| Abstract: | The reaction. of allyl-2-thienyl sulfide with sulfur dichloride yields products of intermolecular- addition of intermediately formed sulfenyl chloride to the starting sulfide, and in the case of allyl-3-thienyl sulfide, intramolecular cyclization also takes place with formation of a compound of the thienodithiin series.Moscow State University, Chemistry Faculty, Moscow 119899. A. N. Nesmeyanov Institute of Organometallic Compounds, Russian Academy of Sciences, Moscow 117813. Translated Khimiya Geterotsiklicheskikh Soedinenii, No. 6, pp. 767–769, June, 1994. Original article submitted April 18, 1994. |
