Zobrazeno 1 - 10
of 15
pro vyhledávání: '"Delphine Blanc"'
Autor:
Delphine Blanc
Publikováno v:
Tr@jectoires, Vol 13 (2020)
Externí odkaz:
https://doaj.org/article/4894f8f6184947c98c3c6dc2fea71b1d
Autor:
Delphine Blanc, Jean Raynaud, Matthieu Humbert, Vincent Monteil, Delphine Crozet, Magali Puillet, David Gajan, James Delorme, Bousquie Magali
Publikováno v:
Catalysis Science & Technology
Catalysis Science & Technology, Royal Society of Chemistry, 2021, 11 (14), pp.4849-4856. ⟨10.1039/D1CY00834J⟩
Catalysis Science & Technology, 2021, 11 (14), pp.4849-4856. ⟨10.1039/D1CY00834J⟩
Catalysis Science & Technology, Royal Society of Chemistry, 2021, 11 (14), pp.4849-4856. ⟨10.1039/D1CY00834J⟩
Catalysis Science & Technology, 2021, 11 (14), pp.4849-4856. ⟨10.1039/D1CY00834J⟩
International audience; Commercially available Ni(II) and Co(II) complexes – M(acac)2 (acac = acetylacetonate) and M(tmhd)2 (tmhd = 2,2,6,6-tetramethyl-3,5-heptanedionato) – exhibit catalytic activity for alkene/vinylsilane dehydrogenative silyla
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::fc83c11c19439cc1485160b1f96d6257
https://doi.org/10.1039/d1cy00834j
https://doi.org/10.1039/d1cy00834j
Publikováno v:
Macromolecular Materials and Engineering. 299:336-343
Le principe d’elaboration des mousses de silicone est base sur une competition entre deux reactions mettant en jeu les fonctions hydrogenosilane portees par le polymere precurseur : la premiere provoque le degagement d’un gaz (a l’origine de la
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::dc8fa65d9379b92eed8f5fa700047f09
https://doi.org/10.1002/mame.201300142
https://doi.org/10.1002/mame.201300142
Autor:
Virginie Ratovelomanana-Vidal, Jean-Pierre Genêt, Delphine Blanc, Angela Marinetti, Sébastien Jus
Publikováno v:
Chemistry - A European Journal. 5:1160-1165
Novel,C2-symmetric 1,2-bis(phosphetano)benzene ligands (see figure) are readily synthesized from the corresponding diol cyclic sulfates. When complexed to ruthenium, they form powerful catalysts for highly selective hydrogenation of β-diketones.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::79fa9456ef72323a597778df23b06d42
https://doi.org/10.1002/(sici)1521-3765(19990401)5:4<1160::aid-chem1160>3.0.co
https://doi.org/10.1002/(sici)1521-3765(19990401)5:4<1160::aid-chem1160>3.0.co
Publikováno v:
Tetrahedron Letters. 38:6603-6606
Asymmetric hydrogenation of prochiral keto groups with (S,S) and (R,R)- SkewphosRuBr2 prepared in situ is described. Good enantiomeric excesses up to 95% were obtained.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::cf5025f32f9928bb9fc4f4a3660248a8
https://doi.org/10.1016/s0040-4039(97)01522-0
https://doi.org/10.1016/s0040-4039(97)01522-0
Publikováno v:
ChemInform. 28
Asymmetric hydrogenation of prochiral keto groups with (S,S) and (R,R)- SkewphosRuBr2 prepared in situ is described. Good enantiomeric excesses up to 95% were obtained.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::30c6353a244405b93ceb06343b06cf75
https://doi.org/10.1002/chin.199751052
https://doi.org/10.1002/chin.199751052
Publikováno v:
ChemInform. 30
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::ec8cb038adc666c09ab47fe5c3597e77
https://doi.org/10.1002/chin.199931039
https://doi.org/10.1002/chin.199931039
Publikováno v:
Synlett. 1999:480-482
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6317d696ae36be0eea0206ec8ed22d5e
https://doi.org/10.1055/s-1999-2631
https://doi.org/10.1055/s-1999-2631
Autor:
Phannarath Phansavath, Florence Popowyck, Jean-Pierre Genêt, Virginie Ratovelomanana-Vidal, Delphine Blanc, Tahar Ayad, Jonathan Madec
Publikováno v:
Advanced Synthesis and Catalysis
Advanced Synthesis and Catalysis, Wiley-VCH Verlag, 2007, pp.943-950. ⟨10.1002/adsc.200600504⟩
Advanced Synthesis and Catalysis, Wiley-VCH Verlag, 2007, pp.943-950. ⟨10.1002/adsc.200600504⟩
Enantioselective syntheses of several paraconic acids have been achieved using catalyzed asymmetric hydrogenation of β-keto esters with SYNPHOS® as a ligand. This strategy allowed the short synthesis of biologically active (-)-methylenolactocin 1,
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::00cac14708eec4e76184a7baef891b21
https://hal.archives-ouvertes.fr/hal-00160294
https://hal.archives-ouvertes.fr/hal-00160294
