Abstract
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.
| Original language | English |
|---|---|
| Pages (from-to) | 4135-4139 |
| Number of pages | 5 |
| Journal | Organic Letters |
| Volume | 27 |
| Issue number | 16 |
| DOIs | |
| Publication status | Published - 25 Apr 2025 |
Bibliographical note
Publisher Copyright:© 2025 The Authors. Published by American Chemical Society
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