Organocatalytic Michael Addition of β-Ketoesters and Ethenesulfonyl Fluoride: Access to Chiral δ-Sultones via SuFEx Chemistry

Abstract Sultones have been gaining popularity within medicinal chemistry due to their vast biological activity; however, access to chiral δ-sultones remains limited. In this study, we have developed an organocatalyzed Michael addition reaction between β-ketoesters and ethenesulfonyl fluoride using a bifunctional thiourea catalyst. This methodology resulted in 11 Michael adducts in yields up to 99% and enantioselectivities up to 84%. Subsequent cyclization under sulfonyl fluoride exchange conditions afforded seven novel chiral δ-sultones in low to moderate yields, generally preserving the enantioselectivity. This work presents an innovative strategy for efficiently synthesizing chiral δ-sultones.

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Publication Details

Journal
Synthesis
Published
2025-12-09
DOI
https://doi.org/10.1055/a-2758-9304
Primary Topic
Organic and Inorganic Chemical Reactions
Type
article
Field-Weighted Citation Impact
0.00
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article

Organocatalytic Michael Addition of β-Ketoesters and Ethenesulfonyl Fluoride: Access to Chiral δ-Sultones via SuFEx Chemistry

Tricia Naicker, Thomas Ebenhan, Kimberleigh B. Govender, Hendrik Gerhardus Kruger et al.
Synthesis
Organic and Inorganic Chemical Reactions
article

Organocatalytic Michael Addition of β-Ketoesters and Ethenesulfonyl Fluoride: Access to Chiral δ-Sultones via SuFEx Chemistry

Tricia Naicker, Thomas Ebenhan, Kimberleigh B. Govender, Hendrik Gerhardus Kruger, Thavendran Govender, Per I. Arvidsson
article en

Abstract

Abstract Sultones have been gaining popularity within medicinal chemistry due to their vast biological activity; however, access to chiral δ-sultones remains limited. In this study, we have developed an organocatalyzed Michael addition reaction between β-ketoesters and ethenesulfonyl fluoride using a bifunctional thiourea catalyst. This methodology resulted in 11 Michael adducts in yields up to 99% and enantioselectivities up to 84%. Subsequent cyclization under sulfonyl fluoride exchange conditions afforded seven novel chiral δ-sultones in low to moderate yields, generally preserving the enantioselectivity. This work presents an innovative strategy for efficiently synthesizing chiral δ-sultones.

SynthesisVol. 58(03)
University of Zululand (ZA), Science for Life Laboratory (SE), Climate Resilience Infrastructure Development Facility (ZA), University of Pretoria (ZA), University of KwaZulu-Natal (ZA)
Openalex Percentile: Top 65%
Organic and Inorganic Chemical Reactions
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