Zobrazeno 1 - 3
of 3
pro vyhledávání: '"Wafaa Chaouni"'
Publikováno v:
ChemInform. 46
New substituted 3-azidothienopyridinecarboxylates (VI) are synthesized via a novel route involving a modified Vilsmeier—Haack—Arnold reaction.
Publikováno v:
European Journal of Medicinal Chemistry
European Journal of Medicinal Chemistry, Elsevier, 2014, 85, pp.450-457. ⟨10.1016/j.ejmech.2014.08.008⟩
European Journal of Medicinal Chemistry, Elsevier, 2014, 85, pp.450-457. ⟨10.1016/j.ejmech.2014.08.008⟩
International audience; Here we describe the synthesis and biological activity of novel amino-pyrazolopyridines with anti-NF-kappa B and pro-apoptotic potential. alpha-Methylene ketones were used as a starting point for synthesis of amino-pyrazolopyr
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::9fd1624cb635c093e4b37cb242aa3972
https://hal.univ-lorraine.fr/hal-01494562
https://hal.univ-lorraine.fr/hal-01494562
Publikováno v:
Zeitschrift fur Naturforschung B
Zeitschrift fur Naturforschung B, Verlag der Zeitschrift Fuer Naturforschung, 2014, 69 (5), pp.509-518. ⟨10.5560/ZNB.2014-3320⟩
Zeitschrift fur Naturforschung B, Verlag der Zeitschrift Fuer Naturforschung, 2014, 69 (5), pp.509-518. ⟨10.5560/ZNB.2014-3320⟩
International audience; The preparation of new substituted methyl 3-azidothieno[2,3-b]pyridine carboxylates by azotization of methyl 3-aminothieno[2,3-b]pyridine and subsequent treatment with sodium azide is described. Via Huisgen's 1,3-dipolar cyclo
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::ddd1902abff44005c7523bce669c6778
https://hal.univ-lorraine.fr/hal-01494560
https://hal.univ-lorraine.fr/hal-01494560