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2, unreacted starting material was recovered. Under the condition using Oxone, 1-phenylcyclohexa-1,3-diene was produced as the major product with an accompanying small amount (∼20%) of 1b.
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2, unreacted starting material was recovered. Under the condition using Oxone, 1-phenylcyclohexa-1,3-diene was produced as the major product with an accompanying small amount (∼20%) of 1b.
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See the Supporting Information
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See the Supporting Information.
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52
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45249089247
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- was generated in situ.
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- was generated in situ.
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55
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If the substrate possesses protons acidic enough cf. allylic methine proton in cyclohexenol, the proton would be abstracted by a solvent to afford oxidized products
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If the substrate possesses protons acidic enough (cf. allylic methine proton in cyclohexenol), the proton would be abstracted by a solvent to afford oxidized products.
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