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the claim
Sulfonyl azides function through diazo or azide transfer mechanisms
the verdict
SUPPORTED
the evidence backs this
refutedsupported
the weight of evidence
3 sources for · 0 against

Sulfonyl azides are widely documented in chemical literature as effective reagents that operate through diazo or azide transfer mechanisms to convert amines to azides or functionalize molecules.

Evidence for · 3
2016 · cited by 64
Paper [0] highlights that sulfonyl azides like imidazole-1-sulfonyl azide serve as valuable reagents for diazo-transfer reactions.
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The analysis

The retrieved papers consistently support the claim that sulfonyl azides function in diazo and azide transfer reactions. Papers [0], [10], and [11] all explicitly discuss or utilize sulfonyl azides in the context of diazo transfer and nitrogen transfer protocols. There are no papers contradicting this established chemical property.

More for · 2
2024 · cited by 2
Paper [10] describes the use of imidazole sulfonyl azide hydrochloride in diazo transfer reactions to prepare chitosan azides.
2025 · cited by 2
Paper [11] demonstrates the use of sulfonyl azides to generate nitrene radical anions for aziridination, establishing their role in nitrogen transfer mechanisms.
Everything we examined (12)
We also searched for evidence AGAINST this claim, not only for it.
  1. An Updated Synthesis of the Diazo-Transfer Reagent Imidazole-1-sulfonyl Azide Hydrogen Sulfate.peer-reviewedsupports
  2. A ‘sulfonyl-azide-free’ (SAFE) aqueous-phase diazo transfer reaction for parallel and diversity-oriented synthesispeer-reviewedno side takennot shown: read and judged not to bear on this claim
  3. Pyrazole Scaffold Synthesis, Functionalization, and Applications in Alzheimer's Disease and Parkinson's Disease Treatment (2011-2020).peer-reviewedno side takennot shown: read and judged not to bear on this claim
  4. Practical Application of the Aqueous ‘Sulfonyl-Azide-Free’ (SAFE) Diazo Transfer Protocol to Less α-C–H Acidic Ketones and Esterspeer-reviewedno side takennot shown: read and judged not to bear on this claim
  5. Synthesis and Application of Bioactive N-Functionalized Aziridines.peer-reviewedno side takennot shown: read and judged not to bear on this claim
  6. Recent advances in the synthesis of <i>N</i>-acyl sulfonamides.peer-reviewedno side takennot shown: read and judged not to bear on this claim
  7. Precise construction of spiro stereocenters <i>via</i> enantioselective radical addition through modulating photocatalysis from redox to energy transfer.peer-reviewedno side takennot shown: read and judged not to bear on this claim
  8. One-pot preparation of methyl 2-diazo-3-oxopropionates comprising an aqueous ‘sulfonyl-azide-free’ (SAFE) diazo transfer steppeer-reviewedno side takennot shown: read and judged not to bear on this claim
  9. Recent Advances in Iodine-Mediated Radical Reactions.peer-reviewedno side takennot shown: read and judged not to bear on this claim
  10. Pyridinium ylides as photocatalytic atom transfer reagents.peer-reviewedno side takennot shown: read and judged not to bear on this claim
  11. Conjugation of CRAMP<sub>18-35</sub> Peptide to Chitosan and Hydroxypropyl Chitosan via Copper-Catalyzed Azide-Alkyne Cycloaddition and Investigation of Antibacterial Activity.peer-reviewedsupports
  12. Photocatalytic Nitrene Radical Anion Generation from Sulfonyl Azides for Intermolecular Aziridination of Unactivated Alkenes.peer-reviewedsupports
The paper trail · every fact has a biography
first checked05 Aug 2026
judged → SUPPORTED · 8605 Aug 2026
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