RNHSO2F as Reliable Azasulfene Precursors for the Construction of Sulfamates

Abstract The utilization of NH-sulfamoyl fluorides (RNHSO2F) as reliable SuFEx synthons for the construction of various sulfamate esters is reported. By using potassium fluoride as base, we were able to convert RNHSO2F into azasulfene intermediates under mild conditions and guarantee their further efficient ligation with phenols and alcohols.

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Publication Details

Journal
Synthesis
Published
2024-12-26
DOI
https://doi.org/10.1055/a-2508-3355
Citations
2
Primary Topic
Sulfur-Based Synthesis Techniques
Type
article
Field-Weighted Citation Impact
0.50
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article

RNHSO2F as Reliable Azasulfene Precursors for the Construction of Sulfamates

Taijie Guo, Jiajia Dong, Long Xu, Wei J. Wang
2 citations
Synthesis
Sulfur-Based Synthesis Techniques
0.50
article

RNHSO2F as Reliable Azasulfene Precursors for the Construction of Sulfamates

Taijie Guo, Jiajia Dong, Long Xu, Wei J. Wang
article en
2 citations

Abstract

Abstract The utilization of NH-sulfamoyl fluorides (RNHSO2F) as reliable SuFEx synthons for the construction of various sulfamate esters is reported. By using potassium fluoride as base, we were able to convert RNHSO2F into azasulfene intermediates under mild conditions and guarantee their further efficient ligation with phenols and alcohols.

SynthesisVol. 57(05)
Shanghai Jiao Tong University (CN), Shanghai Advanced Research Institute (CN), Institute of Natural Science (KP)
Clean water and sanitation
Openalex Percentile: Top 37%
Sulfur-Based Synthesis Techniques
0.50
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