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  1. 2-Iodoxy-5-Methylbenzenesulfonic Acid-Catalyzed Selective Oxidation of 4-Bromobenzyl Alcohol to 4-Bromobenzaldehyde or 4-Bromobenzoic Acid with OxoneOxidation Org. Synth. Vol. 89, p. 105 · Uyanik and Ishihara.*
  2. Methyltrioxorhenium catalyzed oxidation of secondary amines to nitrones: N-benzylidene-benzylamine N-oxideOxidation Org. Synth. Vol. 81, p. 204 · Goti et al.
  3. Mild and selective oxidation of sulfur compounds in trifluoroethanol: diphenyl disulfide and methyl phenyl sulfoxideOxidation Org. Synth. Vol. 80, p. 184 · Ravikumar et al.
  4. Oxidation of 5-aminotetrazoles: benzyl isocyanideOxidation Org. Synth. Coll. Vol. 7, p. 27; Vol. 61, p. 14 · Höfle and Lange
  5. Oxidation of alcohols by methyl sulfide – N-chlorosuccinimide – triethylamine: 4-tert-butylcyclohexanoneOxidation Org. Synth. Coll. Vol. 6, p. 220; Vol. 58, p. 122 · Corey et al.
  6. Oxidation of nerol to neral with iodobenzene diacetate and TEMPOOxidation Org. Synth. Vol. 83, p. 18 · Piancatelli and Leonellia
  7. Oxidation of primary alcohols to carboxylic acids with sodium chlorite catalyzed by TEMPO and bleach: 4-methoxyphenylacetic acidOxidation Org. Synth. Vol. 81, p. 195 · Zhao et al.
  8. Oxidation of secondary amines to nitrones: 6-methyl-2,3,4,5-tetrahydropyridine N-oxideOxidation Org. Synth. Coll. Vol. 9, p. 632; Vol. 70, p. 265 · Murahashi et al.
  9. Oxidation with bis(salicylidene)ethylenediiminocobalt(II) (salcomine): 2,6-di-tert-butyl-p-benzoquinoneOxidation Org. Synth. Coll. Vol. 6, p. 412; Vol. 57, p. 78 · Jonge et al.
  10. Oxidation with the chromium trioxide-pyridine complex prepared in situ:1-decanalOxidation Org. Synth. Coll. Vol. 6, p. 373; Vol. 55, p. 84 · Ratcliffe
  11. Oxidation with the nitrosodisulfonate radical. I. Preparation and use of disodium nitrosodisulfonate: trimethyl-p-benzoquinoneOxidation Org. Synth. Coll. Vol. 6, p. 1010; Vol. 52, p. 83 · Wehrli and Pigott
  12. Polymeric carbodiimide. Moffat oxidation: 4-tert-butylcyclohexanoneOxidation Org. Synth. Coll. Vol. 6, p. 218; Vol. 56, p. 99 · Weinshenker et al.
  13. A practical procedure for carbonyl α-oxidation: synthesis of (2-benzoyloxy)-1,4-cyclohexanedione mono-ethylene ketalOxidation Org. Synth. Vol. 84, p. 233 · Jones and Tomkinson
  14. Preparation of 4-acetylamino-2,2,6,6-tetramethylpiperidine-1-oxoammonium tetrafluoroborate, and the oxidation of geraniol to geranialOxidation Org. Synth. Vol. 82, p. 80 · Bobbitt and Merbouh
  15. Preparation of chiral, nonracemic γ-lactones by enzymecatalyzed oxidation of meso-diols: (+)-(1R,6S)-8-oxabicyclo[4.3.0]nonan-7-oneOxidation Org. Synth. Coll. Vol. 7, p. 406; Vol. 63, p. 10 · Jones and Jakovac
  16. Selective epoxidation of terminal double bonds: 10,11-epoxyfarnesyl acetateOxidation Org. Synth. Coll. Vol. 6, p. 560; Vol. 56, p. 112 · Hanzlik
  17. A selective, heterogeneous oxidation using a mixture of potassium permanganate and cupric sulfate: (3aS,7aR)-hexahydro-(3S,6R)-dimethyl-2(3H)-benzofuranoneOxidation Org. Synth. Coll. Vol. 9, p. 462; Vol. 71, p. 207 · Jefford et al.
  18. A simple and convenient method for the oxidation of organoboranes using sodium perborate: (+)-isopinocampheolOxidation Org. Synth. Coll. Vol. 9, p. 522; Vol. 73, p. 116 · Kabalka et al.
  19. Synthesis of 1-Naphthol via Oxidation of Potassium 1-NaphthyltrifluoroborateOxidation Org. Synth. Vol. 90, p. 153 · Molander et al.
  20. Synthesis of 1,1-dimethylethyl (S)-4-formyl-2,2-dimethyl-3-oxazolidinecarboxylate by oxidation of the alcoholOxidation Org. Synth. Vol. 77, p. 64 · Dondoni and Perrone
  21. Synthesis of 1,2:4,5-di-O-isopropylidene-D-erythro-2,3-hexodiulo-2,6-pyranose. A highly enantioselective ketone catalyst for epoxidationOxidation Org. Synth. Vol. 80, p. 1 · Tu et al.
  22. Tetrahydro-3-benzazepin-2-ones by lead tetraacetate oxidation of isoquinoline enamides: 7,8-dimethoxy-1,3,4,5-tetrahydro-2H-3-benzazepin-2-oneOxidation Org. Synth. Coll. Vol. 9, p. 268; Vol. 70, p. 139 · Lenz and Lessor
  23. The Dess-Martin periodinane: 1,1,1-triacetoxy-1,1-dihydro-1,2-benziodoxol-3(1H)-oneOxidation Org. Synth. Vol. 77, p. 141 · Boeckman et al.