Results 121 to 130 of about 1,851 (175)
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Iptycene-Derived Pyridazines and Phthalazines
The Journal of Organic Chemistry, 2007The synthesis of new heterocyclic oligo(phenylene) analogues based on soluble, nonaggregating 1,2-diazines is reported. Improved palladium-catalyzed reductive coupling methods were developed to allow for the preparation of large quantities of iptycene-derived bipyridazines and biphthalazines, and the controlled synthesis of well-defined oligomers up to
Jean, Bouffard +3 more
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Pyridazine-derived γ-secretase modulators
Bioorganic & Medicinal Chemistry Letters, 2011SAR of a novel series of pyridazine-derived γ-secretase modulators is described. Compound 25 was found to be a potent modulator in vitro, which on further profiling, was found to decrease Aβ42 and Aβ40, and maintain the levels of total Aβ. Furthermore, 25 demonstrated excellent pharmacokinetic parameters as well as good CNS penetration in the rat.
Zehong, Wan +22 more
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Synthesis of α‐(Trifluoromethyl)pyridazine Derivatives
European Journal of Organic Chemistry, 2018Over the last decades, an increasing interest in α‐(trifluoromethyl)pyridazines in medicinal chemistry has been noticed. This interest stems firstly from the recent development of biologically active pyridazines as well as from the capacity of the pyridazine ring to be a bioisoster of other heterocycles.
Feraldi-Xypolia, Alexandra +2 more
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Archiv der Pharmazie, 1989
AbstractThe preparation of a series of 3‐hydrazinocycloalkyl[1,2‐c]‐pyridazines 7 and some derivatives as hydrazones 8, 9, triazoles 10 and pyrroles 11 are described together with their hypotensive activity in normotensive rats.
C, Terán +7 more
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AbstractThe preparation of a series of 3‐hydrazinocycloalkyl[1,2‐c]‐pyridazines 7 and some derivatives as hydrazones 8, 9, triazoles 10 and pyrroles 11 are described together with their hypotensive activity in normotensive rats.
C, Terán +7 more
openaire +2 more sources
Journal für Praktische Chemie, 1969
AbstractDas neuerdings leicht zugängliche 3‐Amino‐4‐hydroxy‐6‐methy1‐pyridazin 1 [1] erschließt einen neuen Zugang zu Derivaten des Pyridazins. Die Umsetzung mit salpetriger Säure liefert in verdünnter Schwefelsäure 3,4‐Dihydroxy‐6‐methyl‐pyridazin 3, in konz. Salzsäure dagegen 3‐Chlor‐4‐hydroxy‐6‐methylpyridazin 2.
H. G. O. Becker, H. Böttcher, J. Koch
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AbstractDas neuerdings leicht zugängliche 3‐Amino‐4‐hydroxy‐6‐methy1‐pyridazin 1 [1] erschließt einen neuen Zugang zu Derivaten des Pyridazins. Die Umsetzung mit salpetriger Säure liefert in verdünnter Schwefelsäure 3,4‐Dihydroxy‐6‐methyl‐pyridazin 3, in konz. Salzsäure dagegen 3‐Chlor‐4‐hydroxy‐6‐methylpyridazin 2.
H. G. O. Becker, H. Böttcher, J. Koch
openaire +1 more source
Synthesis of pyridazine derivatives—XXVIII
Tetrahedron, 1967B. Stanovnik, M. Tišler
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Design, synthesis and biological activity of chalcone derivatives containing pyridazine
Arabian Journal of Chemistry, 2023Yong-Jun Wu, Shuang Feng, Bangcan He
exaly
Pyridazine derivatives as selective COX‐2 inhibitors: A review on recent updates
Drug Development Research, 2023Rasha Ahmed Hassan, Marwa Hassan
exaly

