Abstract
Aryl thenyl and aryl aryl-α-thienylmethyl sulfides have been obtained by the action of oxalic acid esters on an equimolecular mixture of bromomagnesium thienyl or aryl α-thienyl carbinolates and bromomagnesium thiophenolates (or thionaphtholates). Derivatives of the sulfides, sulfoxides and sulfones, are also described.
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For part XX, see [9].
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Lapkin, I.I., Bogoslovskii, N.V. Reactions of halometal alkoxides. Chem Heterocycl Compd 4, 40–44 (1970). https://doi.org/10.1007/BF00478074
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DOI: https://doi.org/10.1007/BF00478074