Issue 0, 1985

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.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1985, 1997-1999

Regioselectivity in the reactions of aryltri-isopropoxytitanium with pyrimidinones.

F. Rise and K. Undheim, J. Chem. Soc., Perkin Trans. 1, 1985, 1997 DOI: 10.1039/P19850001997

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