Fig. 8: Probing the reductive N–O bond cleavage of isoxazolidine. | Nature Communications

Fig. 8: Probing the reductive N–O bond cleavage of isoxazolidine.

From: Harnessing nitroarenes as nitrogen and oxygen sources for general oxo-aminomethylation of alkenes

Fig. 8: Probing the reductive N–O bond cleavage of isoxazolidine.The alternative text for this image may have been generated using AI.

A Effect of protonation on the N–O bond cleavage of isoxazolidine. B Reactivity of the photocatalyst toward N–O bond cleavage of isoxazolidine. C Reactivity of the Ni–H species toward N–O bond cleavage of isoxazolidine. D Reactivity of the Ni0 species toward N–O bond cleavage of isoxazolidine. Me methyl, Cy cyclohexyl.

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