Abstract
Acyclic 2-diazo-1,3-dicarbonyl compounds react at 20–50°С with aromatic thioketones and through a cascade process, involving the cycloaddition of a diazo group dipole with the CS bond, elimination of nitrogen from the arising thiadiazoline, and subsequent [1,5]-electrocyclization of the intermediate СS-ylide, the relevant oxathioles being formed in yields of up to 70%. Carbocyclic 2-diazo-1,3-diketones at room temperature react with thiones much more slowly, but with increasing temperature they partly decompose to produce, via Wolff rearrangement, 2-oxoketenes, which yield [4+2]-cycloaddition products, that is oxathiinones and/or oxoketene dimers.
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