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SYNTHESIS OF NEW PYRIDAZIN- 6-ONES, PYRIDAZIN-6-IMINES, 4-PYRIDAZINALS, AND PYRIDINES

Synthetic Communications, 2002
ABSTRACT 3-Dimethyl-1-[3-methyl-(4H)-5-phenylimidazol[2,1-b]thiazol-2-yl]prop-2-enone 4 couples smoothly with benzenediazonium chloride to yield propanal 5 which is a key intermediate for the synthesis of pyridazinones 9–13, 16 and pyridazine-6-imine 8, 19.
Samia M. Sayed   +3 more
openaire   +1 more source

Pyridazines. XXIII. A novel pyridazine into pyrazole ring transformation

Journal of Heterocyclic Chemistry, 1984
AbstractTreatment of phenyl(4‐pyridazinyl)methanols 1a and 1b with p‐toluenesulfonic acid at elevated temperatures causes transformation into the C‐4 substituted pyrazole derivatives 8a and 8b. Limitations of this novel rearrangement reaction as well as mechanistic considerations are discussed.
Gottfried Heinisch, Richard Waglechner
openaire   +1 more source

[Biotransformation of pyridazines. 1. Pyridazine and 3-methylpyridazine].

Die Pharmazie, 1990
Pyridazin (1) and 3-methylpyridazine (6) undergo oxidative biotransformation in an unexpected high degree. Beside the unchanged compounds, after administration of 1 two isomeric monohydroxylated products (2, 3), 4,5-dihydrodihydroxypyridazine (4) and 4,5-dihydroxypyridazine (5) and after administration of 6 one ringhydroxylated 6-derivative (7), 3 ...
H H, Borchert   +4 more
openaire   +1 more source

Pyridazines. LXXXIV. Studies on borohydride reduction of pyridazine compounds

Journal of Heterocyclic Chemistry, 1976
AbstractImidazo[1,2‐b]pyridazine, s‐triazolo[4,3‐b]pyridazine and tetrazolo[1,5‐b]pyridazine and some derivatives thereof were reduced with sodium borohydride to give the corresponding 5,6,7,8‐tetrahydro derivatives. A mechanism for these reductions is proposed and reduction at the C7‐C8 bond occurs before the reduction of the C6N5 bond.
P. K. Kadaba, B. Stanovnik, M. Tišler
openaire   +1 more source

Pyridazines

2021
ROTH GERALD JUERGEN   +2 more
openaire   +3 more sources

[1,2,4]Triazolo[4,3-b]pyridazine as a building block towards low-sensitivity high-energy materials

Chemical Engineering Journal, 2021
Sitong Chen   +2 more
exaly  

Pyridazines. XXXVII. Pyrimido[1,2-b]pyridazines

The Journal of Organic Chemistry, 1971
Miha Tisler   +2 more
openaire   +1 more source

Pyridazines

1968
M. Tišler, B. Stanovnik
openaire   +1 more source

Imidazo[1,2-b]pyridazine as privileged scaffold in medicinal chemistry: An extensive review

European Journal of Medicinal Chemistry, 2021
Gonzalo Vera   +1 more
exaly  

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