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.

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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
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article

Alkyl and Aryl Thioester Synthesis via N-Heterocyclic Carbene-Catalyzed α-Thio Aldehyde Rearrangement

K. Yamada, Tatsuya Fujiwara, Tsubasa Inokuma
Organic Letters
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
article

Alkyl and Aryl Thioester Synthesis via N-Heterocyclic Carbene-Catalyzed α-Thio Aldehyde Rearrangement

K. Yamada, Tatsuya Fujiwara, Tsubasa Inokuma
article en

Abstract

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.

Organic LettersVol. 28(1)
Tokushima University (JP)
Decent work and economic growth
Openalex Percentile: Top 34%
N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
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