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

Institutions

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

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

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

Baris Yücel, Zeynep Mert, Elif Aydin, Sabri Yılmaz et al.
2 citations
Organic Letters
Synthesis of heterocyclic compounds
1.87
article

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

Baris Yücel, Zeynep Mert, Elif Aydin, Sabri Yılmaz, Hasan Pelit, Mehmet Aytug Sinmaz, Oyku Acelya Ildem, Yigit Efe Turhan, Andrea Mentese
article en
2 citations

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.

Organic LettersVol. 27(16)
Istanbul Technical University (TR)
Türkiye Bilimsel ve Teknolojik Araştırma Kurumu
Openalex Percentile: Top 16%
Synthesis of heterocyclic compounds
1.87
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.