Results 111 to 120 of about 89,598 (163)
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Kondensierte Dihydro‐1,2,4‐triazine
Archiv der Pharmazie, 1987AbstractHydrazone von α‐Aminoketonen mit cyclischem Aminanteil ergeben mit Quecksilber (II)‐EDTA eine Cyclodehydrierung zu entspr. kondensierten Dihydrotriazinen.
Hans Möhrle, Peter Schillings
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, 2020
The treatment of tert-butyl 2-(7-bromo-3-tert-butyl-8-R-4-oxopyrazolo[5,1-c][1,2,4]triazin-1(4H)-yl)acetates (R = CN, CO2Et, NO2) with alkyl lithiums in THF at low temperature led to rapid cascade reactions with the formation of tert-butyl 7-amino-3-tert-
S. M. Ivanov
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The treatment of tert-butyl 2-(7-bromo-3-tert-butyl-8-R-4-oxopyrazolo[5,1-c][1,2,4]triazin-1(4H)-yl)acetates (R = CN, CO2Et, NO2) with alkyl lithiums in THF at low temperature led to rapid cascade reactions with the formation of tert-butyl 7-amino-3-tert-
S. M. Ivanov
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J. Chem. Soc., Perkin Trans. 1, 1976
Synthetic pathways to reduced 1,2,4-triazines have been investigated. The most convenient route involved the reaction of ketones with sodium cyanide and thiosemicarbazide, under acidic conditions, to yield cyanothiosemi-carbazones. These compounds were either converted into the corresponding carboxy-thiosemicarbazones which, in turn, were cyclized in ...
Louis C. March +2 more
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Synthetic pathways to reduced 1,2,4-triazines have been investigated. The most convenient route involved the reaction of ketones with sodium cyanide and thiosemicarbazide, under acidic conditions, to yield cyanothiosemi-carbazones. These compounds were either converted into the corresponding carboxy-thiosemicarbazones which, in turn, were cyclized in ...
Louis C. March +2 more
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Bioorganic chemistry (Print), 2018
A novel 5,6-diaryl-1,2,4-triazine thiazole derivatives (7a-7q) were synthesized and characterized by 1H NMR and 13C NMR and evaluated for their α-glucosidase inhibitory activity.
Guangcheng Wang +3 more
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A novel 5,6-diaryl-1,2,4-triazine thiazole derivatives (7a-7q) were synthesized and characterized by 1H NMR and 13C NMR and evaluated for their α-glucosidase inhibitory activity.
Guangcheng Wang +3 more
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Bioorganic & Medicinal Chemistry Letters, 2020
A series of 6-aminocarbonyl pyrrolo[2,1-f][1,2,4]triazine derivatives were designed by scaffold hopping strategy. The IC50 values of compound 14a against PI3Ks were measured, showing selective activity against p110α and p110δ with IC50s of 122 nM and 119
H. Xiang +6 more
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A series of 6-aminocarbonyl pyrrolo[2,1-f][1,2,4]triazine derivatives were designed by scaffold hopping strategy. The IC50 values of compound 14a against PI3Ks were measured, showing selective activity against p110α and p110δ with IC50s of 122 nM and 119
H. Xiang +6 more
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Merocyaninfarbstoffe aus 1,2,4-Triazin
Monatshefte für Chemie, 1968Hydrazinderivate von 1,2,4-Triazinen liefern mit Acetessigester Pyrazolonderivate. Diese kondensieren sich mit Salzen quartarer heterocyclischer Basen zu Merocyaninfarbstoffen. Darstellung und Spektren von drei Typen solcher Farbstoffe werden beschrieben.
Engelbert Kiša, Jaromír Hadáček
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1,2,4-triazines and condensed derivatives—XIV
Tetrahedron, 1974Abstract 3 - Alkylthio - 6,7 - dihydro - [1.2.4]triazino - [1.6-c]quinazolin - 5 - ium - 1 - olates (3), prepared by condensation of 3 - alkylthio -6-(2- aminophenyl) - 1,2,4 - triazin - 5(2H) - ones (1) with aldehydes, ketones or their equivalents are transformed by thermolysis and/or acid treatment into 3 - alkylthio - [1.2.4]triazino[5.6-b]indoles
G. Doleschall, K. Lempert
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1,2,4-Triazines Are Versatile Bioorthogonal Reagents
Journal of the American Chemical Society, 2015A new class of bioorthogonal reagents, 1,2,4-triazines, is described. These scaffolds are stable in biological media and capable of robust reactivity with trans-cyclooctene (TCO). The enhanced stability of the triazine scaffold enabled its direct use in recombinant protein production.
David N, Kamber +6 more
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European journal of medicinal chemistry, 2018
c-Met and VEGFR-2 have attracted interest as novel targets for treatment of various cancers. Aiming to develop potent dual c-Met and VEGFR-2 inhibitors, a series of pyrrolo[1,2-f][1,2,4]triazine derivatives were designed and synthesized.
W. Shi +5 more
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c-Met and VEGFR-2 have attracted interest as novel targets for treatment of various cancers. Aiming to develop potent dual c-Met and VEGFR-2 inhibitors, a series of pyrrolo[1,2-f][1,2,4]triazine derivatives were designed and synthesized.
W. Shi +5 more
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Zur Chemie der 1,2,4‐Triazine, VII. Reaktionen von 1,2,4‐Triazin‐4‐oxiden
Justus Liebigs Annalen der Chemie, 1976AbstractDie Hydrolyse von 1,2,4‐Triazin‐4‐oxiden 1 verlauft sowohl im sauren als auch im basischen Milieu unter Ringöffnung. Die Oxidation von 1 ergibt 5‐0xo‐1,2,4‐triazin‐4‐oxide 7 und/oder 1,2,4‐Triazin‐1,4‐dioxide 8. Bei der Reaktion von 1 mit Benzoylchlorid in Gegenwart von Wasser werden 1,2,4‐Triazin‐5‐one 5 gebildet.
Hans Neunhoeffer, Volker Böhnisch
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