Zobrazeno 1 - 9
of 9
pro vyhledávání: '"Camille, Remeur"'
Publikováno v:
European Journal of Organic Chemistry. 2018:5869-5877
Publikováno v:
ACS Catalysis. 7:6065-6069
A protocol for the aminomethylation of aryl halides using α-silylamines via Ni/photoredox dual catalysis is described. The low oxidation potential of these silylated species enables facile single electron transfer (SET) oxidation of the amine follow
Autor:
Marc Litaudon, Léa Gauthier, Erell Le Borgne, Brigitte Deguin, Raphaël Grougnet, Camille Remeur, Cyril Poullain
Publikováno v:
Phytochemical Analysis. 28:242-246
Introduction Iridoid glycosides possess highly functionalised monoterpenoid aglycon with several contiguous stereocentres. For the most common, they are often present in quantities reaching several percentage of the fresh plant weight, and thus they
Publikováno v:
Organic and Biomolecular Chemistry
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2015, 13 (19), pp.5520-5531. ⟨10.1039/c5ob00354g⟩
Organic and Biomolecular Chemistry, Royal Society of Chemistry, 2015, 13 (19), pp.5520-5531. ⟨10.1039/c5ob00354g⟩
The synthesis, on a large scale, with very good yield and er via an efficient strategy, of a chiral 4-substituted 2-cyclohexenone intermediate, was a milestone in the synthesis of seven analogues of meiogynin A, a natural sesquiterpenoid dimer. These
Autor:
Camille, Remeur, Erell, Le Borgne, Léa, Gauthier, Raphaël, Grougnet, Brigitte, Deguin, Cyril, Poullain, Marc, Litaudon
Publikováno v:
Phytochemical analysis : PCA. 28(3)
Iridoid glycosides possess highly functionalised monoterpenoid aglycon with several contiguous stereocentres. For the most common, they are often present in quantities reaching several percentage of the fresh plant weight, and thus they may be regard
Autor:
Khalijah Awang, Fanny Roussi, Mohamad Nurul Azmi, Marc Litaudon, Gomathi Chan, Camille Remeur, Tiphaine Péresse
Publikováno v:
Fitoterapia. 109
A phytochemical study of the EtOAc-soluble part of the methanolic extract of the bark of Endiandra kingiana led to the isolation of three new pentacyclic kingianins as racemic mixtures, kingianins O-Q (1-3), together with the known kingianins A, F, K
Publikováno v:
ChemInform. 46
The reaction is performed starting from alkanoates, alkenoates, and benzoates with the corresponding methyl carboxylates providing the highest product yields.
Publikováno v:
SYNLETT
SYNLETT, Georg Thieme Verlag, 2015, 26 (03), pp.385-387. ⟨10.1055/s-0034-1378927⟩
SYNLETT, Georg Thieme Verlag, 2015, 26 (03), pp.385-387. ⟨10.1055/s-0034-1378927⟩
Aliphatic and aromatic esters are efficiently transformed into amides in good to excellent yields, under mild conditions using methylaluminoxane (MAO). This reaction can be performed either at room temperature or by applying microwave irradiation.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c76a7ca4bfaed0cc88d909fc14af2e4
https://hal.archives-ouvertes.fr/hal-01142881
https://hal.archives-ouvertes.fr/hal-01142881
Autor:
Charlotte Gény, Camille Remeur, Fanny Roussi, Nicolas Birlirakis, Bogdan I. Iorga, Vincent Dumontet, Gwladys Rivière, Sandy Desrat, Claire Colas
Publikováno v:
Chemical Communications
Chemical Communications, Royal Society of Chemistry, 2014, 50 (62), pp.8593-8596. ⟨10.1039/c4cc01830c⟩
Chemical Communications, 2014, 50 (62), pp.8593-8596. ⟨10.1039/c4cc01830c⟩
Chemical Communications, Royal Society of Chemistry, 2014, 50 (62), pp.8593-8596. ⟨10.1039/c4cc01830c⟩
Chemical Communications, 2014, 50 (62), pp.8593-8596. ⟨10.1039/c4cc01830c⟩
International audience; The synthesis of one of the most potent dual inhibitors of the anti-apoptotic proteins Bcl-xL and Mcl-1 is reported. This analogue of a natural sesquiterpenoid dimer meiogynin A was elaborated by a convergent asymmetric synthe