Issue 10, 1989

Organotelluriums. Part 21. Amidotellurinylation of olefins and a novel one-pot synthesis of 4,5-dihydro-oxazoles from olefins

Abstract

Benezenetellurinyl trifluoroacetate in the presence of boron trifluoride–diethyl ether effects ready amidotellurinylation of olefins in acetonitrile at room temperature. The resulting β-acetamidoalkyl phenyl telluroxides further suffer an in situ intramolecular substitution at 75 °C to give 4,5-dihydrooxazoles in high yields. These reactions are highly regio- and stereo-selective.

Article information

Article type
Paper

J. Chem. Soc., Perkin Trans. 1, 1989, 1775-1780

Organotelluriums. Part 21. Amidotellurinylation of olefins and a novel one-pot synthesis of 4,5-dihydro-oxazoles from olefins

N. X. Hu, Y. Aso, T. Otsubo and F. Ogura, J. Chem. Soc., Perkin Trans. 1, 1989, 1775 DOI: 10.1039/P19890001775

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