Abstract
The beta-oxo thiosulfines 8, generated by ‘unzipping' of the
corresponding acetyl alpha-chloroalkyl disulfides 11 with
morpholine, are partially converted into the corresponding
thioketones 12 which then cycloadd to 8 to give the observed cis-
and trans-1,2,4-trithiolanes 15. The unsymmetrical Diels-Alder
dimerization of 12 plays only a minor role. The new heterocycles
thus obtained have been characterized spectroscopically and by
X-ray crystallography.
| Original language | English |
|---|---|
| Journal | Acta Chemica Scandinavica |
| Volume | 53 |
| Pages (from-to) | 133-140 |
| Publication status | Published - 1999 |
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