Zobrazeno 1 - 8
of 8
pro vyhledávání: '"Sabine Boisnard"'
Autor:
Thomas Rooney, Philippe Hantraye, Sabine Boisnard, Bertrand Kuhnast, John Allen, Stéphane Demphel, Raphaël Boisgard, Nadia Van Camp, Sébastien Roy, Cyrille Thominiaux, Stéphane Le Helleix, Rivron Luc, Annelaure Damont, Bertrand Tavitian, Hervé Boutin, Jesus Benavides, Fabien Chauveau, Frédéric Dollé
Publikováno v:
Journal of Labelled Compounds and Radiopharmaceuticals. 53:767-773
SSR180575 (7-chloro-N,N,5-trimethyl-4-oxo-3-phenyl-3,5-dihydro-4H-pyridazino[4,5-b]indole-1-acetamide) is the lead compound of an original pyridazinoindole series of potent and highly selective TSPO (peripheral benzodiazepine receptor) ligands. Isoto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::b53bc62817271e5a1788de37a7540e7c
https://doi.org/10.1002/jlcr.1794
https://doi.org/10.1002/jlcr.1794
Publikováno v:
Scopus-Elsevier
Synthesis of fully protected actinoidic acid deriv. I and selectively protected biaryl bisamino acid II, intermediates for vancomycin total synthesis, are reported. [on SciFinder (R)]
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::cf4e953bcdb7db923a4cb2143c8506b2
https://doi.org/10.1021/ol006110s
https://doi.org/10.1021/ol006110s
Publikováno v:
ChemInform. 31
A rapid synthesis of aryl triflate and aryl nonaflate was developed using 4-nitrophenyl triflate and 4-nitrophenyl nonaflate as perfluoroalkanesulfonyl transfer reagents in combination with polymer supported 1,5,7-triazabicyclo[4.4.0]dec-5-ene (PTBD)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::20a9fc45c5183d7952b62b729cd38c69
https://doi.org/10.1002/chin.200001068
https://doi.org/10.1002/chin.200001068
Publikováno v:
ChemInform. 32
Palladium-catalyzed Suzuki cross-coupling, Corey's enantioselective alkylation of glycine template, and macrolactamization are key steps in an efficient synthesis of the 15-membered macrocycle 2.
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::9905f5b33ac3294f2421dc7aa8a68a6d
https://doi.org/10.1002/chin.200141249
https://doi.org/10.1002/chin.200141249
Autor:
Sabine Boisnard, Jieping Zhu
Publikováno v:
ChemInform. 33
Synthesis of a bicyclic A-B-O-C ring system of RP-66453 (I), a neurotensine receptor antagonist, with an endo aryl-aryl and an endo aryl-aryl ether bond is described. An alternative synthetic strategy starting from the construction of functionalized
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::d13fe75049d5e6012c3ec470c5ff306b
https://doi.org/10.1002/chin.200229228
https://doi.org/10.1002/chin.200229228
Publikováno v:
Organic letters. 3(13)
Palladium-catalyzed Suzuki cross-coupling, Corey's enantioselective alkylation of glycine template, and macrolactamization are key steps in an efficient synthesis of the 15-membered macrocycle I, the A-B biaryl macrocyclic component of RP-66453 (II).
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::b725d382b95c61686629825bc5dd043a
https://pubmed.ncbi.nlm.nih.gov/11418049
https://pubmed.ncbi.nlm.nih.gov/11418049
Autor:
Jieping Zhu, Sabine Boisnard
Synthesis of a bicyclic A-B-O-C ring system of RP-66453 (I), a neurotensine receptor antagonist, with an endo aryl-aryl and an endo aryl-aryl ether bond is described. An alternative synthetic strategy starting from the construction of functionalized
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::81ef499081a367d2118bbe731ea56773
https://infoscience.epfl.ch/record/158148
https://infoscience.epfl.ch/record/158148
A rapid synthesis of aryl triflate and aryl nonaflate was developed using 4-nitrophenyl triflate and 4-nitrophenyl nonaflate as perfluoroalkanesulfonyl transfer reagents in combination with polymer supported 1,5,7-triazabicyclo[4.4.0]dec-5-ene (PTBD)
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4b9bb2aab17881437c5ad412df0e41a0
https://infoscience.epfl.ch/record/158172
https://infoscience.epfl.ch/record/158172