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Catalyst-free, direct synthesis of dibenzothiophenes

  • Kim Christopher C. Aganda
  • , Sangcheol Na
  • , Anna Lee*
  • *Corresponding author for this work
  • Jeonbuk National University

Research output: Contribution to journalJournal articlepeer-review

Abstract

A catalyst-free method for the synthesis of dibenzothiophenes has been developed. The nucleophilic intramolecular cyclization of methylthiolated diazonium salts enables the direct synthesis of dibenzothiophenes under mild reaction conditions. The addition of TEMPO is beneficial for improving the reaction yield by suppressing the formation of by-products, which can be formed via a radical-mediated process. This simple method provides an alternative for the synthesis of dibenzothiophenes, which are frequently found in valuable compounds.

Original languageEnglish
Article number154009
JournalTetrahedron Letters
Volume104
DOIs
StatePublished - 2022.08.17

Keywords

  • C[sbnd]S bond formation
  • Diazonium salts
  • Dibenzothiophenes

Quacquarelli Symonds(QS) Subject Topics

  • Engineering - Petroleum
  • Pharmacy & Pharmacology
  • Chemistry
  • Biological Sciences

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