frontiers
Organic Chemistry Frontiers, Royal Society of Chemistry, 2018, 5 (6), pp.948-953. ⟨10.1039/c7qo00878c⟩
Organic Chemistry Frontiers, Royal Society of Chemistry, 2018, 5 (6), pp.948-953. ⟨10.1039/c7qo00878c⟩
International audience; Dirhodium(II)-catalyzed nitrene transfers have been used to prepare a novel synthetic platform bearing the triamino moiety present in pactamycin, jogyamycin and cranomycin. Catalytic intramolecular C(sp3)–H amination and alk
Publikováno v:
Organic Letters. 19:278-281
An efficient enantioselective hypervalent iodine promoted oxylactonization of 4-pentenoic acids has been achieved using stoichiometric or a catalytic amount of chiral aryl-λ3-iodane. This reaction provides straightforward access to a wide range of s
Autor:
Coralie Gelis, Luc Neuville, Guillaume Levitre, Géraldine Masson, Vincent Guérineau, David Touboul
Publikováno v:
European Journal of Organic Chemistry
European Journal of Organic Chemistry, Wiley-VCH Verlag, 2019, 2019 (31-32), pp.5151-5155. ⟨10.1002/ejoc.201900547⟩
European Journal of Organic Chemistry, Wiley-VCH Verlag, 2019, 2019 (31-32), pp.5151-5155. ⟨10.1002/ejoc.201900547⟩
International audience; A new catalytic enantioselective tandem deoxygenation/aza‐Diels‐Alder reaction of nitrones with enecarbamates was serendipitously discovered in the presence of chiral copper(II) diphosphate complexes. This process affords
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::34c30227815c4cae55d3dbb122b8e167
https://hal.archives-ouvertes.fr/hal-02324659
https://hal.archives-ouvertes.fr/hal-02324659