Zobrazeno 1 - 10
of 173
pro vyhledávání: '"Jean-Christophe Plaquevent"'
Autor:
Romain Galy, Stéphanie Ballereau, Yves Génisson, Lionel Mourey, Jean-Christophe Plaquevent, Laurent Maveyraud
Publikováno v:
Pharmaceuticals, Vol 14, Iss 12, p 1282 (2021)
The mycolic acid biosynthetic pathway represents a promising source of pharmacological targets in the fight against tuberculosis. In Mycobacterium tuberculosis, mycolic acids are subject to specific chemical modifications introduced by a set of eight
Externí odkaz:
https://doaj.org/article/869c4c95e0134e7ba56dcb8fa892eb3e
Publikováno v:
Encyclopedia of Reagents for Organic Synthesis. :1-9
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c0bfa441c7bfe71e314b628c2e046aaa
https://doi.org/10.1002/047084289x.rn01221.pub2
https://doi.org/10.1002/047084289x.rn01221.pub2
Autor:
Hélène Vallette, Laurent Ferron, Gérard Coquerel, Frédéric Guillen, Jean-Christophe Plaquevent
Publikováno v:
ARKIVOC, Vol 2006, Iss 4, Pp 200-211 (2006)
Externí odkaz:
https://doaj.org/article/69486a2be32d4fcfa3f231804c8f8304
Autor:
Jean-Christophe Plaquevent, Viacheslav Zgonnik, Frédéric Guillen, Yves Génisson, Taïcir Ben Ayed, Nicolas Galya, Michel Baltas, Khouloud Jebri, Marie-Rose Mazières
Publikováno v:
French-Ukrainian Journal of Chemistry. 4:3-13
This personal account describes our studies regarding peptide synthesis in ionic liquids (PEPSIL). In addition, we summarize our experiments in which the use of ionic liquids gives simple and promising access to unnatural amino acids in an enantiomer
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2ec119bf38988f1430041327de2c2b96
https://doi.org/10.17721/fujcv4i1p3-13
https://doi.org/10.17721/fujcv4i1p3-13
Autor:
Diana Cheshmedzhieva, Jean Rodriguez, Anouk Gaudel-Siri, Jean-Christophe Plaquevent, Maria del Mar Sanchez Duque, Adrien Quintard, Yves Génisson, Xavier Bugaut, Jean-Valère Naubron, Thierry Constantieux
Publikováno v:
Chemistry-A European Journal
Chemistry-A European Journal, Wiley-VCH Verlag, 2015, 21, pp.778-790. ⟨10.1002/chem.201404481⟩
Chemistry-A European Journal, 2015, 21, pp.778-790. ⟨10.1002/chem.201404481⟩
Chemistry-A European Journal, Wiley-VCH Verlag, 2015, 21, pp.778-790. ⟨10.1002/chem.201404481⟩
Chemistry-A European Journal, 2015, 21, pp.778-790. ⟨10.1002/chem.201404481⟩
International audience; The organocatalytic enantioselective conjugate addition of secondary β-ketoamides to α,β-unsaturated carbonyl compounds is reported. Use of bifunctional Takemoto’s thiourea catalyst allows enantiocontrol of the reaction l
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::6c7d82eaecafc6bd54d70d1fd798b32e
https://doi.org/10.1002/chem.201404481
https://doi.org/10.1002/chem.201404481
Autor:
Anne Rouch, Jean Rodriguez, Nathalie Saffon, Jean-Christophe Plaquevent, Thierry Constantieux, Isabelle Fabing, Tessa Castellan, Yves Génisson
Publikováno v:
RSC Advances
RSC Advances, 2013, 3 (2), pp.413-426. ⟨10.1039/C2RA21637J⟩
RSC Advances, 2013, 3 (2), pp.413-426. ⟨10.1039/C2RA21637J⟩
A convenient and general preparative approach for tartrate-derived organic salts with bulky non-coordinating cations is described. This route is based on neutralisation of tartaric acid with cation hydroxides in aqueous solution. A series of 24 tartr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c1d65c075eb421a185d4c083909b8b37
https://doi.org/10.1039/c2ra21637j
https://doi.org/10.1039/c2ra21637j
Autor:
Jean-Christophe Plaquevent
Publikováno v:
Histoire de la recherche contemporaine. :126-133
Les réactions chimiques sont souvent menées en solvants organiques. Leur remplacement ou leur suppression est un enjeu crucial en raison de leur nocivité (toxicité, inflammabilité, émission de COV). Les liquides ioniques répondent aux critère
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::30623ea7745a4f19f32f931968cb754a
https://doi.org/10.4000/hrc.162
https://doi.org/10.4000/hrc.162
Autor:
Jean Rodriguez, Nicolas Isambert, Yves Génisson, Jean-Christophe Plaquevent, Maria del Mar Sanchez Duque, Thierry Constantieux
Publikováno v:
Chemical Society Reviews
Chemical Society Reviews, 2011, 40, pp.1347-1357. ⟨10.1039/c0cs00013b⟩
Chemical Society Reviews, Royal Society of Chemistry, 2011, 40, pp.1347-1357. ⟨10.1039/c0cs00013b⟩
Chemical Society Reviews, 2011, 40, pp.1347-1357. ⟨10.1039/c0cs00013b⟩
Chemical Society Reviews, Royal Society of Chemistry, 2011, 40, pp.1347-1357. ⟨10.1039/c0cs00013b⟩
International audience; The efficiency of a chemical synthesis can be nowadays measured, not only by parameters like selectivity and overall yield, but also by its raw material, time, human resources and energy requirements, as well as the toxicity a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::03eee4d0d49ac68ecb53d291048763aa
https://doi.org/10.1039/c0cs00013b
https://doi.org/10.1039/c0cs00013b
Autor:
Juliette Martin, Jean-Christophe Plaquevent, Marie-Claire Lasne, Jacques Maddaluno, Jacques Rouden
Publikováno v:
European Journal of Organic Chemistry. 2009:5414-5422
A detailed study of the deracemization of pipecolic acid amides is reported. Enantioselective protonation of the lithium enolates of these amides with use of commercially available ephedrines led to enantiomeric excesses (ee values) higher than 99 %.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::94106db2668e2d3e4fa64d1c35a65165
https://doi.org/10.1002/ejoc.200900726
https://doi.org/10.1002/ejoc.200900726
Publikováno v:
Journal of Fluorine Chemistry. 128:889-895
Herein are studied new transformations of ethyl-4,4,4-trifluoroacetoacetate (ETFAA), giving access to a series of enantiopure chirons bearing both a trifluoromethyl group and an amino moiety. The key intermediate is obtained optically pure by a resol
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fc7baeeeea58738c593ae3b639742dde
https://doi.org/10.1016/j.jfluchem.2007.03.007
https://doi.org/10.1016/j.jfluchem.2007.03.007