Zobrazeno 1 - 10
of 18
pro vyhledávání: '"Christian Feasson"'
Autor:
Mathias Ibert, Patrick Fuertes, Nabyl Merbouh, Christian Feasson, Catherine Fiol-Petit, Francis Marsais
Publikováno v:
Electrochimica Acta. 55:3589-3594
The 2,2,6,6-tetramethyl-1-piperidinyloxy free radical (TEMPO) mediated electrochemical oxidation of d -glucose to d -glucaric acid on a synthetically useful scale is reported. Using TEMPO and a graphite felt anode combined with a stainless steel cath
Autor:
Francois D'Hooge, Jean-Charles Quirion, Stéphane Marcotte, Xavier Pannecoucke, Sathunuru Ramadas, Christian Feasson
Publikováno v:
Tetrahedron Letters. 42:5879-5882
A synthesis of gem-difluoromethylene C-glycopyranosides was efficiently achieved via a Reformatsky reaction on an aldehyde and subsequent intramolecular cyclization involving either the opening of an epoxide or an oxymercuration.
Autor:
Christian Feasson, Xavier Pannecoucke, Stéphane Marcotte, Baudoin Gérard, Jean-Charles Quirion
Publikováno v:
Synthesis. 2001:0929-0933
Publikováno v:
Journal of the Chemical Society, Perkin Transactions 1. :701-705
Variously N,N-disubstituted chiral dibromofluoromethylphosphonamides 3 were easily prepared and used for the asymmetric electrosynthesis, in the presence of tert-butyl acrylate, of α-fluorinated cyclopropylphosphonamides 7. The diastereoisomeric exc
Publikováno v:
Synthesis. 1999:1903-1906
Publikováno v:
The Journal of Organic Chemistry. 64:8461-8464
Chiral oxazolidines 2a−e can be diastereoselectively alkylated with BrCF2CO2Et to furnish 3,3-difluoroazetidin-2-ones 3a−e with up to 99% de. Selective cleavage of the chiral appendage provided the corresponding unsubstituted azetidinones. Format
Publikováno v:
Carbohydrate Research
Carbohydrate Research, Elsevier, 2011, 346 (4), pp.512-518. ⟨10.1016/j.carres.2010.12.017⟩
Carbohydrate Research, Elsevier, 2011, 346 (4), pp.512-518. ⟨10.1016/j.carres.2010.12.017⟩
International audience; During the course of the 2,2,6,6-tetramethyl-1-piperidinyloxy free radical-catalyzed electrochemical oxidation of D-glucose to D-glucaric acid a new side-product was observed. This compound was isolated and identified as a tri
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cbb85d9387c61175836a44ab9f2cd182
https://hal.archives-ouvertes.fr/hal-00992147
https://hal.archives-ouvertes.fr/hal-00992147
Publikováno v:
ChemInform. 30
The diastereoselective electrosynthesis of polysubstituted α-chloro cyclopropylphosphonates is efficiently achieved by electroreduction of diisopropropyl trichloromethylphosphonate in the presence of Michael acceptors, in a one-compartment cell equi
Publikováno v:
ChemInform. 30
Publikováno v:
ChemInform. 31
The synthesis of α-fluorinated cyclopropylphosphonates is efficiently achieved for the first time by electroreduction of diisopropyl dibromofluoromethylphosphonate in the presence of Michael acceptors in a one-compartment cell equipped with a magnes