Zobrazeno 1 - 10
of 26
pro vyhledávání: '"Gilles Niel"'
Publikováno v:
Beilstein Journal of Organic Chemistry, Vol 7, Iss 1, Pp 364-368 (2011)
New functional monomers bearing a methacrylate, a bisphosphonate function and, for most, an internal carboxylate group, were prepared for incorporation into copolymers with adhesive or anticorrosive properties. Methanolysis of some trimethylsilyl bis
Externí odkaz:
https://doaj.org/article/7a1d3fc0d9ae49b882415cdec1672ed0
Autor:
Gilles Niel, Arie van der Lee, Eleonora Tosi, Renata Marcia de Figueiredo, Aurélien Lebrun, Kim Spielmann, Jean-Marc Campagne
Publikováno v:
Tetrahedron
Tetrahedron, Elsevier, 2018, 74 (45), pp.6497-6511. ⟨10.1016/j.tet.2018.09.040⟩
Tetrahedron, Elsevier, 2018, 74 (45), pp.6497-6511. ⟨10.1016/j.tet.2018.09.040⟩
International audience; Efficient palladium-catalyzed (3 þ 2)-cycloaddition reactions of cyclic N-sulfonyl imines and vinyl-aziridines (or cyclopropanes) have been achieved. The reactions, with either vinylic substrate, proceed with excellent yields
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ad8daf56e34ada90ca4000445df37c55
https://hal.archives-ouvertes.fr/hal-01892430
https://hal.archives-ouvertes.fr/hal-01892430
Publikováno v:
Chemical Society Reviews
Chemical Society Reviews, Royal Society of Chemistry, 2018, 47, pp.1159-1173. ⟨10.1039/c7cs00449d⟩
Chemical Society Reviews, Royal Society of Chemistry, 2018, 47, pp.1159-1173. 〈10.1039/c7cs00449d〉
Chemical Society Reviews, Royal Society of Chemistry, 2018, 47, pp.1159-1173. ⟨10.1039/c7cs00449d⟩
Chemical Society Reviews, Royal Society of Chemistry, 2018, 47, pp.1159-1173. 〈10.1039/c7cs00449d〉
International audience; After seminal Tsuji-Trost reactions (palladium catalyzed allylation of nucleophiles via -allyl intermediates as electrophiles),the idea of reversal reactivity of -allyl intermediates (i.e. -allyl as nucleophiles) has
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::f34663ebfa7c83335fc020743909a761
https://hal.archives-ouvertes.fr/hal-01678237
https://hal.archives-ouvertes.fr/hal-01678237
Publikováno v:
SYNLETT
SYNLETT, Georg Thieme Verlag, 2012, 23 (2), pp.219-223. ⟨10.1055/s-0031-1290106⟩
SYNLETT, Georg Thieme Verlag, 2012, 23 (2), pp.219-223. ⟨10.1055/s-0031-1290106⟩
International audience; The diastereoselective synthesis of the key C13-C25 fragment of thuggacin A is described. Two Evans aldolization steps and a diastereoselective addition of an allenylstannane control the required all-syn configuration of the f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ce7d7b333a079dd061c9547b2100031a
https://doi.org/10.1055/s-0031-1290106
https://doi.org/10.1055/s-0031-1290106
Publikováno v:
New Journal of Chemistry
New Journal of Chemistry, Royal Society of Chemistry, 2015, 39, pp.8807-8817. ⟨10.1039/C5NJ01077B⟩
New Journal of Chemistry, Royal Society of Chemistry, 2015, 39, pp.8807-8817. ⟨10.1039/C5NJ01077B⟩
International audience; A comparative study of the three main chemical information systems (Scifinder, Web of Science and Scopus) was performed by studying the indexing policies of titles, abstracts and keywords within selected literature articles. V
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::1ad5dd6c31e3e5e579e39f373862e913
https://hal.archives-ouvertes.fr/hal-01203527/document
https://hal.archives-ouvertes.fr/hal-01203527/document
Publikováno v:
Stereoselective Multiple Bond-Forming Transformations in Organic Synthesis
Stereoselective Multiple Bond-Forming Transformations in Organic Synthesis, John Wiley & Sons, Inc, pp.115-156, 2015, ⟨10.1002/9781119006220.ch5⟩
Stereoselective Multiple Bond-Forming Transformations in Organic Synthesis ISBN: 9781119006220
Stereoselective Multiple Bond-Forming Transformations in Organic Synthesis, John Wiley & Sons, Inc, pp.115-156, 2015, ⟨10.1002/9781119006220.ch5⟩
Stereoselective Multiple Bond-Forming Transformations in Organic Synthesis ISBN: 9781119006220
International audience; A review. The syntheses of four-membered carbocycles are much less described than those of three-membered ones. Because of the nature of their structures, domino approaches are clearly the methods of choice for their con
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::75ef5423295a10c55e95135fad68c809
https://hal.archives-ouvertes.fr/hal-01987432
https://hal.archives-ouvertes.fr/hal-01987432
Publikováno v:
Chemical Reviews
Chemical Reviews, American Chemical Society, 2012, 113 (1), pp.PR1-PR40. ⟨10.1021/cr300129n⟩
Chemical Reviews, American Chemical Society, 2012, 113 (1), pp.PR1-PR40. ⟨10.1021/cr300129n⟩
International audience
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::a66b3986e4cb3ab2f1010cac5c429d86
https://hal.archives-ouvertes.fr/hal-00739808
https://hal.archives-ouvertes.fr/hal-00739808
Publikováno v:
Tetrahedron. 50:5345-5360
A stepwise synthesis of dolastatin 10 starting from the dolaphenine residue is described. The chiral dola isoleuine and dolaproine residues were obtained by 5-step procedures from the corresponding N-Boc amino acid. The key steps are respectively the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::67f440545f09bedee0d93ee3468f33b4
https://doi.org/10.1016/s0040-4020(01)80692-x
https://doi.org/10.1016/s0040-4020(01)80692-x
Publikováno v:
ChemInform. 22
Abstraat: Crotyl-boronates add to aldehydes with high simple diastereoselection, such that E-crotyl-boronates give d-homoallyl alcohols, and Z-crotyl-boronates their =-counterparts. This reaction has been extended to stereoselective ring closure reac
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::c2aaa62b84904c47f1b453fcfda77e29
https://doi.org/10.1002/chin.199105346
https://doi.org/10.1002/chin.199105346
Publikováno v:
ChemInform. 25
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5595ed8278e0f3e52720d02c2ad8736c
https://doi.org/10.1002/chin.199438248
https://doi.org/10.1002/chin.199438248