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Published in 2017 at "Tetrahedron"
DOI: 10.1016/j.tet.2016.12.006
Abstract: Tetrafluoropyridazine 1 reacts with a range of oxygen-, nitrogen-, sulfur- and carbon-centred nucleophiles to give, in general, products 2 arising from substitution of fluorine para to ring nitrogen. Subsequent reaction of the trifluoropyridazine derivatives 2…
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Keywords:
ring fused;
fused pyridazine;
polysubstituted ring;
pyridazine systems ... See more keywords