Elsevier, Tetrahedron Letters, 24(44), p. 4459-4462, 2003
DOI: 10.1016/s0040-4039(03)01029-3
Wiley-VCH Verlag, ChemInform, 37(34), 2003
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The efficient one-pot bis-functionalization of the 4,5-positions of the 3-pyridazinone ring has been performed using Suzuki, Sonogashira and Stille cross-coupling reactions assisted by a retro-ene fragmentation. This route allows access in a shorter synthetic sequence to several pharmacologically useful 3(2H)-pyridazinones.