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note
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These alternative conditions were employed due to the base-lability of the allylic acetate moiety within diketone 22.
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40
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77955658796
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note
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Crystallographic data (excluding structure factors) for the structures in this paper have been deposited with the Cambridge Crystallographic Data Center as supplementary publication nos. CCDC 763861.
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77955664370
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Other oxidants were screened but produced Baeyer-Villiger side products.
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0001569250
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For oxidative N-O bond cleavage see Altenative methods for N-O bond cleavage were pursued via ketone i, however all ultimately failed as illustrated below
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