Synthesis of Dithioester Derivatives by Base-Mediated Fragmentation of 1,3-Dithiolanes
Dithioesters are important agents for chain transfer in polymer chemistry and precursors in the synthesis of heterocycles. Straightforward approaches to their synthesis are therefore in demand. Outlined herein is a method to access such compounds in one-pot. 2-Aryl-1,3-dithiolanes undergo ring fragmentation with LiHMDS in CPME to generate aryl-dithiocarboxylates in 5 min at 100 °C. These anions are subsequently captured in the second step by addition of various alkyl halides and diaryliodonium salts to furnish a large library of dithioesters in good yields. The method can be also employed in a one-pot, one-step manner for alkyl bromides and allows the synthesis of dithioesters in gram scale.
Authors
- Baris Yücel (ORCID: https://orcid.org/0000-0002-4785-4113)
- Zeynep Mert
- Elif Aydin
- Sabri Yılmaz (ORCID: https://orcid.org/0000-0002-4789-6663)
- Hasan Pelit
- Mehmet Aytug Sinmaz
- Oyku Acelya Ildem
- Yigit Efe Turhan
- Andrea Mentese
Institutions
- Istanbul Technical University (TR)
Publication Details
- Journal
- Organic Letters
- Published
- 2025-04-14
- DOI
- https://doi.org/10.1021/acs.orglett.5c00666
- Citations
- 2
- Primary Topic
- Synthesis of heterocyclic compounds
- Type
- article
- Field-Weighted Citation Impact
- 1.87
Funders
- Türkiye Bilimsel ve Teknolojik Araştırma Kurumu