Synthesis of [1]benzothiopheno[2,3-b][1]benzothiophene derivatives through iodine-mediated sulfuration reaction of 1,1-diarylethylenes

[Display omitted] •BTBTs are generated at once by the Quadruple CS bond formation.•The addition of molecular iodine accelerates the formation of BTBTs.•3-Arylbenzo[b]thiophenes are also prepared by changing reaction conditions. Acceleration of the reaction for the synthesis of [1]benzothiopheno[2,3-...

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Veröffentlicht in:Tetrahedron letters 2020-02, Vol.61 (6), p.151476, Article 151476
Hauptverfasser: Sakai, Shuta, Sato, Kazuki, Yoshida, Kazuhiro
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Sprache:eng
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Zusammenfassung:[Display omitted] •BTBTs are generated at once by the Quadruple CS bond formation.•The addition of molecular iodine accelerates the formation of BTBTs.•3-Arylbenzo[b]thiophenes are also prepared by changing reaction conditions. Acceleration of the reaction for the synthesis of [1]benzothiopheno[2,3-b][1]benzothiophenes (BTBTs) from 1,1-diarylethylenes was accomplished by the addition of molecular iodine. Postulated intermediates 3-arylbenzo[b]thiophenes were also selectively prepared by simply changing the amount of iodine and the reaction time.
ISSN:0040-4039
1873-3581
DOI:10.1016/j.tetlet.2019.151476