Evaluating the halogen bonding strength of a iodoloisoxazolium(III) salt

Diaryliodonium(III) salts have been established as powerful halogen-bond donors in recent years. Herein, a new structural motif for this compound class was developed: iodoloisoxazolium salts, bearing a cyclic five-membered iodolium core fused with an isoxazole ring. A derivative of this class was synthesized and investigated in the solid state by X-ray crystallography. Finally, the potential as halogen-bonding activator was benchmarked in solution in the gold-catalyzed cyclization of a propargyl amide.

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Publication Details

Journal
Beilstein Journal of Organic Chemistry
Published
2024-09-23
DOI
https://doi.org/10.3762/bjoc.20.204
Citations
3
Primary Topic
Oxidative Organic Chemistry Reactions
Type
article
Field-Weighted Citation Impact
0.75

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article

Evaluating the halogen bonding strength of a iodoloisoxazolium(III) salt

Dominik L. Reinhard, Elric Engelage, Anna Schmidt, Stefan M. Huber et al.
3 citations
Beilstein Journal of Organic Chemistry
Oxidative Organic Chemistry Reactions
0.75
article

Evaluating the halogen bonding strength of a iodoloisoxazolium(III) salt

Dominik L. Reinhard, Elric Engelage, Anna Schmidt, Stefan M. Huber, Julian Wolf, Marc Sons
article en
3 citations

Abstract

Diaryliodonium(III) salts have been established as powerful halogen-bond donors in recent years. Herein, a new structural motif for this compound class was developed: iodoloisoxazolium salts, bearing a cyclic five-membered iodolium core fused with an isoxazole ring. A derivative of this class was synthesized and investigated in the solid state by X-ray crystallography. Finally, the potential as halogen-bonding activator was benchmarked in solution in the gold-catalyzed cyclization of a propargyl amide.

Beilstein Journal of Organic ChemistryVol. 20
Ruhr University Bochum (DE)
Fonds der Chemischen Industrie, Deutsche Forschungsgemeinschaft
Clean water and sanitation
Openalex Percentile: Top 32%
Oxidative Organic Chemistry Reactions
0.75
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