Regioselectivity in the reactions of aryltri-isopropoxytitanium with pyrimidinones.
Abstract
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.
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