Tellurium-based organic synthesis: A novel one-pot formation of 2-oxazolines from alkenes induced by amidotellurinylation

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Abstract

Benzenetellurinyl trifluoroacetate readily reacts with alkenes in acetonitrile in the presence of boron trifluoride etherate at 75 °C to give 2-oxazolines via amidotellurinylation.

Benzenetellurinyl trifluoroacetate readily reacts with alkenes in acetonitrile at 75°C to give 2-oxazolines in one pot.

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