Synthesis of Dithioester Derivatives by Base-Mediated Fragmentation of 1,3-Dithiolanes.

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.

SUBMITTER: Pelit H 

PROVIDER: S-EPMC12038844 | biostudies-literature | 2025 Apr

REPOSITORIES: biostudies-literature