Regioselectivity in the Reactions of Aryltri-isopropoxytitanium with Pyrimidinones.
Complete regioselectivity is observed in the 1:1-adduct formation between aryltri-isopropoxytitanium reagents and pyrimidin-2(1H)ones: the new carbon-carbon-bond is formed at C-4.Dehydrogenation gives the arylated, fully conjugated heterocycle.
Rise, Frode,Undheim, Kjell
p. 1997 - 2000
(2007/10/02)
More Articles about upstream products of 103594-76-9