Zobrazeno 1 - 10
of 49
pro vyhledávání: '"Jean-Louis Canet"'
Autor:
Pierre Adumeau, Arnaud Gautier, Jean-Louis Canet, Rachid Mahiou, Claude Beaudoin, Damien Boyer, Cédric Hesling, Claire Gaillard, Laurent Morel
Publikováno v:
Journal of materials chemistry. B. 1(34)
The facile synthesis of functionalized luminescent nanoparticles from LnL3 lanthanide complexes is described. The luminescence properties of the lanthanide chelates and of the corresponding nanohybrids are reported and compared. For a further applica
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9cb742868c7e44775ffa7bd51f28d42d
https://pubmed.ncbi.nlm.nih.gov/32261027
https://pubmed.ncbi.nlm.nih.gov/32261027
Autor:
Jean-Louis Canet, Damien Boyer, Pierre Adumeau, Arnaud Gautier, Rachid Mahiou, Claire Gaillard
Publikováno v:
European Journal of Inorganic Chemistry. 2015:1233-1242
Several complexes and silica-based nanohybrids of rare-earth ions (Eu3+, Gd3+) have been synthesized from dimethyl 4-azidopyridine-2,6-dicarboxylate (4) following the Click chemistry approach. A complete spectroscopic study indicates that such compou
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ee3f68309d9349c71712a42001566520
https://doi.org/10.1002/ejic.201402617
https://doi.org/10.1002/ejic.201402617
Publikováno v:
Journal of Fluorine Chemistry. 145:8-17
The asymmetric synthesis of trifluoromethyl-piperidine-based γ-aminoacids and of indolizidines bearing a trifluoromethyl group is reported. These rarely described compounds are prepared in a highly enantio-enriched form employing as key step an intr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::98676ddfe4ec54181f8ef516a2efbd63
https://doi.org/10.1016/j.jfluchem.2012.11.006
https://doi.org/10.1016/j.jfluchem.2012.11.006
Autor:
Arnaud Gautier, Federico Cisnetti, Aurélien Chevry, Marie-Laure Teyssot, Jean-Louis Canet, Lionel Nauton
Publikováno v:
European Journal of Organic Chemistry. 2010:3507-03515
Copper(I)-catalysed azide-alkyne cycloaddition (CuAAC) has been successfully conducted under reductant-free conditions. The catalytic system consisted of a combination of a copper(I)-N-heterocyclic carbene complex and aromatic N-donors. The catalyst
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::2aeb66dedb507d9641a94c28b3506acb
https://doi.org/10.1002/ejoc.201000046
https://doi.org/10.1002/ejoc.201000046
Autor:
Gilles Figueredo, Annabelle Bariau, Yves Troin, Cécile Esparcieux, Wahid Bux Jatoi, Jean-Louis Canet
Publikováno v:
Synlett. 2008:1305-1308
The first asymmetric synthesis of (trifluoromethyl)pipecolic acids is reported. The synthetic strategy involves as key step an intramolecular Mannich reaction of a homochiral α-Tfm-β-amino ketal, prepared with a high stereoselectively in four steps
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::eee24b563ecbbac109f2e4edd119a36b
https://doi.org/10.1055/s-2008-1072768
https://doi.org/10.1055/s-2008-1072768
Publikováno v:
European Journal of Organic Chemistry. 2006:3421-3433
The highly diastereoselective synthesis of five trifluoro-substituted analogues of mono-, di-, and trisubstituted piperidine alkaloids was accomplished in two to four steps from 2-trifluoromethyl keto-protected 4-piperidones, prepared by an intramole
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::23bd2751f1f802e515b8c72a9dc926ce
https://doi.org/10.1002/ejoc.200600157
https://doi.org/10.1002/ejoc.200600157
Publikováno v:
Tetrahedron Letters. 45:9003-9006
A new and highly stereoselective access to 4,10b-trans or 4,10b-cis hexahydropyrido[2,1-a]isoindole derivatives is reported, both requiring an intramolecular Mannich-type reaction as key step. The cis diastereoisomer is obtained in three steps from a
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::47c2fbc840c5be80a85f1b8785b3d85f
https://doi.org/10.1016/j.tetlet.2004.10.045
https://doi.org/10.1016/j.tetlet.2004.10.045
Publikováno v:
Tetrahedron: Asymmetry. 15:1561-1567
A highly diastereoselective 1,4-addition involving Davies' lithium amide is employed as the key reaction to prepare, in five steps from ethyl acetoacetate, an enantiomerically pure keto protected β,β ′ -ketoaminoester. This latter was reacted wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::91c96d61d4487601c46005ae98883b52
https://doi.org/10.1016/j.tetasy.2004.04.008
https://doi.org/10.1016/j.tetasy.2004.04.008
Publikováno v:
Tetrahedron Letters. 41:9797-9802
An intramolecular Mannich reaction, involving various achiral aldehydes together with an α-chiral amine is employed as the key step for a stereocontrolled synthesis of highly substituted piperidine systems. Accordingly, 12 new piperidines bearing fo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fac57490d4c345252c153ad5da1cd206
https://doi.org/10.1016/s0040-4039(00)01730-5
https://doi.org/10.1016/s0040-4039(00)01730-5
Publikováno v:
Tetrahedron: Asymmetry. 11:2211-2219
An improved enantioselective synthesis (five steps, 37–44% yield versus seven to 10 steps, 13.5 and 12% yield, respectively) of both enantiomers of keto-protected 4-amino-2-pentanone has been realized, the key step being the microbiological reducti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9a955d2f20d02dab2d08f28f5bf6cd15
https://doi.org/10.1016/s0957-4166(00)00167-1
https://doi.org/10.1016/s0957-4166(00)00167-1