Zobrazeno 1 - 10
of 126
pro vyhledávání: '"Françoise Hénin"'
Publikováno v:
ARKIVOC, Vol 2015, Iss 2, Pp 34-39 (2014)
Externí odkaz:
https://doaj.org/article/7ac57a40793b47649d8623309fde4a12
Publikováno v:
ARKIVOC, Vol 2015, Iss 2, Pp 34-39 (2014)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c3f5cea4ca1077e75b470149110bc821
https://doi.org/10.3998/ark.5550190.p008.805
https://doi.org/10.3998/ark.5550190.p008.805
Autor:
Benjamin Ganchegui, Jacques Muzart, Carole Chevrin, Jean Le Bras, Sandrine Bouquillon, Françoise Hénin
Publikováno v:
Phosphorus, Sulfur, and Silicon and the Related Elements
Phosphorus, Sulfur, and Silicon and the Related Elements, Taylor & Francis, 2007, 181 (11), pp.2635-2639. ⟨10.1080/10426500600781367⟩
Phosphorus, Sulfur, and Silicon and the Related Elements, Taylor & Francis, 2007, 181 (11), pp.2635-2639. ⟨10.1080/10426500600781367⟩
International audience; The synthesis of 2-(2-diphenylphosphinophenyl)-oxazolines from o-fluoroben-zonitrile and (-)-norephedrine or (+)-endo-2-hydroxy-endo-3-aminobornane is described. The Pa-catalyzed alkylation of (E)-1,3-diphenylallyl acetate wit
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::bc70135554fb9a37be2e8804886b7ea8
https://doi.org/10.1080/10426500600781367
https://doi.org/10.1080/10426500600781367
Autor:
Alla Bessmertnykh, Sandrine Bouquillon, Céline Damez, Boris Estrine, Françoise Hénin, Jacques Muzart
Publikováno v:
Journal of Molecular Catalysis A: Chemical
Journal of Molecular Catalysis A: Chemical, Elsevier, 2006, 244 (1-2), pp.93-98. ⟨10.1016/j.molcata.2005.08.041⟩
Journal of Molecular Catalysis A: Chemical, Elsevier, 2006, 244 (1-2), pp.93-98. ⟨10.1016/j.molcata.2005.08.041⟩
International audience; The efficiency and the selectivity of the palladium-catalyzed telomerization of butadiene with d-xylose in DMF were strongly dependent on the presence of triethylamine as additive for low sugar concentrations. The amine influe
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ffb4181d6af7d4582a16b4b381f58a7c
https://doi.org/10.1016/j.molcata.2005.08.041
https://doi.org/10.1016/j.molcata.2005.08.041
Publikováno v:
Journal of Molecular Catalysis A: Chemical
Journal of Molecular Catalysis A: Chemical, Elsevier, 2005, 238 (1-2), pp.199-206. ⟨10.1016/j.molcata.2005.05.020⟩
Journal of Molecular Catalysis A: Chemical, Elsevier, 2005, 238 (1-2), pp.199-206. ⟨10.1016/j.molcata.2005.05.020⟩
Palladium-catalysed telomerization of butadiene with aldoses in an organic medium can be directed towards the formation of mono- or di-octadienyl ethers. The relative reactant ratios and the amounts of dissolved gaseous butadiene have been defined as
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5c8e481b1f853732182988f989530dce
https://doi.org/10.1016/j.molcata.2005.05.020
https://doi.org/10.1016/j.molcata.2005.05.020
Publikováno v:
Synthesis. 2005:2615-2618
Catalytic amounts of the hydrophilic ligand [(HOCH 2 CH 2 NHCOCH 2 ) 2 NCH 2 ] 2 and palladium(II) salts, in the presence of hydrogen peroxide, water and alcohol, allow the direct transformation of 2-allylphenols into 2-(l,2-dihydroxypropyl)phenol de
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fda29a7606b528ebffd516ab24411558
https://doi.org/10.1055/s-2005-872175
https://doi.org/10.1055/s-2005-872175
Publikováno v:
Tetrahedron. 61:8405-8409
The glycosidation of 2,3,4-triacetyl-1-bromo-α- d -xylopyranose with various terpenols occurs at 50 °C in DMF without the requirement of any additive. The decisive role of DMF as solvent on the coupling efficiency is highlighted.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::331b33bef4722a6d32510f3c9bc11c8a
https://doi.org/10.1016/j.tet.2005.06.075
https://doi.org/10.1016/j.tet.2005.06.075
Publikováno v:
The Journal of Organic Chemistry. 69:6528-6532
The monitoring by UV spectroscopy of the Pd-catalyzed hydrogenolysis in acetonitrile of 2-methyl-2-benzyloxycarbonyl-1-indanone and 2-methyl-2-benzyloxycarbonyl-1-tetralone showed the successive formation of corresponding beta-ketoacids and enols to
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::636fee378762a1e6e3ac31dfde75e6f5
https://doi.org/10.1021/jo049464w
https://doi.org/10.1021/jo049464w
Autor:
Anna Pla-Quintana and, Anna Roglans, Jacques Muzart, Roser Pleixats, Jean Le Bras, and Françoise Hénin, Carole Chevrin
Publikováno v:
Organometallics. 23:4796-4799
Allylic substitution of PhCH(OAc)CHCHPh by CH2(COMe)2 in a basic MeOH/H2O mixture could be achieved in the absence of a palladium catalyst and lead to a mixture of PhCH(CH(COMe)2)CHCHPh and PhCH(OMe)CHCHPh in 40% and 55% yields, respectively. The pro
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::a0d21de0691b866878ad25298610f2c5
https://doi.org/10.1021/om0495877
https://doi.org/10.1021/om0495877
Autor:
Sara Gonzalez, Roser Pleixats, Françoise Hénin, Benjamin Ganchegui, Marcial Moreno-Mañas, Jacques Muzart, Jean Le Bras, Mar Tristany, Deb Kumar Mukherjee
Publikováno v:
New J. Chem.. 28:1550-1553
Carbon-carbon double bonds have been selectively hydrogenated at room temperature in the presence of benzyloxy groups using an atmospheric pressure of hydrogen, toluene or [bmim]PF6 as the solvent and palladium nanoparticles stabilized with tetrabuty
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7a90f4b08e385c28befbf560888513a5
https://doi.org/10.1039/b409604e
https://doi.org/10.1039/b409604e