Zobrazeno 1 - 10
of 14
pro vyhledávání: '"Sandrine Langle"'
Publikováno v:
Nuclear Medicine and Biology. :S167-S168
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::7f3ecbe2e5e3182ef10a7b04e56cb267
https://doi.org/10.1016/s0969-8051(22)00353-5
https://doi.org/10.1016/s0969-8051(22)00353-5
Autor:
Kamal Jouad, Julen Ariztia, Cédric Boura, Valérie Jouan-Hureaux, Charlotte Collet, Bertrand Kuhnast, Sandrine LANGLE, Nadia Pellegrini Moïse
Publikováno v:
Nuclear Medicine and Biology. :S42
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::0c14119aa52f6f0c87d72b7ee3082611
https://doi.org/10.1016/s0969-8051(22)00122-6
https://doi.org/10.1016/s0969-8051(22)00122-6
Autor:
Emilien Mengel, Floriane Mangin, Charlotte Collet, Valérie Jouan-Hureaux, Fatiha Maskali, Emilie Roeder, Julien Pierson, Katalin Selmeczi, Cédric Boura, Nadia Pellegrini Moïse, Sandrine Langle
Publikováno v:
Nuclear Medicine and Biology. :S203
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::fb20791f3b6cd0ffac9b8c755cadfb5b
https://doi.org/10.1016/s0969-8051(22)00418-8
https://doi.org/10.1016/s0969-8051(22)00418-8
Publikováno v:
Tetrahedron Letters. 44:9255-9258
Using a double Suzuki cross-coupling reaction ortho - or para -bromobenzyl bromides are easily transformed into unsymmetrical diaryl (or heteroaryl) methanes
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1c48c21777aa51639388ceb3537e2039
https://doi.org/10.1016/j.tetlet.2003.10.080
https://doi.org/10.1016/j.tetlet.2003.10.080
Publikováno v:
Journal of Organometallic Chemistry. 671:113-119
A simple and efficient procedure has been developed for the synthesis of organogermanium compounds and styrenes para-substituted with groups containing an atom of the 14th group by one-pot reaction of halogenosilanes, germanes or stannanes, organic h
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::031b36484ca67e7f7c0b89868de14b27
https://doi.org/10.1016/s0022-328x(03)00053-6
https://doi.org/10.1016/s0022-328x(03)00053-6
Publikováno v:
ChemInform. 43
The regioisomeric dibromides (I) undergo selective cross-coupling at the benzyl site to yield the corresponding bromophenyl derivatives.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::66829ad136d8292b332d6c7c873d33f1
https://doi.org/10.1002/chin.201242066
https://doi.org/10.1002/chin.201242066
Publikováno v:
SYNTHESIS
SYNTHESIS, Georg Thieme Verlag, 2012, 44 (13), pp.2023-2040. ⟨10.1055/s-0031-1290987⟩
SYNTHESIS, Georg Thieme Verlag, 2012, 44 (13), pp.2023-2040. ⟨10.1055/s-0031-1290987⟩
International audience; Regio- and stereoselective reactions of ortho-, meta-, and para-bromobenzyl bromide under Stille and (or) Suzuki cross-coupling reactions are described that provided substituted styrene monomers and biaryls in two steps. By co
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::379ef6ef02ea7744eee851154cb494f0
https://hal.inrae.fr/hal-02650697
https://hal.inrae.fr/hal-02650697
Autor:
Alain Duchêne, Mohamed Abarbri, Samuel Inack Ngi, Jérôme Thibonnet, Sandrine Langle, Elsa Anselmi
Publikováno v:
Organic Syntheses
(E)-2,3-Dibromobut-2-enoic acid (E)-2,3-Dibromooct-2-enoic acid 4-Methoxy-2-butynoic acid Tetrolic acid Pentylpropiolic acid Bromine Keywords: dihalogeno-carboxylic acids; stereoselective synthesis; dibromination; tetrolic acid; alpha; beta-Aceytleni
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::43d7e1269c03eed41556ea204107dc52
https://doi.org/10.1002/0471264229.os085.24
https://doi.org/10.1002/0471264229.os085.24
Publikováno v:
ChemInform. 34
Using double Stille cross-coupling reaction bromo (or chloro)benzylbromide is easily transformed into substituted styrene monomers bearing a wide range of substituents in para position
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1bc1e1c77dee661015e36fd0136c10f8
https://doi.org/10.1002/chin.200320070
https://doi.org/10.1002/chin.200320070
Autor:
Frdric Doll, Sandrine Langle, Galle Roger, Roger R. Fulton, Batrice Lagnel-de Bruin, David J. Henderson, Franoise Hinnen, Taliesha Paine, Mark J. Coster, Heric Valette, Michel Bottlaender, Michael Kassiou
Publikováno v:
Australian Journal of Chemistry; Jun2008, Vol. 61 Issue 6, p438-445, 8p