Alkyl and Aryl Thioester Synthesis via N-Heterocyclic Carbene-Catalyzed α-Thio Aldehyde Rearrangement
We have developed a highly atom economic transformation to provide a thioester. The N-heterocyclic carbene-catalyzed rearrangement of α-thio aldehydes affords thioesters in good yields. This reaction exhibits a broad substrate scope and is applicable to aldehydes bearing either alkylthio or arylthio groups. The optimal combination of catalyst precursor and base is highly dependent on the nature of the S substituent in the starting α-thio aldehyde.
Authors
- K. Yamada
- Tatsuya Fujiwara
- Tsubasa Inokuma (ORCID: https://orcid.org/0000-0002-2331-2758)
Institutions
- Tokushima University (JP)
Publication Details
- Journal
- Organic Letters
- Published
- 2025-12-23
- DOI
- https://doi.org/10.1021/acs.orglett.5c04522
- Primary Topic
- N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
- Type
- article
- Field-Weighted Citation Impact
- 0.00