Formation of 3,6-dihydro-1,2,4-oxathiazines from thioketone S-oxides and a 2H-azirine via a new type of [3,3] cycloaddition reaction

Abstract
Diarylthioketone S-oxides react with the 2H-azirine (1) in the presence of boron trifluoride–diethyl ether to give the oxathiazines (3)via a 1,3-cyclization across the sulphine C–S–O bond; the oxathiazines (3) rearrange thermally to the sulphoxides (5).

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