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Functionalization of 9-thioxanthone at the 1-position: From..:
Mokhtari Brikci-Nigassa, Nahida
;
Nauton, Lionel
;
Moreau, Pascale
...
info:eu-repo/semantics/altIdentifier/doi/10.1016/j.bioorg.2019.103347. , 2020
Link:
https://hal.science/hal-02404054
RT Journal T1
Functionalization of 9-thioxanthone at the 1-position: From arylamino derivatives to [1]benzo(thio)pyrano[4,3,2-de]benzothieno[2,3-b]quinolines of biological interest
UL https://suche.suub.uni-bremen.de/peid=base-ftuniparissaclay:oai:HAL:hal-02404054v1&Exemplar=1&LAN=DE A1 Mokhtari Brikci-Nigassa, Nahida A1 Nauton, Lionel A1 Moreau, Pascale A1 Mongin, Olivier A1 Duval, Raphael, E A1 Picot, Laurent A1 Thiery, Valérie A1 Souab, Mohamed A1 Baratte, Blandine A1 Ruchaud, Sandrine A1 Bach, Stéphane A1 Le Guével, Rémy A1 Bentabed-Ababsa, Ghenia A1 Erb, William A1 Roisnel, Thierry A1 Dorcet, Vincent A1 Mongin, Florence PB HAL CCSD; Elsevier YR 2020 K1 Thioxanthone K1 Kinase inhibition K1 N-arylation K1 Melanoma cells K1 Copper K1 Fluorescence K1 [CHIM.ORGA]Chemical Sciences/Organic chemistry K1 [CHIM.THER]Chemical Sciences/Medicinal Chemistry K1 [SDV.BBM.BC]Life Sciences [q-bio]/Biochemistry K1 Molecular Biology/Biochemistry [q-bio.BM] K1 [SDV.SP.MED]Life Sciences [q-bio]/Pharmaceutical sciences/Medication JF info:eu-repo/semantics/altIdentifier/doi/10.1016/j.bioorg.2019.103347 LK http://dx.doi.org/https://hal.science/hal-02404054 DO https://hal.science/hal-02404054 SF ELIB - SuUB Bremen
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