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Nitrogen-centered free radicals. IX. The ease of formation of thionitroxide radicals

https://doi.org/10.1021/ja00418a031
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Reactions of 5-(alkyl)thianthrenium and other sulfonium salts with nucleophiles
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The Synthesis and Characterization of Stable Radicals Containing the Thiazyl (SN) Fragment and Their Use as Building Blocks for Advanced Functional Materials
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Nitroxides
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NMR and ESR of sulphenic acids and their derivatives
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Thermally Adjustable Dynamic Disulfide Linkages Mediated by Highly Air‐Stable 2,2,6,6‐Tetramethylpiperidine‐1‐sulfanyl (TEMPS) Radicals
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ChemInform Abstract: NITROGEN‐CENTERED FREE RADICALS. IX. THE EASE OF FORMATION OF THIONITROXIDE RADICALS
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One‐Pot Synthesis of 3‐Sulfenyl/Selenylimidazo[1,5‐a]quinolines from 2‐Methylquinolines, Aliphatic Amines/Amino Acids, and Dichalcogenides
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TEMPS, the Chalcogen Cousin of the Infamous Stable Radical TEMPO, Traps Radicals via Substitution on Its Dimer (TEMPS)2
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inferred← citeshttps://doi.org/10.1002/marc.202400303openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/marc.202400460openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/mrc.1260280302openalex-snapshot
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inferred← citeshttps://doi.org/10.1002/smll.202310682openalex-snapshot
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inferred← citeshttps://doi.org/10.1007/10201276_169openalex-snapshot
6.45 Thio nitroxides
inferred← citeshttps://doi.org/10.1007/10201276_170openalex-snapshot
60Ulb1 - 72Mot1
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inferred← citeshttps://doi.org/10.1007/10201373_58openalex-snapshot
6.3 Aminothiyl radicals, RRNS, iminothiyl radicals, RR’C=NS, and related species
inferred← citeshttps://doi.org/10.1007/10201373_59openalex-snapshot
References for 6.1 - 6.3
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10.1.1 Thiyl radicals
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Transforming Cyclic/Linear Polymer Topologies: Emerging Techniques and Opportunities
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inferred← citeshttps://doi.org/10.1021/acs.macromol.3c02515openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/bi00459a042openalex-snapshot
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inferred← citeshttps://doi.org/10.1021/jm960644aopenalex-snapshot
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