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1 es and diorganyl dichalcogenides promoted by Oxone.
2 functionality to the corresponding acid with oxone.
3 peracetic acid, m-chloroperbenzoic acid, and OXONE.
4 on with use of more ketone catalyst and less Oxone.
5 d in situ from a fructose-derived ketone and Oxone.
6 cleavage of an osmate ester by the action of oxone.
7 m glycoconjugates by a simple treatment with Oxone.
8 ,6-tetramethyl-2-iodobenzoic acid (TetMe-IA)/oxone.
9 mol 1)(-1) hr(-1) and K(M) = 53 +/- 5 mM for oxone ([1] = 7.5 microM), and V(max) = 6.5 +/- 0.3 mol O
10 to catalyze the epoxidation of alkenes using Oxone (2KHSO(5)+KHSO(4)+K(2)SO(4)), and significant leve
11 acid and arenes by a one-pot procedure using Oxone (2KHSO5.KHSO4.K2SO4) as an inexpensive and environ
12 oxyarylacrylic acids has been developed with Oxone (2KHSO5.KHSO4.K2SO4); the oxidation reaction invol
13 , very important synthons, by treatment with Oxone, a cheap, stable, and nonpollutant oxidizing reage
14 keto esters and 1,3-diketones mediated by an Oxone/aluminum trichloride system.
15  dependent on the relative concentrations of oxone and 1.
16                                   The use of Oxone and a palladium(II) catalyst enables the efficient
17 -linking in the presence of oxidants such as oxone and monoperoxyphthalic acid (MMPP).
18 metallic alternative to ozonolysis utilizing oxone and OsO(4) is presented.
19  diorganyl diselenides or ditellurides using Oxone as a green oxidant and acetonitrile as solvent in
20  were performed under mild conditions, using Oxone as a green oxidant to promote the cleavage of the
21 the presence of diorganyl diselenides, using Oxone as a green oxidizing agent.
22 trimethylsilyl enol ethers is possible using Oxone as a stoichiometric oxidant and sodium hydrogen ph
23 m hydrogen sulfate from 2-iodobiphenyl using Oxone as an inexpensive and environmentally safe oxidant
24  using 1-iodo-4-nitrobenzene as catalyst and oxone as an inexpensive and environmentally safe termina
25 angement of carboxamides to carbamates using Oxone as an oxidant can be efficiently catalyzed by iodo
26 ination of tetrabutylammonium iodide (TBAI), Oxone as non-nucleophilic and easy to handle co-oxidant,
27 ble glucose-derived ketone 2 as catalyst and Oxone as oxidant to form cis-propargyl epoxides in high
28 zolidinone-containing ketone as catalyst and Oxone as oxidant via a sequential asymmetric epoxidation
29 tose-derived chiral ketone 1 as catalyst and Oxone as oxidant.
30 NaI) as halogen source and K(2)S(2)O(8) (or) oxone as promoter.
31 , and environmentally benign peroxide-based "oxone" as the sole oxidant.
32  peptides using potassium peroxymonosulfate (oxone) as an oxidant.
33 imethylammonium permanganate (CTAP), RuCl(3)/Oxone/base or Ag(+)/oxalic acid each generate distinctiv
34                         The CTAP and RuCl(3)/Oxone/base oxidations also generate a unique open chain
35 d, and tested in heterogeneous activation of Oxone for phenol degradation in aqueous solution.
36 -5-iodoimidazole using a cheap and available Oxone/H(2)SO(4) oxidative system.
37 ve catalysts for asymmetric epoxidation with Oxone has been evaluated.
38 azole compounds using commercially available oxone improves the energetic properties and reveals a st
39  catalytic amount (10 mol %) of TetMe-IA and oxone in acetonitrile-water mixture (1:1, v/v) at rt.
40 lenes, phenanthrenes, anthracenes, etc. with Oxone in an acetonitrile-water mixture (1:1, v/v) at rt.
41  conversion of cyclic ketones to lactones by Oxone in neutral buffered water is extended to heterocyc
42 ted in situ from catalytic amount of PhI and Oxone in the presence of 1,1,1,3,3,3-hexafluoroisopropan
43 he corresponding perfluoroalkyl iodides with Oxone in trifluoroacetic acid at room temperature and su
44 The operational parameters, such as MnO2 and Oxone loading, phenol concentration and temperature, wer
45                               A novel iodine/oxone-mediated three-component coupling reaction of 2-me
46 h could then competitively react with either oxone or water/hydroxide to produce O(2).
47 (2) evolution from either KHSO(5) (potassium oxone) or NaOCl.
48 ly oxidized to the corresponding oxides 2 by OXONE over silica gel or alumina, as well as by (CH(3))(
49                                              OXONE over silica gel or, in some cases, alumina has bee
50 s initial dihydroxylation of the olefin with oxone, oxidative cleavage by the in situ-generated 3,4,5
51                                              Oxone (potassium peroxomonosulfate) is an efficient oxid
52 catalyzed reactions (sulfite and oxygen, and oxone) produce an imine intermediate that spontaneously
53 dation to iodine by peroxymonosulfate (i.e., Oxone reagent).
54 ne not only acts as a PTC but also activates Oxone, through hydrogen bonding, toward electrophilic at
55 y showed varying activities in activation of Oxone to generate sulfate radicals for phenol degradatio
56 2-(diphenylmethyl)pyrrolidine 1 reacted with Oxone to give a mixture of ammonium salts containing the
57 cal reaction: see text] Biacetyl reacts with oxone to give bis-dioxirane [3,3'-dimethyl-3,3'-bidioxir
58 benign reagent KHSO(5), prepared easily from Oxone, to diesters in one simple transformation.
59 s for asymmetric epoxidation of alkenes with Oxone, via a dioxirane intermediate.
60 ) complexes to cleave DNA in the presence of Oxone was strongly dependent on both the nature and the
61                                         When oxone was used, oxygen was not required for the deaminat
62 uickly and selectively oxidized with aqueous Oxone without the need for protection of most peptide si