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- W2056519776 abstract "The presence of a nitro group in the p-phenyl position dramatically slows down the oxygenation of isobenzofuranyl radicals. However, both unsubstituted and m-substituted phenyl rings have no appreciable influence on the reactivity toward oxygen. Spin delocalization on the nitro group is proposed to explain the stability of the carbon-centered radical generated. [reaction: see text]" @default.
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- W2056519776 date "2003-04-09" @default.
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- W2056519776 title "Reactivity toward Oxygen of Isobenzofuranyl Radicals: Effect of Nitro Group Substitution" @default.
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- W2056519776 doi "https://doi.org/10.1021/ol034307p" @default.
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