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For a recent article that elegantly employs these oxidants in an enantioselective epoxidation using a different amine catalyst, see Ref. 17.
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For an example of a 1,4-addition with iodosobenzene, see:
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37
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33750472927
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For examples of nucleophilic attack by the oxygen of iodosobenzene, see:
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1H NMR.
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42
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33750455039
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For a discussion of substituent effects on the phenyl ring of hypervalent iodides, see:
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2, o-Me, and o-Cl) were found to be much less efficient than unfunctionalized iodosobenzene.
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46
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33750467523
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For examples of non-metal mediated oxidations by iodosobenzene, see:
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Concentrations of iodosobenzene species were calculated relative to benzyl methyl ether (internal standard) and were determined after removal of oligomeric iodosobenzene by filtration through Celite.
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